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Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Can lumbar spine bone mineral density predict readmission in denosumab-treated patients with chronic kidney disease?
Ben-Chung Cheng1,2, Ying-Chou Chen3
1Department of Nephrology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Insights
Patients with chronic kidney disease (CKD) receiving denosumab therapy face higher readmission risks with lower bone mineral density (BMD). A lumbar spine T-score below -3 is a key predictor of readmission, indicating a need for improved prevention strategies.
Area of Science:
- Nephrology
- Endocrinology
- Geriatrics
Background:
- Osteoporosis is prevalent in chronic kidney disease (CKD) patients.
- Denosumab is used to treat osteoporosis in CKD.
- Readmission risk in CKD patients on denosumab requires further investigation.
Purpose of the Study:
- To determine if bone mineral density (BMD) impacts readmission risk in CKD patients treated with denosumab.
- To identify BMD as a predictor of readmission in this population.
Main Methods:
- Retrospective case review of 121 CKD patients on denosumab.
- Dual energy X-ray absorptiometry (DXA) for lumbar spine and hip BMD measurement.
- Logistic regression analysis to assess readmission risk factors.
Main Results:
- Lower lumbar spine BMD (T-score -2.94) was observed in readmitted patients compared to non-readmitted patients (T-score -2.09).
- A lumbar spine T-score below -3 was identified as a significant predictor of readmission.
- Decreased BMD correlated with a higher risk of fracture-related readmission.
Conclusions:
- Osteoporosis in CKD patients treated with denosumab is linked to increased readmission.
- Lumbar spine T-score is a critical predictor of readmission risk post-denosumab therapy.
- Optimizing prevention strategies for osteoporosis in CKD patients is crucial for reducing readmissions and improving outcomes.
Abstract:
This study investigated whether bone mineral density (BMD) affects readmission risk in patients with chronic kidney diseases (CKD) who received denosumab therapy. The study design was a retrospective case review of patients with CKD. Baseline age, sex, and body mass index were recorded for all patients included in the study. All comorbidities were recorded. All subjects underwent dual energy X-ray absorptiometry assay of the lumbar spine and right hip for BMD. The primary outcome was readmission. Predictive variables were categorized and compared between readmitted and non-readmitted patients. Logistic regression was used for multivariable analysis. A total of 121 patients with CKD who received denosumab therapy were enrolled. Of these, 29 were readmitted within 2 years, and 92 had no readmission. The lumbar BMD differed between the readmission (-2.94±0.68) and non-readmission (-2.09±1.48) groups. The readmission group had a lower T score than the non-readmission group. When adjusted for potential confounding factors, a decreased lumbar BMD had a higher readmission risk. When the cut-off points determined by receiver operating characteristic curve analysis were applied, the most precise point was set at a T score of -3. Osteoporosis in patients with CKD is associated with a high risk of readmission; the best predictor after denosumab therapy was the lumbar spine T score. A lower T score (especially if <-3) was associated with a higher probability of fracture readmission. It is essential to optimize primary and secondary prevention in these patients to improve their quality of life.
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