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维生素B12和叶酸缺乏及/或一碳代谢遗传性疾病所致中度和重度高同型半胱氨酸血症的心血管表现:对连续患者进行的3.5年回顾性横断面研究

Cardiovascular manifestations of intermediate and major hyperhomocysteinemia due to vitamin B12 and folate deficiency and/or inherited disorders of one-carbon metabolism: a 3.5-year retrospective cross-sectional study of consecutive patients.

作者信息

Levy Julien, Rodriguez-Guéant Rosa-Maria, Oussalah Abderrahim, Jeannesson Elise, Wahl Denis, Ziuly Stéphane, Guéant Jean-Louis

机构信息

Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital (CHRU) of Nancy, Nancy, France.

Reference Centre for Inborn Errors of Metabolism (ORPHA67872), University Hospital (CHRU) of Nancy, Nancy, France.

出版信息

Am J Clin Nutr. 2021 May 8;113(5):1157-1167. doi: 10.1093/ajcn/nqaa432.

Abstract

BACKGROUND

The association of moderate hyperhomocysteinemia (HHcy) (15-30 μmol/L) with cardiovascular diseases (CVD) has been challenged by the lack of benefit of vitamin supplementation to lowering homocysteine. Consequently, the results of interventional studies have confused the debate regarding the management of patients with intermediate/severe HHcy.

OBJECTIVE

We sought to evaluate the association of intermediate (30-100 μmol/L) and severe (>100 μmol/L) HHcy related to vitamin deficiencies and/or inherited disorders with CVD outcomes.

METHODS

We performed a retrospective cross-sectional study on consecutive patients who underwent a homocysteine assay in a French University Regional Hospital Center. Patients with CVD outcomes were assessed for vitamin B12, folate, Hcy, methylmalonic acid, and next-generation clinical exome sequencing.

RESULTS

We evaluated 165 patients hospitalized for thromboembolic and other cardiovascular (CV) manifestations among 1006 patients consecutively recruited. Among them, 84% (138/165) had Hcy >30 μmol/L, 27% Hcy >50 μmol/L (44/165) and 3% Hcy >100 μmol/L (5/165). HHcy was related to vitamin B12 and/or folate deficiency in 55% (87/165), mutations in one or more genes of one-carbon and/or vitamin B12 metabolisms in 11% (19/165), and severe renal failure in 15% (21/141) of the studied patients. HHcy was the single vascular risk retrieved in almost 9% (15/165) of patients. Sixty % (101/165) of patients received a supplementation to treat HHcy, with a significant decrease in median Hcy from 41 to 17 µmol/L (IQR: 33.6-60.4 compared with 12.1-28). No recurrence of thromboembolic manifestations was observed after supplementation and antithrombotic treatment of patients who had HHcy as a single risk, after ∼4 y of follow-up.

CONCLUSION

The high frequency of intermediate/severe HHcy differs from the frequent moderate HHcy reported in previous observational studies of patients with pre-existing CVD. Our study points out the importance of diagnosing and treating nutritional deficiencies and inherited disorders to reverse intermediate/severe HHcy associated with CVD outcomes.

摘要

背景

中度高同型半胱氨酸血症(HHcy)(15 - 30 μmol/L)与心血管疾病(CVD)之间的关联因补充维生素对降低同型半胱氨酸水平缺乏益处而受到质疑。因此,干预性研究的结果使关于中度/重度HHcy患者管理的争论变得混乱。

目的

我们试图评估中度(30 - 100 μmol/L)和重度(>100 μmol/L)HHcy与维生素缺乏和/或遗传性疾病相关联对CVD结局的影响。

方法

我们对在法国大学地区医院中心接受同型半胱氨酸检测的连续患者进行了一项回顾性横断面研究。对有CVD结局的患者进行维生素B12、叶酸、同型半胱氨酸、甲基丙二酸检测以及下一代临床外显子组测序。

结果

我们评估了连续招募的1006例患者中因血栓栓塞和其他心血管(CV)表现而住院的165例患者。其中,84%(138/165)的患者同型半胱氨酸>30 μmol/L,27%(44/165)的患者同型半胱氨酸>50 μmol/L,3%(5/165)的患者同型半胱氨酸>100 μmol/L。55%(87/165)的HHcy与维生素B12和/或叶酸缺乏有关,11%(19/165)的患者与一碳和/或维生素B12代谢的一个或多个基因突变有关,15%(21/141)的研究患者与严重肾衰竭有关。在近9%(15/165)的患者中,HHcy是唯一检测到的血管风险因素。60%(101/165)的患者接受了治疗HHcy的补充剂,同型半胱氨酸中位数从41 μmol/L显著降至17 μmol/L(四分位间距:33.6 - 60.4与12.1 - 28相比)。在对以HHcy作为单一风险因素的患者进行补充剂治疗和抗血栓治疗后,经过约4年的随访,未观察到血栓栓塞表现复发。

结论

中度/重度HHcy的高发生率与先前对已有CVD患者的观察性研究中频繁报道的中度HHcy不同。我们的研究指出了诊断和治疗营养缺乏及遗传性疾病以逆转与CVD结局相关的中度/重度HHcy的重要性。

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