Bibliographic Details
Title: |
GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease |
Authors: |
Chung-Hsing Wang, Yu‐Nan Huang, Wen-Ling Liao, Ai-Ru Hsieh, Wei-De Lin, Kai-Wen Liu, Wen-Li Lu, Chieh‐Chen Huang, Yin-Hsiu Chien, Ni-Chung Lee, Pen-Hua Su, Fuu-Jen Tsai |
Source: |
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024) |
Publisher Information: |
BMC, 2024. |
Publication Year: |
2024 |
Collection: |
LCC:Medicine |
Subject Terms: |
Gaucher disease, GBA1, Osteoclastogenesis, Inflammasome, Endoplasmic reticulum stress, Osteoporosis, Medicine |
More Details: |
Abstract Background Osteoporosis and its primary complication, fragility fractures, contribute to substantial global morbidity and mortality. Gaucher disease (GD) is caused by glucocerebrosidase (GBA1) deficiency, leading to skeletal complications. This study aimed to investigate the impact of the GBA1 gene on osteoporosis progression in GD patients and the specific populations. Methods We selected 8115 patients with osteoporosis (T-score ≤ − 2.5) and 55,942 healthy individuals (T-score > − 1) from a clinical database (N = 95,223). Monocytes from GD patients were evaluated in relation to endoplasmic reticulum (ER) stress, inflammasome activation, and osteoclastogenesis. An in vitro model of GD patient’s cells treated with adeno-associated virus 9 (AAV9)-GBA1 to assess GBA1 enzyme activity, chitotriosidase activity, ER stress, and osteoclast differentiation. Longitudinal dual-energy X-ray absorptiometry (DXA) data tracking bone density in patients with Gaucher disease (GD) undergoing enzyme replacement therapy (ERT) over an extended period. Results The GBA1 gene variant rs11264345 was significantly associated [P |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
1750-1172 |
Relation: |
https://doaj.org/toc/1750-1172 |
DOI: |
10.1186/s13023-024-03132-x |
Access URL: |
https://doaj.org/article/0c1baf8b9b3b4b928fe4f713814a049b |
Accession Number: |
edsdoj.0c1baf8b9b3b4b928fe4f713814a049b |
Database: |
Directory of Open Access Journals |
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