Raras
Buscar doenças, sintomas, genes...
Alteração da oxidação do ácido graxo mitocondrial
ORPHA:309115CID-11 · 5C52.01DOENÇA RARA

A carnitina, L-carnitina ou levocarnitina é um composto quaternário de amónio envolvido no metabolismo da maior parte dos mamíferos, plantas e algumas bactérias. Encontrada em quase todas as células do organismo, atua na geração de energia (ATP), a partir de ácidos graxos (gordura). Ela ajuda a melhorar os níveis de colesterol bom (HDL) melhorando o funcionamento do coração e da circulação sanguínea.

Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

📋

Doença rara que afeta a metabolização de gorduras nas mitocôndrias, levando a quadros de encefalopatia aguda, acidose metabólica e atraso no desenvolvimento. Pode manifestar-se com insuficiência respiratória, problemas cardíacos e renais, além de alterações visuais.

🏥
SUS: Cobertura mínimaScore: 5%
Triagem neonatal (Fase 2)
Você se identifica com essa condição?
O Raras está aqui pra te apoiar — com ou sem diagnóstico

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Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🧠
Neurológico
31 sintomas
❤️
Coração
24 sintomas
🫃
Digestivo
23 sintomas
💪
Músculos
21 sintomas
📏
Crescimento
18 sintomas
👁️
Olhos
13 sintomas

+ 104 sintomas em outras categorias

Características mais comuns

Encefalopatia aguda
Escoliose
Insuficiência respiratória
Atraso do neurodesenvolvimento
Oligúria
Acidose metabólica episódica
273sintomas
Sem dados (273)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 273 características clínicas mais associadas, ordenadas por frequência.

Encefalopatia agudaAcute encephalopathy
EscolioseScoliosis
Insuficiência respiratóriaRespiratory failure
Atraso do neurodesenvolvimentoNeurodevelopmental delay
OligúriaOliguria

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa11
Últimos 10 anos117publicações
Pico202517 papers
Linha do tempo
20202015Hoje · 2026📈 2025Ano de pico
Publicações por ano (últimos 10 anos)

Triagem neonatal (Teste do Pezinho)

👶
Teste: MS/MS — acilcarnitinas
Fase 2 do PNTNin_rollout
Incidência no Brasil: 1:15.000

A triagem neonatal permite diagnóstico precoce e início imediato do tratamento.

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

15 genes identificados com associação a esta condição.

SLC25A32Solute carrier family 25 member 32Candidate gene tested inTolerante
FUNÇÃO

Facilitates flavin adenine dinucleotide (FAD) translocation across the mitochondrial inner membrane into the mitochondrial matrix where it acts as a redox cofactor to assist flavoenzyme activities in fundamental metabolic processes including fatty acid beta-oxidation, amino acid and choline metabolism as well as mitochondrial electron transportation. In particular, provides FAD to DLD dehydrogenase of the glycine cleavage system, part of mitochondrial one-carbon metabolic pathway involved in neu

LOCALIZAÇÃO

Mitochondrion inner membrane

VIAS BIOLÓGICAS (1)
Metabolism of folate and pterines
MECANISMO DE DOENÇA

Exercise intolerance, riboflavin-responsive

A riboflavin-responsive form of exercise intolerance, a condition characterized by failure to maintain an expected level of force during sustained or repeated muscle contraction, resulting in an overwhelming sense of tiredness, lack of energy and feeling of exhaustion. RREI transmission pattern is consistent with autosomal recessive inheritance.

EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
37.6 TPM
Fibroblastos
37.6 TPM
Cervix Ectocervix
29.4 TPM
Fallopian Tube
26.8 TPM
Tecido adiposo
26.7 TPM
INTERAÇÕES PROTEICAS (2)
OUTRAS DOENÇAS (2)
exercise intolerance, riboflavin-responsivemultiple acyl-CoA dehydrogenase deficiency, mild type
HGNC:29683UniProt:Q9H2D1
ETFDHElectron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Accepts electrons from ETF and reduces ubiquinone

LOCALIZAÇÃO

Mitochondrion inner membrane

VIAS BIOLÓGICAS (1)
Respiratory electron transport
MECANISMO DE DOENÇA

Glutaric aciduria 2C

An autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.

EXPRESSÃO TECIDUAL(Ubíquo)
Coração - Ventrículo esquerdo
51.2 TPM
Fígado
43.3 TPM
Glândula adrenal
41.9 TPM
Músculo esquelético
41.7 TPM
Coração - Átrio
38.5 TPM
OUTRAS DOENÇAS (3)
multiple acyl-CoA dehydrogenase deficiencymultiple acyl-CoA dehydrogenase deficiency, severe neonatal typemultiple acyl-CoA dehydrogenase deficiency, mild type
HGNC:3483UniProt:Q16134
SLC22A5Organic cation/carnitine transporter 2Disease-causing germline mutation(s) inTolerante
FUNÇÃO

Sodium-ion dependent, high affinity carnitine transporter. Involved in the active cellular uptake of carnitine. Transports one sodium ion with one molecule of carnitine (PubMed:10454528, PubMed:10525100, PubMed:10966938, PubMed:17509700, PubMed:20722056, PubMed:33124720). Also transports organic cations such as tetraethylammonium (TEA) without the involvement of sodium. Relative uptake activity ratio of carnitine to TEA is 11.3 (PubMed:10454528, PubMed:10525100, PubMed:10966938). In intestinal e

LOCALIZAÇÃO

Cell membraneApical cell membraneBasal cell membraneEndoplasmic reticulum

VIAS BIOLÓGICAS (2)
Carnitine shuttleSLC-mediated transport of organic cations
MECANISMO DE DOENÇA

Systemic primary carnitine deficiency

Autosomal recessive disorder of fatty acid oxidation caused by defective carnitine transport. Present early in life with hypoketotic hypoglycemia and acute metabolic decompensation, or later in life with skeletal myopathy or cardiomyopathy.

EXPRESSÃO TECIDUAL(Ubíquo)
Músculo esquelético
50.3 TPM
Cerebelo
38.3 TPM
Cérebro - Hemisfério cerebelar
37.8 TPM
Pituitária
28.6 TPM
Próstata
25.9 TPM
INTERAÇÕES PROTEICAS (1)
OUTRAS DOENÇAS (1)
systemic primary carnitine deficiency disease
HGNC:10969UniProt:O76082
ACADVLVery long-chain acyl-CoA dehydrogenase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Very long-chain specific acyl-CoA dehydrogenase is one of the acyl-CoA dehydrogenases that catalyze the first step of mitochondrial fatty acid beta-oxidation (FAO), breaking down fatty acids into acetyl-CoA and allowing the production of energy from fats (PubMed:17564966, PubMed:18227065, PubMed:7668252, PubMed:9461620, PubMed:9599005, PubMed:9839948). The first step of FAO consists in the proR-proR stereospecific alpha, beta-dehydrogenation of fatty acyl-CoA thioesters using the electron transf

LOCALIZAÇÃO

Mitochondrion inner membrane

VIAS BIOLÓGICAS (2)
Beta oxidation of palmitoyl-CoA to myristoyl-CoAXBP1(S) activates chaperone genes
MECANISMO DE DOENÇA

Acyl-CoA dehydrogenase very long-chain deficiency

An inborn error of mitochondrial fatty acid beta-oxidation which leads to impaired long-chain fatty acid beta-oxidation. It is clinically heterogeneous, with three major phenotypes: a severe childhood form characterized by early onset, high mortality and high incidence of cardiomyopathy; a milder childhood form with later onset, characterized by hypoketotic hypoglycemia, low mortality and rare cardiomyopathy; an adult form, with isolated skeletal muscle involvement, rhabdomyolysis and myoglobinuria, usually triggered by exercise or fasting.

OUTRAS DOENÇAS (1)
very long chain acyl-CoA dehydrogenase deficiency
HGNC:92UniProt:P49748
HMGCS2Hydroxymethylglutaryl-CoA synthase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Catalyzes the first irreversible step in ketogenesis, condensing acetyl-CoA to acetoacetyl-CoA to form HMG-CoA, which is converted by HMG-CoA reductase (HMGCR) into mevalonate

LOCALIZAÇÃO

Mitochondrion

VIAS BIOLÓGICAS (3)
Synthesis of Ketone BodiesPPARA activates gene expressionMitochondrial protein degradation
MECANISMO DE DOENÇA

3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency

A metabolic disorder characterized by severe hypoketotic hypoglycemia, encephalopathy, and hepatomegaly.

EXPRESSÃO TECIDUAL(Tecido-específico)
Fígado
748.5 TPM
Cólon transverso
218.1 TPM
Testículo
67.2 TPM
Estômago
59.6 TPM
Glândula salivar
47.1 TPM
OUTRAS DOENÇAS (1)
3-hydroxy-3-methylglutaryl-CoA synthase deficiency
HGNC:5008UniProt:P54868
HADHHydroxyacyl-coenzyme A dehydrogenase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Mitochondrial fatty acid beta-oxidation enzyme that catalyzes the third step of the beta-oxidation cycle for medium and short-chain 3-hydroxy fatty acyl-CoAs (C4 to C10) (PubMed:10231530, PubMed:11489939, PubMed:16725361). Plays a role in the control of insulin secretion by inhibiting the activation of glutamate dehydrogenase 1 (GLUD1), an enzyme that has an important role in regulating amino acid-induced insulin secretion (By similarity). Plays a role in the maintenance of normal spermatogenesi

LOCALIZAÇÃO

Mitochondrion matrix

VIAS BIOLÓGICAS (6)
Beta oxidation of butanoyl-CoA to acetyl-CoABeta oxidation of hexanoyl-CoA to butanoyl-CoABeta oxidation of octanoyl-CoA to hexanoyl-CoABeta oxidation of decanoyl-CoA to octanoyl-CoA-CoABeta oxidation of lauroyl-CoA to decanoyl-CoA-CoA
MECANISMO DE DOENÇA

3-alpha-hydroxyacyl-CoA dehydrogenase deficiency

An autosomal recessive, metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.

EXPRESSÃO TECIDUAL(Ubíquo)
Músculo esquelético
55.6 TPM
Adipose Visceral Omentum
50.9 TPM
Coração - Ventrículo esquerdo
49.9 TPM
Tecido adiposo
48.5 TPM
Artéria tibial
45.6 TPM
OUTRAS DOENÇAS (2)
hyperinsulinemic hypoglycemia, familial, 43-hydroxyacyl-CoA dehydrogenase deficiency
HGNC:4799UniProt:Q16836
HMGCLHydroxymethylglutaryl-CoA lyase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA lyase that catalyzes a cation-dependent cleavage of (S)-3-hydroxy-3-methylglutaryl-CoA into acetyl-CoA and acetoacetate, a key step in ketogenesis. Terminal step in leucine catabolism. Ketone bodies (beta-hydroxybutyrate, acetoacetate and acetone) are essential as an alternative source of energy to glucose, as lipid precursors and as regulators of metabolism

LOCALIZAÇÃO

Mitochondrion matrixPeroxisome

VIAS BIOLÓGICAS (1)
Synthesis of Ketone Bodies
MECANISMO DE DOENÇA

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

An autosomal recessive disease affecting ketogenesis and L-leucine catabolism. The disease usually appears in the first year of life after a fasting period and its clinical acute symptoms include vomiting, seizures, metabolic acidosis, hypoketotic hypoglycemia and lethargy. These symptoms sometimes progress to coma, with fatal outcome in some cases.

EXPRESSÃO TECIDUAL(Ubíquo)
Fígado
77.6 TPM
Glândula adrenal
34.4 TPM
Rim - Medula
31.9 TPM
Tireoide
29.5 TPM
Rim - Córtex
28.9 TPM
OUTRAS DOENÇAS (1)
3-hydroxy-3-methylglutaric aciduria
HGNC:5005UniProt:P35914
ACADMMedium-chain specific acyl-CoA dehydrogenase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Medium-chain specific acyl-CoA dehydrogenase is one of the acyl-CoA dehydrogenases that catalyze the first step of mitochondrial fatty acid beta-oxidation (FAO), breaking down fatty acids into acetyl-CoA and allowing the production of energy from fats (PubMed:1970566, PubMed:21237683, PubMed:2251268, PubMed:8823175). The first step of FAO consists in the proR-proR stereospecific alpha, beta-dehydrogenation of fatty acyl-CoA thioesters using the electron transfer flavoprotein (ETF) as their physi

LOCALIZAÇÃO

Mitochondrion matrix

VIAS BIOLÓGICAS (4)
Beta oxidation of octanoyl-CoA to hexanoyl-CoABeta oxidation of decanoyl-CoA to octanoyl-CoA-CoAmitochondrial fatty acid beta-oxidation of unsaturated fatty acidsPPARA activates gene expression
MECANISMO DE DOENÇA

Acyl-CoA dehydrogenase medium-chain deficiency

An inborn error of mitochondrial fatty acid beta-oxidation which causes fasting hypoglycemia, hepatic dysfunction and encephalopathy, often resulting in death in infancy.

OUTRAS DOENÇAS (1)
medium chain acyl-CoA dehydrogenase deficiency
HGNC:89UniProt:P11310
FLAD1Bifunctional FAD diphosphatase/FAD synthaseCandidate gene tested inTolerante
FUNÇÃO

This enzyme has two activities: FAD diphosphatase activity and FAD synthase activity (PubMed:16643857, PubMed:21924249, PubMed:21951714, PubMed:23443125, PubMed:25135855, PubMed:26277395, PubMed:27259049, PubMed:31351152, PubMed:38688286). FAD diphosphatase acts on FAD and NADH to produce FMN and NMNH(2-), respectively (PubMed:26277395, PubMed:31351152, PubMed:38688286). FAD synthase catalyzes the adenylation of flavin mononucleotide (FMN) to form flavin adenine dinucleotide (FAD) coenzyme (PubM

LOCALIZAÇÃO

NucleusMitochondrion matrixCytoplasm, cytosol

VIAS BIOLÓGICAS (1)
Vitamin B2 (riboflavin) metabolism
MECANISMO DE DOENÇA

Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency

An autosomal recessive, inborn error of metabolism characterized by variable mitochondrial dysfunction. Clinical features range from severe cardiac and respiratory insufficiency with onset in infancy and resulting in early death, to mild muscle weakness with onset in adulthood. Some patients show significant improvement with riboflavin treatment. Analysis of skeletal muscle show multiple mitochondrial respiratory chain deficiency and a lipid storage myopathy in most patients.

EXPRESSÃO TECIDUAL(Ubíquo)
Skin Not Sun Exposed Suprapubic
24.3 TPM
Skin Sun Exposed Lower leg
24.2 TPM
Tireoide
22.7 TPM
Baço
22.1 TPM
Útero
21.3 TPM
OUTRAS DOENÇAS (3)
myopathy with abnormal lipid metabolismmultiple acyl-CoA dehydrogenase deficiency, severe neonatal typemultiple acyl-CoA dehydrogenase deficiency, mild type
HGNC:24671UniProt:Q8NFF5
HADHATrifunctional enzyme subunit alpha, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Mitochondrial trifunctional enzyme catalyzes the last three of the four reactions of the mitochondrial beta-oxidation pathway (PubMed:1550553, PubMed:29915090, PubMed:30850536, PubMed:8135828, PubMed:31604922). The mitochondrial beta-oxidation pathway is the major energy-producing process in tissues and is performed through four consecutive reactions breaking down fatty acids into acetyl-CoA (PubMed:29915090). Among the enzymes involved in this pathway, the trifunctional enzyme exhibits specific

LOCALIZAÇÃO

MitochondrionMitochondrion inner membrane

VIAS BIOLÓGICAS (8)
Acyl chain remodeling of CLBeta oxidation of hexanoyl-CoA to butanoyl-CoABeta oxidation of octanoyl-CoA to hexanoyl-CoABeta oxidation of decanoyl-CoA to octanoyl-CoA-CoABeta oxidation of lauroyl-CoA to decanoyl-CoA-CoA
MECANISMO DE DOENÇA

Mitochondrial trifunctional protein deficiency 1

An autosomal recessive metabolic disorder of long-chain fatty acid oxidation, biochemically characterized by loss of all enzyme activities of the mitochondrial trifunctional protein complex. The disease phenotype ranges from a fatal form characterized by early-onset cardiomyopathy, cardiac failure and early death to less severe, late-onset forms with myopathy, recurrent rhabdomyolysis, and sensorimotor axonal neuropathy as key features.

EXPRESSÃO TECIDUAL(Ubíquo)
Músculo esquelético
343.5 TPM
Coração - Ventrículo esquerdo
215.7 TPM
Linfócitos
203.7 TPM
Fibroblastos
194.0 TPM
Esôfago - Muscular
182.5 TPM
OUTRAS DOENÇAS (4)
long chain 3-hydroxyacyl-CoA dehydrogenase deficiencymitochondrial trifunctional protein deficiency 1mitochondrial trifunctional protein deficiencyacute fatty liver of pregnancy
HGNC:4801UniProt:P40939
ETFBElectron transfer flavoprotein subunit betaDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Heterodimeric electron transfer flavoprotein that accepts electrons from several mitochondrial dehydrogenases, including acyl-CoA dehydrogenases, glutaryl-CoA and sarcosine dehydrogenase (PubMed:15159392, PubMed:15975918, PubMed:25416781). It transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (Probable). Required for normal mitochondrial fatty acid oxidation and normal amino acid metabolism (PubMed:12815589, PubMed:7912128). ETFB binds an AMP mo

LOCALIZAÇÃO

Mitochondrion matrix

VIAS BIOLÓGICAS (2)
Respiratory electron transportProtein methylation
MECANISMO DE DOENÇA

Glutaric aciduria 2B

An autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.

EXPRESSÃO TECIDUAL(Ubíquo)
Fígado
61.0 TPM
Coração - Ventrículo esquerdo
46.4 TPM
Glândula adrenal
45.8 TPM
Fibroblastos
41.3 TPM
Coração - Átrio
39.7 TPM
OUTRAS DOENÇAS (3)
multiple acyl-CoA dehydrogenase deficiencymultiple acyl-CoA dehydrogenase deficiency, mild typemultiple acyl-CoA dehydrogenase deficiency, severe neonatal type
HGNC:3482UniProt:P38117
SLC25A20Mitochondrial carnitine/acylcarnitine carrier proteinDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Mediates the electroneutral exchange of acylcarnitines (O-acyl-(R)-carnitine or L-acylcarnitine) of different acyl chain lengths (ranging from O-acetyl-(R)-carnitine to long-chain O-acyl-(R)-carnitines) with free carnitine ((R)-carnitine or L-carnitine) across the mitochondrial inner membrane, via a ping-pong mechanism (Probable) (PubMed:12892634, PubMed:18307102). Key player in the mitochondrial oxidation pathway, it translocates the fatty acids in the form of acylcarnitines into the mitochondr

LOCALIZAÇÃO

Mitochondrion inner membrane

VIAS BIOLÓGICAS (1)
Carnitine shuttle
MECANISMO DE DOENÇA

Carnitine-acylcarnitine translocase deficiency

A rare long-chain fatty acid oxidation disorder. Metabolic consequences include hypoketotic hypoglycemia under fasting conditions, hyperammonemia, elevated creatine kinase and transaminases, dicarboxylic aciduria, very low free carnitine and abnormal acylcarnitine profile with marked elevation of the long-chain acylcarnitines. Clinical features include neurologic abnormalities, cardiomyopathy, arrhythmias, skeletal muscle damage, liver dysfunction and episodes of life-threatening coma, which eventually lead to death. Most patients become symptomatic in the neonatal period with a rapidly progressive deterioration and a high mortality rate.

VIAS REACTOME (1)
EXPRESSÃO TECIDUAL(Ubíquo)
Fígado
70.3 TPM
Músculo esquelético
49.1 TPM
Glândula adrenal
45.7 TPM
Coração - Ventrículo esquerdo
39.5 TPM
Baço
38.9 TPM
OUTRAS DOENÇAS (1)
carnitine-acylcarnitine translocase deficiency
HGNC:1421UniProt:O43772
ACADSShort-chain specific acyl-CoA dehydrogenase, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Short-chain specific acyl-CoA dehydrogenase is one of the acyl-CoA dehydrogenases that catalyze the first step of mitochondrial fatty acid beta-oxidation, an aerobic process breaking down fatty acids into acetyl-CoA and allowing the production of energy from fats (By similarity). The first step of fatty acid beta-oxidation consists in the removal of one hydrogen from C-2 and C-3 of the straight-chain fatty acyl-CoA thioester, resulting in the formation of trans-2-enoyl-CoA (By similarity). Among

LOCALIZAÇÃO

Mitochondrion matrix

VIAS BIOLÓGICAS (2)
Beta oxidation of butanoyl-CoA to acetyl-CoABeta oxidation of hexanoyl-CoA to butanoyl-CoA
MECANISMO DE DOENÇA

Acyl-CoA dehydrogenase short-chain deficiency

An inborn error of mitochondrial fatty acid beta-oxidation resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.

OUTRAS DOENÇAS (1)
short chain acyl-CoA dehydrogenase deficiency
HGNC:90UniProt:P16219
ETFAElectron transfer flavoprotein subunit alpha, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Heterodimeric electron transfer flavoprotein that accepts electrons from several mitochondrial dehydrogenases, including acyl-CoA dehydrogenases, glutaryl-CoA and sarcosine dehydrogenase (PubMed:10356313, PubMed:15159392, PubMed:15975918, PubMed:27499296, PubMed:9334218). It transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase) (PubMed:9334218). Required for normal mitochondrial fatty acid oxidation and normal amino acid metabol

LOCALIZAÇÃO

Mitochondrion matrix

VIAS BIOLÓGICAS (1)
Respiratory electron transport
MECANISMO DE DOENÇA

Glutaric aciduria 2A

An autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.

EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
144.9 TPM
Músculo esquelético
109.5 TPM
Glândula adrenal
101.8 TPM
Coração - Ventrículo esquerdo
98.5 TPM
Fígado
90.9 TPM
OUTRAS DOENÇAS (3)
multiple acyl-CoA dehydrogenase deficiencymultiple acyl-CoA dehydrogenase deficiency, mild typemultiple acyl-CoA dehydrogenase deficiency, severe neonatal type
HGNC:3481UniProt:P13804
ACAD9Complex I assembly factor ACAD9, mitochondrialDisease-causing germline mutation(s) inTolerante
FUNÇÃO

Together with NDUFAF1 and ECSIT, forms part of the mitochondrial complex I (MCIA),which is required for the biogenesis of respiratory Complex I (CI) and is therefore crucial for the activation of the oxidative phosphorylation system (PubMed:20816094, PubMed:24158852, PubMed:32320651, PubMed:38086790). ECSIT binding triggers a large conformational change, switching ACAD9 from a fatty acid oxidation (FAO) enzyme to a CI assembly factor (PubMed:38086790). The function in CI assembly is independent

LOCALIZAÇÃO

Mitochondrion inner membrane

VIAS BIOLÓGICAS (1)
Complex I biogenesis
MECANISMO DE DOENÇA

Mitochondrial complex I deficiency, nuclear type 20

An autosomal recessive metabolic disorder associated with mitochondrial complex I deficiency, resulting in multisystemic and variable manifestations. Clinical features include infantile onset of acute metabolic acidosis, Reye-like episodes (brain edema and vomiting that may rapidly progress to seizures, coma and death), exercise intolerance, hypertrophic cardiomyopathy, liver failure, muscle weakness, and neurologic dysfunction.

VIAS REACTOME (1)
OUTRAS DOENÇAS (1)
acyl-CoA dehydrogenase 9 deficiency
HGNC:21497UniProt:Q9H845

Variantes genéticas (ClinVar)

891 variantes patogênicas registradas no ClinVar.

🧬 SLC25A32: NM_030780.5(SLC25A32):c.392-84C>T ()
🧬 SLC25A32: GRCh37/hg19 8q22.3(chr8:104418038-105005666)x1 ()
🧬 SLC25A32: GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 ()
🧬 SLC25A32: NM_030780.5(SLC25A32):c.698T>C (p.Leu233Pro) ()
🧬 SLC25A32: NM_030780.5(SLC25A32):c.103T>G (p.Leu35Val) ()
Ver todas no ClinVar

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

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Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Alteração da oxidação do ácido graxo mitocondrial

🗺️

Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

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Publicações mais relevantes

Timeline de publicações
0 papers (10 anos)
#1

Distinct effects of ketogenic and non-ketogenic weight-loss diets on hepatic steatosis and mitochondrial metabolism in MASLD.

Journal of hepatology2026 Feb 06

Weight loss is the cornerstone of therapy for metabolic dysfunction-associated steatotic liver disease (MASLD). However, the optimal dietary approach for reducing intrahepatic triglycerides (IHTG) and the mechanisms underlying steatosis resolution remain poorly defined. We investigated whether weight loss via a ketogenic diet (KD) compared with a non-ketogenic diet (ND) differentially affects IHTG content, hepatic mitochondrial metabolism, and the circulating metabolome. Individuals with varying IHTG content underwent short-term hypocaloric KD and ND in a crossover design. Before and after each diet, IHTG was quantified by proton magnetic resonance spectroscopy and liver stiffness by magnetic resonance elastography. We used state-of-the-art isotope tracer methodology to compare in vivo rates of hepatic mitochondrial tricarboxylic acid (TCA) cycle oxidation, endogenous glucose production, and β-hydroxybutyrate production (ketogenesis). Targeted plasma metabolomics by NMR and LC-MS was used to evaluate systemic metabolic responses. Despite similar energy deficits and body fat loss, IHTG decreased 45% more with KD than ND (-29% vs. -20%), accompanied by a threefold greater improvement in hepatic insulin sensitivity (59% vs. 21%). KD, but not ND, markedly reduced serum insulin concentrations (-54%), thereby promoting lipolysis and intrahepatic fatty acid partitioning toward mitochondrial β-oxidation, increasing hepatic mitochondrial [NADH]/[NAD+] (redox state) (+51%), and decreasing rates of hepatic mitochondrial TCA cycle oxidation (-34%). KD, but not ND, increased plasma concentrations of branched-chain amino acids, acylcarnitines, and TCA cycle intermediates. Both diets ameliorated MASLD, but KD produced a greater reduction in IHTG owing to a starvation-like metabolic state. However, the benefits of KD were accompanied by increased hepatic mitochondrial redox state and suppression of TCA cycle oxidation, which are features previously linked to progressive liver injury. This study provides mechanistic justification for considering dietary composition, in addition to caloric restriction, as a key determinant of steatosis resolution in metabolic dysfunction-associated steatotic liver disease (MASLD). The findings highlight a potential trade-off between greater short-term reductions in liver fat and the emergence of metabolic features previously associated with increased susceptibility to liver injury. While a ketogenic diet may facilitate rapid liver fat reduction in selected clinical contexts, its use should be approached cautiously, particularly in individuals with advanced MASLD. These results underscore the need for systematic evaluation of dietary composition as a determinant of both efficacy and safety of nutritional interventions for MASLD. NCT03737071.

#2

Renal Ketogenesis Protects Against Ischemic Kidney Injury.

Journal of the American Society of Nephrology : JASN2026 Jan 21

Proximal tubular expression of hydroxymethylglutaryl-CoA synthase 2 (HMGCS2) during ischemic injury increases kidney ketone and prostaglandin content. Kidney HMGCS2 deficiency emerged as both a biomarker and contributor to kidney disease. Renal ketogenesis supported the maintenance of proximal tubular fatty acid oxidation. Abnormal renal fatty acid oxidation in kidney disease suggests that dysregulated metabolism is a key component of kidney disease pathogenesis. While the liver is the main ketogenic organ, the rate-limiting enzyme for ketogenesis, mitochondrial hydroxymethylglutaryl-CoA synthase 2 (HMGCS2), is induced in the proximal tubule of the kidney during fasting. We previously demonstrated that HMGCS2 induced in the kidney does not contribute to the circulating pool of ketones during fasting and cannot compensate for hepatic ketogenic deficiency. We hypothesized that kidney HMGCS2 may be acting locally within the kidney to maintain normal function during metabolic stress or injury. Mice with kidney- or liver-specific deletion of Hmgcs2 were subjected to ischemia/reperfusion injury (IRI). Kidney histology, metabolomics, and lipidomics were analyzed. Mice were placed on a ketogenic diet for 4 days to increase plasma and kidney ketone content. Using novel mouse models with proximal tubular hemagglutinin-tagged mitochondria with or without Hmgcs2 deletion, proximal tubular-specific mitochondria were isolated, and fatty acid oxidation capacity was measured after IRI. Mice with kidney-specific Hmgcs2 deletion had significantly more kidney injury after IRI compared with wild-type controls. Kidneys lacking HMGCS2 exhibited a decrease in ketone content and an increase in lipid droplet accumulation after IRI. Proximal tubular-specific mitochondria lacking HMGCS2 had significantly lower fatty acid oxidation capacity both at baseline and after ischemic injury. Administration of a ketogenic diet for 4 days before IRI was sufficient to decrease kidney injury and augment mitochondrial fatty acid oxidation in kidney Hmgcs2 knockout mice. Kidney tissue lipidomics revealed that the loss of kidney HMGCS2 was associated with a decrease in both arachidonic acid containing phospholipids and prostaglandin levels. Loss of renal HMGCS2 and resultant ketogenesis increased ischemia-induced injury and decreased mitochondrial fatty acid oxidation capacity, suggesting a role in renal ketogenesis in limiting AKI. The primary energy source shifts from glucose to fat during periods of fasting or starvation, when carbohydrate intake is markedly reduced. Adipose tissue releases stored triglycerides, which are hydrolyzed into free fatty acids (FFAs) and glycerol. FFAs are transported to the liver, where they undergo β-oxidation, generating large amounts of acetyl-CoA. Accumulation occurs when acetyl-CoA production exceeds the liver’s oxidative capacity in the citric acid cycle. This imbalance is partly driven by decreased availability of oxaloacetate, which is diverted toward gluconeogenesis. Excess acetyl-CoA cannot be fully oxidized or redirected into fatty acid synthesis. The metabolic bottleneck channels acetyl-CoA into ketogenesis, in which the liver converts acetyl-CoA into ketone bodies, primarily acetoacetate and β-hydroxybutyrate (see Image. Ketogenesis Pathway). Ketone bodies are released into the circulation and serve as an alternative energy substrate for peripheral tissues, particularly the brain, during prolonged carbohydrate deficiency. Plasma concentrations rise when the rate of ketone body production surpasses peripheral utilization, resulting in ketonemia. Progressive accumulation leads to urinary excretion, termed "ketonuria." Marked ketonemia and ketonuria are most frequently associated with uncontrolled type 1 diabetes mellitus. In this setting, absolute insulin deficiency limits glucose uptake, promotes unregulated lipolysis, and accelerates ketogenesis. The resulting overproduction of acidic ketone bodies can exceed the buffering capacity of blood, causing metabolic acidosis. This condition, known as diabetic ketoacidosis (DKA), constitutes a serious and potentially life-threatening complication requiring prompt treatment. Mastery of the ketogenesis pathway enables clinicians to link biochemical findings with clinical presentations. This integrative approach enhances decision-making in metabolic, endocrine, and nutritional disorders.

#3

β‑hydroxybutyric acid as a potential therapeutic metabolite for type 2 diabetes mellitus (Review).

International journal of molecular medicine2026 Jan

Type 2 diabetes mellitus (T2DM) is a major metabolic disease that poses a threat to human health; therefore, the development of new pharmaceutical therapies for the treatment of T2DM is of great importance. β‑hydroxybutyric acid (β‑HB) is the primary ketone body present in the human body. β‑HB not only serves as an energy substrate to maintain the metabolic homeostasis of the body but also acts as a signaling molecule, exerting multiple biological functions both inside and outside cells. The present review summarizes the research progress and latest findings of β‑HB in T2DM models from the perspective of metabolism, physiological effects and potential as a therapeutic agent. Research indicates that β‑HB exerts protective effects against T2DM by regulating glucose and lipid metabolism, preserving the integrity of pancreatic β‑cells and improving insulin resistance (IR). Additionally, β‑HB can alleviate the core pathological conditions of T2DM and related complications by enhancing the stability of cellular proteins, reducing oxidative stress and controlling inflammatory responses and endoplasmic reticulum stress (ERS), while regulating mitochondrial biogenesis, autophagy and apoptosis. Furthermore, the present review also describes the application of β‑HB in clinical research on T2DM. Research indicates that regulating β‑HB levels through endogenous and exogenous ketogenesis approaches can influence body weight, fasting blood glucose levels, IR and memory ability in T2DM patients. These results suggest that β‑HB is a potential metabolite for T2DM treatment.

#4

Hepatic Ketogenesis Regulates Lipid Homeostasis via ACSL1-mediated Fatty Acid Partitioning.

Cellular and molecular gastroenterology and hepatology2025

Liver-derived ketone bodies play an essential role in energy homeostasis during fasting by supplying fuel to the brain and peripheral tissues. Ketogenesis also helps to remove excess acetyl-CoA generated from fatty acid oxidation, thereby protecting against diet-induced hepatic steatosis. Despite this, the role of ketogenesis in fasting-associated hepatocellular lipid metabolism has not been thoroughly investigated. We used mice with liver-specific knockout of HMGCS2 mice to determine how ACSL1-mediated esterification contributes to fasting-induced steatosis and performed biochemical assays, gene expression profiling, Western blotting, and histologic analyses. We further investigated the association between HMGCS2 expression, lipid re-esterification, and steatosis using human primary hepatocytes and liver samples from patients with metabolic dysfunction-associated steatohepatitis. We show that ketogenic insufficiency, achieved through disrupting hepatic HMGCS2, worsens liver steatosis in both fasted chow-fed and high-fat-fed mice. Our findings indicate that hepatic steatosis arises from increased fatty acid partitioning to the endoplasmic reticulum (ER) for re-esterification, a process mediated by acyl-CoA synthetase long-chain family member 1 (ACSL1). Mechanistically, the accumulation of acetyl-CoA because of impaired hepatic ketogenesis drives the elevated translocation of ACSL1 to the ER. Furthermore, our study reveals heightened ER-localized ACSL1 and lipid re-esterification in human metabolic dysfunction-associated steatohepatitis cases exhibiting impaired hepatic ketogenesis. We also demonstrate that L-carnitine, which buffers excess acetyl-CoA, reduces ER-associated ACSL1 and alleviates hepatic steatosis. Hepatic ketogenesis plays a crucial role in maintaining intracellular acetyl-CoA balance, regulating lipid partitioning, and preventing the development of fasting-induced hepatic steatosis.

#5

The Multifaceted Influence of Beta-Hydroxybutyrate on Autophagy, Mitochondrial Metabolism, and Epigenetic Regulation.

Journal of cellular biochemistry2025 Jun

Beta-hydroxybutyrate (BHB), a key ketone body produced during fatty acid metabolism, plays critical roles in various physiological and pathological conditions. Synthesized in the liver through ketogenesis, BHB serves as an essential energy substrate during glucose deprivation, supporting survival by efficiently utilizing fat reserves. It crosses the blood-brain barrier, providing energy for neuronal function, enhancing cognitive processes such as learning and memory, and offering neuroprotection by modulating synaptic plasticity and neurotransmitter levels. BHB's impact extends to cellular pathways, including autophagy, mitochondrial biogenesis, and epigenetic regulation. By modulating autophagy, BHB ensures mitochondrial integrity and function through intricate molecular pathways involving AMPK, mTOR, PINK1/Parkin, and others. This regulation plays vital roles in neurodegenerative diseases, metabolic disorders, cancer, and cardiovascular diseases, reducing oxidative stress and preventing cellular dysfunction. Epigenetically, BHB acts as an endogenous histone deacetylase inhibitor, inducing beneficial histone modifications that enhance cellular resilience and stress responses. This epigenetic influence is crucial in conditions like diabetes and cancer, aiding insulin secretion, protecting pancreatic beta cells, and impacting cancer cell gene expression and survival. Furthermore, BHB's therapeutic potential is evident in its ability to improve mitochondrial function across various tissues, including neurons, muscle, and liver. By enhancing mitochondrial respiration, reducing oxidative stress, and altering metabolic pathways, BHB mitigates conditions such as ICU-acquired weakness, nonalcoholic fatty liver disease, and cardiovascular diseases. BHB's modulation of autophagy and epigenetic regulation underscores its comprehensive role in cellular homeostasis and health across multiple physiological contexts, providing a foundation for future therapeutic strategies.

📚 EuropePMCmostrando 117

2026

Distinct effects of ketogenic and non-ketogenic weight-loss diets on hepatic steatosis and mitochondrial metabolism in MASLD.

Journal of hepatology
2026

Renal Ketogenesis Protects Against Ischemic Kidney Injury.

Journal of the American Society of Nephrology : JASN
2026

β‑hydroxybutyric acid as a potential therapeutic metabolite for type 2 diabetes mellitus (Review).

International journal of molecular medicine
2025

Minimum Dietary Fat Threshold for Effective Ketogenesis and Obesity Control in Mice.

Nutrients
2025

Perioperative Anesthetic Considerations in HMG-CoA Lyase Deficiency: Case Report and Literature Review.

Journal of clinical medicine
2025

Breaking the metabolic-inflammatory vicious cycle in polycystic ovary syndrome: a comparative review of ketogenic and high-fat diets.

Lipids in health and disease
2025

Mechanisms of SIRT3 Regulation of Aging and Aging-Related Diseases and Advances in Drug Therapy.

Gerontology
2025

Hepatic Ketogenesis Regulates Lipid Homeostasis via ACSL1-mediated Fatty Acid Partitioning.

Cellular and molecular gastroenterology and hepatology
2025

Glial adaptations to high-fat diet in the mediobasal hypothalamus and effects on metabolic control.

Physiology & behavior
2025

The Multifaceted Influence of Beta-Hydroxybutyrate on Autophagy, Mitochondrial Metabolism, and Epigenetic Regulation.

Journal of cellular biochemistry
2025

Liver Metabolism at the Crossroads: The Reciprocal Control of Nutrient-Sensing Nuclear Receptors and Autophagy.

International journal of molecular sciences
2025

Dietary lipids, not ketone body metabolites, influence intestinal tumorigenesis in a ketogenic diet.

bioRxiv : the preprint server for biology
2025

Sustained Glucose Turnover Flux Distinguishes Cancer Cachexia from Nutrient Limitation.

bioRxiv : the preprint server for biology
2025

Induction of Fructose Mediated De Novo Lipogenesis Coexists with the Upregulation of Mitochondrial Oxidative Function in Mice Livers.

The Journal of nutrition
2025

Fatty acid metabolism: The crossroads in intestinal homeostasis and tumor.

Metabolism: clinical and experimental
2025

Ketogenesis mitigates metabolic dysfunction-associated steatotic liver disease through mechanisms that extend beyond fat oxidation.

The Journal of clinical investigation
2025

The Heart Has Intrinsic Ketogenic Capacity that Mediates NAD+ Therapy in HFpEF.

Circulation research
2025

The Influence of Physical Exercise, Ketogenic Diet, and Time-Restricted Eating on De Novo Lipogenesis: A Narrative Review.

Nutrients
2025

Impact of Dapagliflozin on Hepatic Lipid Metabolism and a Dynamic Model of Ketone Body Levels.

The AAPS journal
2025

Identification of chikusetsusaponin IVa as a novel lysine-specific demethylase 1 inhibitor that ameliorates high fat diet-induced MASLD in mice.

Acta pharmacologica Sinica
2024

Branched-chain amino acids alleviate NAFLD via inhibiting de novo lipogenesis and activating fatty acid β-oxidation in laying hens.

Redox biology
2024

Adipocyte metabolic state regulates glial phagocytic function.

bioRxiv : the preprint server for biology
2024

Ethnic differences in postprandial fatty acid trafficking and utilization between overweight and obese White European and Black African-Caribbean men.

American journal of physiology. Endocrinology and metabolism
2024

Metabolic aspects of glycogenolysis with special attention to McArdle disease.

Molecular genetics and metabolism
2024

The interplay between glucose and ketone bodies in neural stem cell metabolism.

Journal of neuroscience research
2024

Restoration of HMGCS2-mediated ketogenesis alleviates tacrolimus-induced hepatic lipid metabolism disorder.

Acta pharmacologica Sinica
2024

Adaptive Metabolic Responses Facilitate Blood-Brain Barrier Repair in Ischemic Stroke via BHB-Mediated Epigenetic Modification of ZO-1 Expression.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
2024

Hepatic signal transducer and activator of transcription-3 signalling drives early-stage pancreatic cancer cachexia via suppressed ketogenesis.

Journal of cachexia, sarcopenia and muscle
2024

Relationship between serum β-hydroxybutyrate and hepatic fatty acid oxidation in individuals with obesity and NAFLD.

American journal of physiology. Endocrinology and metabolism
2023

[Ketone Body Metabolism and Renal Diseases].

Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition
2023

Ketone bodies mediate alterations in brain energy metabolism and biomarkers of Alzheimer's disease.

Frontiers in neuroscience
2023

Dietary pattern and hepatic lipid metabolism.

Liver research (Beijing, China)
2023

Changes in Plasma Pyruvate and TCA Cycle Metabolites upon Increased Hepatic Fatty Acid Oxidation and Ketogenesis in Male Wistar Rats.

International journal of molecular sciences
2023

From common to rare: repurposing of bempedoic acid for the treatment of glycogen storage disease type 1.

Genes & nutrition
2024

Identification of 3H-benzo[b] [1,4] diazepine derivatives as PPARα agonists by in silico studies and biochemical evaluation.

Journal of biomolecular structure & dynamics
2023

Dietary Regulation of Hepatic Triacylglycerol Content-the Role of Eucaloric Carbohydrate Restriction with Fat or Protein Replacement.

Advances in nutrition (Bethesda, Md.)
2023

Transcriptome Analysis Reveals the Molecular Basis of Overfeeding-Induced Diabetes in Zebrafish.

International journal of molecular sciences
2023

PAQR9 regulates glucose homeostasis in diabetic mice and modulates insulin secretion in β cells in vitro under stress conditions.

Molecular and cellular endocrinology
2023

MLX plays a key role in lipid and glucose metabolism in humans: Evidence from in vitro and in vivo studies.

Metabolism: clinical and experimental
2023

Persistent fasting lipogenesis links impaired ketogenesis with citrate synthesis in humans with nonalcoholic fatty liver.

The Journal of clinical investigation
2023

A Young Female With Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD): A Case Report.

Cureus
2023

Renal and Cardiovascular Metabolic Impact Caused by Ketogenesis of the SGLT2 Inhibitors.

International journal of molecular sciences
2022

The metabolomics of a protein kinase C delta (PKCδ) knock-out mouse model.

Metabolomics : Official journal of the Metabolomic Society
2022

Circadian clock controls rhythms in ketogenesis by interfering with PPARα transcriptional network.

Proceedings of the National Academy of Sciences of the United States of America
2022

Integrating the contributions of mitochondrial oxidative metabolism to lipotoxicity and inflammation in NAFLD pathogenesis.

Biochimica et biophysica acta. Molecular and cell biology of lipids
2022

CoA in Health and Disease.

International journal of molecular sciences
2022

Mitochondrial Dysfunction and Acute Fatty Liver of Pregnancy.

International journal of molecular sciences
2022

Schisandrin B mitigates hepatic steatosis and promotes fatty acid oxidation by inducing autophagy through AMPK/mTOR signaling pathway.

Metabolism: clinical and experimental
2022

Ketogenesis acts as an endogenous protective programme to restrain inflammatory macrophage activation during acute pancreatitis.

EBioMedicine
2022

The Role of l-Carnitine in Mitochondria, Prevention of Metabolic Inflexibility and Disease Initiation.

International journal of molecular sciences
2022

What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children.

Molecular genetics and metabolism
2022

Basal Autophagy Is Necessary for A Pharmacologic PPARα Transactivation.

Cells
2022

Detecting de novo Hepatic Ketogenesis Using Hyperpolarized [2-13C] Pyruvate.

Frontiers in physiology
2022

Metabolites and Genes behind Cardiac Metabolic Remodeling in Mice with Type 1 Diabetes Mellitus.

International journal of molecular sciences
2021

Blueberry Counteracts Prediabetes in a Hypercaloric Diet-Induced Rat Model and Rescues Hepatic Mitochondrial Bioenergetics.

Nutrients
2021

Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency.

Frontiers in pediatrics
2022

Multi-omics of a pre-clinical model of diabetic cardiomyopathy reveals increased fatty acid supply impacts mitochondrial metabolic selectivity.

Journal of molecular and cellular cardiology
2021

Status epilepticus and coma leading to death in a boy caused by Medium-chainacyl-coA dehydrogenase deficiency.

Iranian journal of child neurology
2022

Hepatocyte-specific fibroblast growth factor 21 overexpression ameliorates high-fat diet-induced obesity and liver steatosis in mice.

Laboratory investigation; a journal of technical methods and pathology
2022

Metabolism as Disease Tolerance: Implications for Sepsis-Associated Acute Kidney Injury.

Nephron
2020

Gallic Acid Ameliorated Impaired Lipid Homeostasis in a Mouse Model of High-Fat Diet-and Streptozotocin-Induced NAFLD and Diabetes through Improvement of β-oxidation and Ketogenesis.

Frontiers in pharmacology
2021

Plasma 3-hydroxyisobutyrate (3-HIB) and methylmalonic acid (MMA) are markers of hepatic mitochondrial fatty acid oxidation in male Wistar rats.

Biochimica et biophysica acta. Molecular and cell biology of lipids
2020

ChREBP-Mediated Regulation of Lipid Metabolism: Involvement of the Gut Microbiota, Liver, and Adipose Tissue.

Frontiers in endocrinology
2021

Proteome and phosphoproteome characterization of liver in the postprandial state from diet-induced obese and lean mice.

Journal of proteomics
2020

CR reprograms acetyl-CoA metabolism and induces long-chain acyl-CoA dehydrogenase and CrAT expression.

Aging cell
2020

Contributions of Fat and Carbohydrate Metabolism to Glucose Homeostasis in Childhood Change With Age and Puberty: A 12-Years Cohort Study (EARLYBIRD 77).

Frontiers in nutrition
2020

Metabolic alterations in dairy cows with subclinical ketosis after treatment with carboxymethyl chitosan-loaded, reduced glutathione nanoparticles.

Journal of veterinary internal medicine
2020

Branched chain amino acids and carbohydrate restriction exacerbate ketogenesis and hepatic mitochondrial oxidative dysfunction during NAFLD.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
2020

Role of ketogenic starvation sensors in mediating the renal protective effects of SGLT2 inhibitors in type 2 diabetes.

Journal of diabetes and its complications
2020

ADSA Foundation Scholar Award: Influencing hepatic metabolism: Can nutrient partitioning be modulated to optimize metabolic health in the transition dairy cow?

Journal of dairy science
2020

Effect of a ketogenic diet on hepatic steatosis and hepatic mitochondrial metabolism in nonalcoholic fatty liver disease.

Proceedings of the National Academy of Sciences of the United States of America
2020

Role of Deranged Energy Deprivation Signaling in the Pathogenesis of Cardiac and Renal Disease in States of Perceived Nutrient Overabundance.

Circulation
2019

Hepatic Mitochondrial Oxidative Metabolism and Lipogenesis Synergistically Adapt to Mediate Healthy Embryonic-to-Neonatal Transition in Chicken.

Scientific reports
2020

Liver Activation of Hepatocellular Nuclear Factor-4α by Small Activating RNA Rescues Dyslipidemia and Improves Metabolic Profile.

Molecular therapy. Nucleic acids
2020

PPARA/RXRA signalling regulates the fate of hepatic non-esterified fatty acids in a sheep model of maternal undernutrition.

Biochimica et biophysica acta. Molecular and cell biology of lipids
2019

Ketogenic Diet: A New Light Shining on Old but Gold Biochemistry.

Nutrients
2020

Mitochondrial dysfunction, AMPK activation and peroxisomal metabolism: A coherent scenario for non-canonical 3-methylglutaconic acidurias.

Biochimie
2019

Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models.

Nutrients
2019

Adipose tissue protects against sepsis-induced muscle weakness in mice: from lipolysis to ketones.

Critical care (London, England)
2019

Multi-omics insights into functional alterations of the liver in insulin-deficient diabetes mellitus.

Molecular metabolism
2019

Linking bioenergetic function of mitochondria to tissue-specific molecular fingerprints.

American journal of physiology. Endocrinology and metabolism
2019

Maternal undernutrition induces fetal hepatic lipid metabolism disorder and affects the development of fetal liver in a sheep model.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
2019

Impaired ketogenesis and increased acetyl-CoA oxidation promote hyperglycemia in human fatty liver.

JCI insight
2019

Role of ketone signaling in the hepatic response to fasting.

American journal of physiology. Gastrointestinal and liver physiology
2019

Ketogenic and anaplerotic dietary modifications ameliorate seizure activity in Drosophila models of mitochondrial encephalomyopathy and glycolytic enzymopathy.

Molecular genetics and metabolism
2019

Metabolic effects of glucagon in humans.

Journal of clinical & translational endocrinology
2018

Persistent Hypoglycemia in Children: Targeted Gene Panel Improves the Diagnosis of Hypoglycemia Due to Inborn Errors of Metabolism.

The Journal of pediatrics
2018

Oral nitrite restores age-dependent phenotypes in eNOS-null mice.

JCI insight
2018

Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection.

Molecular genetics and metabolism
2017

Emulsification Increases the Acute Ketogenic Effect and Bioavailability of Medium-Chain Triglycerides in Humans: Protein, Carbohydrate, and Fat Metabolism.

Current developments in nutrition
2018

Hepatic ketogenic insufficiency reprograms hepatic glycogen metabolism and the lipidome.

JCI insight
2018

Acetylcholinesterase Inhibitor Donepezil Effects on Plasma β-Hydroxybutyrate Levels in the Treatment of Alzheimer's Disease.

Current Alzheimer research
2018

Acetyl-CoA Carboxylase Inhibition Reverses NAFLD and Hepatic Insulin Resistance but Promotes Hypertriglyceridemia in Rodents.

Hepatology (Baltimore, Md.)
2018

Dendritic peptide bolaamphiphiles for siRNA delivery to primary adipocytes.

Biomaterials
2018

DEPP/DEPP1/C10ORF10 regulates hepatic glucose and fat metabolism partly via ROS-induced FGF21.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
2018

Exercise decreases CLK2 in the liver of obese mice and prevents hepatic fat accumulation.

Journal of cellular biochemistry
2018

Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features.

JIMD reports
2017

Nrg4 promotes fuel oxidation and a healthy adipokine profile to ameliorate diet-induced metabolic disorders.

Molecular metabolism
2018

High non-esterified fatty acid concentrations promote expression and secretion of fibroblast growth factor 21 in calf hepatocytes cultured in vitro.

Journal of animal physiology and animal nutrition
2017

Hepatic lipid accumulation: cause and consequence of dysregulated glucoregulatory hormones.

The Journal of endocrinology
2017

The desert gerbil Psammomys obesus as a model for metformin-sensitive nutritional type 2 diabetes to protect hepatocellular metabolic damage: Impact of mitochondrial redox state.

PloS one
2017

Diagnosis of LCHAD/TFP deficiency in an at risk newborn using umbilical cord blood acylcarnitine analysis.

Molecular genetics and metabolism reports
2016

Medium-chain acyl-Coenzyme A dehydrogenase deficiency (MCADD): a cause of severe hypoglycaemia in an apparently well child.

BMJ case reports
2017

Tanycytes and a differential fatty acid metabolism in the hypothalamus.

Glia
2016

Metabolomic Profile of Low-Copy Number Carriers at the Salivary α-Amylase Gene Suggests a Metabolic Shift Toward Lipid-Based Energy Production.

Diabetes
2016

Inhibition of Pyruvate Dehydrogenase Kinase 2 Protects Against Hepatic Steatosis Through Modulation of Tricarboxylic Acid Cycle Anaplerosis and Ketogenesis.

Diabetes
2016

Medium-chain plasma acylcarnitines, ketone levels, cognition, and gray matter volumes in healthy elderly, mildly cognitively impaired, or Alzheimer's disease subjects.

Neurobiology of aging
2016

Measuring changes in substrate utilization in the myocardium in response to fasting using hyperpolarized [1-(13)C]butyrate and [1-(13)C]pyruvate.

Scientific reports
2016

Hyperketonemia and ketosis increase the risk of complications in type 1 diabetes.

Free radical biology & medicine
2016

Fatty acids and their therapeutic potential in neurological disorders.

Neurochemistry international
2016

Lipotoxicity in steatohepatitis occurs despite an increase in tricarboxylic acid cycle activity.

American journal of physiology. Endocrinology and metabolism
2015

Longitudinal Metabolomic Profiling of Amino Acids and Lipids across Healthy Pregnancy.

PloS one
2015

Exercise and the Regulation of Hepatic Metabolism.

Progress in molecular biology and translational science
2016

PCB126-Induced Disruption in Gluconeogenesis and Fatty Acid Oxidation Precedes Fatty Liver in Male Rats.

Toxicological sciences : an official journal of the Society of Toxicology
2017

Role of the Wnt/β-Catenin Pathway in the Pathogenesis of Alcoholic Liver Disease.

Current molecular pharmacology
2015

Ketone Body Therapy Protects From Lipotoxicity and Acute Liver Failure Upon Pparα Deficiency.

Molecular endocrinology (Baltimore, Md.)
2015

Phosphorylation of the nuclear receptor corepressor 1 by protein kinase B switches its corepressor targets in the liver in mice.

Hepatology (Baltimore, Md.)

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Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Distinct effects of ketogenic and non-ketogenic weight-loss diets on hepatic steatosis and mitochondrial metabolism in MASLD.
    Journal of hepatology· 2026· PMID 41655910mais citado
  2. Renal Ketogenesis Protects Against Ischemic Kidney Injury.
    Journal of the American Society of Nephrology : JASN· 2026· PMID 41568909mais citado
  3. β‑hydroxybutyric acid as a potential therapeutic metabolite for type 2 diabetes mellitus (Review).
    International journal of molecular medicine· 2026· PMID 41201041mais citado
  4. Hepatic Ketogenesis Regulates Lipid Homeostasis via ACSL1-mediated Fatty Acid Partitioning.
    Cellular and molecular gastroenterology and hepatology· 2025· PMID 40692014mais citado
  5. The Multifaceted Influence of Beta-Hydroxybutyrate on Autophagy, Mitochondrial Metabolism, and Epigenetic Regulation.
    Journal of cellular biochemistry· 2025· PMID 40583323mais citado

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  1. ORPHA:309115(Orphanet)
  2. MONDO:0017713(MONDO)
  3. GARD:21317(GARD (NIH))
  4. Variantes catalogadas(ClinVar)
  5. Q55787301(Wikidata)

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Alteração da oxidação do ácido graxo mitocondrial

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