Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati–Engelmann Disease: Assessed by HR‐pQCT. (28th September 2021)
- Record Type:
- Journal Article
- Title:
- Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati–Engelmann Disease: Assessed by HR‐pQCT. (28th September 2021)
- Main Title:
- Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati–Engelmann Disease: Assessed by HR‐pQCT
- Authors:
- Li, Qian
Zhao, Zhen
Wu, Bo
Pang, Qianqian
Cui, Lijia
Zhang, Li
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiaoping
Hu, Yingying
Yu, Wei
Meng, Xunwu
Jiajue, Ruizhi
Xia, Weibo - Abstract:
- ABSTRACT: Camurati‐Engelmann disease (CED) is a rare autosomal‐dominant skeletal dysplasia caused by mutations in the transforming growth factor‐β1 ( 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 strengthABSTRACT: Camurati‐Engelmann disease (CED) is a rare autosomal‐dominant skeletal dysplasia caused by mutations in the transforming growth factor‐β1 ( 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. © 2021 American Society for Bone and Mineral Research (ASBMR). … (more)
- Is Part Of:
- Journal of bone and mineral research. Volume 37:Number 1(2022)
- Journal:
- Journal of bone and mineral research
- Issue:
- Volume 37:Number 1(2022)
- Issue Display:
- Volume 37, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 37
- Issue:
- 1
- Issue Sort Value:
- 2022-0037-0001-0000
- Page Start:
- 78
- Page End:
- 86
- Publication Date:
- 2021-09-28
- Subjects:
- BONE MICROSTRUCTURE -- CAMURATI‐ENGELMANN DISEASE -- HR‐pQCT -- PROGRESSIVE DIAPHYSEAL DYSPLASIA -- TRANSFORMING GROWTH FACTOR‐Β1
Bones -- Metabolism -- Periodicals
Mineral metabolism -- Periodicals
612.392 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1523-4681 ↗
http://www.jbmr-online.com ↗ - DOI:
- 10.1002/jbmr.4436 ↗
- Languages:
- English
- ISSNs:
- 0884-0431
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4954.255530
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26360.xml