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Risk of chemotherapy-associated liver injury (CALI) in PNPLA3 p.148M allele carriers: Preliminary results of a transient elastography-based study.
Casper, Markus; Zimmermann, Simone; Weber, Susanne N; Arslanow, Anita; Lammert, Frank; Krawczyk, Marcin.
Afiliação
  • Casper M; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany.
  • Zimmermann S; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany.
  • Weber SN; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany.
  • Arslanow A; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany; Department of Internal Medicine I, University Medical Centre of the Johannes Gutenberg-University, Mainz, Germany.
  • Lammert F; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany.
  • Krawczyk M; Department of Medicine II, Saarland University Medical Centre, Saarland University, Homburg, Germany; Laboratory of Metabolic Liver Diseases, Centre for Preclinical Research, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, Warsaw, Poland. Electronic address: marcin
Dig Liver Dis ; 52(1): 102-106, 2020 01.
Article em En | MEDLINE | ID: mdl-31669075
ABSTRACT
BACKGROUND AND

AIMS:

Liver steatosis is one of the side effects of chemotherapy. The PNPLA3 p.I148M, TM6SF2 p.E167K and MBOAT7 p.G17E variants represent genetic determinants for progressive liver diseases. Here, we investigate their association with chemotherapy-associated steatosis. PATIENTS AND

METHODS:

Prospectively, we recruited 87 patients undergoing systemic chemotherapy for gastrointestinal cancers. Hepatic fat (controlled attenuation parameter, CAP) and liver stiffness (LSM) were measured non-invasively before the initiation of chemotherapy (T0) and after at least two (T1) and four cycles (T2). Genetic variants were genotyped using allelic discrimination assays.

RESULTS:

In the final dataset (n = 60) patients demonstrated the following CAP values T0 - 215.0 ±â€¯55.7 dB/m, T1 - 223.3 ±â€¯53.6 dB/m, T2 - 223.4 ±â€¯56.7 dB/m, consistent with mild steatosis. Initial CAP correlated with BMI (P < 0.01) and serum triglyceride concentrations (P = 0.03). Whereas at T0 none of the variants was associated with CAP or LSM, carriers of the prosteatotic PNPLA3 p.148M allele showed significantly (P = 0.008) higher steatosis at T1 as compared to patients carrying the homozygous wild-type genotype [II].

CONCLUSIONS:

Our preliminary results show that patients carrying the PNPLA3 p.I148 M risk allele might be prone to hepatic fat accumulation during chemotherapy. Further studies are be needed to validate the clinical value of these findings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aciltransferases / Fígado Gorduroso / Lipase / Proteínas de Membrana / Antineoplásicos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Dig Liver Dis Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aciltransferases / Fígado Gorduroso / Lipase / Proteínas de Membrana / Antineoplásicos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Dig Liver Dis Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha