Sandhu Roopinder K, Ezekowitz Justin A, Hijazi Ziad, Westerbergh Johan, Aulin Julia, Alexander John H, Granger Christopher B, Halvorsen Sigrun, Hanna Michael S, Lopes Renato D, Siegbahn Agneta, Wallentin Lars
Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada.
Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.
Open Heart. 2018 Nov 1;5(2):e000908. doi: 10.1136/openhrt-2018-000908. eCollection 2018.
We investigated the association between obesity and biomarkers indicating cardiac or renal dysfunction or inflammation and their interaction with obesity and outcomes.
A total of 14 753 patients in the Apixaban for Reduction In STroke and Other ThromboemboLic Events in Atrial Fibrillation (ARISTOTLE) trial provided plasma samples at randomisation to apixaban or warfarin. Median follow-up was 1.9 years. Body Mass Index (BMI) was measured at baseline and categorised as normal, 18.5-25 kg/m; overweight, >25 to <30 kg/m; and obese, ≥30 kg/m. We analysed the biomarkers high-sensitivity C reactive protein (hs-CRP), interleukin 6 (IL-6), growth differentiation factor-15 (GDF-15), troponin T and N-terminal B-type natriuretic peptide (NT-pro-BNP). Outcomes included stroke/systemic embolism (SE), myocardial infarction (MI), composite (stroke/SE, MI, or all-cause mortality), all-cause and cardiac mortality, and major bleeding.
Compared with normal BMI, obese patients had significantly higher levels of hs-CRP and IL-6 and lower levels of GDF-15, troponin T and NT-pro-BNP. In multivariable analyses, higher compared with normal BMI was associated with a lower risk of all-cause mortality (overweight: HR 0.73 (95% CI 0.63 to 0.86); obese: 0.67 (0.56 to 0.80), p<0.0001), cardiac death (overweight: HR 0.74 (95% CI 0.60 to 0.93); obese: 0.71 (0.56 to 0.92), p=0.01) and composite endpoint (overweight: 0.80 (0.70 to 0.92); obese: 0.72 (0.62 to 0.84), p<0.0001).
Regardless of biomarkers indicating inflammation or cardiac or renal dysfunction, obesity was independently associated with an improved survival in anticoagulated patients with AF.
NCT00412984.
我们研究了肥胖与提示心脏或肾脏功能障碍或炎症的生物标志物之间的关联,以及它们与肥胖和预后的相互作用。
在阿哌沙班用于降低房颤患者中风和其他血栓栓塞事件(ARISTOTLE)试验中,共有14753名患者在随机分组接受阿哌沙班或华法林治疗时提供了血浆样本。中位随访时间为1.9年。在基线时测量体重指数(BMI),并分为正常(18.5 - 25kg/m²)、超重(>25至<30kg/m²)和肥胖(≥30kg/m²)。我们分析了生物标志物高敏C反应蛋白(hs-CRP)、白细胞介素6(IL-6)、生长分化因子-15(GDF-15)、肌钙蛋白T和N末端B型利钠肽(NT-pro-BNP)。结局包括中风/全身性栓塞(SE)、心肌梗死(MI)、复合终点(中风/SE、MI或全因死亡率)、全因和心脏死亡率以及大出血。
与正常BMI相比,肥胖患者的hs-CRP和IL-6水平显著更高,而GDF-15、肌钙蛋白T和NT-pro-BNP水平更低。在多变量分析中,与正常BMI相比,较高的BMI与全因死亡率较低相关(超重:风险比[HR] 0.73(95%置信区间[CI] 0.63至0.86);肥胖:0.67(0.56至0.80),p<0.0001)、心脏死亡(超重:HR 0.74(95% CI 0.60至0.93);肥胖:0.71(0.56至0.92),p = 0.01)和复合终点(超重:0.80(0.70至0.92);肥胖:0.72(0.62至0.84),p<0.0001)。
无论生物标志物提示炎症或心脏或肾脏功能障碍如何,肥胖与接受抗凝治疗的房颤患者生存率提高独立相关。
NCT00412984。