Higher need for polycystic liver disease therapy in female patients: Sex-specific association between liver volume and need for therapy

Author:

Barten Thijs R.M.12ORCID,Atsma Femke3,van der Meer Adriaan J.4,Gansevoort Ron5,Nevens Frederik26,Drenth Joost P.H.12,Gevers Tom J.G.278

Affiliation:

1. Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands

2. European Reference Network RARE-LIVER, Germany

3. Scientific Institute for Quality of Healthcare, Radboud University Medical Center, Nijmegen, The Netherlands

4. Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands

5. Department of Nephrology, University Medical Centre Groningen, University Hospital Groningen, Groningen, Netherlands

6. Department of Hepatology, University Hospitals KU Leuven, Leuven, Belgium

7. Department of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, The Netherlands

8. Nutrim School for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands

Abstract

Background and Aims: Prognostic tools or biomarkers are urgently needed in polycystic liver disease (PLD) to monitor disease progression and evaluate treatment outcomes. Total liver volume (TLV) is currently used to assess cross-sectional disease severity, and female patients typically have larger livers than males. Therefore, this study explores the sex-specific association between TLV and volume-reducing therapy (VRT). Approach and Results: In this prospective cohort study, we included patients with PLD from European treatment centers. We explored sex-specific differences in the association between baseline TLV and initiation of volume-reducing therapy and determined the cumulative incidence rates of volume-reducing therapy in our cohort. We included 358 patients, of whom 157 (43.9%) received treatment. Treated patients had a higher baseline TLV (median TLV 2.16 vs. 4.34 liter, p < 0.001), were more frequently female (69.7% vs. 89.8%, p < 0.001), and had a higher risk of liver events (HR 4.381, p < 0.001). The cumulative volume-reducing therapy rate at 1 year of follow-up was 21.0% for females compared to 9.1% for males. Baseline TLV was associated with volume-reducing therapy, and there was an interaction with sex (HR females 1.202, p < 0.001; HR males 1.790, p < 0.001; at 1.5 l). Conclusion: Baseline TLV is strongly associated with volume-reducing therapy initiation at follow-up in patients with PLD, with sex-specific differences in this association. Disease staging systems should use TLV to predict the need for future volume-reducing therapy in PLD separately for males and females.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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