急性失代偿性心力衰竭患者的认知障碍及其与循环生物标志物的关系

Ying‐Chang Tung, Fu-Chih Hsiao, Chia-Pin Lin, W. Hsu, Pao-Hsien Chu
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引用次数: 4

摘要

背景:认知障碍(CI)在心力衰竭(HF)患者中很常见,但CI与HF或HF患者认知能力下降相关的生物标志物之间的关系尚不清楚。方法:本前瞻性观察性研究调查了急性失代偿性心衰住院的左室射血分数< 40%患者CI的发生率、随后的认知变化以及CI与新型生物标志物之间的关系。分别用Mini-Mental State Examination (MMSE)和Mini-Cog、Beck Depression Inventory (BDI)-II和Kansas City Cardiomyopathy Questionnaire (KCCQ)评估患者的CI、抑郁症状和生活质量。主要终点是一年内全因死亡率或HF住院率的综合。结果:145例入组患者中,54例基线CI(37.2%)。在3个月和1年的随访中,平均MMSE显著增加,BDI-II下降,KCCQ评分增加。MMSE评分的改善主要发生在CI患者。在所检测的生物标志物中,只有生长/分化因子(GDF)-15 > 1621.1 pg/mL与CI显著相关(曲线下面积= 0.64;P = 0.003)。每1000单位GDF-15的增加与主要终点的风险增加相关(风险比= 1.42;95%置信区间:1.17-1.73;P < 0.001)。结论:在伴有CI的HF患者中,认知功能、抑郁和生活质量指标在3个月和1年的随访中有所改善。GDF-15预测CI具有中等判别能力,与较差的HF结局相关。
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Cognitive impairment and its association with circulating biomarkers in patients with acute decompensated heart failure
BACKGROUND Cognitive impairment (CI) is common in patients with heart failure (HF), but the association between CI and biomarkers related to HF or cognitive decline in patients with HF remains unclear. METHODS This prospective observational study investigated the incidence of CI, subsequent cognitive changes, and the association between CI and novel biomarkers in patients with left ventricular ejection fraction < 40% who were hospitalized for acute decompensated HF. Patients were evaluated for CI, depressive symptoms, and quality of life with the Mini-Mental State Examination (MMSE) and the Mini-Cog, Beck Depression Inventory (BDI)-II, and Kansas City Cardiomyopathy Questionnaire (KCCQ), respectively. The primary endpoint was a composite of all-cause mortality or hospitalization for HF at one year. RESULTS Among the 145 patients enrolled in this study, 54 had CI (37.2%) at baseline. The mean MMSE increased significantly at the 3-month and 1-year follow-up, accompanied by decreased BDI-II and increased KCCQ scores. The improvement in the MMSE scores mainly occurred in patients with CI. Among the biomarkers assayed, only growth/differentiation factor (GDF)-15 > 1621.1 pg/mL was significantly associated with CI (area under the curve = 0.64; P = 0.003). An increase in GDF-15 per 1000 units was associated with an increased risk of the primary endpoint (hazard ratio = 1.42; 95% confidence interval: 1.17–1.73; P < 0.001). CONCLUSIONS In patients with HF with CI, cognitive function, depression, and quality of life measures improved at the 3-month and 1-year follow-up. GDF-15 predicted CI with moderate discrimination capacity and was associated with worse HF outcomes.
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