Center for Liver Diseases, Department of Medicine, Inova Fairfax Hospital.
Betty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church.
J Clin Gastroenterol. 2019 Oct;53(9):693-698. doi: 10.1097/MCG.0000000000001120.
Although relatively, primary biliary cholangitis (PBC) is an important cause of nonalcoholic chronic liver disease which may lead to liver transplantation. PBC patients with alkaline phosphatase (ALP) ≥1.5× the upper limit of normal (ULN) tend to have a more aggressive course. The study was designed to identify factors associated with ALP≥1.5×ULN or cirrhosis in PBC and to evaluate concomitant health care resource utilization.
We used a large real-world database that contained comprehensive and continuous electronic medical recored/claims data from over 500 health care practices or systems from the United States.
Of 195 million patients included in the database, 36,317 were adults with PBC. After applying exclusion criteria, 15,875 patients comprised the final PBC cohort (63.0±13.5 y, 78% female, 71% privately insured, 5% covered by Medicaid, 57% with other autoimmune diseases, 46% with cirrhosis); 6083 (38%) had ALP≥1.5×ULN. Patients with ALP≥1.5×ULN were more frequently female, less covered by Medicaid, had more pruritus, cirrhosis, and other autoimmune diseases (P<0.05). In multivariate analysis, older age, female gender, the presence of other autoimmune diseases, and having compensated or decompensated cirrhosis were independently associated with having ALP≥1.5×ULN in PBC (P<0.05). In contrast, being male was associated with higher risk of cirrhosis in PBC [odds ratio 2.3 (95% confidence interval, 2.1-2.5)]. Patients with ALP≥1.5×ULN and/or with cirrhosis also incurred substantially more health care resource utilization (P<0.05).
Many clinical, sociodemographic, and economic factors are associated with a potentially more aggressive profile of PBC with elevated ALP. These data may inform clinicians to implement management strategies to optimize care of these patients.
尽管原发性胆汁性胆管炎(PBC)相对而言是导致非酒精性慢性肝病的一个重要原因,可能需要进行肝移植,但碱性磷酸酶(ALP)≥正常值上限(ULN)1.5 倍的 PBC 患者往往具有更具侵袭性的病程。本研究旨在确定与 PBC 中 ALP≥1.5×ULN 或肝硬化相关的因素,并评估同时发生的医疗保健资源利用情况。
我们使用了一个大型真实世界数据库,该数据库包含来自美国 500 多个医疗保健机构或系统的全面且连续的电子病历/索赔数据。
在数据库包含的 1.95 亿患者中,有 36317 名成年人患有 PBC。在应用排除标准后,最终纳入了 15875 名患者作为 PBC 队列(63.0±13.5 岁,78%为女性,71%为私人保险,5%为医疗补助保险,57%患有其他自身免疫性疾病,46%患有肝硬化);其中 6083 名(38%)患者的 ALP≥1.5×ULN。ALP≥1.5×ULN 的患者更常为女性,较少受医疗补助保险覆盖,瘙痒、肝硬化和其他自身免疫性疾病更为常见(P<0.05)。多变量分析显示,年龄较大、女性、存在其他自身免疫性疾病以及代偿性或失代偿性肝硬化与 PBC 中 ALP≥1.5×ULN 独立相关(P<0.05)。相比之下,男性患有 PBC 时肝硬化的风险更高[比值比 2.3(95%置信区间,2.1-2.5)]。ALP≥1.5×ULN 和/或肝硬化的患者还会产生更多的医疗保健资源利用(P<0.05)。
许多临床、社会人口统计学和经济因素与 ALP 升高的 PBC 更具侵袭性特征相关。这些数据可能为临床医生提供信息,以便实施管理策略来优化这些患者的治疗。