Primary Sclerosing Cholangitis is not Rare Among Blacks in a Multi-Center North American Consortium.
Robert S. Rahimi M.D.
Goldberg, D., C. Levy, K. Yimam, S. Gordon, L. Forman, E. Verna, L. Yu, R. Rahimi, K. Schwarz, B. Eksteen, D. Pratt, T. Boyer, D. Assis and C. Bowlus (2017). “Primary sclerosing cholangitis is not rare among blacks in a multi-center north american consortium.” Clin Gastroenterol Hepatol: 1-9.
In this multi-center North American consortium, we demonstrate that PSC is not rare among black patients. The proportional representation of PSC in black patients compared to each center’s MSA was variable across the 13 centers. Thus although these data do not demonstrate that PSC is as common in black and white patients, PSC in blacks is not as rare as what would be interpreted based on published data. This suggests that existing literature may reflect selection bias related to the demographics of the underlying population from where these studies emerge, rather than a clinical disease largely restricted to white patients. The existing literature bias could prevent adequate evaluation and diagnosis of PSC in non-white patients by practicing clinicians. We were not able to compare the clinical characteristics of PSC in black versus white patients at each center, but have highlighted potential differences of PSC in black patients compared to published data of solely white patients: 1) 58.8% had IBD, compared to 75-80% in white patients; 8 2) 52.2% had isolated intra-hepatic bile duct involvement (diagnosed using cholangiograms per AASLD guidelines), compared to 20-30% in white patients; and 3) 51.3% were male, compared to 60-65% in whites.1 The time from diagnosis to transplant or death was similar to data from published cohort studies of white patients with PSC from tertiary care centers. 1,2,7