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carnitine and Deficiency Diseases

carnitine has been researched along with Deficiency Diseases in 28 studies

Deficiency Diseases: A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed)

Research Excerpts

ExcerptRelevanceReference
"To explore the incidence and independent risk-factors of secondary carnitine deficiency in Chinese children with epilepsy on valproate monotherapy."7.88Carnitine Deficiency in Chinese Children with Epilepsy on Valproate Monotherapy. ( Hong, J; Qiliang, L; Wenqi, S, 2018)
"Sepsis is defined as the dysregulated host response to an infection resulting in life-threatening organ dysfunction."6.58A review of micronutrients in sepsis: the role of thiamine, l-carnitine, vitamin C, selenium and vitamin D. ( Belsky, JB; Jacob, V; Lee, PJ; Sather, JE; Wira, CR, 2018)
"To explore the incidence and independent risk-factors of secondary carnitine deficiency in Chinese children with epilepsy on valproate monotherapy."3.88Carnitine Deficiency in Chinese Children with Epilepsy on Valproate Monotherapy. ( Hong, J; Qiliang, L; Wenqi, S, 2018)
"Sepsis is defined as the dysregulated host response to an infection resulting in life-threatening organ dysfunction."2.58A review of micronutrients in sepsis: the role of thiamine, l-carnitine, vitamin C, selenium and vitamin D. ( Belsky, JB; Jacob, V; Lee, PJ; Sather, JE; Wira, CR, 2018)
"Carnitine was approved by the US Food and Drug Administration in 1985 for treatment of 'primary carnitine deficiency', and later in 1992 for treatment of 'secondary carnitine deficiency', a definition that included the majority of relevant metabolic disorders associated with low or abnormal plasma carnitine levels."2.53Historical Perspective on Clinical Trials of Carnitine in Children and Adults. ( Buist, NR, 2016)
"Glutaric aciduria type I is an autosomal recessive disorder resulting from a deficiency of glutaryl-CoA dehydrogenase."2.43Glutaric aciduria types I and II. ( Gordon, N, 2006)
"Carnitine depletion was associated with a 30% decrease soleus muscle weight, whereas contractile function (expressed per gram of muscle), free coenzyme A, and water content remained unaltered from CON."1.42Contractile function and energy metabolism of skeletal muscle in rats with secondary carnitine deficiency. ( Bonifacio, A; Bouitbir, J; Kaufmann, P; Krähenbühl, S; Roberts, PA; Singh, F; Urwyler, A, 2015)
"This lysine-derived label was incorporated only into the butyrate carbon chain."1.25Biosynthesis of carnitine and 4-N-trimethylaminobutyrate from lysine. ( Cox, RA; Hoppel, CL, 1973)

Research

Studies (28)

TimeframeStudies, this research(%)All Research%
pre-19909 (32.14)18.7374
1990's2 (7.14)18.2507
2000's4 (14.29)29.6817
2010's13 (46.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Qiliang, L1
Wenqi, S1
Hong, J1
Belsky, JB1
Wira, CR1
Jacob, V1
Sather, JE1
Lee, PJ1
Hayashi, H1
Tokuriki, S1
Okuno, T1
Shigematsu, Y1
Yasushi, A1
Matsuyama, G1
Sawada, K1
Ohshima, Y1
Fukami, K1
Yamagishi, S1
Sakai, K1
Kaida, Y1
Yokoro, M1
Ueda, S1
Wada, Y1
Takeuchi, M1
Shimizu, M1
Yamazaki, H1
Okuda, S1
Roberts, PA1
Bouitbir, J1
Bonifacio, A1
Singh, F1
Kaufmann, P1
Urwyler, A1
Krähenbühl, S1
Longo, N2
Armenian, SH2
Winter, S1
Buist, NR2
Lopaschuk, G1
Wasilewska, A1
Lopaschuk, GD1
Dessein, AF1
Fontaine, M1
Andresen, BS1
Gregersen, N1
Brivet, M1
Rabier, D1
Napuri-Gouel, S1
Dobbelaere, D1
Mention-Mulliez, K1
Martin-Ponthieu, A1
Briand, G1
Millington, DS1
Vianey-Saban, C1
Wanders, RJ1
Vamecq, J1
Stratton, SL2
Horvath, TD2
Bogusiewicz, A2
Matthews, NI1
Henrich, CL1
Spencer, HJ1
Moran, JH1
Mock, DM2
Boysen, G1
Bartlett, K1
Pourfarzam, M1
Cam, H1
Yildirim, B1
Aydin, A1
Say, A1
Gordon, N1
Bove, KE1
Sugie, H1
Sugie, Y1
Tsurui, S1
Ito, M1
Miyamoto, R1
Matsuda, F1
Nagao, M1
Tsuchiyama, A1
Mori, T1
Agatsuma, Y1
Oyanagi, K1
Rudman, D2
Feller, A1
Penn, D1
Schmidt-Sommerfeld, E1
Williams, PJ1
Tanphaichitr, V3
Broquist, HP3
Cox, RA1
Hoppel, CL1

Reviews

9 reviews available for carnitine and Deficiency Diseases

ArticleYear
A review of micronutrients in sepsis: the role of thiamine, l-carnitine, vitamin C, selenium and vitamin D.
    Nutrition research reviews, 2018, Volume: 31, Issue:2

    Topics: Ascorbic Acid; Carnitine; Deficiency Diseases; Dietary Supplements; Humans; Micronutrients; Nutritio

2018
Primary Carnitine Deficiency and Newborn Screening for Disorders of the Carnitine Cycle.
    Annals of nutrition & metabolism, 2016, Volume: 68 Suppl 3

    Topics: Cardiomyopathies; Carnitine; Deficiency Diseases; Denmark; Dietary Supplements; Genetic Testing; Hum

2016
Anthracycline-Induced Cardiotoxicity in Young Cancer Patients: The Role of Carnitine.
    Annals of nutrition & metabolism, 2016, Volume: 68 Suppl 3

    Topics: Anthracyclines; Antineoplastic Agents; Cardiomyopathies; Cardiotoxicity; Carnitine; Child; Deficienc

2016
Fatty Acid Oxidation and Its Relation with Insulin Resistance and Associated Disorders.
    Annals of nutrition & metabolism, 2016, Volume: 68 Suppl 3

    Topics: Animals; Carnitine; Carnitine Acyltransferases; Deficiency Diseases; Diabetes Mellitus; Diet, High-F

2016
Historical Perspective on Clinical Trials of Carnitine in Children and Adults.
    Annals of nutrition & metabolism, 2016, Volume: 68 Suppl 3

    Topics: Administration, Intravenous; Adult; Cardiomyopathies; Carnitine; Carnitine Acyltransferases; Child;

2016
Defects of beta-oxidation including carnitine deficiency.
    International review of neurobiology, 2002, Volume: 53

    Topics: Biological Transport; Carnitine; Carnitine O-Palmitoyltransferase; Deficiency Diseases; Humans; Meta

2002
Glutaric aciduria types I and II.
    Brain & development, 2006, Volume: 28, Issue:3

    Topics: Carnitine; Deficiency Diseases; Genes, Recessive; Glutarates; Glutaryl-CoA Dehydrogenase; Humans

2006
Nutrient deficiencies during total parenteral nutrition.
    Nutrition reviews, 1985, Volume: 43, Issue:1

    Topics: Adolescent; Adult; Aged; Animals; Biotin; Carnitine; Child; Choline Deficiency; Chromium; Copper; Cy

1985
Formation of carnitine from lysine in the rat.
    Nutrition reviews, 1972, Volume: 30, Issue:5

    Topics: Animal Nutritional Physiological Phenomena; Animals; Butyrates; Carnitine; Deficiency Diseases; Diet

1972

Other Studies

19 other studies available for carnitine and Deficiency Diseases

ArticleYear
Carnitine Deficiency in Chinese Children with Epilepsy on Valproate Monotherapy.
    Indian pediatrics, 2018, 03-15, Volume: 55, Issue:3

    Topics: Anticonvulsants; Beijing; Carnitine; Case-Control Studies; Child, Preschool; Deficiency Diseases; Ep

2018
Biotin and carnitine deficiency due to hypoallergenic formula nutrition in infants with milk allergy.
    Pediatrics international : official journal of the Japan Pediatric Society, 2014, Volume: 56, Issue:2

    Topics: Biotin; Carnitine; Deficiency Diseases; Female; Humans; Infant; Infant Formula; Male; Milk Hypersens

2014
Oral L-carnitine supplementation increases trimethylamine-N-oxide but reduces markers of vascular injury in hemodialysis patients.
    Journal of cardiovascular pharmacology, 2015, Volume: 65, Issue:3

    Topics: Administration, Oral; Aged; Biomarkers; Carnitine; Case-Control Studies; Deficiency Diseases; Dietar

2015
Contractile function and energy metabolism of skeletal muscle in rats with secondary carnitine deficiency.
    American journal of physiology. Endocrinology and metabolism, 2015, Aug-01, Volume: 309, Issue:3

    Topics: Animals; Apoptosis; Biomarkers; Carnitine; Deficiency Diseases; Disease Models, Animal; Energy Metab

2015
Round Table Discussion.
    Annals of nutrition & metabolism, 2016, Volume: 68 Suppl 3

    Topics: Adolescent; Autistic Disorder; Biomedical Research; Cardiomyopathies; Carnitine; Child; Congresses a

2016
A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.
    Orphanet journal of rare diseases, 2010, Oct-05, Volume: 5

    Topics: Acyl-CoA Dehydrogenase; Adult; Carnitine; Cells, Cultured; Child, Preschool; Deficiency Diseases; Fa

2010
Plasma concentration of 3-hydroxyisovaleryl carnitine is an early and sensitive indicator of marginal biotin deficiency in humans.
    The American journal of clinical nutrition, 2010, Volume: 92, Issue:6

    Topics: Adult; Aged; Biomarkers; Biotin; Carbon-Carbon Ligases; Carnitine; Deficiency Diseases; Egg White; F

2010
Measurement of acylcarnitine substrate to product ratios specific to biotin-dependent carboxylases offers a combination of indicators of biotin status in humans.
    The Journal of nutrition, 2012, Volume: 142, Issue:9

    Topics: Acetyl-CoA Carboxylase; Biomarkers; Biotin; Carbon-Carbon Ligases; Carbon-Nitrogen Ligases; Carnitin

2012
L-carnitine.
    The Medical letter on drugs and therapeutics, 2004, Nov-22, Volume: 46, Issue:1196

    Topics: Carnitine; Controlled Clinical Trials as Topic; Deficiency Diseases; Dietary Supplements; Double-Bli

2004
Carnitine levels in neonatal hypoxia.
    Journal of tropical pediatrics, 2005, Volume: 51, Issue:2

    Topics: Asphyxia Neonatorum; Carnitine; Case-Control Studies; Deficiency Diseases; Female; Humans; Infant, N

2005
The metabolic crisis: a diagnostic challenge [editoria; comment].
    The Journal of pediatrics, 1997, Volume: 131, Issue:2

    Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Deficiency Diseases; Energy Metabolism; Fatty Acid Desatur

1997
[Secondary carnitine deficiency due to antibiotics therapy using pivaloxyl methyl cephem].
    No to hattatsu = Brain and development, 1992, Volume: 24, Issue:1

    Topics: Administration, Oral; Carnitine; Cefmenoxime; Deficiency Diseases; Humans; Prodrugs; Respiratory Tra

1992
Neonatal hyperammonemia associated with carnitine deficiency.
    The Tohoku journal of experimental medicine, 1989, Volume: 158, Issue:4

    Topics: Ammonia; Carnitine; Deficiency Diseases; Female; Humans; Infant, Newborn; Male

1989
Evidence for deficiencies of conditionally essential nutrients during total parenteral nutrition.
    Journal of the American College of Nutrition, 1986, Volume: 5, Issue:2

    Topics: Carnitine; Choline Deficiency; Cysteine; Deficiency Diseases; Humans; Parenteral Nutrition, Total; T

1986
The carnitine-deprived newborn rabbit: a potential model to study carnitine deficiency.
    The Journal of nutrition, 1988, Volume: 118, Issue:12

    Topics: Adipose Tissue, Brown; Animals; Animals, Newborn; Carnitine; Deficiency Diseases; Diet; Disease Mode

1988
Site of carnitine biosynthesis in the rat.
    The Journal of nutrition, 1974, Volume: 104, Issue:12

    Topics: Animals; Betaine; Butyrates; Carbon Radioisotopes; Carnitine; Deficiency Diseases; Epididymis; Injec

1974
Lysine deficiency in the rat: concomitant impairement in carnitine biosynthesis.
    The Journal of nutrition, 1973, Volume: 103, Issue:1

    Topics: Anemia; Animals; Blood Proteins; Body Weight; Carnitine; Deficiency Diseases; Dietary Proteins; Eryt

1973
Role of lysine and -N-trimethyllysine in carnitine biosynthesis. II. Studies in the rat.
    The Journal of biological chemistry, 1973, Mar-25, Volume: 248, Issue:6

    Topics: Animal Nutritional Physiological Phenomena; Animals; Betaine; Brain; Butyrates; Carbon Isotopes; Car

1973
Biosynthesis of carnitine and 4-N-trimethylaminobutyrate from lysine.
    The Biochemical journal, 1973, Volume: 136, Issue:4

    Topics: Animals; Betaine; Butyrates; Carbon Radioisotopes; Carnitine; Choline; Chromatography; Chromatograph

1973
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