Osteoporosis and Fragility Fractures in Patients with Liver Cirrhosis: Usefulness of FRAX® as a Screening Tool

Author:

Sánchez-Delgado Jordi12ORCID,Profitós Joaquim3,Arévalo Marta4,Lira Alba1,Mármol Carlos5,Miquel Mireia126ORCID,Casas Meritxell1,Vergara Mercedes12,Calvet Xavier12ORCID,Berlanga Eugenio7,del Rio Luís del8,Valero Oliver9,Costa Ester4,Larrosa Marta4,Casado Burgos Enrique4ORCID

Affiliation:

1. Hepatology Unit, Digestive Disease Department, University Hospital Parc Taulí, I3PT Institute Research, Universitat Autònoma de Barcelona, 08208 Sabadell, Spain

2. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Instituto Carlos III, 28029 Madrid, Spain

3. Hospital Consorci de Terrassa, 08227 Terrassa, Spain

4. Rheumatology Department, University Hospital Parc Taulí, I3PT Institute Research, Universitat Autònoma de Barcelona, 08208 Sabadell, Spain

5. Hospital Sant Joan de Déu, 08950 Manresa, Spain

6. Department de Medicina, Universitat de Vic—Universitat Central de Catalunya (UVic-UCC), 08500 Vic, Spain

7. Clinical Analytics Department, University Hospital Parc Taulí, 08208 Sabadell, Spain

8. CETIR Ascires Centre Mèdic, 08029 Barcelona, Spain

9. Department of Statistics, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain

Abstract

Purpose: The purpose of this study is to assess the prevalence of osteoporosis and fragility fractures in patients with liver cirrhosis (LC) and determine the associated risk factors, evaluating the usefulness of FRAX® as a screening method to identify patients at a higher risk of fracture. Methods: This was a cross-sectional study. Demographic, clinical, and analytical data were collected in a randomized sample of LC patients attending the Hepatology Department of a university hospital. We assessed the absolute risk of fracture at 10 years (FRAX®) and based on the bone mineral density (BMD), the presence of morphometric vertebral fracture with a vertebral fracture assessment (VFA), or a thoracic and lumbar X-ray and bone microarchitecture with a trabecular bone score (TBS). Results: Ninety-two patients were included (71% male); the mean age was 63 ± 11.3 years. The main etiology of LC was alcoholism (52.2%), and most patients were Child–Pugh A (80.4%), with a mean model for end-stage liver disease (MELD) score of 10.1 ± 3.6. Sixteen patients (17.4%) had osteoporosis, and fifty-four (58.7%) had osteopenia. Eight patients (8.7%) had suffered at least one fragility fracture. The absolute risk of a major fracture according to FRAX without the BMD was 5.7 ± 4.5%. Risk factors associated with osteoporosis were age and the female sex. BMI > 30 was a protective factor. A FRAX cut-off point for a major fracture > 6.6% had a sensitivity of 69% and a specificity of 85% for a diagnosis of osteoporosis. Conclusions: The prevalence of osteoporosis and fractures in patients with LC is high, particularly in older women. FRAX® may be a useful method to identify candidates for bone densitometry. A FRAX value below 6.6% without the BMD can avoid unnecessary testing.

Funder

grant for initiation to research of the Societat Catalana de Digestologia 2015

Publisher

MDPI AG

Subject

General Medicine

Reference46 articles.

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