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叶酸状态是维持性透析患者空腹血浆总同型半胱氨酸水平的主要决定因素。

Folate status is the major determinant of fasting total plasma homocysteine levels in maintenance dialysis patients.

作者信息

Bostom A G, Shemin D, Lapane K L, Nadeau M R, Sutherland P, Chan J, Rozen R, Yoburn D, Jacques P F, Selhub J, Rosenberg I H

机构信息

Vitamin Bioavailability Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts New England Medical Center, Boston MA 02111, USA.

出版信息

Atherosclerosis. 1996 Jun;123(1-2):193-202. doi: 10.1016/0021-9150(96)05809-1.

Abstract

Limited data are available on the determinants of homocysteinemia or the association between plasma homocysteine (Hcy) levels and prevalent cardiovascular disease (CVD) in maintenance dialysis patients. We assessed etiology of renal failure, residual renal function and dialysis adequacy-related variables, and vitamin status, as determinants of fasting total plasma homocysteine (Hcy) in 75 maintenance dialysis patients. We also assessed the potential interactive effect on plasma Hcy of folate status and a common mutation (ala to val; homozygous val-val frequency approximately 10%) in methylenetetrahydrofolate reductase (MTHFR), a folate-dependent enzyme crucial for the remethylation of homocysteine (Hcy) to methionine. Lastly, we evaluated whether the Hcy levels differed amongst these patients in the presence or absence of prevalent CVD, after adjustment for the traditional CVD risk factors. Fasting total plasma Hcy, folate, pyridoxal 5'-phosphate (PLP; active B6), B12, creatinine, glucose, total and HDL cholesterol levels, and presence of the ala to val MTHFR mutation were determined, and clinical CVD and CVD risk factor prevalence were ascertained. General linear modelling/analysis of covariance revealed: (1) folate status and serum creatinine were the only significant independent predictors of fasting Hcy; (2) there was a significant interaction between presence of the val mutation and folate status, i.e., among patients with plasma folate below the median (< 29.2 ng/ml), geometric mean Hcy levels were 33% greater (29.0 vs. 21.8 microM, P = 0.012) in the pooled homozygotes (val-val) and heterozygotes (ala-val) for the ala to val mutation, vs. normals (ala-ala); (3) there was no association between prevalent CVD and plasma Hcy. Given potentially intractable survivorship effects, prospective cohort studies will be required to clarify the relationship between plasma Hcy or any putative CVD risk factor, and incident CVD in dialysis patients. If a positive association between plasma Hcy and incident CVD can be established in maintenance dialysis patients, the current data provide a rationale for additional folic acid supplementation in this patient population.

摘要

关于维持性透析患者高同型半胱氨酸血症的决定因素,或血浆同型半胱氨酸(Hcy)水平与心血管疾病(CVD)患病率之间的关联,目前可获得的数据有限。我们评估了75例维持性透析患者的肾衰竭病因、残余肾功能和透析充分性相关变量,以及维生素状态,将其作为空腹总血浆同型半胱氨酸(Hcy)的决定因素。我们还评估了叶酸状态与亚甲基四氢叶酸还原酶(MTHFR)中一个常见突变(丙氨酸突变为缬氨酸;纯合缬氨酸 - 缬氨酸频率约为10%)对血浆Hcy的潜在交互作用,MTHFR是一种对同型半胱氨酸(Hcy)再甲基化为甲硫氨酸至关重要的叶酸依赖性酶。最后,我们在对传统CVD危险因素进行校正后,评估了这些患者中存在或不存在CVD时Hcy水平是否存在差异。测定了空腹总血浆Hcy、叶酸、5'-磷酸吡哆醛(PLP;活性B6)、B12、肌酐、葡萄糖、总胆固醇和高密度脂蛋白胆固醇水平,以及丙氨酸到缬氨酸MTHFR突变的存在情况,并确定了临床CVD和CVD危险因素的患病率。一般线性模型/协方差分析显示:(1)叶酸状态和血清肌酐是空腹Hcy仅有的显著独立预测因素;(2)缬氨酸突变的存在与叶酸状态之间存在显著交互作用,即血浆叶酸低于中位数(<29.2 ng/ml)的患者中,丙氨酸到缬氨酸突变的纯合子(缬氨酸 - 缬氨酸)和杂合子(丙氨酸 - 缬氨酸)的几何平均Hcy水平比正常(丙氨酸 - 丙氨酸)高33%(29.0对21.8 microM,P = 0.012);(3)CVD患病率与血浆Hcy之间无关联。鉴于可能存在难以处理的生存效应,需要进行前瞻性队列研究以阐明血浆Hcy或任何假定的CVD危险因素与透析患者新发CVD之间的关系。如果能够在维持性透析患者中确立血浆Hcy与新发CVD之间的正相关关系,那么当前数据为该患者群体额外补充叶酸提供了理论依据。

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