Literature DB >> 20207827

Pegvisomant-induced liver injury is related to the UGT1A1*28 polymorphism of Gilbert's syndrome.

Ignacio Bernabeu1, Mónica Marazuela, Tomás Lucas, Lourdes Loidi, Cristina Alvarez-Escolá, Manuel Luque-Ramírez, Eva Fernandez-Rodriguez, Amalia-Elisa Paniagua, Celsa Quinteiro, Felipe F Casanueva.   

Abstract

CONTEXT: Pegvisomant (PEG) therapy has been associated with drug-induced liver dysfunction in acromegalic patients. The mechanism of its toxicity remains unknown.
OBJECTIVE: The primary objective was to determine whether or not the UGT1A1*28 polymorphism associated with Gilbert's syndrome influences the development of liver dysfunction during PEG treatment. DESIGN AND
SETTING: A cross-sectional study was conducted in four Spanish university hospitals. PATIENTS: Thirty-six acromegalic patients with active disease, resistant to somatostatin analogs, participated.
RESULTS: The prevalence of the UGT1A1*28 homozygous and heterozygous genotypes in acromegalic patients was 14 and 44%, respectively. Ten patients (28%) developed liver function test (LFT) abnormalities. There was a tendency for more frequent liver function abnormalities in males (70% males vs. 30% females, P = 0.058). Carriers of the UGT1A1*28 polymorphism had a higher incidence of LFT abnormalities than the UGT1A1 wild type (43% carriers vs. 7% wild type, P = 0.024). This difference persisted when adjusted in an all-factors multiple regression analysis [coefficient of determination (R(2)) = 0.463; P = 0.008] for age, gender, alcohol consumption, and UGT1A1*28 polymorphism. A stepwise multivariate likelihood binary logistic regression analysis (R(2) = 0.40; P = 0.003) identified male gender (beta = 7.21; P = 0.033) and UGT1A1*28 polymorphism (beta = 14.1; P = 0.028) as the only significant predictors for the development of LFT abnormalities.
CONCLUSIONS: The UGT1A1*28 genotype and male gender predict an increased incidence of LFT abnormalities during PEG therapy in acromegaly.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20207827     DOI: 10.1210/jc.2009-2547

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  7 in total

1.  ACROSTUDY: the Italian experience.

Authors:  S Grottoli; P Maffei; F Bogazzi; S Cannavò; A Colao; E Ghigo; R Gomez; E Graziano; M Monterubbianesi; P Jonsson; L De Marinis
Journal:  Endocrine       Date:  2014-08-23       Impact factor: 3.633

Review 2.  Uridine 5'-diphospho-glucronosyltrasferase: Its role in pharmacogenomics and human disease.

Authors:  Celia N Sanchez-Dominguez; Hugo L Gallardo-Blanco; Mauricio A Salinas-Santander; Rocio Ortiz-Lopez
Journal:  Exp Ther Med       Date:  2018-05-18       Impact factor: 2.447

3.  Safety of long-term treatment with Pegvisomant: analysis of Spanish patients included in global ACROSTUDY.

Authors:  I Bernabeu; A Pico; E Venegas; J Aller; C Alvarez-Escolá; J A García-Arnés; M Marazuela; P Jonsson; N Mir; M García Vargas
Journal:  Pituitary       Date:  2016-04       Impact factor: 4.107

4.  Medical therapy of acromegaly.

Authors:  U Plöckinger
Journal:  Int J Endocrinol       Date:  2012-04-10       Impact factor: 3.257

5.  Use of Pegvisomant in acromegaly. An Italian Society of Endocrinology guideline.

Authors:  A Giustina; M R Ambrosio; P Beck Peccoz; F Bogazzi; S Cannavo'; L De Marinis; E De Menis; S Grottoli; R Pivonello
Journal:  J Endocrinol Invest       Date:  2014-09-23       Impact factor: 4.256

Review 6.  Combined treatment of somatostatin analogues with pegvisomant in acromegaly.

Authors:  S E Franck; A Muhammad; A J van der Lely; S J C M M Neggers
Journal:  Endocrine       Date:  2015-12-10       Impact factor: 3.633

7.  Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 (⁎) 28 Mutation.

Authors:  Maria Susana Mallea-Gil; Ignacio Bernabeu; Adriana Spiraquis; Alejandra Avangina; Lourdes Loidi; Carolina Ballarino
Journal:  Case Rep Endocrinol       Date:  2016-02-09
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.