High incidence of two methylenetetrahydrofolate reductase mutations (C677T and A1298C) in Hispanics

被引:7
作者
Chowdary, D
Streck, D
Schwalb, MN
Dermody, JJ
机构
[1] UMDNJ, New Jersey Med Sch, Dept Microbiol & Mol Genet, Newark, NJ 07103 USA
[2] UMDNJ, New Jersey Med Sch, Ctr Human & Mol Genet, Newark, NJ 07103 USA
来源
GENETIC TESTING | 2003年 / 7卷 / 03期
关键词
D O I
10.1089/109065703322537296
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mutations in the 5,10-methylenetetrahydrofolate reductase (MTHFR) and coagulation factors II and V genes have been found at high frequencies in European and American Caucasian populations and are associated with increased risk for thrombophilia, premature coronary artery disease, and a variety of adverse pregnancy outcomes. Hispanic populations in the United States exhibit high levels of some of these conditions, so we initiated a population-based study to determine the frequency of these mutations (MTHFR C677T and A1298C, Factor II G20210A and Factor V G1691A) in this group. We find comparable frequencies of the Factors II and V mutations, but a high incidence of the two MTHFR mutations in a diverse sample of American Hispanics compared to those reported in Caucasians. Prospective studies of Hispanic women with these mutations and pregnancy outcomes will establish if there is a causal relationship.
引用
收藏
页码:255 / 257
页数:3
相关论文
共 37 条
[1]  
Arruda VR, 1997, THROMB HAEMOSTASIS, V77, P818
[2]   Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas Hispanic population [J].
Barber, R ;
Shalat, S ;
Hendricks, K ;
Joggerst, B ;
Larsen, R ;
Suarez, L ;
Finnell, R .
MOLECULAR GENETICS AND METABOLISM, 2000, 70 (01) :45-52
[3]   Venous thrombosis - The interaction of genes and environment [J].
Bertina, RM ;
Rosendaal, FR .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (25) :1840-1841
[4]  
Canfield MA, 1996, AM J EPIDEMIOL, V143, P1
[5]  
Chavez G F, 1988, MMWR CDC Surveill Summ, V37, P17
[6]   The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy [J].
de Franchis, R ;
Buoninconti, A ;
Mandato, C ;
Pepe, A ;
Sperandeo, MP ;
Del Gado, R ;
Capra, V ;
Salvaggio, E ;
Andria, G ;
Mastroiacovo, P .
JOURNAL OF MEDICAL GENETICS, 1998, 35 (12) :1009-1013
[7]  
deVries JIP, 1997, BRIT J OBSTET GYNAEC, V104, P1248
[8]  
DURNWALD FC, 2000, OBSTET GYNECOL, V95, P11
[9]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[10]  
Gregg JP, 1997, AM J MED GENET, V73, P334, DOI 10.1002/(SICI)1096-8628(19971219)73:3<334::AID-AJMG20>3.0.CO