Literature DB >> 29066370

Factors Associated With Prevalence and Treatment of Primary Biliary Cholangitis in United States Health Systems.

Mei Lu1, Jia Li2, Irina V Haller3, Robert J Romanelli4, Jeffrey J VanWormer5, Carla V Rodriguez6, Marsha A Raebel7, Joseph A Boscarino8, Mark A Schmidt9, Yihe G Daida10, Amandeep Sahota11, Jennifer Vincent12, Christopher L Bowlus13, Keith Lindor14, Loralee B Rupp15, Stuart C Gordon16.   

Abstract

BACKGROUND & AIMS: Reported prevalence of primary biliary cholangitis (PBC) varies widely. Demographic features and treatment patterns are not well characterized in the United States (US). We analyzed data from the Fibrotic Liver Disease (FOLD) Consortium, drawn from 11 geographically diverse health systems, to investigate epidemiologic factors and treatment of PBC in the US.
METHODS: We developed a validated electronic health record-based classification model to identify patients with PBC in the FOLD database from 2003 through 2014. We used multivariable modeling to assess the effects of factors associated with PBC prevalence and treatment with ursodeoxycholic acid (UDCA).
RESULTS: We identified 4241 PBC cases among over 14.5 million patients in FOLD health systems; median follow-up was 5 years. Accuracy of the classification model was excellent, with an area under the receiver operating characteristic curve value of 93%, 94% sensitivity, and 87% specificity. The average patient age at diagnosis was 60 years; 21% were Hispanic, 8% were African American, and 7% were Asian American/American Indian/Pacific Islander. Half of the cohort (49%) had elevated levels of alkaline phosphatase, and overall, 70% were treated with UDCA. The estimated 12-year prevalence of PBC was 29.3 per 100,000 persons. Adjusted prevalence values were highest among women (42.8 per 100,000), White patients (29.6 per 100,000), and patients 60-70 years old (44.7 per 100,000). Prevalence was significantly lower among men and African Americans (10.7 and 19.7 per 100,000, respectively) than women and whites; men and African Americans were also less likely to receive UDCA treatment (odds ratios, 0.6 and 0.5, respectively; P < .05).
CONCLUSIONS: In an analysis of a large cohort of patients with PBC receiving routine clinical care, we observed significant differences in PBC prevalence and treatment by gender, race, and age.
Copyright © 2018 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Autoimmune Disease; Classification and Regression Trees; Electronic Health Records; Gender; Primary Biliary Cirrhosis; Racial Disparities

Mesh:

Substances:

Year:  2017        PMID: 29066370     DOI: 10.1016/j.cgh.2017.10.018

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  9 in total

1.  Epidemiology and clinical course of primary biliary cholangitis in the Asia-Pacific region: a systematic review and meta-analysis.

Authors:  Na Zeng; Weijia Duan; Sha Chen; Shanshan Wu; Hong Ma; Xiaojuan Ou; Hong You; Yuanyuan Kong; Jidong Jia
Journal:  Hepatol Int       Date:  2019-09-25       Impact factor: 6.047

2.  Update on New Drugs and Those in Development for the Treatment of Primary Biliary Cholangitis.

Authors:  Runalia Bahar; Kimberly A Wong; Chung H Liu; Christopher L Bowlus
Journal:  Gastroenterol Hepatol (N Y)       Date:  2018-03

3.  Validity of an Automated Algorithm to Identify Cirrhosis Using Electronic Health Records in Patients with Primary Biliary Cholangitis.

Authors:  Mei Lu; Christopher L Bowlus; Keith Lindor; Carla V Rodriguez-Watson; Robert J Romanelli; Irina V Haller; Heather Anderson; Jeffrey J VanWormer; Joseph A Boscarino; Mark A Schmidt; Yihe G Daida; Amandeep Sahota; Jennifer Vincent; Jia Li; Sheri Trudeau; Loralee B Rupp; Stuart C Gordon
Journal:  Clin Epidemiol       Date:  2020-11-10       Impact factor: 4.790

4.  Metabolomic biomarkers are associated with mortality in patients with cirrhosis caused by primary biliary cholangitis or primary sclerosing cholangitis.

Authors:  Ayse L Mindikoglu; Cristian Coarfa; Antone R Opekun; Vijay H Shah; Juan P Arab; Konstantinos N Lazaridis; Nagireddy Putluri; Chandrashekar R Ambati; Matthew J Robertson; Sridevi Devaraj; Prasun K Jalal; Abbas Rana; John A Goss; Thomas C Dowling; Matthew R Weir; Stephen L Seliger; Jean-Pierre Raufman; David W Bernard; John M Vierling
Journal:  Future Sci OA       Date:  2019-12-17

5.  Widespread gaps in the quality of care for primary biliary cholangitis in UK.

Authors:  Mathuri Sivakumar; Akash Gandhi; Eathar Shakweh; Yu Meng Li; Niloufar Safinia; Belinda Claire Smith; Aileen Marshall; Lucy Turner; Ashis Mukhopadhya; Hasan Nadim Haboubi; Rebecca Vincent; Huey Kuan Tan; Laith Alrubaiy; David E J Jones
Journal:  Frontline Gastroenterol       Date:  2021-03-09

6.  Disease burden of primary biliary cholangitis and associated pruritus based on a cross-sectional US claims analysis.

Authors:  Usha Gungabissoon; Daniel C Gibbons; Gema Requena; Andrea Ribeiro de Souza; Helen Smith
Journal:  BMJ Open Gastroenterol       Date:  2022-08

7.  Factors Explaining the Coincidence of Smoldering Multiple Myeloma and Primary Biliary Cholangitis: A Case Report.

Authors:  Mirna El Dirani; Julius M Nagaratnam; Samer Kholoki
Journal:  Cureus       Date:  2022-07-13

8.  External Validation of UDCA Response Score in Slovak and Croatian Patients with Primary Biliary Cholangitis.

Authors:  Jakub Gazda; Martin Janicko; Sylvia Drazilova; Ivica Grgurevic; Tajana Filipec Kanizaj; Tomas Koller; Beatrica Bodorovska; Maja Mijic; Ivana Mikolasevic; Ivana Knezevic Stromar; Branislav Kucinsky; Matej Gazda; Peter Jarcuska
Journal:  Can J Gastroenterol Hepatol       Date:  2021-06-22

Review 9.  Emerging therapies for PBC.

Authors:  David Maxwell Hunter Chascsa; Keith Douglas Lindor
Journal:  J Gastroenterol       Date:  2020-01-22       Impact factor: 7.527

  9 in total

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