Kulkarni Chiraag, Cholankeril George, Fardeen Touran, Rathkey Joseph, Khan Samir, Murag Soumya, Lerrigo Robert, Kamal Ahmad, Mannalithara Ajitha, Jalal Prasun, Ahmed Aijaz, Vierling John, Goel Aparna, Sinha Sidhartha R
Division of Gastroenterology & Hepatology, Department of Medicine, Stanford University, Palo Alto, California, USA.
Section of Gastroenterology & Hepatology, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
Clin Transl Gastroenterol. 2025 Apr 1;16(4):e00816. doi: 10.14309/ctg.0000000000000816.
Patients with primary sclerosing cholangitis (PSC) are at increased risk of acute cholangitis. The epidemiological risks of cholangitis are poorly studied despite the high morbidity associated with this infection. The aim of this study was to understand the impact of statins on acute cholangitis in PSC.
This multicenter, retrospective cohort study assessed data from 294 patients with PSC at Stanford Medical Center, Baylor Medical Center, and Valley Medical Center. Clinical factors associated with the development of cholangitis were identified using multivariable Cox regression.
The patients were predominantly male (68.7%) with a median age at enrollment of 48 years (interquartile range [IQR]: 31.0-60.8). Fifty patients (17.0%) were prescribed statins. The median follow-up time was 6 years (IQR: 2.0-12.0), in which 29.6% (n = 87) developed cholangitis. In multivariable analysis, statins were associated with an 81% reduction in cholangitis (HR 0.19, 95% confidence interval 0.03-0.64). Statins were associated with a lower adjusted incidence of cholangitis at 36 months compared with patients not on statin therapy (incidence of 2.8% vs 12.2%, P < 0.001). Statins were also associated with increased time-to-stricture ( P = 0.004), an outcome known to be associated with PSC complications.
Statin therapy is associated with reduced risk of cholangitis in PSC, possibly by delaying the time to develop dominant or high-grade strictures. In patients with PSC, use of statin therapy may be a beneficial modality to prevent the development of cholangitis and warrants further investigation.
原发性硬化性胆管炎(PSC)患者发生急性胆管炎的风险增加。尽管这种感染的发病率很高,但胆管炎的流行病学风险仍研究不足。本研究的目的是了解他汀类药物对PSC患者急性胆管炎的影响。
这项多中心回顾性队列研究评估了斯坦福医疗中心、贝勒医疗中心和山谷医疗中心294例PSC患者的数据。使用多变量Cox回归确定与胆管炎发生相关的临床因素。
患者以男性为主(68.7%),入组时的中位年龄为48岁(四分位间距[IQR]:31.0 - 60.8)。50例患者(17.0%)服用他汀类药物。中位随访时间为6年(IQR:2.0 - 12.0),其中29.6%(n = 87)发生胆管炎。在多变量分析中,他汀类药物与胆管炎风险降低81%相关(风险比0.19,95%置信区间0.03 - 0.64)。与未接受他汀类药物治疗的患者相比,服用他汀类药物的患者在36个月时调整后的胆管炎发病率更低(发病率分别为2.8%和12.2%,P < 0.001)。他汀类药物还与狭窄发生时间延长相关(P = 0.004),这是一种已知与PSC并发症相关的结果。
他汀类药物治疗与PSC患者胆管炎风险降低相关,可能是通过延迟显性或高度狭窄的发生时间。在PSC患者中,使用他汀类药物治疗可能是预防胆管炎发生的有益方式,值得进一步研究。