Literature DB >> 35814506

Does Treatment of Erectile Dysfunction With PDE 5 Inhibitor Tadalafil Improve Quality of Life in Male Patients With Compensated Chronic Liver Disease? A Prospective Pilot Study.

Alok Kumar1, Vivek Saraswat1, Gaurav Pande1, Rajesh Kumar2.   

Abstract

Background and aims: Erectile dysfunction (ED) is common in patients with compensated cirrhosis but its impact on the quality of life (QOL) is usually overlooked. This study aimed at determining the frequency of ED in male patients with compensated chronic liver disease (CLD), assessing their QOL and the response to treatment with tadalafil. A secondary aim was to assess the effect of the tadalafil therapy on liver fibrosis, if any.
Methods: Consecutive patients with compensated CLD and advanced liver fibrosis were screened at the baseline with the International Index of Erectile Function-5 (IIEF-5), QOL questionnaire (WHOQOL-BREF), liver stiffness measurements (LSM) made with Fibroscan™ (Echosens, France), and fibrosis index based on 4 factors (FIB-4) scores. Patients with ED meeting eligibility criteria were prescribed PDE5 inhibitor tadalafil 20 mg on alternate days. During the follow-up, IIEF-5, LSM, and FIB-4 were monitored after 3 and 6 months while the WHOQOL-BREF questionnaire was administered at the baseline and at 6 months.
Results: Among 89 patients with CLD and advanced liver fibrosis, ED was present in 43 (48%) and tadalafil was prescribed to 34 patients (38%) meeting exclusion and inclusion criteria. At 3 months follow-up, the mean IIEF 5 score increased from 15.57 ± 4 to 20.78 ± 3.6, (P = 0.0001) and the improvement persisted at 6 months (IIEF-5 score 21.87 ± 2.2; P = 0.12). The physical, social relationships, and environment domains in the WHOQOL-BREF questionnaire showed significant improvement at six months (P < 0.05) but not the psychological domain (P = ns). From a baseline value of 12.69 ± 3.1 kPa, the mean LSM decreased to 11.37 ± 3.9 kPa, (P = 0.02) after 3 months on tadalafil. After 6 months, the LSM further decreased from 11 ± 0.9 to 8.2 ± 3.2 kPa (P = 0.034). FIB-4 values showed a decline from the baseline at 3 months, from 1.52 ± 0.58 to 1.32 ± 0.55, P < 0.05 and at 6 months, from 1.25 ± 0.53 to 0.97 ± 0.36, P > 0.05. The CAP values did not show any significant change. There was an insignificant decline in the SGOT and SGPT levels (P > 0.05) with no significant change in CTP or MELD scores. Conclusions: In the short term, tadalafil improves ED and QOL in patients with CLD and advanced liver fibrosis. It may also reduce liver fibrosis in them. Further studies that include liver histology are needed to confirm this preliminary observation of a possible antifibrotic effect.
© 2022 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALD, alcoholic liver disease; CLD, chronic liver disease; ED, Erectile dysfunction; FIB-4; FIB-4, fibrosis index based on 4 factors; HRQOL, health-related quality of life; IIEF-5; IIEF-5, the International Index of Erectile Function-5; LC, liver cirrhosis; LSM, liver stiffness measurement; MAP, mean arterial pressure; PDE-5 I; PDE5-I, phosphodiesterase inhibitors; PDEs, phosphodiesterases; PPH, porto-pulmonary hypertension; QOL, quality of life; SMT, standard medical therapy; TAA, thioacetamide; TE, transient elastography; WHOQOL-BREF; cAMP, cyclic adenosine monophosphate; cGMP, cyclic guanosine monophosphate; erectile dysfunction

Year:  2022        PMID: 35814506      PMCID: PMC9257884          DOI: 10.1016/j.jceh.2022.01.009

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  45 in total

1.  The anti-inflammatory and anti-fibrotic effects of tadalafil in thioacetamide-induced liver fibrosis in rats.

Authors:  Heba M Mansour; Abeer A A Salama; Rania M Abdel-Salam; Naglaa A Ahmed; Noha N Yassen; Hala F Zaki
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2.  Vitamin D inhibits proliferation and profibrotic marker expression in hepatic stellate cells and decreases thioacetamide-induced liver fibrosis in rats.

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4.  Sildenafil has no effect on portal pressure but lowers arterial pressure in patients with compensated cirrhosis.

Authors:  Puneeta Tandon; Irteza Inayat; Michael Tal; Marcelo Spector; Martha Shea; Roberto J Groszmann; Guadalupe Garcia-Tsao
Journal:  Clin Gastroenterol Hepatol       Date:  2010-02-06       Impact factor: 11.382

5.  An evaluation of an alternative dosing regimen with tadalafil, 3 times/week, for men with erectile dysfunction: SURE study in 14 European countries.

Authors:  Vincenzo Mirone; Pierre Costa; Jan-Erik Damber; Simon Holmes; Ignacio Moncada; Hermann Van Ahlen; Eric Wespes; William H Cordell; Melanie Chan; Danilo Lembo; Lucio Varanese
Journal:  Eur Urol       Date:  2005-03-09       Impact factor: 20.096

6.  Weight Loss Through Lifestyle Modification Significantly Reduces Features of Nonalcoholic Steatohepatitis.

Authors:  Eduardo Vilar-Gomez; Yadina Martinez-Perez; Luis Calzadilla-Bertot; Ana Torres-Gonzalez; Bienvenido Gra-Oramas; Licet Gonzalez-Fabian; Scott L Friedman; Moises Diago; Manuel Romero-Gomez
Journal:  Gastroenterology       Date:  2015-04-10       Impact factor: 22.682

7.  Long-term efficacy of sildenafil and tachyphylaxis effect.

Authors:  R El-Galley; H Rutland; R Talic; T Keane; H Clark
Journal:  J Urol       Date:  2001-09       Impact factor: 7.450

8.  Sildenafil Citrate, a Selective Phosphodiesterase Type 5 Inhibitor:

Authors: 
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Review 9.  Nitric oxide synthases: regulation and function.

Authors:  Ulrich Förstermann; William C Sessa
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10.  Erectile dysfunction in cirrhosis is impacted by liver dysfunction, portal hypertension, diabetes and arterial hypertension.

Authors:  Rafael Paternostro; Birgit B Heinisch; Thomas Reiberger; Mattias Mandorfer; Remy Schwarzer; Berit Seeland; Michael Trauner; Markus Peck-Radosavljevic; Arnulf Ferlitsch
Journal:  Liver Int       Date:  2018-02-20       Impact factor: 5.828

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