TY - JOUR
T1 - Contribution of bone turnover markers (BTMs) and vitamin D to bone health in Iranian elderly women
AU - Gharibzadeh, Safoora
AU - Fahimfar, Noushin
AU - Goudarzi, Samira
AU - Yarmohammadi, Hossein
AU - Razi, Farideh
AU - Khashayar, Patricia
AU - Shafiee, Gita
AU - Heshmat, Ramin
AU - Moradi, Nahid
AU - Sanjari, Mahnaz
AU - Khalagi, Kazem
AU - Raeisi, Alireza
AU - Nabipour, Iraj
AU - Larijani, Bagher
AU - Ostovar, Afshin
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Tehran University of Medical Sciences 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Purpose: While only a few postmenopausal women exhibit biochemical signs of hypovitaminosis D, it has been shown that vitamin D insufficiency has detrimental effects on the overall skeleton mineralization, bone turnover rate, and may be a significant risk factor for osteoporosis and fracture. We evaluated the concurrent effect of Vitamin D levels and biochemical markers of bone turnover on bone health of postmenopausal women. Methods: The present study was conducted within the framework of the Bushehr Elderly Health (BEH) program, a population-based prospective cohort study being conducted in Bushehr, a southern province of Iran. In summary, 400 persons from participants of the second stage were selected; serum bone turnover markers (bone-specific alkaline phosphatase (bALP), amino‐terminal procollagen propeptides of type I collagen (P1NP), osteocalcin (OC), tartrate‐resistant acid phosphatase isoenzyme 5b (TRAP)) and vitamin D were measured. Vitamin D deficiency was defined as serum 25(OH) D below 20 ng/ml, and Bone health was considered in terms of Osteoporosis and degraded bone microarchitecture. Results: The number of partially or significantly degraded microstructure based on TBS was higher than the number of osteoporotic women based on BMD. Women with higher CTX levels were more prone to being degraded microarchitecture. Although we couldn’t find any association between vitamin D deficiency and bone health, when we considered the vitamin D levels in univariable modelling, the effect of it was significant. Conclusions: In this study, only CTX was found to be significantly correlated with TBS while BMD was associated with CTX, OC, and TRAP.
AB - Purpose: While only a few postmenopausal women exhibit biochemical signs of hypovitaminosis D, it has been shown that vitamin D insufficiency has detrimental effects on the overall skeleton mineralization, bone turnover rate, and may be a significant risk factor for osteoporosis and fracture. We evaluated the concurrent effect of Vitamin D levels and biochemical markers of bone turnover on bone health of postmenopausal women. Methods: The present study was conducted within the framework of the Bushehr Elderly Health (BEH) program, a population-based prospective cohort study being conducted in Bushehr, a southern province of Iran. In summary, 400 persons from participants of the second stage were selected; serum bone turnover markers (bone-specific alkaline phosphatase (bALP), amino‐terminal procollagen propeptides of type I collagen (P1NP), osteocalcin (OC), tartrate‐resistant acid phosphatase isoenzyme 5b (TRAP)) and vitamin D were measured. Vitamin D deficiency was defined as serum 25(OH) D below 20 ng/ml, and Bone health was considered in terms of Osteoporosis and degraded bone microarchitecture. Results: The number of partially or significantly degraded microstructure based on TBS was higher than the number of osteoporotic women based on BMD. Women with higher CTX levels were more prone to being degraded microarchitecture. Although we couldn’t find any association between vitamin D deficiency and bone health, when we considered the vitamin D levels in univariable modelling, the effect of it was significant. Conclusions: In this study, only CTX was found to be significantly correlated with TBS while BMD was associated with CTX, OC, and TRAP.
KW - Bone health
KW - Bone turnover markers (BTMs)
KW - Bushehr elderly health (BEH) program
KW - Osteoporosis
KW - Trabecular bone score (TBS)
KW - Vitamin D deficiency
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U2 - 10.1007/s40200-024-01436-0
DO - 10.1007/s40200-024-01436-0
M3 - Article
C2 - 39610511
AN - SCOPUS:85195296859
SN - 2251-6581
VL - 23
SP - 1871
EP - 1877
JO - Journal of Diabetes and Metabolic Disorders
JF - Journal of Diabetes and Metabolic Disorders
IS - 2
ER -