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代谢综合征和种族对 SPRINT 队列中强化血压控制与心血管结局关系的影响。

Influence of metabolic syndrome and race on the relationship between intensive blood pressure control and cardiovascular outcomes in the SPRINT cohort.

机构信息

Division of Endocrinology, Diabetes and Metabolism, Ohio State University, Columbus, Ohio.

Department of Biostatistics, Wake Forest School of Medicine, Winston-Salem, North Carolina.

出版信息

Diabetes Obes Metab. 2018 Mar;20(3):629-637. doi: 10.1111/dom.13127. Epub 2017 Nov 9.

DOI:10.1111/dom.13127
PMID:29024310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5812782/
Abstract

AIMS

To determine whether baseline metabolic syndrome (MetS) modifies the effect of intensive blood pressure control on cardiovascular (CV) outcomes, and whether the effects varied by race/ethnicity.

METHODS

We performed post hoc analyses among non-Hispanic black, non-hispanic white and Hispanic participants, with and without MetS, in the Systolic Blood Pressure Intervention Trial (SPRINT), who were randomized to a systolic blood pressure (SBP) target of <120 mm Hg (intensive group, N = 4544) or an SBP target of <140 mm Hg (standard group, N = 4553). The median follow-up was 3.26 years. The primary outcome was the composite of the first occurrence of myocardial infarction, stroke, heart failure, non-myocardial infarction acute coronary syndrome or CV death.

RESULTS

Overall, 3521/9097 participants (38.7%) met the criteria for MetS at baseline. Baseline characteristics were similar in the two SBP target groups within each MetS subgroup, except body mass index was slightly higher in the standard arm of the MetS subgroup (33.3 ± 5.6 vs 33.0 ± 5.3 kg/m ; P < .01), but were similar across treatment arms in the non-MetS subgroup. The hazard ratio for the primary outcome was similarly reduced in participants with or without baseline MetS: 0.75 (95% confidence interval [CI] 0.57, 0.96) and 0.71 (95% CI 0.57, 0.87), respectively (adjusted P value for treatment by subgroup interaction = .98). Similarly, there was no evidence of treatment × MetS subgroup interaction for all-cause mortality (adjusted interaction P value = .98). The findings were also similar across race/ethnic subgroups.

CONCLUSIONS

In this analysis the CV benefit of intensive SBP control did not differ among participants by baseline MetS status, regardless of race/ethnicity.

摘要

目的

确定基线代谢综合征(MetS)是否会改变强化血压控制对心血管(CV)结局的影响,以及这种影响是否因种族/民族而异。

方法

我们对非西班牙裔黑种人、非西班牙裔白种人和西班牙裔参与者进行了事后分析,这些参与者在收缩期血压干预试验(SPRINT)中患有或不患有 MetS,他们被随机分配到收缩压(SBP)目标值<120mmHg(强化组,N=4544)或 SBP 目标值<140mmHg(标准组,N=4553)。中位随访时间为 3.26 年。主要结局是首次发生心肌梗死、卒中和心力衰竭、非心肌梗死急性冠脉综合征或 CV 死亡的复合事件。

结果

总体而言,9097 名参与者中有 3521 名(38.7%)在基线时符合 MetS 标准。在每个 MetS 亚组的两个 SBP 目标组内,基线特征相似,除了 MetS 亚组的标准治疗组的体重指数稍高(33.3±5.6 vs 33.0±5.3kg/m2;P<.01),但在非 MetS 亚组中,两个治疗组的体重指数相似。基线有或无 MetS 的参与者的主要结局风险比相似降低:0.75(95%置信区间[CI]0.57,0.96)和 0.71(95%CI0.57,0.87)(调整后的亚组间治疗 P 值交互检验为 0.98)。同样,全因死亡率也没有治疗×MetS 亚组相互作用的证据(调整后的交互 P 值为 0.98)。种族/民族亚组的结果也相似。

结论

在这项分析中,强化 SBP 控制的 CV 获益在基线 MetS 状态不同的参与者中没有差异,无论种族/民族如何。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e2d/5812782/e229cfcec324/nihms917055f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e2d/5812782/c3d72a0c6fc3/nihms917055f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e2d/5812782/e229cfcec324/nihms917055f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e2d/5812782/c3d72a0c6fc3/nihms917055f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e2d/5812782/e229cfcec324/nihms917055f2.jpg

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