Constipation is associated with an increased risk of major adverse cardiac events in a UK population.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of physiology. Heart and circulatory physiology Pub Date : 2024-10-01 Epub Date: 2024-08-16 DOI:10.1152/ajpheart.00519.2024
Tenghao Zheng, Leticia Camargo Tavares, Mauro D'Amato, Francine Z Marques
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Abstract

Traditional cardiovascular risk factors, including hypertension, only explain part of major adverse cardiac events (MACEs). Understanding what other risk factors contribute to MACE is essential for prevention. Constipation shares common risk factors with hypertension and is associated with an increased risk of several cardiovascular diseases. We hypothesized that constipation is an underappreciated risk factor for MACE. We used the population healthcare and genomic data in the UK Biobank (n = 408,354) to study the contribution of constipation (ICD10 K59.0) to the risk of MACE, defined by any episode of acute coronary syndrome (ACS), ischemic stroke, and heart failure (HF). Analyses were controlled for traditional cardiovascular risk factors. We also assessed genetic correlations (rg) between constipation and MACE. Constipation cases (n = 23,814) exhibited a significantly higher risk of MACE compared with those with normal bowel habits [odds ratio (OR) = 2.15, P < 1.00 × 10-300]. Constipation was also significantly associated with individual MACE subgroups, in order: HF (OR = 2.72, P < 1.00 × 10-300), ischemic stroke (OR = 2.36, P = 2.02 × 10-230), and ACS (OR = 1.62, P = 5.82 × 10-113). In comparison with patients with constipation-free hypertension, patients with hypertension with constipation showed significantly higher odds of MACE (OR = 1.68, P = 1.05 × 10-136) and a 34% increased risk of MACE occurrence (P = 2.3 × 10-50) after adjustment for medications that affect gut motility and other traditional cardiovascular risk factors. Finally, we detected positive genetic correlations between constipation and MACE subgroups ACS (rg = 0.27, P = 2.12 × 10-6), ischemic stroke (rg = 0.23, P = 0.011), and HF (rg = 0.21, P = 0.0062). We identified constipation as a potential risk factor independently associated with higher MACE prevalence. These findings warrant further studies on their causal relationship and identification of pathophysiological mechanisms.NEW & NOTEWORTHY Analyzing 408,354 participants of the UK Biobank, we show that constipation cases exhibited a significantly higher risk of major adverse cardiac events (MACEs) than those with regular bowel habits. In comparison with patients with constipation-free hypertension, patients with hypertension with constipation showed significantly higher odds of MACE and a 34% increased risk of subsequent MACE occurrence. Finally, we detected positive genetic correlations between constipation and MACE. This association holds potential for therapeutic exploitation and prevention based on individuals' risk assessment.

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在英国人群中,便秘与重大心脏不良事件的风险增加有关。
背景:包括高血压在内的传统心血管风险因素只能解释重大心脏不良事件(MACE)的部分原因。了解导致 MACE 的其他风险因素对于预防至关重要。便秘与高血压有着共同的风险因素,并与多种心血管疾病的风险增加有关。我们假设便秘是 MACE 的一个未被充分重视的风险因素:我们利用英国生物库(UKBB)(n=408,354)中的人口医疗保健和基因组数据研究了便秘(ICD-10 K59.0)对MACE风险的影响,MACE是指急性冠状动脉综合征(ACS)、缺血性中风和心力衰竭(HF)的任何发作。分析控制了传统的心血管风险因素。我们还评估了便秘与MACE之间的遗传相关性(rg):结果:与排便习惯正常的患者相比,便秘患者(N=23,814)发生 MACE 的风险明显更高(OR=2.15,P-300)。便秘还与各个 MACE 亚组有明显关联,依次为HF(OR=2.72,P-300)、缺血性中风(OR=2.36,P=2.02×10-230)和 ACS(OR=1.62,P=5.82×10-113)。与无便秘的高血压患者相比,有便秘的高血压患者发生 MACE 的几率明显更高(OR=1.68,P=1.05×10-136),在调整了影响肠道蠕动的药物和其他传统心血管风险因素后,发生 MACE 的风险增加了 34%(P=2.3×10-50)。最后,我们发现便秘与MACE亚组ACS(rg=0.27,P=2.12×10-6)、缺血性中风(rg=0.23,P=0.011)和HF(rg=0.21,P=0.0062)之间存在正遗传相关性:我们发现便秘是与 MACE 发生率较高相关的潜在风险因素。这些发现值得进一步研究其因果关系并确定病理生理机制。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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