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Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry
Rod Carlo Agram Columbres1,2, Vu Luu1,3, Minh Nguyen1
1Division of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of California, Irvine, California, USA.
Introduction/Aims:
VCP multisystem proteinopathy 1 (MSP1), encompassing inclusion body myopathy (IBM), Paget's disease of bone (PDB) and frontotemporal dementia (FTD) (IBMPFD), features progressive muscle weakness, fatty infiltration, and disorganized bone structure in Pagetic bones. The aim of this study is to utilize dual-energy x-ray absorptiometry (DXA) parameters to examine it as a biomarker of muscle and bone disease in MSP1.
Methods:
DXA scans were obtained in 28 patients to assess body composition parameters (bone mineral density [BMD], T-score, total fat, and lean mass) across different groups: total VCP disease (n = 19), including myopathy without Paget's ("myopathy"; n = 12) and myopathy with Paget's ("Paget"; n = 7), and unaffected first-degree relatives serving as controls (n = 6).
Results:
In the VCP disease group, significant declines in left hip BMD and Z-scores were noted versus the control group (p ≤ .03). The VCP disease group showed decreased whole body lean mass % (p = .04), and increased total body fat % (p = .04) compared to controls. Subgroup comparisons indicated osteopenia in 33.3% and osteoporosis in 8.3% of the myopathy group, with 14.3% exhibiting osteopenia in the Paget group. Moreover, the Paget group displayed higher lumbar L1-L4 T-score values than the myopathy group.
Discussion:
In MSP1, DXA revealed reduced bone and lean mass, and increased fat mass. These DXA insights could aid in monitoring disease progression of muscle loss and secondary osteopenia/osteoporosis in MSP1, providing value both clinically and in clinical research.
Insights
Dual-energy x-ray absorptiometry (DXA) reveals reduced bone and lean mass, alongside increased fat mass in VCP multisystem proteinopathy 1 (MSP1). These DXA findings can help monitor muscle loss and bone density changes in MSP1 patients.
Area of Science:
- Biomedical research
- Skeletal and muscle physiology
- Genetic disorders
Background:
- VCP multisystem proteinopathy 1 (MSP1) involves muscle weakness, bone abnormalities, and cognitive decline.
- Current biomarkers for MSP1's muscle and bone manifestations are limited.
Purpose of the Study:
- To evaluate dual-energy x-ray absorptiometry (DXA) parameters as potential biomarkers for muscle and bone disease in MSP1.
- To assess body composition changes in MSP1 patients compared to healthy controls.
Main Methods:
- DXA scans were performed on 28 individuals: 19 with VCP disease (12 myopathy, 7 myopathy with Paget's disease) and 6 controls.
- Body composition parameters including bone mineral density (BMD), T-score, total fat, and lean mass were analyzed.
Main Results:
- VCP disease patients exhibited significantly lower left hip BMD and Z-scores compared to controls.
- The VCP disease group showed decreased whole-body lean mass and increased total body fat percentage.
- Osteopenia and osteoporosis were prevalent in the myopathy subgroup, while the Paget group had higher lumbar spine T-scores.
Conclusions:
- DXA effectively identifies reduced bone and lean mass, and increased fat mass in MSP1.
- DXA parameters show promise for monitoring disease progression, including muscle atrophy and secondary bone loss, in MSP1.
- These findings support the clinical utility of DXA in MSP1 management and research.
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