carnitine has been researched along with Complications, Pregnancy in 34 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The crucial role of L-carnitine in pregnancy metabolism suggests that nutritional supplementation of this amino acid can be offered to women who are either overweight or obese at the beginning of the pregnancy." | 7.79 | Lowered serum total L-carnitine levels are associated with obesity at term pregnancy. ( Arioz, DT; Kanat-Pektas, M; Koken, G; Koken, T; Tipi-Akbas, P; Yilmazer, M, 2013) |
| "Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a mitochondrial fatty acid beta-oxidation defect characterized by accumulation of long-chain hydroxyacylcarnitine intermediates and female carriers of this disorder are in risk for pregnancy complications." | 7.76 | Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication? ( Eskelin, PM; Laitinen, KA; Tyni, TA, 2010) |
| "Close observation of plasma amino acid, carnitine, and acylcarnitine profiles was performed in a patient with IVA that completed uneventful pregnancy." | 7.76 | Maternal isovaleric acidemia: observation of distinctive changes in plasma amino acids and carnitine profiles during pregnancy. ( Castelnovi, C; Moseley, K; Yano, S, 2010) |
| "We report management through pregnancy and delivery of a patient with carnitine deficiency who had reduced carnitine transport in fibroblasts, but no mutations in the OCTN2 gene." | 7.74 | Carnitine deficiency in pregnancy. ( Abdenur, JE; Donnelly, CT; Hameed, AB; Wing, DA, 2007) |
| "We report on a favourable pregnancy in a woman affected by mut- methylmalonic acidaemia." | 7.71 | Successful pregnancy in a woman with mut- methylmalonic acidaemia. ( Baiocco, F; Boenzi, S; Deodato, F; Dionisi-Vici, C; Rizzo, C; Sabetta, G, 2002) |
| "In this study the correlations between the concentration of carnitine and an increasing glucose intolerance in women with untreated, non insulin dependent gestational diabetes (GDM) were examined." | 7.71 | [The concentration of carnitine in the last trimester of pregnancy subject to glucose tolerance]. ( Günter, HH; Oehler, K; Peulecke, W; Scharf, A; Schumann, G; Sohn, C, 2002) |
| "We report on 2 women with organic acidemias, one with classical maple syrup urine disease and another with mild propionic acidemia in which protein restricted diets and carnitine supplementation were successfully employed to manage pregnancies." | 7.68 | Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia. ( Barness, LA; Davidson, SR; Harding, CO; Van Calcar, SC; Wolff, JA, 1992) |
| "Although frank symptomatic biotin deficiency is rare, some evidence suggests that marginal biotin deficiency occurs spontaneously in a substantial proportion of women during normal human pregnancy and might confer an increased risk of birth defects." | 4.95 | Biotin: From Nutrition to Therapeutics. ( Mock, DM, 2017) |
| "21]) were associated with higher odds of antepartum depression and 4 metabolites (betaine [OR = =0." | 3.96 | Metabolomic markers of antepartum depression and suicidal ideation. ( Clish, C; Gelaye, B; Larrabure-Torrealva, GT; Mitro, SD; Molsberry, SA; Sanchez, SE; Williams, MA, 2020) |
| "Targeted metabolomic assays of clinical metabolites, amino acids, and acylcarnitines were performed on fasting and 1-h postglucose serum samples from European ancestry, Afro-Caribbean, Thai, and Mexican American mothers (400 from each ancestry group) who participated in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study and underwent an oral glucose tolerance test at ∼28 weeks gestation." | 3.85 | Targeted Metabolomics Demonstrates Distinct and Overlapping Maternal Metabolites Associated With BMI, Glucose, and Insulin Sensitivity During Pregnancy Across Four Ancestry Groups. ( Bain, JR; Ilkayeva, OR; Jacob, S; Lowe, LP; Lowe, WL; Metzger, BE; Muehlbauer, MJ; Newgard, CB; Nodzenski, M; Reisetter, AC; Scholtens, DM; Stevens, RD, 2017) |
| "The crucial role of L-carnitine in pregnancy metabolism suggests that nutritional supplementation of this amino acid can be offered to women who are either overweight or obese at the beginning of the pregnancy." | 3.79 | Lowered serum total L-carnitine levels are associated with obesity at term pregnancy. ( Arioz, DT; Kanat-Pektas, M; Koken, G; Koken, T; Tipi-Akbas, P; Yilmazer, M, 2013) |
| "Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a mitochondrial fatty acid beta-oxidation defect characterized by accumulation of long-chain hydroxyacylcarnitine intermediates and female carriers of this disorder are in risk for pregnancy complications." | 3.76 | Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication? ( Eskelin, PM; Laitinen, KA; Tyni, TA, 2010) |
| "Close observation of plasma amino acid, carnitine, and acylcarnitine profiles was performed in a patient with IVA that completed uneventful pregnancy." | 3.76 | Maternal isovaleric acidemia: observation of distinctive changes in plasma amino acids and carnitine profiles during pregnancy. ( Castelnovi, C; Moseley, K; Yano, S, 2010) |
| "We report management through pregnancy and delivery of a patient with carnitine deficiency who had reduced carnitine transport in fibroblasts, but no mutations in the OCTN2 gene." | 3.74 | Carnitine deficiency in pregnancy. ( Abdenur, JE; Donnelly, CT; Hameed, AB; Wing, DA, 2007) |
| "We report on a favourable pregnancy in a woman affected by mut- methylmalonic acidaemia." | 3.71 | Successful pregnancy in a woman with mut- methylmalonic acidaemia. ( Baiocco, F; Boenzi, S; Deodato, F; Dionisi-Vici, C; Rizzo, C; Sabetta, G, 2002) |
| "In this study the correlations between the concentration of carnitine and an increasing glucose intolerance in women with untreated, non insulin dependent gestational diabetes (GDM) were examined." | 3.71 | [The concentration of carnitine in the last trimester of pregnancy subject to glucose tolerance]. ( Günter, HH; Oehler, K; Peulecke, W; Scharf, A; Schumann, G; Sohn, C, 2002) |
| "We report on 2 women with organic acidemias, one with classical maple syrup urine disease and another with mild propionic acidemia in which protein restricted diets and carnitine supplementation were successfully employed to manage pregnancies." | 3.68 | Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia. ( Barness, LA; Davidson, SR; Harding, CO; Van Calcar, SC; Wolff, JA, 1992) |
| "Obesity is an important worldwide public health problem and considered a disease of chronic low-grade inflammation." | 2.80 | Effect of L-carnitine supplementation in comparison with moderate aerobic training on serum inflammatory parameters in healthy obese women. ( Jafari, A; Karimi, M; Rafraf, M, 2015) |
| "Birth weight was higher in the G allele homozygotes of the CHDH rs2289205 than in the minor allele carriers: GG: 3398 ± 64 g; GA+AA: 3193 ± 76 g." | 1.48 | PEMT rs12325817 and PCYT1A rs7639752 polymorphisms are associated with betaine but not choline concentrations in pregnant women. ( Barlik, M; Chmurzynska, A; Drews, K; Jagodziński, PP; Kurzawińska, G; Malinowska, AM; Radziejewska, A; Różycka, A; Seremak-Mrozikiewicz, A; Szwengiel, A, 2018) |
| "Her pregnancy was uncomplicated." | 1.40 | Methylmalonic acidaemia in pregnancy. ( Den Hartog, M; Eyskens, F; Jacquemyn, Y, 2014) |
| "Although vitamin B12 deficiency is not a primary target of newborn screening (NBS) programs, measurements of propionylcarnitine (C3) and its ratios with acetylcarnitine (C3/C2) and palmitoylcarnitine (C3/C16) may incidentally identify vitamin B12-deficient newborns." | 1.40 | Serum vitamin B12 levels during the first trimester of pregnancy correlate with newborn screening markers of vitamin B12 deficiency. ( Dayaldasani, A; Pérez-Valero, V; Rodríguez-Espinosa, M; Rueda, I; Ruiz-Escalera, J; Yahyaoui, R, 2014) |
| "The pregnancy was uneventful and the delivery at term." | 1.36 | Treatment of cobalamin C (cblC) deficiency during pregnancy. ( Brunel-Guitton, C; Costa, T; Lambert, M; Mitchell, GA, 2010) |
| "She had no phenotypic feature of holocarboxylase synthetase deficiency, most importantly no episodes ever of acute metabolic acidosis." | 1.35 | Positive newborn screen in the biochemically normal infant of a mother with treated holocarboxylase synthetase deficiency. ( Barshop, BA; Gangoiti, J; Nyhan, WL; Willis, M, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (14.71) | 18.7374 |
| 1990's | 3 (8.82) | 18.2507 |
| 2000's | 9 (26.47) | 29.6817 |
| 2010's | 16 (47.06) | 24.3611 |
| 2020's | 1 (2.94) | 2.80 |
| Authors | Studies |
|---|---|
| Mitro, SD | 1 |
| Larrabure-Torrealva, GT | 1 |
| Sanchez, SE | 1 |
| Molsberry, SA | 1 |
| Williams, MA | 1 |
| Clish, C | 1 |
| Gelaye, B | 1 |
| Jacob, S | 1 |
| Nodzenski, M | 1 |
| Reisetter, AC | 1 |
| Bain, JR | 1 |
| Muehlbauer, MJ | 1 |
| Stevens, RD | 1 |
| Ilkayeva, OR | 1 |
| Lowe, LP | 1 |
| Metzger, BE | 1 |
| Newgard, CB | 1 |
| Scholtens, DM | 1 |
| Lowe, WL | 1 |
| Mock, DM | 1 |
| Chmurzynska, A | 1 |
| Seremak-Mrozikiewicz, A | 1 |
| Malinowska, AM | 1 |
| Różycka, A | 1 |
| Radziejewska, A | 1 |
| Szwengiel, A | 1 |
| Kurzawińska, G | 1 |
| Barlik, M | 1 |
| Jagodziński, PP | 1 |
| Drews, K | 1 |
| Rossi, C | 1 |
| Cicalini, I | 1 |
| Zucchelli, M | 1 |
| di Ioia, M | 1 |
| Onofrj, M | 1 |
| Federici, L | 1 |
| Del Boccio, P | 1 |
| Pieragostino, D | 1 |
| Tipi-Akbas, P | 1 |
| Arioz, DT | 1 |
| Kanat-Pektas, M | 1 |
| Koken, T | 1 |
| Koken, G | 1 |
| Yilmazer, M | 1 |
| Jacquemyn, Y | 1 |
| Den Hartog, M | 1 |
| Eyskens, F | 1 |
| Scolamiero, E | 1 |
| Villani, GR | 1 |
| Ingenito, L | 1 |
| Pecce, R | 1 |
| Albano, L | 1 |
| Caterino, M | 1 |
| di Girolamo, MG | 1 |
| Di Stefano, C | 1 |
| Franzese, I | 1 |
| Gallo, G | 1 |
| Ruoppolo, M | 1 |
| Romigi, A | 1 |
| Liguori, C | 1 |
| Izzi, F | 1 |
| Albanese, M | 1 |
| Marchi, A | 1 |
| Mancini, C | 1 |
| Tarquini, E | 1 |
| Mercuri, NB | 1 |
| Placidi, F | 1 |
| Rafraf, M | 1 |
| Karimi, M | 1 |
| Jafari, A | 1 |
| Dayaldasani, A | 1 |
| Ruiz-Escalera, J | 1 |
| Rodríguez-Espinosa, M | 1 |
| Rueda, I | 1 |
| Pérez-Valero, V | 1 |
| Yahyaoui, R | 1 |
| Nyhan, WL | 1 |
| Willis, M | 1 |
| Barshop, BA | 1 |
| Gangoiti, J | 1 |
| Eskelin, PM | 1 |
| Laitinen, KA | 1 |
| Tyni, TA | 1 |
| Mendez-Figueroa, H | 1 |
| Shchelochkov, OA | 1 |
| Shaibani, A | 1 |
| Aagaard-Tillery, K | 1 |
| Shinawi, MS | 1 |
| Castelnovi, C | 1 |
| Moseley, K | 1 |
| Yano, S | 1 |
| Brunel-Guitton, C | 1 |
| Costa, T | 1 |
| Mitchell, GA | 1 |
| Lambert, M | 1 |
| Sarafoglou, K | 1 |
| Rodgers, J | 1 |
| Hietala, A | 1 |
| Matern, D | 1 |
| Bentler, K | 1 |
| Ituk, US | 1 |
| Allen, TK | 1 |
| Habib, AS | 1 |
| Deodato, F | 1 |
| Rizzo, C | 1 |
| Boenzi, S | 1 |
| Baiocco, F | 1 |
| Sabetta, G | 1 |
| Dionisi-Vici, C | 1 |
| Günter, HH | 1 |
| Peulecke, W | 1 |
| Oehler, K | 1 |
| Scharf, A | 1 |
| Schumann, G | 1 |
| Sohn, C | 1 |
| Bok, LA | 1 |
| Vreken, P | 1 |
| Wijburg, FA | 1 |
| Wanders, RJ | 1 |
| Gregersen, N | 1 |
| Corydon, MJ | 1 |
| Waterham, HR | 1 |
| Duran, M | 1 |
| Wu, SP | 1 |
| Shyu, MK | 1 |
| Liou, HH | 1 |
| Gau, CS | 1 |
| Lin, CJ | 1 |
| Campbell, CD | 1 |
| Ganesh, J | 1 |
| Ficicioglu, C | 1 |
| Donnelly, CT | 1 |
| Hameed, AB | 1 |
| Abdenur, JE | 1 |
| Wing, DA | 1 |
| Kong, XF | 1 |
| Zhang, XX | 1 |
| Yu, YY | 1 |
| Shi, Q | 1 |
| La, DD | 1 |
| Zhu-Ge, CD | 1 |
| Deng, L | 1 |
| Gong, QM | 1 |
| Shen, BY | 1 |
| Peng, CH | 1 |
| Li, HW | 1 |
| Bargen-Lockner, C | 1 |
| Hahn, P | 1 |
| Wittmann, B | 1 |
| Treem, WR | 2 |
| Rinaldo, P | 1 |
| Hale, DE | 1 |
| Stanley, CA | 1 |
| Millington, DS | 1 |
| Hyams, JS | 1 |
| Jackson, S | 1 |
| Turnbull, DM | 1 |
| Borum, PR | 1 |
| Broquist, HP | 1 |
| Salonen, V | 1 |
| Nikoskelainen, J | 1 |
| Heinonen, OJ | 1 |
| Kalimo, H | 1 |
| Aula, P | 1 |
| Van Calcar, SC | 1 |
| Harding, CO | 1 |
| Davidson, SR | 1 |
| Barness, LA | 1 |
| Wolff, JA | 1 |
| Nagao, M | 1 |
| Tsuchiyama, A | 1 |
| Aoyama, T | 1 |
| Mori, T | 1 |
| Oyanagi, K | 1 |
| Acosta, PB | 1 |
| Stepnick-Gropper, S | 1 |
| Salzer, H | 1 |
| Lohninger, A | 1 |
| Sevelda, P | 1 |
| Legenstein, E | 1 |
2 reviews available for carnitine and Complications, Pregnancy
| Article | Year |
|---|---|
Biotin: From Nutrition to Therapeutics.
Topics: Animals; Biotin; Biotinylation; Carnitine; Female; Gene Expression; Hormones; Humans; Multiple Scler | 2017 |
New developments in the pathophysiology, clinical spectrum, and diagnosis of disorders of fatty acid oxidation.
Topics: Acetyl Coenzyme A; Carnitine; Fatty Acids; Female; Fetal Diseases; Humans; Infant; Lipid Metabolism, | 2000 |
1 trial available for carnitine and Complications, Pregnancy
| Article | Year |
|---|---|
Effect of L-carnitine supplementation in comparison with moderate aerobic training on serum inflammatory parameters in healthy obese women.
Topics: Adult; Biomarkers; Body Mass Index; C-Reactive Protein; Carnitine; Dietary Supplements; Double-Blind | 2015 |
31 other studies available for carnitine and Complications, Pregnancy
| Article | Year |
|---|---|
Metabolomic markers of antepartum depression and suicidal ideation.
Topics: 5-Hydroxytryptophan; Adult; Betaine; Biomarkers; Carnitine; Citrulline; Cross-Sectional Studies; Dep | 2020 |
Targeted Metabolomics Demonstrates Distinct and Overlapping Maternal Metabolites Associated With BMI, Glucose, and Insulin Sensitivity During Pregnancy Across Four Ancestry Groups.
Topics: Amino Acids; Blood Glucose; Body Mass Index; Carnitine; Cohort Studies; Female; Gestational Age; Glu | 2017 |
PEMT rs12325817 and PCYT1A rs7639752 polymorphisms are associated with betaine but not choline concentrations in pregnant women.
Topics: Adolescent; Adult; Alleles; Betaine; Birth Weight; Carnitine; Choline; Choline-Phosphate Cytidylyltr | 2018 |
Metabolomic Signature in Sera of Multiple Sclerosis Patients during Pregnancy.
Topics: Adult; Amino Acids; Biomarkers; Carnitine; Case-Control Studies; Female; Gonadal Steroid Hormones; H | 2018 |
Lowered serum total L-carnitine levels are associated with obesity at term pregnancy.
Topics: Adult; Body Height; Body Mass Index; Carnitine; Dietary Supplements; Female; Fetal Weight; Gestation | 2013 |
Methylmalonic acidaemia in pregnancy.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Calcium Carbonate; Carnitine; Diet, Protein-Restricted; | 2014 |
Maternal vitamin B12 deficiency detected in expanded newborn screening.
Topics: Carnitine; Female; Folic Acid; Homocysteine; Humans; Infant, Newborn; Methylmalonic Acid; Neonatal S | 2014 |
Oral L-carnitine as treatment for narcolepsy without cataplexy during pregnancy: a case report.
Topics: Adult; Carnitine; Female; Humans; Narcolepsy; Pregnancy; Pregnancy Complications | 2015 |
Serum vitamin B12 levels during the first trimester of pregnancy correlate with newborn screening markers of vitamin B12 deficiency.
Topics: Acetylcarnitine; Adolescent; Adult; Biomarkers; Carnitine; Diet; Female; Gestational Age; Humans; In | 2014 |
Positive newborn screen in the biochemically normal infant of a mother with treated holocarboxylase synthetase deficiency.
Topics: Adult; Biotin; Carnitine; False Positive Reactions; Female; Holocarboxylase Synthetase Deficiency; H | 2009 |
Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication?
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acute Disease; Adult; Carnitine; Fatty Liver; Female; Humans; Lipi | 2010 |
Clinical and biochemical improvement of very long-chain acyl-CoA dehydrogenase deficiency in pregnancy.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Female; Humans; Infant, Newborn; Lipid Metabolism, In | 2010 |
Maternal isovaleric acidemia: observation of distinctive changes in plasma amino acids and carnitine profiles during pregnancy.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Carnitine; Female; Humans; Infant, Newborn; Isova | 2010 |
Treatment of cobalamin C (cblC) deficiency during pregnancy.
Topics: Amino Acid Metabolism, Inborn Errors; Aspirin; Carnitine; Carrier Proteins; Cells, Cultured; Combine | 2010 |
Expanded newborn screening for detection of vitamin B12 deficiency.
Topics: Carnitine; Female; Humans; Infant, Newborn; Minnesota; Neonatal Screening; Pregnancy; Pregnancy Comp | 2011 |
The peripartum management of a patient with glutaric aciduria type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Anesthesia, Obstetrical; Anesthesia, Spinal; Brain Diseases, M | 2013 |
Successful pregnancy in a woman with mut- methylmalonic acidaemia.
Topics: Adult; Carnitine; Female; Humans; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnancy; Pregnanc | 2002 |
[The concentration of carnitine in the last trimester of pregnancy subject to glucose tolerance].
Topics: Adult; Biomarkers; Blood Glucose; Carnitine; Diabetes, Gestational; Female; Glucose Intolerance; Glu | 2002 |
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
Topics: Amino Acid Substitution; Anemia, Hemolytic; Butyryl-CoA Dehydrogenase; Carnitine; Consanguinity; DNA | 2003 |
Interaction between anticonvulsants and human placental carnitine transporter.
Topics: Acetates; Amines; Aminoisobutyric Acids; Anticonvulsants; Carnitine; Carrier Proteins; Culture Techn | 2004 |
Two newborns with nutritional vitamin B12 deficiency: challenges in newborn screening for vitamin B12 deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Anemia, Pernicious; Autoimmune Diseases; Biomarkers; Carnitine; | 2005 |
Carnitine deficiency in pregnancy.
Topics: Adult; Carnitine; Cesarean Section; Female; Fibroblasts; Humans; Pregnancy; Pregnancy Complications; | 2007 |
No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adult; Carnitine; Cytosine; Family; Fatty Liver; Female; Guanine; | 2007 |
Plasma carnitine in pregnancy.
Topics: Adolescent; Adult; Carnitine; Female; Fetus; Humans; Maternal-Fetal Exchange; Pregnancy; Pregnancy C | 1981 |
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acute Disease; Adult; Carnitine; Cells, Cultured; Child; Child, Pr | 1994 |
Lysine deficiency and carnitine in male and female rats.
Topics: Animals; Body Weight; Carnitine; Dietary Proteins; Epididymis; Female; Glutens; Liver; Lysine; Male; | 1977 |
[Carnitine deficiency and severe nausea-induced thiamine deficiency causing a metabolic crisis].
Topics: Adult; Carnitine; Female; Humans; Hyperemesis Gravidarum; Lipid Metabolism; Metabolic Diseases; Naus | 1992 |
Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia.
Topics: Adult; Amino Acids; Carbon-Carbon Ligases; Carnitine; Citrates; Citric Acid; Female; Fetal Growth Re | 1992 |
Secondary carnitine deficiency in the newborn period in twins of a mother with partial ornithine transcarbamylase deficiency.
Topics: Carnitine; Diseases in Twins; Female; Humans; Infant, Newborn; Ornithine Carbamoyltransferase Defici | 1989 |
Problems related to diet management of maternal phenylketonuria.
Topics: alpha-Linolenic Acid; Carnitine; Cations, Divalent; Cell Membrane Permeability; Cholesterol; Dietary | 1986 |
[Carnitine for the stimulation of fetal lung maturation. Clinical case report].
Topics: Adult; Betamethasone; Carnitine; Female; Fetal Organ Maturity; Humans; Infant, Newborn; Lung; Male; | 1985 |