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The Covert Surge: Murine Bile Acid Levels Are Associated With Pruritus in Pediatric Autoimmune Sclerosing Cholangitis.
Meinel, Katharina; Szabo, Doloresz; Dezsofi, Antal; Pohl, Sina; Strini, Tanja; Greimel, Theresa; Aguiriano-Moser, Victor; Haidl, Harald; Wagner, Martin; Schlagenhauf, Axel; Jahnel, Jörg.
Afiliación
  • Meinel K; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Szabo D; First Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Dezsofi A; First Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Pohl S; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Strini T; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Greimel T; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Aguiriano-Moser V; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Haidl H; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Wagner M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Schlagenhauf A; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
  • Jahnel J; Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Front Pediatr ; 10: 903360, 2022.
Article en En | MEDLINE | ID: mdl-35633951
ABSTRACT

Objectives:

The exact etiology of pruritus in chronic cholestasis is unknown. Pruritus intensity does not correlate with common biochemical indices and there is a lack of biomarkers guiding diagnosis and treatment. We explored profiles of bile acids (BA) and muricholic acids (MCA) as well as autotaxin (ATX) antigen levels as potential circulating biomarkers of pruritus in pediatric patients.

Methods:

In 27 pediatric cholestatic patients [autoimmune sclerosing cholangitis (ASC) n = 20 (with pruritus n = 6, without pruritus n = 14); progressive familial intrahepatic cholestasis (PFIC) n = 7 (with pruritus n = 5, without pruritus n = 2)] and 23 age-matched controls pruritus was assessed by a visual analog scale of pruritus (PVAS). We obtained profiles of serum human BA including MCA using a mass-spectrometry assay and ATX antigen levels with a commercial ELISA.

Results:

PFIC and ASC patients exhibited significantly higher BA-, and MCA levels, than healthy controls, but only PFIC patients showed elevated ATX antigen levels higher [median 1,650 ng/ml, interquartile rang (IQR) 776.9-3,742] compared to controls (median 315.9 ng/ml, IQR 251.1-417.2; PFIC p = 0.0003). ASC patients with pruritus showed only a minor increase in total BA (tBA) levels (median 76.5 µmol/L, IQR 54.7-205), but strikingly higher T-conjugated BA (median 16.4 µmol/L, IQR 8.9-41.4) and total MCA (tMCA) (median 1.15 µmol/L, IQR 0.77-2.44) levels compared to ASC patients without pruritus (tBA median 24.3 µmol/L, IQR 16.2-80.8; p < 0.0408; T-conjugated BA median 1.3 µmol/L, IQR 0.8-4.9; p = 0.0023; tMCA median 0.30 µmol/L, IQR 0.13-0.64, p = 0.0033). BA/MCA profiles distinctly differed depending on presence/absence of pruritus. Different from PFIC patients, ATX antigen levels were not significantly elevated in ASC patients with (median 665.8 ng/ml, IQR 357.8-1,203) and without pruritus (median 391.0 ng/ml, IQR 283.2-485.6). In ASC patients, tBA, tMCA, and ATX antigen levels did not correlate with pruritus severity.

Conclusion:

Despite the same underlying disease, pediatric ASC patients with pruritus exhibit significantly altered BA profiles and MCA levels compared to ASC patients without pruritus. ATX antigen levels seem to have little diagnostic or prognostic meaning in ASC patients. An increased ATX activity alone seems not to be causal for pruritus genesis in ASC patients. Clinical Trial Registration [www.drks.de], identifier [DRKS00026913].
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Risk_factors_studies Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Risk_factors_studies Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: Austria