Thermolabile MTHFR genotype and retinal vascular occlusive disease

被引:25
作者
Cahill, M
Karabatzaki, M
Donoghue, C
Meleady, R
Mynett-Johnson, LA
Mooney, D
Graham, IM
Whitehead, AS
Shields, DC
机构
[1] Royal Victoria Eye & Ear Hosp, Res Fdn, Dublin 2, Ireland
[2] Univ Dublin Trinity Coll, Dept Genet, Dublin 2, Ireland
[3] Natl Childrens Hosp, Adelaide Meath Hosp, Dept Cardiol, Dublin 24, Ireland
[4] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Med, Ctr Pharmacogenet, Philadelphia, PA 19104 USA
[6] Royal Coll Surg Ireland, Dept Clin Pharmacol, Dublin 2, Ireland
关键词
D O I
10.1136/bjo.85.1.88
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background-Raised levels of total plasma homocysteine (tHcy) are associated with an increased risk of retinal vascular occlusive disease. A thermolabile form of a pivotal enzyme in homocysteine metabolism, methylenetetrahydrofolate reductase (MTHFR), has been associated with vascular occlusive disease and raised tHcy levels. The relation between thermolabile MTHFR genotype, tHcy, and retinal vascular occlusive disease has not been determined. Methods-A retrospective case-control study involving hospital based controls and cases with retinal vascular occlusions in whom tHcy levels had been determined was undertaken. Genotyping for the MTHFR 677 C-T mutation that specifies the thermolabile form of the enzyme was performed by established methods in all subjects. The relation between homozygosity for thermolabile MTHFR genotype (TT), raised tHcy levels, and risk of retinal vascular occlusive disease was examined. Results-87 cases of retinal vascular occlusive disease (mean age 68.7 years) comprising 26 cases of retinal artery occlusion and 61 of retinal vein occlusion were compared with 87 controls (mean age 70.2 years). The TT genotype did not confer a significantly increased risk of retinal vascular occlusive disease. The mean tHcy level was significantly higher in the cases than in the controls (p<0.0001). Overall, and in both the cases and controls, the frequency of the TT genotype was higher in those with normal tHcy levels than in those with increased levels of tHcy. However, the TT genotype did not significantly alter the risk of increased tHcy levels in these patients. Conclusions-The TT genotype is not associated with an increased risk of retinal vascular occlusive disease or increased tHcy levels in this group of elderly patients. In older patients, nutritional rather than genetic factors may be more important in increasing tHcy levels, a known risk factor for retinal vascular occlusive disease.
引用
收藏
页码:88 / 90
页数:3
相关论文
共 32 条
  • [1] A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction
    Anderson, JL
    King, GJ
    Thomson, MJ
    Todd, M
    Bair, TL
    Muhlestein, JB
    Carlquist, JF
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (05) : 1206 - 1211
  • [2] Arruda VR, 1997, THROMB HAEMOSTASIS, V77, P818
  • [3] Retinal vein occlusion and transient monocular visual loss associated with hyperhomocystinemia
    Biousse, V
    Newman, NJ
    Sternberg, P
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1997, 124 (02) : 257 - 260
  • [4] A QUANTITATIVE ASSESSMENT OF PLASMA HOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE - PROBABLE BENEFITS OF INCREASING FOLIC-ACID INTAKES
    BOUSHEY, CJ
    BERESFORD, SAA
    OMENN, GS
    MOTULSKY, AG
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (13): : 1049 - 1057
  • [5] A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction
    Brugada, R
    Marian, AJ
    [J]. ATHEROSCLEROSIS, 1997, 128 (01) : 107 - 112
  • [6] Raised plasma homocysteine as a risk factor for retinal vascular occlusive disease
    Cahill, M
    Karabatzaki, M
    Meleady, R
    Refsum, H
    Ueland, P
    Shields, D
    Mooney, D
    Graham, I
    [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 2000, 84 (02) : 154 - 157
  • [7] Clark ZE, 1998, CLIN CHEM, V44, P2360
  • [8] Clarke R, 1998, J Cardiovasc Risk, V5, P249, DOI 10.1097/00043798-199808000-00007
  • [9] Common mutation in methylenetetrahydrofolate reductase - Correlation with homocysteine metabolism and late-onset vascular disease
    Deloughery, TG
    Evans, A
    Sadeghi, A
    McWilliams, J
    Henner, WD
    Taylor, LM
    Press, RD
    [J]. CIRCULATION, 1996, 94 (12) : 3074 - 3078
  • [10] FISKERSTRAND T, 1993, CLIN CHEM, V39, P263