Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School, Boston, MA
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School, Boston, MA.
J Am Heart Assoc. 2018 May 18;7(11):e008517. doi: 10.1161/JAHA.117.008517.
The aim of this study was to determine whether reducing plasma homocysteine concentrations with long-term, combined treatment with folic acid, vitamin B, and vitamin B alters plasma biomarkers of inflammation and endothelial dysfunction in women at increased risk of cardiovascular disease.
We conducted a blood substudy of 300 treatment-adherent participants (150 in the active treatment group, 150 in the placebo group) in the WAFACS (Women's Antioxidant and Folic Acid Cardiovascular Study), a randomized, double-blind, placebo-controlled trial testing a daily combination of folic acid (2.5 mg), vitamin B (50 mg), vitamin B (1 mg), or matching placebo, in cardiovascular disease prevention among women at increased risk of cardiovascular disease. Plasma concentration of 3 biomarkers of inflammation (C-reactive protein, interleukin-6, and fibrinogen) and a biomarker of endothelial dysfunction (intercellular adhesion molecule 1) were measured at baseline and at the end of treatment and follow-up. After 7.3 years of combined treatment with folic acid, vitamin B, and vitamin B, homocysteine concentrations were reduced by 18% in the active treatment group as compared with the placebo group (<0.001). However, there was no difference between treatment groups in change in blood concentration from baseline to follow-up for C-reactive protein (=0.77), interleukin-6 (=0.91), intercellular adhesion molecule 1 (=0.38), or fibrinogen (=0.68).
These findings indicate that long-term, combined treatment with folic acid, vitamin B, and vitamin B lowers homocysteine concentrations, but does not alter major biomarkers of vascular inflammation, consistent with the lack of clinical cardiovascular disease benefit in the trial.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00000541.
本研究旨在确定长期联合应用叶酸、维生素 B₁₂ 和维生素 B₁ 治疗以降低血浆同型半胱氨酸水平是否会改变心血管疾病风险增加的女性的血浆炎症和内皮功能障碍生物标志物。
我们对 WAFACS(女性抗氧化剂和叶酸心血管研究)中 300 名治疗依从性参与者(活性治疗组 150 名,安慰剂组 150 名)进行了血液亚研究,这是一项随机、双盲、安慰剂对照试验,测试了叶酸(2.5mg)、维生素 B₁₂(50mg)、维生素 B₁(1mg)的每日联合应用或匹配的安慰剂在心血管疾病风险增加的女性中的心血管疾病预防作用。在基线时和治疗结束及随访时测量了 3 种炎症生物标志物(C 反应蛋白、白细胞介素 6 和纤维蛋白原)和 1 种内皮功能障碍生物标志物(细胞间黏附分子 1)的血浆浓度。在叶酸、维生素 B₁₂ 和维生素 B₁ 的联合治疗 7.3 年后,与安慰剂组相比,活性治疗组的同型半胱氨酸浓度降低了 18%(<0.001)。然而,从基线到随访,治疗组之间的 C 反应蛋白(=0.77)、白细胞介素 6(=0.91)、细胞间黏附分子 1(=0.38)或纤维蛋白原(=0.68)的血液浓度变化无差异。
这些发现表明,长期联合应用叶酸、维生素 B₁₂ 和维生素 B₁ 可降低同型半胱氨酸水平,但不会改变主要的血管炎症生物标志物,与试验中缺乏临床心血管疾病获益一致。