尼古丁酰胺暴露后发生重大不良心血管事件的风险:队列研究

Lee Wheless, Ranya Guennoun, Basia M Michalski, Katlyn M Gonzalez, Rachel Weiss, Siwei Zhang, Lydia Yao, Christopher Madden, Hua-Chang Chen, Jefferson Triozzi, Ran Tao, Otis D Wilson, Quinn S Wells, Adriana M Hung, Kristin Bibee, Rebecca I Hartman, Yaomin Xu, Million Veteran Program
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引用次数: 0

摘要

重要性。尼古丁酰胺代谢物最近被认为增加了主要心血管事件(MACE)的风险。目前尚缺乏有关烟酰胺使用者 MACE 临床风险的支持性数据。确定使用烟酰胺是否会导致 MACE 增加。对范德比尔特大学医学中心(VUMC)和退伍军人计划(MVP)两组患者进行回顾性队列研究。将暴露于烟酰胺的患者发生坏死性脑损伤的风险与未暴露于烟酰胺的患者发生坏死性脑损伤的风险进行比较。在VUMC队列中,根据 "烟酰胺 "或 "烟酸 "的关键字输入和人工查看病历,有1228名患者接触过烟酰胺,253名患者未接触过烟酰胺,但有使用建议记录。在 MVP 队列中,有 1594 名患者接触过烟酰胺,与 2694 名未接触过烟酰胺的患者进行了倾向评分匹配。暴露。VUMC 队列中的主要暴露是在病历审查中确认暴露于烟酰胺。MVP 队列的主要暴露是 "烟酰胺 "或 "烟酰胺 "的用药记录。主要结果和测量指标。主要结果是根据验证的表型发生 MACE。两个队列共纳入 6039 名患者,其中 5125 人为男性,平均年龄为 63.2 岁。尼古丁酰胺暴露组和未暴露组在平均年龄、性别、种族和民族方面均无明显差异。在 VUMC 队列中,尼古丁酰胺暴露与 MACE 这一主要结果之间没有明显关联(HR 0.76,95% CI 0.46 - 1.25,p = 0.28)。尼古丁酰胺暴露前的 MACE 与随后的 MACE 密切相关(HR 9.01,95% CI 5.90 - 13.70,p <0.001)。在 MVP 队列中,我们将 MACE 风险因素作为潜在混杂变量进行了调整,结果显示尼古丁酰胺暴露与 MACE 之间无显著相关性(HR 1.00 95% CI 0.75 - 1.32),而既往 MACE 史仍与随后的 MACE 密切相关(HR 9.50,95% CI 6.38 - 14.1)。结论和相关性。在这项对来自两个不同患者群体的 6039 名成人进行的回顾性队列研究中,我们发现尼古丁酰胺暴露的患者发生 MACE 的风险并没有增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Major Adverse Cardiovascular Events following Nicotinamide Exposure: Cohort Study
IMPORTANCE. Nicotinamide metabolites have recently been implicated in increased risk of major cardiovascular events (MACE). Supportive data about clinical risk of MACE for nicotinamide users is lacking. OBJECTIVE. To determine whether nicotinamide use results in an increase of MACE. DESIGN, SETTING, PARTICIPANTS. Retrospective cohort study of two patient cohorts, Vanderbilt University Medical Center (VUMC) and Military Veteran Program (MVP). The risk of MACE in patients exposed to nicotinamide was compared to the risk of MACE in unexposed patients. In the VUMC cohort, 1228 patients were exposed to nicotinamide based on keyword entry for 'nicotinamide' or 'niacinamide' and hand-review of charts, while 253 were unexposed but had documented recommendation for use. In the MVP cohort, there were 1594 with exposure to nicotinamide propensity score matched to 2694 without exposure. EXPOSURES. The primary exposure for the VUMC cohort was a confirmed exposure to nicotinamide in chart review. The primary exposure for the MVP cohort was medication entry for 'nicotinamide' or 'niacinamide'. MAIN OUTCOME(S) AND MEASURE(S). The primary outcome was development of MACE based on a validated phenotype. RESULTS. Between both cohorts, 6039 patients were included, of whom 5125 were male with a mean age of 63.2 years. Neither cohort had significant differences in mean age, sex, race and ethnicity between the nicotinamide exposed and unexposed groups. In the VUMC cohort, there was no significant association between nicotinamide exposure and the primary outcome of MACE (HR 0.76, 95% CI 0.46 - 1.25, p = 0.28). MACE prior to nicotinamide exposure was strongly associated with subsequent MACE (HR 9.01, 95% CI 5.90 - 13.70, p < 0.001). In the MVP cohort, we adjusted for MACE risk factors as potential confounding variables and saw no significant association between nicotinamide exposure and MACE (HR 1.00 95% CI 0.75 - 1.32), while history of prior MACE remained strongly associated with subsequent MACE (HR 9.50, 95% CI 6.38 - 14.1). CONCLUSIONS AND RELEVANCE. In this retrospective cohort study of 6039 adults from two different patient populations, we found no increased risk of MACE in patients with nicotinamide exposure.
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