时间标签：数据日期 2026-11-03 · 生成时间 2026-11-03 05:30（Asia/Shanghai）｜ 检索窗口 PubMed edat 2026/10/31 – 2026/11/03 ｜ 情报发生日期 2026-11-03
研究问题
However, further studies are needed to determine their incremental value beyond SA alone.；Thus, various studies have been conducted to investigate the correlation between SA levels and different types of CVDs ( Fig.；Although the physiological functions of albumin are well reported, the optimal SA level in elderly patients with CAD remains unclear.
方法
In an epidemiological cross-sectional study, 5,879 elderly Chinese patients (mean age, ≥ 65 years) were included.；A cross-sectional study was conducted from 2009 to 2018 by the National Health and Nutrition Examination Survey involving 17,303 participants.；A prospective observational study was conducted involving 50 patients (mean age, 61.50 ± 9.77 years) with ACS from May 2021 to December 2021.
核心结论
These findings suggested that SA levels may provide additional prognostic information in elderly patients with stable CAD [ 45 ].；SA levels were significantly associated with the incidence of major adverse cardiovascular events (MACEs; hazard ratio (HR), 1.74 per 1 g/dL decrease; 95% CI, 1.34–2.26) and all-cause mortality (HR, 1.74; 95% CI, 1.30–2.33).；Overall, these findings indicate that increased SA levels are associated with better prognosis and survival among elderly patients with CAD; however, this association should be interpreted with caution, as the available evidence is primarily derived from observational studies.
局限
The etiology of CVD is considered to be multifactorial and cannot be described by a single factor.；However, low serum albumin (SA) level remains a prognostic indicator in patients with CVD [ 10 – 12 ].
对本项目的价值
中等价值：属「免疫衰老 / 炎症衰老」方向；血管 / 心血管老化栏目可用作本项目文献库与综述素材。 ｜ 价值分 2.2/5（★★☆☆☆）
全文来源
PubMed PMC JATS（正文 50,466 字符，题名指纹 0.75，已过 DOI 逐字 + 题名指纹 + 正文长度三重归属校验）
原文题录
- 中文题名：血清白蛋白在老年心血管疾病管理中的预后价值
- 英文标题：Prognostic Value of Serum Albumin in Elderly Cardiovascular Disease Management.
- 期刊与标识：Cardiol Res · PMID 42964411 · DOI 10.14740/cr2286 · PMC PMC13719653 · EDAT 2026-10-31