Tien Ni, Wu Tien-Yuan, Lin Cheng-Li, Wu Chia-Jui, Hsu Chung-Y, Fang Yi-Jen, Lim Yun-Ping
Department of Laboratory Medicine, China Medical University Hospital, Taichung, Taiwan.
Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
Front Med (Lausanne). 2022 Jun 13;9:910623. doi: 10.3389/fmed.2022.910623. eCollection 2022.
Patients with inflammatory bowel disease (IBD) present a higher risk of developing cardiovascular diseases (CVDs) due to chronic inflammation, which plays an essential role in atherogenesis. Hyperlipidemia is another risk factor for CVDs; however, the association between IBD, IBD medications, and hyperlipidemia remains controversial. We conducted a nationwide, population-based, retrospective, cohort study to examine the effect of IBD and IBD medications on the risk of developing hyperlipidemia. The effects of IBD medications on the expression of lipogenesis-related hepatic genes were also evaluated. We obtained data from the Longitudinal Health Insurance Database of Taiwan from patients with new-onset IBD and a comparison cohort of patients without IBD. A Cox proportional hazards regression model was used to analyze the difference in the risk of developing hyperlipidemia between the two cohorts. We also examined the influence of IBD medications on the expression of lipogenesis-related hepatic genes. After adjusting for comorbidities and confounding factors, the case group ( = 14,524) had a higher risk for hyperlipidemia than the control group ( = 14,524) [adjusted hazards ratio (aHR), 2.18]. Patients with IBD that did not receive IBD medications exhibited a significantly higher risk of hyperlipidemia (aHR, 2.20). In those treated with IBD medications, the risk of developing hyperlipidemia was significantly lowered than those without such medications (all aHR ≤ 0.45). Gene expression analysis indicated that IBD medications downregulated the expression of lipogenesis-related genes. Screening blood lipids in IBD patients is needed to explore the specific role and impact of IBD medications in the development of CVD.
炎症性肠病(IBD)患者由于慢性炎症而呈现出更高的患心血管疾病(CVD)风险,慢性炎症在动脉粥样硬化形成中起着至关重要的作用。高脂血症是CVD的另一个风险因素;然而,IBD、IBD药物与高脂血症之间的关联仍存在争议。我们进行了一项全国性的、基于人群的回顾性队列研究,以检验IBD和IBD药物对发生高脂血症风险的影响。还评估了IBD药物对肝脏脂肪生成相关基因表达的影响。我们从台湾纵向健康保险数据库中获取了新发IBD患者以及无IBD的对照队列患者的数据。采用Cox比例风险回归模型分析两组发生高脂血症风险的差异。我们还研究了IBD药物对肝脏脂肪生成相关基因表达的影响。在调整合并症和混杂因素后,病例组(n = 14,524)患高脂血症的风险高于对照组(n = 14,524)[调整后风险比(aHR),2.18]。未接受IBD药物治疗的IBD患者患高脂血症的风险显著更高(aHR,2.20)。在接受IBD药物治疗的患者中,发生高脂血症的风险显著低于未接受此类药物治疗的患者(所有aHR≤0.45)。基因表达分析表明,IBD药物下调了脂肪生成相关基因的表达。需要对IBD患者进行血脂筛查,以探索IBD药物在CVD发生发展中的具体作用和影响。