Fifteen-year clinical prognosis and cardiovascular or limb event associated with homocysteine levels in peripheral arterial disease

医学 内科学 狼牙棒 心脏病学 四分位间距 同型半胱氨酸 糖尿病 体质指数 严重肢体缺血 比例危险模型 前瞻性队列研究 2型糖尿病 血管疾病 心肌梗塞 内分泌学 经皮冠状动脉介入治疗 动脉疾病
作者
Hisao Kumakura,Ryuichi Funada,Yae Matsuo,Tadaaki Iwasaki,Kuniki Nakashima,Eitoshi Tsuboi,Shûichi Ichikawa
出处
期刊:Journal of Cardiology [Elsevier BV]
卷期号:82 (5): 423-428
标识
DOI:10.1016/j.jjcc.2023.04.021
摘要

There are limited reports on the relationship between plasma homocysteine (Hcy) levels and long-term all-cause death (ACD), cardiovascular events, or limb events in patients with peripheral arterial disease (PAD). We examined the relationship between plasma Hcy levels and 15-year these events in PAD patients.We performed a prospective cohort study in 955 PAD patients. The patients were divided into four groups based on plasma Hcy levels with median (interquartile range). The endpoints were cumulative incidences of ACD, major adverse cardiovascular events (MACE), and MACE plus limb events (MACLE).The incidences of ACD, MACE, and MACLE were correlated with plasma Hcy levels (P < 0.05). In multiple regression analysis, plasma Hcy had positive correlations with C-reactive protein (CRP), men, and critical limb ischemia (CLI) and negative correlations with estimated glomerular filtration rate (eGFR) and high-density lipoprotein cholesterol (p < 0.05). In Cox multivariate analysis, higher Hcy (HR 1.614, 95 % CI 1.229-2.119, p = 0.001), age, CRP, brain natriuretic peptide (BNP), D-dimer, lower body mass index, ankle brachial pressure index (ABI), serum albumin, eGFR, CLI, coronary heart disease (CHD), cerebrovascular disease, and diabetes were related to ACD; higher Hcy (HR 1.242, 95 % CI 1.004-1.535, p = 0.045), age, BNP, lower ABI, serum albumin, diabetes, and CHD were related to MACE; and higher Hcy (HR 1.290, 95 % CI 1.057-1.574, p = 0.012), BNP, lower ABI, serum albumin, CHD, and diabetes were related to MACLE (P < 0.05). Statins improved ACD, MACE, and MACLE (p < 0.01).Plasma Hcy was a risk factor for 15-year ACD, MACE, and MACLE in patients with PAD.
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