# Bone Health and Anti-Osteoporotic Medication Eligibility in Postmenopausal Women Undergoing Bariatric Surgery: The Impact of Age and Modifiable Risk Factors

**Authors:** Line Abdulghani, Hélène Verkindt, Laurine Cadart, Cécile Philippoteaux, Robert Caiazzo, Julien Paccou

PMC · DOI: 10.1007/s00223-026-01484-z · 2026-01-31

## TL;DR

This study finds that nearly one in five older postmenopausal women undergoing bariatric surgery may need anti-osteoporotic medication due to poor bone health.

## Contribution

The study identifies age, smoking, and specific biomarkers as key predictors of anti-osteoporotic medication eligibility in postmenopausal women undergoing bariatric surgery.

## Key findings

- 30.1% of women aged 60 or older were eligible for anti-osteoporotic medication compared to 16.8% of younger women.
- Age ≥60 years, active smoking, and low appendicular lean mass index were independent predictors of medication eligibility.
- Early lifestyle interventions and bone health assessments are recommended to reduce fracture risk in this population.

## Abstract

Postoperative complications after metabolic and bariatric surgery (MBS) increase with age, yet data on bone health in older postmenopausal women remain limited. The 2022 European Calcified Tissue Society (ECTS) position statement recommend anti-osteoporotic medication (AOM) for patients with a T-score ≤ −2 and/or a fragility fracture within the past two years. This study evaluated the prevalence of AOM eligibility according to age (< 60 vs. ≥ 60 years) in postmenopausal women and identified associated risk factors.

We conducted a cross-sectional, observational, single-center study at Lille University Hospital including postmenopausal women referred for bone health evaluation before or after MBS. AOM eligibility was defined according to the 2022 ECTS criteria.

Among 306 postmenopausal women, 173 were < 60 years (group 1) and 133 were ≥ 60 years (group 2). Overall, 69 patients (22.5%) were eligible for AOM, with a significantly higher prevalence in women ≥ 60 years (30.1% vs. 16.8%, p = 0.006). In multivariate analysis, independent predictors of AOM eligibility were age ≥ 60 years (OR = 2.34, 95% CI: 1.19–4.61), active smoking (OR = 2.98, 95% CI: 1.27–7.02), reduced appendicular lean mass index (ALMI < 5.5 kg/m2; OR = 3.72, 95% CI: 1.78–7.78), and elevated iPTH (OR = 1.15, 95% CI: 1.05–1.25 per 10 ng/mL increase).

Nearly one in five postmenopausal women undergoing MBS were eligible for AOM based on the ECTS position statement, with prevalence doubling after 60 years (OR = 2.34). Active smoking, secondary hyperparathyroidism, and low ALMI were key independent risk factors. These findings underscore the importance of systematic bone health assessment and early implementation of lifestyle interventions, alongside AOM, to reduce fracture risk in this vulnerable population.

## Linked entities

- **Diseases:** osteoporosis (MONDO:0005298)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}
- **Diseases:** chronic malnutrition (MESH:D044342), cardiovascular disease (MESH:D002318), fragility fracture (MESH:D005600), Physical inactivity (MESH:C564765), bone loss (MESH:D001847), dyslipidemia (MESH:D050171), fracture (MESH:D050723), rheumatic diseases (MESH:D012216), inflammatory (MESH:D007249), MBS (MESH:D008659), smoking (MESH:D015208), bone resorption (MESH:D001862), estrogen deficiency (MESH:D056828), RYGB (MESH:D013272), chronic kidney disease (MESH:D051436), excess adiposity (MESH:D018205), Sarcopenia (MESH:D055948), musculoskeletal (MESH:D009140), AOM (MESH:D058866), Hypertension (MESH:D006973), obstructive sleep apnea (MESH:D020181), anastomotic strictures (MESH:D003251), ALMI (MESH:D013851), Obesity (MESH:D009765), alcoholism (MESH:D000437), hyperthyroidism (MESH:D006980), Osteoporosis (MESH:D010024), BMD (MESH:D001851), vertebral fractures (MESH:C535781), hip fracture (MESH:D006620), sleep apnea (MESH:D012891), T2DM (MESH:D003924), gastrointestinal ulcers (MESH:D014456), cancers (MESH:D009369), vitamin D deficiency (MESH:D014808), secondary hyperparathyroidism (MESH:D006962)
- **Chemicals:** iPTH (MESH:D010281), vitamin D (MESH:D014807), Alcohol (MESH:D000438), prednisone (MESH:D011241), hydroxyapatite (MESH:D017886), Calcium (MESH:D002118), creatinine (MESH:D003404), 25(OH) vitamin D (-)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858525/full.md

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Source: https://tomesphere.com/paper/PMC12858525