Resolution of subclinical porphyria cutanea tarda after hepatitis C eradication with direct‐acting anti‐virals
Open Access
- 15 April 2020
- journal article
- research article
- Published by Wiley in Alimentary Pharmacology & Therapeutics
- Vol. 51 (10), 968-973
- https://doi.org/10.1111/apt.15703
Abstract
Background Hepatitis C virus (HCV) is a risk factor for porphyria cutanea tarda (PCT), a rare disease originating in the liver characterised by overproduction of porphyrins. Although hepatitis C infection is highly prevalent among patients with porphyria, only a minority of hepatitis C patients develop PCT. Aims To explore the presence of porphyrin abnormalities in a cohort of asymptomatic hepatitis C‐infected patients and the impact of anti‐viral therapy. Methods Eighty‐four consecutive patients with HCV infection treated with direct‐acting antivirals after 1 January 2018 were longitudinally evaluated for the presence of porphyrin abnormalities. Those patients with biochemical abnormalities at baseline were additionally evaluated at follow‐up. Porphyrins in urine were screened by fluorometry and isomer separation was performed by liquid chromatography. Results In five patients, all of them asymptomatic, porphyrin profile abnormalities were detected: three presented significant increased urinary porphyrins with a typical PCT profile, and two showed normal levels of urinary porphyrins, but abnormal porphyria‐like profiles. Urine evaluation after hepatitis C cure showed complete normalisation of the urinary porphyrins in all patients, confirming the biochemical cure of the disease. Conclusions We document the existence of rare cases of hepatitis C‐infected patients with significant uroporphyrinuria in the absence of dermatological manifestations. Anti‐viral therapy normalises the biochemical disorder, preventing patients from presenting PCT associated complications.Funding Information
- CERCA Programme/Generalitat de Catalunya
- Secretaria d'Universitats i Recerca del Departament d'Economia i Coneixement (2017_SGR_1753 (XF))
This publication has 26 references indexed in Scilit:
- Establishing a network of specialist Porphyria centres - effects on diagnostic activities and servicesOrphanet Journal of Rare Diseases, 2012
- Familial and Sporadic Porphyria Cutanea TardaMedicine, 2010
- A porphomethene inhibitor of uroporphyrinogen decarboxylase causes porphyria cutanea tardaProceedings of the National Academy of Sciences, 2007
- Porphyria Cutanea Tarda in a Swedish Population: Risk Factors and ComplicationsActa Dermato-Venereologica, 2005
- Population screening for hemochromatosis: a study in 5370 Spanish blood donorsJournal of Hepatology, 2003
- Upregulation of Interleukin-12 and -17 in Active Inflammatory Bowel DiseaseScandinavian Journal of Gastroenterology, 2003
- Porphyria cutanea tarda, hepatitis C, and HFE gene mutations in north america†Hepatology, 1998
- Porphyria Cutanea TardaSeminars in Liver Disease, 1998
- Hepatitis C Virus and Porphyria Cutanea Tarda: Evidence of A Strong AssociationHepatology, 1992
- The Enzymatic Defect in Porphyria Cutanea TardaNew England Journal of Medicine, 1982