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01.02.2015 | Review Article

“Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis”

Erschienen in: Metabolic Brain Disease | Ausgabe 1/2015

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Abstract

Epidemiological studies have evaluated the association between maternal methylenetetrahydrofolate reductase (MTHFR) C677T, A1298C and methionine synthase reductase (MTRR) A66G polymorphisms and risk of neural tube defects (NTDs) in offspring. However, the results from the published studies on the association between these three polymorphisms and NTD risk are conflicting. To derive a clearer picture of association between these three maternal polymorphisms and risk of NTD, we performed meta-analysis. A comprehensive search was conducted to identify all case–control studies of maternal MTHFR and MTRR polymorphisms and NTD risk. We used odds ratios (ORs) with 95 % confidence intervals (CIs) to assess the strength of the association. Overall, we found that maternal MTHFR C677T polymorphism (ORTvsC =1.20; 95 % CI = 1.13–1.28) and MTRR A66G polymorphism (ORGvsA = 1.21; 95 % CI = 0.98–1.49) were risk factors for producing offspring with NTD but maternal MTHFR A1298C polymorphism (ORCvsA = 0.91; 95 % CI = 0.78–1.07) was not associated with NTD risk. However, in stratified analysis by geographical regions, we found that the maternal C677T polymorphism was significantly associated with the risk of NTD in Asian (ORTvsC = 1.43; 95 % CI: 1.05–1.94), European (ORTvsC = 1.13; 95 % CI: 1.04–1.24) and American (ORTvsC = 1.26; 95 % CI: 1.13–1.41) populations. In conclusion, present meta-analysis supports that the maternal MTHFR C677T and MTRR A66G are polymorphisms contributory to risk for NTD.
Literatur
Zurück zum Zitat Akar N, Akar E, Deda G, Arsan S (2000) Spina bifida and common mutations at the homocysteine metabolism pathway. Clin Genet 57(3):230–231 Akar N, Akar E, Deda G, Arsan S (2000) Spina bifida and common mutations at the homocysteine metabolism pathway. Clin Genet 57(3):230–231
Zurück zum Zitat Arbour L, Christensen B, Delormier T, Platt R, Gilfix B, Forbes P, Kovitch I, Morel J, Rozen R (2002) Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population. Int J Circumpolar Health 61(4):341–351PubMedCrossRef Arbour L, Christensen B, Delormier T, Platt R, Gilfix B, Forbes P, Kovitch I, Morel J, Rozen R (2002) Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population. Int J Circumpolar Health 61(4):341–351PubMedCrossRef
Zurück zum Zitat Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R (2000) Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population. Mol Genet Metab 70(1):45–52PubMedCrossRef Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R (2000) Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population. Mol Genet Metab 70(1):45–52PubMedCrossRef
Zurück zum Zitat Bax L, Yu LM, Ikeda N, Tsuruta H, Moons KG (2006) Development and validation of MIX: comprehensive free software for meta-analysis of causal research data. BMC Med Res Methodol 6:50PubMedCentralPubMedCrossRef Bax L, Yu LM, Ikeda N, Tsuruta H, Moons KG (2006) Development and validation of MIX: comprehensive free software for meta-analysis of causal research data. BMC Med Res Methodol 6:50PubMedCentralPubMedCrossRef
Zurück zum Zitat Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci U S A 94:3290–3295PubMedCentralPubMedCrossRef Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci U S A 94:3290–3295PubMedCentralPubMedCrossRef
Zurück zum Zitat Boduroğlu K, Alikaşifoğlu M, Anar B, Tunçbilek E (1999) Association of the 677C– > T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. J Child Neurol 14(3):159–161 Boduroğlu K, Alikaşifoğlu M, Anar B, Tunçbilek E (1999) Association of the 677C– > T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. J Child Neurol 14(3):159–161
Zurück zum Zitat Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E (2005) Analysis of MTHFR 1298A > C in addition to MTHFR 677C > T polymorphism as a risk factor for neural tube defects in the Turkish population. Turk J Pediatr 47(4):327–333PubMed Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E (2005) Analysis of MTHFR 1298A > C in addition to MTHFR 677C > T polymorphism as a risk factor for neural tube defects in the Turkish population. Turk J Pediatr 47(4):327–333PubMed
Zurück zum Zitat Candito M, Rivet R, Herbeth B, Boisson C, Rudigoz RC, Luton D, Journel H, Oury JF, Roux F, Saura R, Vernhet I, Gaucherand P, Muller F, Guidicelli B, Heckenroth H, Poulain P, Blayau M, Francannet C, Roszyk L, Brustié C, Staccini P, Gérard P, Fillion-Emery N, Guéant-Rodriguez RM, Van Obberghen E, Guéant JL (2008) Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: a multicenter case–control study. Am J Med Genet A 146A(9):1128–1133PubMedCrossRef Candito M, Rivet R, Herbeth B, Boisson C, Rudigoz RC, Luton D, Journel H, Oury JF, Roux F, Saura R, Vernhet I, Gaucherand P, Muller F, Guidicelli B, Heckenroth H, Poulain P, Blayau M, Francannet C, Roszyk L, Brustié C, Staccini P, Gérard P, Fillion-Emery N, Guéant-Rodriguez RM, Van Obberghen E, Guéant JL (2008) Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: a multicenter case–control study. Am J Med Genet A 146A(9):1128–1133PubMedCrossRef
Zurück zum Zitat Ceyhan ST, Beyan C, Bahce M, Baser I, Kaptan K, Ifran A, Egin Y, Akar N (2008) Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects. Int J Gynaecol Obstet 101(2):188–189PubMedCrossRef Ceyhan ST, Beyan C, Bahce M, Baser I, Kaptan K, Ifran A, Egin Y, Akar N (2008) Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects. Int J Gynaecol Obstet 101(2):188–189PubMedCrossRef
Zurück zum Zitat Choi SW, Mason JB (2000) Folate and carcinogenesis: an integrated scheme. J Nutr 130:129–132PubMed Choi SW, Mason JB (2000) Folate and carcinogenesis: an integrated scheme. J Nutr 130:129–132PubMed
Zurück zum Zitat Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, Rozen R (1999) Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Am J Med Genet 84(2):151–157PubMedCrossRef Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, Rozen R (1999) Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Am J Med Genet 84(2):151–157PubMedCrossRef
Zurück zum Zitat Cunha AL, Hirata MH, Kim CA, Guerra-Shinohara EM, Nonoyama K, Hirata RD (2002) Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects. Clin Chim Acta 318(1–2):139–143PubMedCrossRef Cunha AL, Hirata MH, Kim CA, Guerra-Shinohara EM, Nonoyama K, Hirata RD (2002) Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects. Clin Chim Acta 318(1–2):139–143PubMedCrossRef
Zurück zum Zitat Czeizel AE, Dudás I (1992) Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 327(26):1832–1835PubMedCrossRef Czeizel AE, Dudás I (1992) Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 327(26):1832–1835PubMedCrossRef
Zurück zum Zitat Dalal A, Pradhan M, Tiwari D, Behari S, Singh U, Mallik GK, Das V, Agarwal S (2007) MTHFR 677C– > T and 1298A– > C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect. Gynecol Obstet Invest 63(3):146–150PubMedCrossRef Dalal A, Pradhan M, Tiwari D, Behari S, Singh U, Mallik GK, Das V, Agarwal S (2007) MTHFR 677C– > T and 1298A– > C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect. Gynecol Obstet Invest 63(3):146–150PubMedCrossRef
Zurück zum Zitat Daly LE, Kirke PN, Molloy A, Weir DG, Scott JM (1995) Folate levels and neural tube defects. Implications for prevention. JAMA 274(21):1698–1702PubMedCrossRef Daly LE, Kirke PN, Molloy A, Weir DG, Scott JM (1995) Folate levels and neural tube defects. Implications for prevention. JAMA 274(21):1698–1702PubMedCrossRef
Zurück zum Zitat Dávalos IP, Olivares N, Castillo MT, Cantú JM, Ibarra B, Sandoval L, Morán MC, Gallegos MP, Chakraborty R, Rivas F (2000) The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations. Ann Genet 43(2):89–92PubMedCrossRef Dávalos IP, Olivares N, Castillo MT, Cantú JM, Ibarra B, Sandoval L, Morán MC, Gallegos MP, Chakraborty R, Rivas F (2000) The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations. Ann Genet 43(2):89–92PubMedCrossRef
Zurück zum Zitat De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V (2001) Polymorphisms in genes involved in folate metabolism as risk factors for NTDs. Eur J Pediatr Surg 11 Suppl 1:S14–S17 De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V (2001) Polymorphisms in genes involved in folate metabolism as risk factors for NTDs. Eur J Pediatr Surg 11 Suppl 1:S14–S17
Zurück zum Zitat De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2002) Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet 47(6):319–324PubMedCrossRef De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2002) Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet 47(6):319–324PubMedCrossRef
Zurück zum Zitat De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2003) Reduced folate carrier polymorphism (80A– > G) and neural tube defects. Eur J Hum Genet 11(3):245–252 De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V (2003) Reduced folate carrier polymorphism (80A– > G) and neural tube defects. Eur J Hum Genet 11(3):245–252
Zurück zum Zitat Deb R, Arora J, Meitei SY, Gupta S, Verma V, Saraswathy KN, Saran S, Kalla AK (2011) Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India. Metab Brain Dis 26(3):241–246PubMedCrossRef Deb R, Arora J, Meitei SY, Gupta S, Verma V, Saraswathy KN, Saran S, Kalla AK (2011) Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India. Metab Brain Dis 26(3):241–246PubMedCrossRef
Zurück zum Zitat DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7:177–188PubMedCrossRef DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7:177–188PubMedCrossRef
Zurück zum Zitat Elsayed GM, El Assiouty L, El Sobky ES (2013) The importance of rapid aneuploidy screening and prenatal diagnosis in the detection of numerical chromosomal abnormalities. Springer Plus 2(1):1–8CrossRef Elsayed GM, El Assiouty L, El Sobky ES (2013) The importance of rapid aneuploidy screening and prenatal diagnosis in the detection of numerical chromosomal abnormalities. Springer Plus 2(1):1–8CrossRef
Zurück zum Zitat Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S (2010) C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects. Genet Mol Res 9(2):1197–1203PubMedCrossRef Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S (2010) C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects. Genet Mol Res 9(2):1197–1203PubMedCrossRef
Zurück zum Zitat Félix TM, Leistner S, Giugliani R (2004) Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil. Birth Defects Res A Clin Mol Teratol 70(7):459–63PubMedCrossRef Félix TM, Leistner S, Giugliani R (2004) Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil. Birth Defects Res A Clin Mol Teratol 70(7):459–63PubMedCrossRef
Zurück zum Zitat Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Mathews RG, Boers GJH, den Heijer M, Kluijtmans LAJ, van den Heuvel LP, Rozen R (1995) A candidate genetic risk factor for vascular disease: a common mutation in methelenetetrahydrofolate reductase. (Letter). Nat Genet 10:111–113PubMedCrossRef Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Mathews RG, Boers GJH, den Heijer M, Kluijtmans LAJ, van den Heuvel LP, Rozen R (1995) A candidate genetic risk factor for vascular disease: a common mutation in methelenetetrahydrofolate reductase. (Letter). Nat Genet 10:111–113PubMedCrossRef
Zurück zum Zitat Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N, Suresh S, Sheth J, Chandak GR, Yajnik CS (2011) Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India. Birth Defects Res A Clin Mol Teratol 91(9):848–856 Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N, Suresh S, Sheth J, Chandak GR, Yajnik CS (2011) Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India. Birth Defects Res A Clin Mol Teratol 91(9):848–856
Zurück zum Zitat González-Herrera L, García-Escalante G, Castillo-Zapata I, Canto-Herrera J, Ceballos-Quintal J, Pinto-Escalante D, Díaz-Rubio F, Del Angel RM, Orozco-Orozco L (2002) Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico. Clin Genet 62(5):394–398PubMedCrossRef González-Herrera L, García-Escalante G, Castillo-Zapata I, Canto-Herrera J, Ceballos-Quintal J, Pinto-Escalante D, Díaz-Rubio F, Del Angel RM, Orozco-Orozco L (2002) Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico. Clin Genet 62(5):394–398PubMedCrossRef
Zurück zum Zitat Gonzalez-Herrera L, Castillo-Zapata I, Garcia-Escalante G, Pinto-Escalante D (2007) A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico. Birth Defects Res A Clin Mol Teratol 79(8):622–626PubMedCrossRef Gonzalez-Herrera L, Castillo-Zapata I, Garcia-Escalante G, Pinto-Escalante D (2007) A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico. Birth Defects Res A Clin Mol Teratol 79(8):622–626PubMedCrossRef
Zurück zum Zitat Gos M, Sliwerska E, Szpecht-Potocka A (2004) Mutation incidence in folate metabolism genes and regulatory genes in polish families with neural tube defects. J Appl Genet 45(3):363–368PubMed Gos M, Sliwerska E, Szpecht-Potocka A (2004) Mutation incidence in folate metabolism genes and regulatory genes in polish families with neural tube defects. J Appl Genet 45(3):363–368PubMed
Zurück zum Zitat Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, Chan M, Rozen R (1998) Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR). Mamm Genome 9(8):652–656PubMedCrossRef Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, Chan M, Rozen R (1998) Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR). Mamm Genome 9(8):652–656PubMedCrossRef
Zurück zum Zitat Grandone E, Corrao AM, Colaizzo D, Vecchione G, Di Girgenti C, Paladini D, Sardella L, Pellegrino M, Zelante L, Martinelli P, Margaglione M (2006) Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants. Prenat Diagn 26(1):1–5PubMedCrossRef Grandone E, Corrao AM, Colaizzo D, Vecchione G, Di Girgenti C, Paladini D, Sardella L, Pellegrino M, Zelante L, Martinelli P, Margaglione M (2006) Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants. Prenat Diagn 26(1):1–5PubMedCrossRef
Zurück zum Zitat Guenther BD, Sheppard CA, Tran P, Rozen R, Matthews RG, Ludwig ML (1999) The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia. Nat Struct Biol 6:359–365PubMedCrossRef Guenther BD, Sheppard CA, Tran P, Rozen R, Matthews RG, Ludwig ML (1999) The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia. Nat Struct Biol 6:359–365PubMedCrossRef
Zurück zum Zitat Harisha PN, Devi BI, Christopher R, Kruthika-Vinod TP (2010) Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects. J Neurosurg Pediatr 6(4):364–367PubMedCrossRef Harisha PN, Devi BI, Christopher R, Kruthika-Vinod TP (2010) Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects. J Neurosurg Pediatr 6(4):364–367PubMedCrossRef
Zurück zum Zitat Hegele RA, Tully C, Young TK, Connelly PW (1997) V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit. Lancet 349(9060):1221–1222PubMedCrossRef Hegele RA, Tully C, Young TK, Connelly PW (1997) V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit. Lancet 349(9060):1221–1222PubMedCrossRef
Zurück zum Zitat Houcher B, Bourouba R, Djabi F, Yilmaz E, Eğin Y, Akar N (2009) Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Pediatr Neurosurg 45(6):472–477PubMedCrossRef Houcher B, Bourouba R, Djabi F, Yilmaz E, Eğin Y, Akar N (2009) Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Pediatr Neurosurg 45(6):472–477PubMedCrossRef
Zurück zum Zitat Jakobkiewicz-Banecka J, Kloska A, Stepnowsk M, Banecki B, Wegrzyn A, Wegrzyn G (2005) A bacterial model for studying effects of human mutations in vivo: Escherichia coli strains mimicking a common polymorphism in the human MTHFR gene. Mutat Res 578:175–186PubMedCrossRef Jakobkiewicz-Banecka J, Kloska A, Stepnowsk M, Banecki B, Wegrzyn A, Wegrzyn G (2005) A bacterial model for studying effects of human mutations in vivo: Escherichia coli strains mimicking a common polymorphism in the human MTHFR gene. Mutat Res 578:175–186PubMedCrossRef
Zurück zum Zitat James SJ, Pogribny IP, Pogribna M, Miller BJ, Jernigan S, Melnyk S (2003) Mechanisms of DNA damage, DNA hypomethylation, and tumor progression in the folate/methyl-deficient rat model of hepatocarcinogenesis. J Nutr 133(11Suppl.1):37 James SJ, Pogribny IP, Pogribna M, Miller BJ, Jernigan S, Melnyk S (2003) Mechanisms of DNA damage, DNA hypomethylation, and tumor progression in the folate/methyl-deficient rat model of hepatocarcinogenesis. J Nutr 133(11Suppl.1):37
Zurück zum Zitat Kirke PN, Molloy AM, Daly LE, Burke H, Weir DG, Scott JM (1993) Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. QJ Med 86:703–708 Kirke PN, Molloy AM, Daly LE, Burke H, Weir DG, Scott JM (1993) Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. QJ Med 86:703–708
Zurück zum Zitat Lacasaña M, Blanco-Muñoz J, Borja-Aburto VH, Aguilar-Garduño C, Rodríguez-Barranco M, Sierra-Ramirez JA, Galaviz-Hernandez C, Gonzalez-Alzaga B, Garcia-Cavazos R (2012) Effect on risk of anencephaly of gene-nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile. Public Health Nutr 15(8):1419–1428PubMedCrossRef Lacasaña M, Blanco-Muñoz J, Borja-Aburto VH, Aguilar-Garduño C, Rodríguez-Barranco M, Sierra-Ramirez JA, Galaviz-Hernandez C, Gonzalez-Alzaga B, Garcia-Cavazos R (2012) Effect on risk of anencephaly of gene-nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile. Public Health Nutr 15(8):1419–1428PubMedCrossRef
Zurück zum Zitat Lee BH, Cheong HI, Shin YS, Cho BK, Wang KC (2000) The effect of C677T mutation of methylene tetrahydrofolate reductase gene and plasma folate level on hyperhomocysteinemia in patients with meningomyelocele. Childs Nerv Syst 16(9):559–563PubMedCrossRef Lee BH, Cheong HI, Shin YS, Cho BK, Wang KC (2000) The effect of C677T mutation of methylene tetrahydrofolate reductase gene and plasma folate level on hyperhomocysteinemia in patients with meningomyelocele. Childs Nerv Syst 16(9):559–563PubMedCrossRef
Zurück zum Zitat Li K, Zheng D, Xue Y, Sun Y, Chen L, Guo J, Zhang G, Li P (2000) The common C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with neural tube defects and preeclampsia. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 17(2):76–78 Li K, Zheng D, Xue Y, Sun Y, Chen L, Guo J, Zhang G, Li P (2000) The common C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with neural tube defects and preeclampsia. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 17(2):76–78
Zurück zum Zitat Liu ZZ, Zhang JT, Liu D, Hao YH, Chang BM, Xie J, Li PZ (2013) Interaction between maternal 5, 10-methylenetetrahydrofolate reductase C677T and methionine synthase A2756G gene variants to increase the risk of fetal neural tube defects in a Shanxi Han population. Chin Med J (Engl) 126(5):865–869 Liu ZZ, Zhang JT, Liu D, Hao YH, Chang BM, Xie J, Li PZ (2013) Interaction between maternal 5, 10-methylenetetrahydrofolate reductase C677T and methionine synthase A2756G gene variants to increase the risk of fetal neural tube defects in a Shanxi Han population. Chin Med J (Engl) 126(5):865–869
Zurück zum Zitat Lucock M, Daskalakis I, Briggs D, Yates Z, Levene M (2000) Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c – > t methylenetetrahydrofolate reductase and 2756a – > g methionine synthase genotypes. Mol Genet Metab 70(1):27–44PubMedCrossRef Lucock M, Daskalakis I, Briggs D, Yates Z, Levene M (2000) Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c – > t methylenetetrahydrofolate reductase and 2756a – > g methionine synthase genotypes. Mol Genet Metab 70(1):27–44PubMedCrossRef
Zurück zum Zitat Lucock M, Daskalakis I, Hinkins M, Yates Z (2001) An examination of polymorphic genes and folate metabolism in mothers affected by a spina bifida pregnancy. Mol Genet Metab 73(4):322–332 Lucock M, Daskalakis I, Hinkins M, Yates Z (2001) An examination of polymorphic genes and folate metabolism in mothers affected by a spina bifida pregnancy. Mol Genet Metab 73(4):322–332
Zurück zum Zitat Mantel N, Haenszel W (1959) Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 22(4):719–748PubMed Mantel N, Haenszel W (1959) Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 22(4):719–748PubMed
Zurück zum Zitat Martínez de Villarreal LE, Delgado-Enciso I, Valdéz-Leal R, Ortíz-López R, Rojas-Martínez A, Limón-Benavides C, Sánchez-Peña MA, Ancer-Rodríguez J, Barrera-Saldaña HA, Villarreal-Pérez JZ (2001) Folate levels and N(5), N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case–control study. Arch Med Res 32(4):277–282PubMedCrossRef Martínez de Villarreal LE, Delgado-Enciso I, Valdéz-Leal R, Ortíz-López R, Rojas-Martínez A, Limón-Benavides C, Sánchez-Peña MA, Ancer-Rodríguez J, Barrera-Saldaña HA, Villarreal-Pérez JZ (2001) Folate levels and N(5), N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case–control study. Arch Med Res 32(4):277–282PubMedCrossRef
Zurück zum Zitat Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, Scott JM (1995) Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 345(8943):149–151PubMedCrossRef Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, Scott JM (1995) Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 345(8943):149–151PubMedCrossRef
Zurück zum Zitat Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM (1998) Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor. Am J Med Genet 78(2):155–159 Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM (1998) Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor. Am J Med Genet 78(2):155–159
Zurück zum Zitat Morrison K, Papapetrou C, Hol FA, Mariman EC, Lynch SA, Burn J, Edwards YH (1998) Susceptibility to spina bifida; an association study of five candidate genes. Ann Hum Genet 62(Pt5):379–396PubMedCrossRef Morrison K, Papapetrou C, Hol FA, Mariman EC, Lynch SA, Burn J, Edwards YH (1998) Susceptibility to spina bifida; an association study of five candidate genes. Ann Hum Genet 62(Pt5):379–396PubMedCrossRef
Zurück zum Zitat Muñoz JB, Lacasaña M, Cavazos RG, Borja-Aburto VH, Galavíz-Hernández C, Garduño CA (2007) Methylenetetrahydrofolate reductase gene polymorphisms and the risk of anencephaly in Mexico. Mol Hum Reprod 13(6):419–424PubMedCrossRef Muñoz JB, Lacasaña M, Cavazos RG, Borja-Aburto VH, Galavíz-Hernández C, Garduño CA (2007) Methylenetetrahydrofolate reductase gene polymorphisms and the risk of anencephaly in Mexico. Mol Hum Reprod 13(6):419–424PubMedCrossRef
Zurück zum Zitat Naushad SM, Devi AR (2010) Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India. J Perinat Med 38(1):63–69PubMedCrossRef Naushad SM, Devi AR (2010) Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India. J Perinat Med 38(1):63–69PubMedCrossRef
Zurück zum Zitat O’Leary VB, Mills JL, Pangilinan F, Kirke PN, Cox C, Conley M, Weiler A, Peng K, Shane B, Scott JM, Parle-McDermott A, Molloy AM, Brody LC; Members of the Birth Defects Research Group (2005) Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association. Mol Genet Metab 85(3):220–227CrossRef O’Leary VB, Mills JL, Pangilinan F, Kirke PN, Cox C, Conley M, Weiler A, Peng K, Shane B, Scott JM, Parle-McDermott A, Molloy AM, Brody LC; Members of the Birth Defects Research Group (2005) Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association. Mol Genet Metab 85(3):220–227CrossRef
Zurück zum Zitat Olteanu H, Munson T, Banerjee R (2002) Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase. Biochemistry 41(45):13378–13385PubMedCrossRef Olteanu H, Munson T, Banerjee R (2002) Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase. Biochemistry 41(45):13378–13385PubMedCrossRef
Zurück zum Zitat Olteanu H, Wolthers KR, Munro AW, Scrutton NS, Banerjee R (2004) Kinetic and thermodynamic characterization of the common polymorphic variants of human methionine synthase reductase. Biochemistry 43(7):1988–9197PubMedCrossRef Olteanu H, Wolthers KR, Munro AW, Scrutton NS, Banerjee R (2004) Kinetic and thermodynamic characterization of the common polymorphic variants of human methionine synthase reductase. Biochemistry 43(7):1988–9197PubMedCrossRef
Zurück zum Zitat Ouyang S, Li Y, Liu Z, Chang H, Wu J (2013) Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis. Gene 515(2):308–312 Ouyang S, Li Y, Liu Z, Chang H, Wu J (2013) Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis. Gene 515(2):308–312
Zurück zum Zitat Parle-McDermott A, Mills JL, Kirke PN, O’Leary VB, Swanson DA, Pangilinan F, Conley M, Molloy AM, Cox C, Scott JM, Brody LC (2003) Analysis of the MTHFR 1298A– > C and 677C- > T polymorphisms as risk factors for neural tube defects. J Hum Genet 48(4):190–193PubMedCrossRef Parle-McDermott A, Mills JL, Kirke PN, O’Leary VB, Swanson DA, Pangilinan F, Conley M, Molloy AM, Cox C, Scott JM, Brody LC (2003) Analysis of the MTHFR 1298A– > C and 677C- > T polymorphisms as risk factors for neural tube defects. J Hum Genet 48(4):190–193PubMedCrossRef
Zurück zum Zitat Peerbooms OL, van Os J, Drukker M, Kenis G, Hoogveld L; MTHFR in Psychiatry Group, de Hert M, Delespaul P, van Winkel R, Rutten BP (2011) Meta-analysis of MTHFR gene variants in schizophrenia, bipolar disorder and unipolar depressive disorder: evidence for a common genetic vulnerability? Brain Behav Immun 25(8):1530–1543CrossRef Peerbooms OL, van Os J, Drukker M, Kenis G, Hoogveld L; MTHFR in Psychiatry Group, de Hert M, Delespaul P, van Winkel R, Rutten BP (2011) Meta-analysis of MTHFR gene variants in schizophrenia, bipolar disorder and unipolar depressive disorder: evidence for a common genetic vulnerability? Brain Behav Immun 25(8):1530–1543CrossRef
Zurück zum Zitat Pejchal R, Campbell E, Guenther BD, Lennon BW, Matthews RG, Ludwig ML (2006) Structural perturbations in the Ala f Val polymorphism of Methylenetetrahydrofolate Reductase: how binding of folates may protect against inactivation. Biochemistry 45:4808–4818PubMedCentralPubMedCrossRef Pejchal R, Campbell E, Guenther BD, Lennon BW, Matthews RG, Ludwig ML (2006) Structural perturbations in the Ala f Val polymorphism of Methylenetetrahydrofolate Reductase: how binding of folates may protect against inactivation. Biochemistry 45:4808–4818PubMedCentralPubMedCrossRef
Zurück zum Zitat Pepe G, Camacho Vanegas O, Giusti B, Brunelli T, Marcucci R, Attanasio M, Rickards O, De Stefano GF, Prisco D, Gensini GF, Abbate R (1998) Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase. Am J Hum Genet 63(3):917–920PubMedCentralPubMedCrossRef Pepe G, Camacho Vanegas O, Giusti B, Brunelli T, Marcucci R, Attanasio M, Rickards O, De Stefano GF, Prisco D, Gensini GF, Abbate R (1998) Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase. Am J Hum Genet 63(3):917–920PubMedCentralPubMedCrossRef
Zurück zum Zitat Perez AB, D’Almeida V, Vergani N, de Oliveira AC, de Lima FT, Brunoni D (2003) Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida. Am J Med Genet A 119A(1):20–25PubMedCrossRef Perez AB, D’Almeida V, Vergani N, de Oliveira AC, de Lima FT, Brunoni D (2003) Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida. Am J Med Genet A 119A(1):20–25PubMedCrossRef
Zurück zum Zitat Pietrzyk JJ, Bik-Multanowski M, Sanak M, Twardowska M (2003) Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida. J Appl Genet 44(1):111–113PubMed Pietrzyk JJ, Bik-Multanowski M, Sanak M, Twardowska M (2003) Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida. J Appl Genet 44(1):111–113PubMed
Zurück zum Zitat Pogribny IP, James SJ, Jernigan S, Pogribna M (2004) Genomic hypomethylation is specific for preneoplastic liver in folate/methyl deficient rats and does not occur in non-target tissues. Mutat Res 548(1–2):53–59PubMedCrossRef Pogribny IP, James SJ, Jernigan S, Pogribna M (2004) Genomic hypomethylation is specific for preneoplastic liver in folate/methyl deficient rats and does not occur in non-target tissues. Mutat Res 548(1–2):53–59PubMedCrossRef
Zurück zum Zitat Rai V, Yadav U, Kumar P (2012) Genotype prevalence and allele frequencies of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T mutation in two caste groups of India. Cell Mol Biol (Noisy-le-Grand) 58 Suppl:OL1695–1701 Rai V, Yadav U, Kumar P (2012) Genotype prevalence and allele frequencies of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T mutation in two caste groups of India. Cell Mol Biol (Noisy-le-Grand) 58 Suppl:OL1695–1701
Zurück zum Zitat Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC; NTD Collaborative Group (2003) Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clin Genet 63(3):210–214CrossRef Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC; NTD Collaborative Group (2003) Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clin Genet 63(3):210–214CrossRef
Zurück zum Zitat Razin A, Kantor B (2005) DNA methylation in epigenetic control of gene expression. Prog Mol Subcell Biol 38:151–167PubMedCrossRef Razin A, Kantor B (2005) DNA methylation in epigenetic control of gene expression. Prog Mol Subcell Biol 38:151–167PubMedCrossRef
Zurück zum Zitat Relton CL, Wilding CS, Jonas PA, Lynch SA, Tawn EJ, Burn J (2003) Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype. Clin Genet 64(5):424–428PubMedCrossRef Relton CL, Wilding CS, Jonas PA, Lynch SA, Tawn EJ, Burn J (2003) Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype. Clin Genet 64(5):424–428PubMedCrossRef
Zurück zum Zitat Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J (2004a) Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population. J Med Genet 41(4):256–260PubMedCentralPubMedCrossRef Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J (2004a) Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population. J Med Genet 41(4):256–260PubMedCentralPubMedCrossRef
Zurück zum Zitat Relton CL, Wilding CS, Laffling AJ, Jonas PA, Burgess T, Binks K, Tawn EJ, Burn J (2004b) Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy. Mol Genet Metab 81(4):273–281 Relton CL, Wilding CS, Laffling AJ, Jonas PA, Burgess T, Binks K, Tawn EJ, Burn J (2004b) Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy. Mol Genet Metab 81(4):273–281
Zurück zum Zitat Sadewa AH, Sutomo R, Istiadjid M, Nishiyama K, Shirakawa T, Matsuo M, Nishio H (2004) C677T mutation in the MTHFR gene was not found in patients with frontoethmoidal encephalocele in East Java, Indonesia. Pediatr Int 46(4):409–414PubMedCrossRef Sadewa AH, Sutomo R, Istiadjid M, Nishiyama K, Shirakawa T, Matsuo M, Nishio H (2004) C677T mutation in the MTHFR gene was not found in patients with frontoethmoidal encephalocele in East Java, Indonesia. Pediatr Int 46(4):409–414PubMedCrossRef
Zurück zum Zitat Selvì N, Ergun R, Gube O, Yìldirim U, Tetik A, Gunduz C, Ulman I, Eroglu Z (2010) Genetic polymorphism of methylenetetrahydrofolate reductase as a risk factor for lumbosacral neutral tube defects. MEJSR 6:93–98 Selvì N, Ergun R, Gube O, Yìldirim U, Tetik A, Gunduz C, Ulman I, Eroglu Z (2010) Genetic polymorphism of methylenetetrahydrofolate reductase as a risk factor for lumbosacral neutral tube defects. MEJSR 6:93–98
Zurück zum Zitat Shang Y, Zhao H, Niu B, Li WI, Zhou R, Zhang T, Xie J (2008) Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China. Birth Defects Res A Clin Mol Teratol 82(1):3–7PubMedCrossRef Shang Y, Zhao H, Niu B, Li WI, Zhou R, Zhang T, Xie J (2008) Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China. Birth Defects Res A Clin Mol Teratol 82(1):3–7PubMedCrossRef
Zurück zum Zitat Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS (1999) The “thermolabile” variant of methylenetetrahydrofolate reductase and neural tube defects: an evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Am J Hum Genet 64(4):1045–1055PubMedCentralPubMedCrossRef Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS (1999) The “thermolabile” variant of methylenetetrahydrofolate reductase and neural tube defects: an evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Am J Hum Genet 64(4):1045–1055PubMedCentralPubMedCrossRef
Zurück zum Zitat Sözen MA, Hecht JT, Spritz RA (2009) Mutation analysis of the PVRL1 gene in caucasians with nonsyndromic cleft lip/palate. Genet Test Mol Biomark 13(5):617–621CrossRef Sözen MA, Hecht JT, Spritz RA (2009) Mutation analysis of the PVRL1 gene in caucasians with nonsyndromic cleft lip/palate. Genet Test Mol Biomark 13(5):617–621CrossRef
Zurück zum Zitat Speer MC, Worley G, Mackey JF, Melvin E, Oakes WJ, George TM (1997) The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD collaborative group. Neurogenetics 1(2):149–150PubMedCrossRef Speer MC, Worley G, Mackey JF, Melvin E, Oakes WJ, George TM (1997) The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD collaborative group. Neurogenetics 1(2):149–150PubMedCrossRef
Zurück zum Zitat Speer MC, Nye J, McLone D, Worley G, Melvin EC, Viles KD, Franklin A, Drake C, Mackey J, George TM (1999) Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group. Clin Genet 56(2):142–144 Speer MC, Nye J, McLone D, Worley G, Melvin EC, Viles KD, Franklin A, Drake C, Mackey J, George TM (1999) Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group. Clin Genet 56(2):142–144
Zurück zum Zitat Stuck AE, Rubenstein LZ, Wieland D (1998) Bias in meta-analysis detected by a simple, graphical test. Asymmetry detected in funnel plot was probably due to true heterogeneity. BMJ 316:469PubMedCentralPubMedCrossRef Stuck AE, Rubenstein LZ, Wieland D (1998) Bias in meta-analysis detected by a simple, graphical test. Asymmetry detected in funnel plot was probably due to true heterogeneity. BMJ 316:469PubMedCentralPubMedCrossRef
Zurück zum Zitat Ubbink JB, Christianson A, Bester MJ, Van Allen MI, Venter PA, Delport R, Blom HJ, van der Merwe A, Potgieter H, Vermaak WJ (1999) Folate status, homocysteine metabolism, and methylene tetrahydrofolate reductase genotype in rural South African blacks with a history of pregnancy complicated by neural tube defects. Metabolism 48(2):269–274PubMedCrossRef Ubbink JB, Christianson A, Bester MJ, Van Allen MI, Venter PA, Delport R, Blom HJ, van der Merwe A, Potgieter H, Vermaak WJ (1999) Folate status, homocysteine metabolism, and methylene tetrahydrofolate reductase genotype in rural South African blacks with a history of pregnancy complicated by neural tube defects. Metabolism 48(2):269–274PubMedCrossRef
Zurück zum Zitat van der Linden IJ, den Heijer M, Afman LA, Gellekink H, Vermeulen SH, Kluijtmans LA, Blom HJ (2006) The methionine synthase reductase 66A > G polymorphism is a maternal risk factor for spina bifida. J Mol Med (Berl) 84(12):1047–1054CrossRef van der Linden IJ, den Heijer M, Afman LA, Gellekink H, Vermeulen SH, Kluijtmans LA, Blom HJ (2006) The methionine synthase reductase 66A > G polymorphism is a maternal risk factor for spina bifida. J Mol Med (Berl) 84(12):1047–1054CrossRef
Zurück zum Zitat van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ (1995) Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346(8982):1070–1071PubMedCrossRef van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ (1995) Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346(8982):1070–1071PubMedCrossRef
Zurück zum Zitat van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ (1996) Decreased methylene tetrahydrofolate reductase activity due to the 677C– > T mutation in families with spina bifida offspring. J Mol Med (Berl) 74(11):691–694CrossRef van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ (1996) Decreased methylene tetrahydrofolate reductase activity due to the 677C– > T mutation in families with spina bifida offspring. J Mol Med (Berl) 74(11):691–694CrossRef
Zurück zum Zitat van der Put NM, Gabreëls F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ (1998) A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet 62(5):1044–1051PubMedCentralPubMedCrossRef van der Put NM, Gabreëls F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ (1998) A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet 62(5):1044–1051PubMedCentralPubMedCrossRef
Zurück zum Zitat van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ (2001) Folate, homocysteine and neural tube defects: an overview. Exp Biol Med (Maywood) 226(4):243–270 van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ (2001) Folate, homocysteine and neural tube defects: an overview. Exp Biol Med (Maywood) 226(4):243–270
Zurück zum Zitat Verkleij-Hagoort A, Bliek J, Sayed-Tabatabaei F, Ursem N, Steegers E, Steegers-Theunissen R (2007) Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: a meta-analysis. Am J Med Genet A 143A(9):952–960PubMedCrossRef Verkleij-Hagoort A, Bliek J, Sayed-Tabatabaei F, Ursem N, Steegers E, Steegers-Theunissen R (2007) Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: a meta-analysis. Am J Med Genet A 143A(9):952–960PubMedCrossRef
Zurück zum Zitat Volcik KA, Blanton SH, Tyerman GH, Jong ST, Rott EJ, Page TZ, Romaine NK, Northrup H (2000) Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics. Am J Med Genet 95(1):21–7 Volcik KA, Blanton SH, Tyerman GH, Jong ST, Rott EJ, Page TZ, Romaine NK, Northrup H (2000) Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics. Am J Med Genet 95(1):21–7
Zurück zum Zitat Wang F, Yang YF, Li PZ (2008) A case-control study on the risk factors of neural tube defects in Shanxi province. Zhonghua Liu Xing Bing Xue Za Zhi 29(8):771–774 Wang F, Yang YF, Li PZ (2008) A case-control study on the risk factors of neural tube defects in Shanxi province. Zhonghua Liu Xing Bing Xue Za Zhi 29(8):771–774
Zurück zum Zitat Wang XW, Luo YL, Wang W, Zhang Y, Chen Q, Cheng YL (2012) Association between MTHFR A1298C polymorphism and neural tube defect susceptibility: a meta-analysis. Am J Obstet Gynecol 206(3):251.e1–7 Wang XW, Luo YL, Wang W, Zhang Y, Chen Q, Cheng YL (2012) Association between MTHFR A1298C polymorphism and neural tube defect susceptibility: a meta-analysis. Am J Obstet Gynecol 206(3):251.e1–7
Zurück zum Zitat Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methelenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 94:169–172CrossRef Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methelenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 94:169–172CrossRef
Zurück zum Zitat Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R (1999) A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol Genet Metab 67(4):317–323PubMedCrossRef Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R (1999) A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol Genet Metab 67(4):317–323PubMedCrossRef
Zurück zum Zitat Wu J, Springett A, Morris JK (2013) Survival of trisomy 18 (Edwards syndrome) and trisomy 13 (Patau Syndrome) in England and Wales: 2004-2011. Am J Med Genet A 161(10):2512–2518 Wu J, Springett A, Morris JK (2013) Survival of trisomy 18 (Edwards syndrome) and trisomy 13 (Patau Syndrome) in England and Wales: 2004-2011. Am J Med Genet A 161(10):2512–2518
Zurück zum Zitat Xuan C, Bai XY, Gao G, Yang Q, He GW (2011) Association between polymorphism of methylenetetrahydrofolate reductase (MTHFR) C677T and risk of myocardial infarction: a meta-analysis for 8,140 cases and 10,522 controls. Arch Med Res 42(8):677–685PubMedCrossRef Xuan C, Bai XY, Gao G, Yang Q, He GW (2011) Association between polymorphism of methylenetetrahydrofolate reductase (MTHFR) C677T and risk of myocardial infarction: a meta-analysis for 8,140 cases and 10,522 controls. Arch Med Res 42(8):677–685PubMedCrossRef
Zurück zum Zitat Yadav U, Kumar P, Rai V (2011) Docking study of MTHFR with FAD by Hex. J Comput Intell Bioinforma 4(1):171–178 Yadav U, Kumar P, Rai V (2011) Docking study of MTHFR with FAD by Hex. J Comput Intell Bioinforma 4(1):171–178
Zurück zum Zitat Yamada K, Zhoutao C, Rima R, Mathews RG (2001) Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase. Proc Natl Acad Sci U S A 98:14853–14858PubMedCentralPubMedCrossRef Yamada K, Zhoutao C, Rima R, Mathews RG (2001) Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase. Proc Natl Acad Sci U S A 98:14853–14858PubMedCentralPubMedCrossRef
Zurück zum Zitat Yan L, Zhao L, Long Y, Zou P, Ji G, Gu A, Zhao P (2012) Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies. PLoS One 7(10):e41689 Yan L, Zhao L, Long Y, Zou P, Ji G, Gu A, Zhao P (2012) Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies. PLoS One 7(10):e41689
Zurück zum Zitat Yang S, Zhang J, Feng C, Huang G (2013) MTHFR 677T variant contributes to diabetic nephropathy risk in Caucasian individuals with type 2 diabetes: a meta-analysis. Metabolism 62(4):586–594PubMedCrossRef Yang S, Zhang J, Feng C, Huang G (2013) MTHFR 677T variant contributes to diabetic nephropathy risk in Caucasian individuals with type 2 diabetes: a meta-analysis. Metabolism 62(4):586–594PubMedCrossRef
Zurück zum Zitat Yu J, Chen B, Zhang G, Fu S, Li P (2000) The 677 C– > T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groups. Hum Hered 50(4):268–270PubMedCrossRef Yu J, Chen B, Zhang G, Fu S, Li P (2000) The 677 C– > T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groups. Hum Hered 50(4):268–270PubMedCrossRef
Zurück zum Zitat Zidan HE, Rezk NA, Mohammed D (2013) MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases. Gene 529(1):119–124PubMedCrossRef Zidan HE, Rezk NA, Mohammed D (2013) MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases. Gene 529(1):119–124PubMedCrossRef
Zurück zum Zitat Zhang T, Lou J, Zhong R, Wu J, Zou L, Sun Y, Lu X, Liu L, Miao X, Xiong G (2013) Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature. PLoS One 8(4):e59570 Zhang T, Lou J, Zhong R, Wu J, Zou L, Sun Y, Lu X, Liu L, Miao X, Xiong G (2013) Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature. PLoS One 8(4):e59570
Zurück zum Zitat Zhu H, Wicker NJ, Shaw GM, Lammer EJ, Hendricks K, Suarez L, Canfield M, Finnell RH (2003) Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab 78(3):216–221 Zhu H, Wicker NJ, Shaw GM, Lammer EJ, Hendricks K, Suarez L, Canfield M, Finnell RH (2003) Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab 78(3):216–221
Metadaten
Titel
“Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis”
Publikationsdatum
01.02.2015
Erschienen in
Metabolic Brain Disease / Ausgabe 1/2015
Print ISSN: 0885-7490
Elektronische ISSN: 1573-7365
DOI
https://doi.org/10.1007/s11011-014-9575-7

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