S2572 Association of Vitamin D Supplementation in the Development of Osteoporosis and Osteoporosis-Related Fractures in Primary Biliary Cholangitis

Introduction: Vitamin D supplementation is recommended for osteoporosis with chronic liver disease, targeting calcium homeostasis and bone mineralization. Despite widespread use of Vitamin D supplementation, its clinical efficacy in osteoporosis progression and development of fractures has not been rigorously evaluated in PBC population. Methods: We conducted a retrospective cohort study using data from 2 U.S.-based tertiary centers from 2005–2025. Participants included postmenopausal women aged >65 years with primary biliary cholangitis (PBC) and age- and baseline serum vitamin D level-matched controls. All participants maintained consistent vitamin D supplementation (800–1000 IU/day) for ≥1 year. Fracture incidence was ascertained via comprehensive medical record review. Risk factors for fractures were evaluated using univariate and multivariate logistic regression analyses, while longitudinal fracture outcomes were modeled with mixed-effects regression modelling. Results: Among 101 PBC and 208 matched-control patients receiving vitamin D supplementation, PBC patients demonstrated lower mean T-scores (-1.98 vs -1.63; P = 0.05) and lumbar mineral density scores (0.99 vs 1.07; P = 0.01) despite comparable osteopenia and osteoporosis prevalence. Fracture prevalence was higher in PBC compared to controls (56.0% vs 36.1%), with significantly increased risk of multiple fractures (OR = 1.29, P < 0.001). Osteoporosis medication reduced fracture risk (OR = 0.80, P = 0.05). Mixed-effects models revealed diverging 10-year trajectories with only marginal risk reduction in PBC patients from 75% to 62% while substantial risk reduction from 59% to 24% in controls. Conclusion: Standard vitamin D supplementation may not adequately protect PBC patients from fractures, as evidenced by persistently elevated rates and marginal long-term risk reduction. However, in combination with osteoporosis medications, Vitamin D supplementation partially reduced risk of osteoporosis-related fractures. Further studies are needed to identify risk factors of metabolic bone disease progression and fracture development in PBC to individualize prevention and treatment approach in this population.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001137748.76665.f0
Primary Topic
Liver Diseases and Immunity
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

S2572 Association of Vitamin D Supplementation in the Development of Osteoporosis and Osteoporosis-Related Fractures in Primary Biliary Cholangitis

Hussam Kawas, Xaralambos Zervos, Leandro Sierra, Richard McNulty et al.
The American Journal of Gastroenterology
Liver Diseases and Immunity
article

S2572 Association of Vitamin D Supplementation in the Development of Osteoporosis and Osteoporosis-Related Fractures in Primary Biliary Cholangitis

Hussam Kawas, Xaralambos Zervos, Leandro Sierra, Richard McNulty, Omar T. Sims, Sara Osorio Valencia, Juan Armijos, John McMichael, Dian Chiang
article en

Abstract

Introduction: Vitamin D supplementation is recommended for osteoporosis with chronic liver disease, targeting calcium homeostasis and bone mineralization. Despite widespread use of Vitamin D supplementation, its clinical efficacy in osteoporosis progression and development of fractures has not been rigorously evaluated in PBC population. Methods: We conducted a retrospective cohort study using data from 2 U.S.-based tertiary centers from 2005–2025. Participants included postmenopausal women aged >65 years with primary biliary cholangitis (PBC) and age- and baseline serum vitamin D level-matched controls. All participants maintained consistent vitamin D supplementation (800–1000 IU/day) for ≥1 year. Fracture incidence was ascertained via comprehensive medical record review. Risk factors for fractures were evaluated using univariate and multivariate logistic regression analyses, while longitudinal fracture outcomes were modeled with mixed-effects regression modelling. Results: Among 101 PBC and 208 matched-control patients receiving vitamin D supplementation, PBC patients demonstrated lower mean T-scores (-1.98 vs -1.63; P = 0.05) and lumbar mineral density scores (0.99 vs 1.07; P = 0.01) despite comparable osteopenia and osteoporosis prevalence. Fracture prevalence was higher in PBC compared to controls (56.0% vs 36.1%), with significantly increased risk of multiple fractures (OR = 1.29, P < 0.001). Osteoporosis medication reduced fracture risk (OR = 0.80, P = 0.05). Mixed-effects models revealed diverging 10-year trajectories with only marginal risk reduction in PBC patients from 75% to 62% while substantial risk reduction from 59% to 24% in controls. Conclusion: Standard vitamin D supplementation may not adequately protect PBC patients from fractures, as evidenced by persistently elevated rates and marginal long-term risk reduction. However, in combination with osteoporosis medications, Vitamin D supplementation partially reduced risk of osteoporosis-related fractures. Further studies are needed to identify risk factors of metabolic bone disease progression and fracture development in PBC to individualize prevention and treatment approach in this population.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 48%
Liver Diseases and Immunity
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.