Changes in bone mineral density in Down syndrome individuals: a systematic review and meta-analysis
- 12.08.2021
- Review
- Verfasst von
- Y. Zhang
- Z. Tian
- S. Ye
- Q. Mu
- X. Wang
- S. Ren
- X. Hou
- W. Yu
- J. Guo
- Erschienen in
- Osteoporosis International | Ausgabe 1/2022
Abstract
Data evaluating changes in bone mineral density (BMD) in Down syndrome (DS) individuals remains controversial. Therefore, we conducted a systematic review and meta-analysis to better understand associations between BMD and DS. A systematic literature search of PubMed, EMBASE, Web of Science, and the Cochrane Library up until 1st January 2021 was conducted. We used the keywords “bone mineral density” and “Down Syndrome.” Fifteen studies were included. Overall, our results showed a significant decrease in BMD of total body (TB BMD) [MD = − 0.18; 95% CI (− 0.23 and − 0.12), P < 0.00001, I2 = 89%], total hip (TH BMD) [MD = − 0.12; 95% CI (− 0.15 and − 0.10), P < 0.00001, I2 = 0%], lumbar spine (LS BMD) [MD = − 0.12; 95% CI (− 0.14 and − 0.09), P < 0.00001, I2 = 18%], and femoral neck (FN BMD) [MD = − 0.08; 95% CI (− 0.10 and − 0.06), P < 0.00001, I2 = 0%] in DS individuals when compared with controls. Moreover, the volumetric BMD of lumbar spine (LS vBMD) [MD = − 0.01; 95% CI (− 0.02 and − 0.01), P = 0.0004, I2 = 19%] also showed a decreasing tendency while the volumetric BMD of the femoral neck (FN vBMD) [MD = 0.01; 95% CI (0.00 and 0.02), P = 0.02, I2 = 0%] was elevated in DS individuals versus controls. These findings demonstrated that individuals with DS had a decreased total and regional (TH, LS, and FN) BMD when compared with the general population. Additionally, when BMD was adjusted for skeletal volume, LS vBMD was also lower, while FN vBMD was elevated in DS individuals versus controls.
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- Titel
- Changes in bone mineral density in Down syndrome individuals: a systematic review and meta-analysis
- Verfasst von
-
Y. Zhang
Z. Tian
S. Ye
Q. Mu
X. Wang
S. Ren
X. Hou
W. Yu
J. Guo
- Publikationsdatum
- 12.08.2021
- Verlag
- Springer London
- Erschienen in
-
Osteoporosis International / Ausgabe 1/2022
Print ISSN: 0937-941X
Elektronische ISSN: 1433-2965 - DOI
- https://doi.org/10.1007/s00198-021-06070-7
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