Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry

被引:0
作者
Columbres, Rod Carlo Agram [1 ,2 ]
Luu, Vu [1 ,3 ]
Nguyen, Minh [1 ]
Kimonis, Virginia [1 ,4 ,5 ,6 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Pediat, Div Genet & Metab, Irvine, CA USA
[2] William Carey Univ, Coll Osteopath Med, Hattiesburg, MS USA
[3] Western Univ Hlth Sci, Coll Osteopath Med Pacific, Pomona, CA USA
[4] Univ Calif Irvine, Sch Med, Dept Neurol, Irvine, CA USA
[5] Univ Calif Irvine, Sch Med, Dept Pathol, Irvine, CA USA
[6] Univ Calif Irvine, Dept Pediat, Div Genet & Genom Med, Irvine, CA 92697 USA
关键词
DXA; IBMPFD; MSP1; myopathy; VCP/p97; BONE-MINERAL DENSITY; PAGETS-DISEASE; MUSCULAR-DYSTROPHY; BODY-COMPOSITION; SPINE; MUTATIONS; PHENOTYPE; STRENGTH; MASS; DXA;
D O I
10.1002/mus.28095
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 <= 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.
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页码:699 / 707
页数:9
相关论文
共 49 条
[1]   Genotype-phenotype study in patients with valosin-containing protein mutations associated with multisystem proteinopathy [J].
Al-Obeidi, E. ;
Al-Tahan, S. ;
Surampalli, A. ;
Goyal, N. ;
Wang, A. K. ;
Hermann, A. ;
Omizo, M. ;
Smith, C. ;
Mozaffar, T. ;
Kimonis, V. .
CLINICAL GENETICS, 2018, 93 (01) :119-125
[2]   Novel valosin-containing protein mutations associated with multisystem proteinopathy [J].
Al-Tahan, Sejad ;
Al-Obeidi, Ebaa ;
Yoshioka, Hiroshi ;
Lakatos, Anita ;
Weiss, Lan ;
Grafe, Marjorie ;
Palmio, Johanna ;
Wicklund, Matt ;
Harati, Yadollah ;
Omizo, Molly ;
Udd, Bjarne ;
Kimonis, Virginia .
NEUROMUSCULAR DISORDERS, 2018, 28 (06) :491-501
[3]   The role of fat and lean mass in bone loss in older men: Findings from the CHAMP study [J].
Bleicher, Kerrin ;
Cumming, Robert G. ;
Naganathan, Vasikaran ;
Travison, Thomas G. ;
Sambrook, Philip N. ;
Blyth, Fiona M. ;
Handelsman, David J. ;
Le Couteur, David G. ;
Waite, Louise M. ;
Creasey, Helen M. ;
Seibel, Markus J. .
BONE, 2011, 49 (06) :1299-1305
[4]   Pitfalls in the measurement of muscle mass: a need for a reference standard [J].
Buckinx, Fanny ;
Landi, Francesco ;
Cesari, Matteo ;
Fielding, Roger A. ;
Visser, Marjolein ;
Engelke, Klaus ;
Maggi, Stefania ;
Dennison, Elaine ;
Al-Daghri, Nasser M. ;
Allepaerts, Sophie ;
Bauer, Jurgen ;
Bautmans, Ivan ;
Brandi, Maria Luisa ;
Bruyere, Olivier ;
Cederholm, Tommy ;
Cerreta, Francesca ;
Cherubini, Antonio ;
Cooper, Cyrus ;
Cruz-Jentoft, Alphonso ;
McCloskey, Eugene ;
Dawson-Hughes, Bess ;
Kaufman, Jean-Marc ;
Laslop, Andrea ;
Petermans, Jean ;
Reginster, Jean-Yves ;
Rizzoli, Rene ;
Robinson, Sian ;
Rolland, Yves ;
Rueda, Ricardo ;
Vellas, Bruno ;
Kanis, John A. .
JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE, 2018, 9 (02) :269-278
[5]   Body composition in patients with congenital myotonic dystrophy [J].
Ceballos-Saenz, Delia ;
Zapata-Aldana, Eugenio ;
Singeris, Stephanie ;
Hicks, Rhiannon ;
Johnson, Nicholas ;
Campbell, Craig .
MUSCLE & NERVE, 2019, 60 (02) :176-179
[6]   Effect of Paget's disease of bone on areal lumbar spine bone mineral density measured by DXA, and density of cortical and trabecular bone measured by quantitative CT [J].
Cherian, RA ;
Haddaway, MJ ;
Davie, MWJ ;
McCall, IW ;
Cassar-Pullicino, VN .
BRITISH JOURNAL OF RADIOLOGY, 2000, 73 (871) :720-726
[7]   Novel Variants in the VCP Gene Causing Multisystem Proteinopathy 1 [J].
Columbres, Rod Carlo Agram ;
Chin, Yue ;
Pratti, Sanjana ;
Quinn, Colin ;
Gonzalez-Cuyar, Luis F. ;
Weiss, Michael ;
Quintero-Rivera, Fabiola ;
Kimonis, Virginia .
GENES, 2023, 14 (03)
[8]   The spine in Paget's disease [J].
Dell'Atti, C. ;
Cassar-Pullicino, V. N. ;
Lalam, R. K. ;
Tins, B. J. ;
Tyrrell, P. N. M. .
SKELETAL RADIOLOGY, 2007, 36 (07) :609-626
[9]  
Diaz-Manera Jordi, 2015, Acta Myol, V34, P95
[10]   The muscular dystrophies [J].
Emery, AEH .
LANCET, 2002, 359 (9307) :687-695