Community-living nonagenarians in Northern Ireland have lower plasma homocysteine but similar methylenetetrahydrofolate reductase thermolabile genotype prevalence compared to 70-89-year-old subjects

被引:26
作者
Rea, IM
McMaster, D
Woodside, JV
Young, IS
Archbold, GPR
Linton, T
Lennox, S
McNulty, H
Harmon, DL
Whitehead, AS
机构
[1] Queens Univ Belfast, Cardiovasc Res Ctr, Belfast, Antrim, North Ireland
[2] UCL, Dept Surg, London, England
[3] Belfast City Hosp, Biochem Lab, Belfast BT9 7AD, Antrim, North Ireland
[4] Univ Ulster, No Ireland Ctr Diet & Hlth, Coleraine BT52 1SA, Londonderry, North Ireland
[5] Univ Coll Dublin, Dept Pathol, Dublin 2, Ireland
[6] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
关键词
homocysteine; aging; nonagenarian; GFR; MTHFR; B vitamins;
D O I
10.1016/S0021-9150(99)00417-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This cross-sectional study assessed relationships between plasma homocysteine, 'thermolabile' methylenetetrahydrofolatereductase (MTHFR) genotype, B vitamin status and measures of renal function in elderly (70-89 years) and nonagenarian (90 + years) subjects, with the hypothesis that octo/nonagenarian subjects who remain healthy into old age as defined by 'Senieur' status might show reduced genetic or environmental risk factors usually associated with hyperhomocysteinaemia. Plasma homocysteine was 9.1 mu mol/l (geometric mean [GM]) for all elderly subjects. Intriguingly, homocysteine was significantly lower in 90 + (GM; 8.2 mu mol/l) compared to 70-89-year-old subjects (GM; 9.8 mu mol/l) despite significantly lower glomerular filtration rate (GFR) and serum B12 in nonagenarian subjects and comparable MTHFR thermolabile (TT) genotype frequency, folate and B6 status to 70-89-year-olds. For all elderly subjects, the odds ratio and 95% confidence intervals for plasma homocysteine being in the highest versus lowest quartile was 4.27 (2.04-8.92) for age < 90 compared > 90 years, 3.4 (1.5-7.8) for serum folate < 10.7 compared > 10.7nmol/l, 3.0 (0.9-10.2) for creatinine > 140 compared < 140 umol/l and 2.1 (1.0-4.4) for male sex. This study shows that plasma homocysteine does not invariably increase with age. Compared to similarly enlisted 70-89-year-olds, apparently well, mentally alert, community-living 90 + year olds approximating 'Senieur' status, show lower homocysteine, which is unexplained by renal function, TT genotype and B vitamin status, suggesting that lower homocysteine may be associated with survival. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:207 / 214
页数:8
相关论文
共 48 条
[1]   Plasma total homocysteine in a representative sample of 972 British men and women aged 65 and over [J].
Bates, CJ ;
Mansoor, MA ;
vanderPols, J ;
Prentice, A ;
Cole, TJ ;
Finch, S .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 1997, 51 (10) :691-697
[2]   A QUANTITATIVE ASSESSMENT OF PLASMA HOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE - PROBABLE BENEFITS OF INCREASING FOLIC-ACID INTAKES [J].
BOUSHEY, CJ ;
BERESFORD, SAA ;
OMENN, GS ;
MOTULSKY, AG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (13) :1049-1057
[3]   Vitamins as homocysteine-lowering agents [J].
Brattstrom, L .
JOURNAL OF NUTRITION, 1996, 126 (04) :S1276-S1280
[4]   Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease -: The result of a meta-analysis [J].
Brattström, L ;
Wilcken, DEL ;
Öhrvik, J ;
Brudin, L .
CIRCULATION, 1998, 98 (23) :2520-2526
[5]   A common methylenetetrahydrofolate reductase gene mutation and longevity [J].
Brattström, L ;
Zhang, Y ;
Hurtig, M ;
Refsum, H ;
Östensson, S ;
Fransson, L ;
Jonés, K ;
Landgren, F ;
Brudin, L ;
Ueland, PM .
ATHEROSCLEROSIS, 1998, 141 (02) :315-319
[6]   HOMOCYSTEINE AND CYSTEINE - DETERMINANTS OF PLASMA-LEVELS IN MIDDLE-AGED AND ELDERLY SUBJECTS [J].
BRATTSTROM, L ;
LINDGREN, A ;
ISRAELSSON, B ;
ANDERSSON, A ;
HULTBERG, B .
JOURNAL OF INTERNAL MEDICINE, 1994, 236 (06) :633-641
[7]  
Brattström L, 1998, BMJ-BRIT MED J, V316, P894, DOI 10.1136/bmj.316.7135.894
[8]   HYPERHOMOCYSTEINEMIA - AN INDEPENDENT RISK FACTOR FOR VASCULAR-DISEASE [J].
CLARKE, R ;
DALY, L ;
ROBINSON, K ;
NAUGHTEN, E ;
CAHALANE, S ;
FOWLER, B ;
GRAHAM, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (17) :1149-1155
[9]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[10]  
Department of Health, 1991, DIET REF VAL FOOD EN