Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
Clin Gastroenterol Hepatol. 2018 Aug;16(8):1342-1350.e1. doi: 10.1016/j.cgh.2017.12.033. Epub 2017 Dec 23.
BACKGROUND & AIMS: There are few data from longitudinal studies of trends in primary biliary cholangitis (PBC) among patients under routine clinical care in the United States. We collected data from the Fibrotic Liver Disease consortium to investigate changes in the incidence and prevalence of PBC and the effects of patient demographics, clinical features, and treatment on mortality.
We collected demographic and clinical data for the general patient population as well as PBC patients receiving care from 11 health systems in different regions of the United States (Northeast, Midwest, Northwest, and South) from January 1, 2003, through December 31, 2014. Annual percentage changes in PBC prevalence and incidence were estimated using join-point Poisson regression. Differences based on race, age, and gender were calculated with rate ratios. All-cause mortality was estimated using Cox regression with adjustment for patient characteristics and treatment with ursodeoxycholic acid (UDCA). Propensity scores were used to adjust for treatment selection bias. Analyses were adjusted by geographic regions.
In our racially diverse cohort of 3488 patients with PBC (21% Hispanic, 8% African American, 7% Asian American), 70% had ever received UDCA. From 2006 through 2014, the prevalence of PBC increased from 21.7 to 39.2 per 100,000 persons. Adjusted annual percentage changes in prevalence differed among age groups (≤40 y, 41-50 y, 51-60 y, 61-70 y, and >70 y), ranging from 3.0% to 7.5% (P < .05). Incidence did not change significantly during the study period (4.2 vs 4.3 per 100,000 person-years in 2006 and 2014, respectively; P = .98). Ratios of prevalence for women vs men (3.9:1) and incidence for women vs men (3.2:1) were consistent over the study period. Among African Americans, the prevalence of PBC increased from 16.9 to 30.8 per 100,000 during the study period, and annual incidence ranged from 2.6 to 6.6 per 100,000 person-years. In adjusted analyses, an increased level of alkaline phosphatase at baseline was associated with significantly higher mortality (adjusted hazard ratios [aHR], 1.24; 95% CI, 1.04-1.48 for patients with levels 1-2 times the upper limit of normal and aHR, 2.27; 95% CI, 1.88-2.73 for patients with levels more than 3 times the upper limit of normal). UDCA treatment was associated with significantly reduced mortality (aHR, 0.57; 95% CI, 0.52-0.64).
In an analysis of data from patients receiving routine clinical care in Fibrotic Liver Disease Consortium health systems, we found that the prevalence of PBC increased from 2004 through 2014, despite steady incidence. Patient demographic and clinical characteristics, as well as UDCA treatment, affected mortality.
在美国,常规临床护理中很少有关于原发性胆汁性胆管炎(PBC)趋势的纵向研究数据。我们从纤维化肝脏疾病联盟收集数据,以调查 PBC 的发病率和患病率的变化,以及患者人口统计学、临床特征和治疗对死亡率的影响。
我们从美国 11 个不同地区(东北部、中西部、西北部和南部)的 11 个卫生系统收集了一般患者人群以及接受治疗的 PBC 患者的人口统计学和临床数据。使用连接点泊松回归估计 PBC 患病率和发病率的年变化百分比。根据种族、年龄和性别计算差异的比率。使用 Cox 回归估计所有原因死亡率,并调整患者特征和熊去氧胆酸(UDCA)治疗的影响。使用倾向评分调整治疗选择偏差。分析按地理区域进行调整。
在我们的种族多样化队列中,有 3488 名 PBC 患者(21%为西班牙裔,8%为非裔美国人,7%为亚裔美国人),其中 70%曾接受过 UDCA 治疗。从 2006 年到 2014 年,PBC 的患病率从每 100000 人 21.7 增加到 39.2。不同年龄组(≤40 岁、41-50 岁、51-60 岁、61-70 岁和>70 岁)的患病率调整年变化百分比差异显著,范围为 3.0%至 7.5%(P<.05)。在研究期间,发病率没有显著变化(2006 年和 2014 年分别为每 100000 人 4.2 比 4.3);P=0.98)。女性与男性的患病率比(3.9:1)和女性与男性的发病率比(3.2:1)在整个研究期间保持一致。在非裔美国人中,PBC 的患病率从研究期间的每 100000 人 16.9 增加到 30.8,年发病率范围为每 100000 人 2.6 至 6.6。在调整分析中,基线碱性磷酸酶水平升高与死亡率显著相关(调整后的危险比[aHR],1.24;95%CI,1.04-1.48,水平为正常上限的 1-2 倍;aHR,2.27;95%CI,1.88-2.73,水平为正常上限的 3 倍以上)。UDCA 治疗与死亡率显著降低相关(aHR,0.57;95%CI,0.52-0.64)。
在对纤维化肝脏疾病联盟卫生系统接受常规临床护理的患者数据进行分析时,我们发现尽管发病率稳定,但从 2004 年到 2014 年,PBC 的患病率仍在增加。患者的人口统计学和临床特征以及 UDCA 治疗影响死亡率。