Does MTHFR C677T polymorphism predispose asthma? A North Indian study

被引:0
作者
Muthuswamy, Srinivasan [1 ]
Awasthi, Shally [2 ]
Dixit, Pratibha [2 ]
Agarwal, Sarita [1 ]
机构
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Med Genet, Lucknow, Uttar Pradesh, India
[2] Chatrapathi Shahuji Maharaj Med Univ, Dept Pediat, Lucknow, Uttar Pradesh, India
关键词
Asthma; MTHFR; C677T polymorphism; case-control study; METHYLENETETRAHYDROFOLATE REDUCTASE; POSITIONAL CLONING; COMMON MUTATION; FOLATE STATUS; ASSOCIATION; ENVIRONMENT; LOCUS;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Involvement of impaired folate metabolism has been hypothesized to be a potential risk factor for the predisposition of asthma. The reports are conflicting on the potential association between atopic disease and polymorphism of the methylene-tetrahydrofolate reductase (MTHFR)-gene. Objective: We designed the study to investigate the association of C677T polymorphism of the MTHFR gene with asthma in the Indian population. Methodology: This was a hospital based case control study in which 200 asthmatic cases and 329 controls from North India population were enrolled and the MTHFR gene C677T polymorphism was genotyped by PCR-RFLP method. Result: We observed 92.85% of control group as wildtype homozygous, 11.24% and 1.51% as heterozygous and mutant homozygous respectively, while 98.25% and 3.75% of case group as wildtype homozygous and heterozygous respectively. Conclusion: Our finding suggests a lack of association of MTHFR C677T polymorphism with asthma. Further association studies in worldwide populations, involving different ethnic group samples with narrowly defined phenotypes of asthma, could contribute to the understanding of genetic susceptibility to asthma.
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页码:107 / 111
页数:5
相关论文
共 25 条
  • [1] Positional cloning of a novel gene influencing asthma from Chromosome 2q14
    Allen, M
    Heinzmann, A
    Noguchi, E
    Abecasis, G
    Broxholme, J
    Ponting, CP
    Bhattacharyya, S
    Tinsley, J
    Zhang, YM
    Holt, R
    Jones, EY
    Lench, N
    Carey, A
    Jones, H
    Dickens, NJ
    Dimon, C
    Nicholls, R
    Baker, C
    Xue, LZ
    Townsend, E
    Kabesch, M
    Weiland, SK
    Carr, D
    von Mutius, E
    Adcock, IM
    Barnes, PJ
    Lathrop, GM
    Edwards, M
    Moffatt, MF
    Cookson, WOCM
    [J]. NATURE GENETICS, 2003, 35 (03) : 258 - 263
  • [2] [Anonymous], 2010, MED BIOL RES, V43, P1
  • [3] Association of CFTR gene mutation with bronchial asthma and its severity in Indian children: A case-control study
    Awasthi, Shally
    Maurya, Nutan
    Agarwal, Sarita
    Dixit, Pratibha
    Muthuswamy, Srinivasan
    Singh, Shweta
    [J]. ANNALS OF HUMAN BIOLOGY, 2012, 39 (02) : 113 - 121
  • [4] Brustolin S, GENETICS HOMOCYSTEIN
  • [5] Genetics and genomics of core short tandem repeat loci used in human identity testing
    Butler, JM
    [J]. JOURNAL OF FORENSIC SCIENCES, 2006, 51 (02) : 253 - 265
  • [6] The consanguinity effect on QF-PCR diagnosis of autosomal anomalies
    Choueiri, Michel B.
    Makhoul, Nadine J.
    Zreik, Tony G.
    Mattar, Farid
    Adra, Abdallah M.
    Eid, Raymond
    Mroueh, Adnan M.
    Zalloua, Pierre A.
    [J]. PRENATAL DIAGNOSIS, 2006, 26 (05) : 409 - 414
  • [7] The alliance of genes and environment in asthma and allergy
    Cookson, W
    [J]. NATURE, 1999, 402 (6760) : B5 - B11
  • [8] The immunogenetics of asthma and eczema: A new focus on the epithelium
    Cookson, W
    [J]. NATURE REVIEWS IMMUNOLOGY, 2004, 4 (12) : 978 - 988
  • [9] EDWARDS A, 1991, AM J HUM GENET, V49, P746
  • [10] A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE
    FROSST, P
    BLOM, HJ
    MILOS, R
    GOYETTE, P
    SHEPPARD, CA
    MATTHEWS, RG
    BOERS, GJH
    DENHEIJER, M
    KLUIJTMANS, LAJ
    VANDENHEUVEL, LP
    ROZEN, R
    [J]. NATURE GENETICS, 1995, 10 (01) : 111 - 113