Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati-Engelmann Disease: Assessed by HR-pQCT

被引:6
作者
Li, Qian [1 ]
Zhao, Zhen [1 ]
Wu, Bo [1 ]
Pang, Qianqian [1 ]
Cui, Lijia [1 ]
Zhang, Li [1 ]
Jiang, Yan [1 ]
Wang, Ou [1 ]
Li, Mei [1 ]
Xing, Xiaoping [1 ]
Hu, Yingying [1 ]
Yu, Wei [2 ]
Meng, Xunwu [1 ]
Jiajue, Ruizhi [1 ]
Xia, Weibo [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Endocrinol, Key Lab Endocrinol,NHC,State Key Lab Complex Seve, Shuaifuyuan 1, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Radiol, Beijing, Peoples R China
基金
国家重点研发计划;
关键词
BONE MICROSTRUCTURE; CAMURATI-ENGELMANN DISEASE; HR-pQCT; PROGRESSIVE DIAPHYSEAL DYSPLASIA; TRANSFORMING GROWTH FACTOR-Beta 1; LATENCY-ASSOCIATED PEPTIDE; TRANSFORMING-GROWTH-FACTOR; PHENOTYPIC VARIABILITY; TGF-BETA-1; MUTATION;
D O I
10.1002/jbmr.4436
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Camurati-Engelmann disease (CED) is a rare autosomal-dominant skeletal dysplasia caused by mutations in the transforming growth factor-beta 1 (TGFB1) gene. In this study, a retrospective review of patients with CED evaluated at Peking Union Medical College Hospital in Beijing, China, between November 30, 2000 and November 30, 2020 was conducted. Data including demographic data, manifestations, and examination results were characterized. Furthermore, bone geometry, density, and microarchitecture were assessed and bone strength was estimated by HR-pQCT. Results showed the median age at onset was 2.5 years. Common manifestations included pain in the lower limbs (94%, 17/18), abnormal gait (89%, 16/18), genu valgum (89%, 16/18), reduced subcutaneous fat (78%, 14/18), delayed puberty (73%, 8/11), muscle weakness (67%, 12/18), hearing loss (39%, 7/18), hepatosplenomegaly (39%, 7/18), exophthalmos or impaired vision or visual field defect (33%, 6/18), and anemia (33%, 7/18). Twenty-five percent (4/16) of patients had short stature. Serum level of alkaline phosphatase was elevated in 41% (7/17) of patients whereas beta-C-terminal telopeptide was elevated in 91% of patients (10/11). Among 12 patients, the Z-scores of two patients were greater than 2.5 at the femur neck and the Z-scores of five patients were lower than -2.5 at the femur neck and/or lumbar spine. HR-pQCT results showed lower volumetric BMD (vBMD), altered bone microstructure and lower estimated bone strength at the distal radius and tibia in patients with CED compared with controls. In addition, total volume bone mineral density and cortical volumetric bone mineral density at the radius were negatively correlated with age in patients with CED, but positively correlated with age in controls. In conclusion, the largest case series of CED with characterized clinical features in a Chinese population was reported here. In addition, HR-pQCT was used to investigate bone microstructure at the distal radius and tibia in nine patients with CED, and the alteration of bone density, microstructure, and strength was shown for the first time. (c) 2021 American Society for Bone and Mineral Research (ASBMR).
引用
收藏
页码:78 / 86
页数:9
相关论文
共 34 条
  • [1] Advances in bone imaging for osteoporosis
    Adams, Judith E.
    [J]. NATURE REVIEWS ENDOCRINOLOGY, 2013, 9 (01) : 28 - 42
  • [2] Delayed puberty versus hypogonadism: a challenge for the pediatrician
    Bozzola, Mauro
    Bozzola, Elena
    Montalbano, Chiara
    Stamati, Filomena Andreina
    Ferrara, Pietro
    Villani, Alberto
    [J]. ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2018, 23 (02) : 57 - 61
  • [3] High-resolution Computed Tomography for Clinical Imaging of Bone Microarchitecture
    Burghardt, Andrew J.
    Link, Thomas M.
    Majumdar, Sharmila
    [J]. CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2011, 469 (08) : 2179 - 2193
  • [4] Phenotypic variability at the TGF-β1 locus in Camurati-Engelmann disease
    Campos-Xavier, AB
    Saraiva, JM
    Savarirayan, R
    Verloes, A
    Feingold, J
    Faivre, L
    Munnich, A
    Le Merrer, M
    Cormier-Daire, V
    [J]. HUMAN GENETICS, 2001, 109 (06) : 653 - 658
  • [5] Geometric indices of hip bone strength in obese, overweight, and normal-weight adolescent boys
    El Hage, R.
    [J]. OSTEOPOROSIS INTERNATIONAL, 2012, 23 (05) : 1593 - 1600
  • [6] Sex-, Ethnic-, and Age-Specific Centile Curves for pQCT- and HR-pQCT-Derived Measures of Bone Structure and Strength in Adolescents and Young Adults
    Gabel, Leigh
    Macdonald, Heather M.
    Nettlefold, Lindsay A.
    McKay, Heather A.
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2018, 33 (06) : 987 - 1000
  • [7] Biochemical markers of bone turnover in Camurati-Engelmann disease: A report on four cases in one family
    Hernandez, MV
    Peris, P
    Guanabens, N
    Alvarez, L
    Monegal, A
    Pons, F
    Ponce, A
    MunozGomez, J
    [J]. CALCIFIED TISSUE INTERNATIONAL, 1997, 61 (01) : 48 - 51
  • [8] TYPE-BETA TRANSFORMING GROWTH-FACTOR CONTROLS THE ADIPOGENIC DIFFERENTIATION OF 3T3 FIBROBLASTS
    IGNOTZ, RA
    MASSAGUE, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (24) : 8530 - 8534
  • [9] Mutations in the gene encoding the latency-associated peptide of TGF-β1 cause Camurati-Engelmann disease
    Janssens, K
    Gershoni-Baruch, R
    Guañabens, N
    Migone, N
    Ralston, S
    Bonduelle, M
    Lissens, W
    Van Maldergem, L
    Vanhoenacker, F
    Verbruggen, L
    Van Hul, W
    [J]. NATURE GENETICS, 2000, 26 (03) : 273 - 275
  • [10] Camurati-Engelmann disease:: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment
    Janssens, K
    Vanhoenacker, F
    Bonduelle, M
    Verbruggen, L
    Van Maldergem, L
    Ralston, S
    Guañabens, N
    Migone, N
    Wientroub, S
    Divizia, MT
    Bergmann, C
    Bennett, C
    Simsek, S
    Melançon, S
    Cundy, T
    Van Hul, W
    [J]. JOURNAL OF MEDICAL GENETICS, 2006, 43 (01) : 1 - 11