2005
DOI: 10.1016/j.maturitas.2005.01.009
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Ovarian aging and bone metabolism in menstruating women aged 35–50 years

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Cited by 27 publications
(29 citation statements)
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“…Our research has confirmed that serum FSH and LH levels in Chinese women are positively correlated with both bone formation indicators (BAP and OC) and bone resorption indicators (sNTX, sCTX, uNTX, uCTX, and uDPD), suggesting that the bone turnover speed becomes more rapid in women with increasing FSH and LH levels in circulation; this finding is similar to those of other studies [10,[27][28][29]. In contrast, however, Vural et al [15] found that serum FSH and LH levels are not correlated with the bone formation marker OC. Our results also demonstrate that bone turnover markers in quartile groups with high serum FSH and LH levels (Q3 and Q4) are higher than those in quartile groups with lower serum FSH and LH g sNTX=15.169+0.051×(LH), R 2 =0.018 (P=0.001).…”
Section: Discussionsupporting
confidence: 91%
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“…Our research has confirmed that serum FSH and LH levels in Chinese women are positively correlated with both bone formation indicators (BAP and OC) and bone resorption indicators (sNTX, sCTX, uNTX, uCTX, and uDPD), suggesting that the bone turnover speed becomes more rapid in women with increasing FSH and LH levels in circulation; this finding is similar to those of other studies [10,[27][28][29]. In contrast, however, Vural et al [15] found that serum FSH and LH levels are not correlated with the bone formation marker OC. Our results also demonstrate that bone turnover markers in quartile groups with high serum FSH and LH levels (Q3 and Q4) are higher than those in quartile groups with lower serum FSH and LH g sNTX=15.169+0.051×(LH), R 2 =0.018 (P=0.001).…”
Section: Discussionsupporting
confidence: 91%
“…However, from a physiopathological perspective, increased bone loss and bone resorption caused by early menopause and gonadal dysfunction should be attributed not just to a decrease in sex hormones because serum estrogen levels are not correlated with bone resorption indicators [4,39]. Increased premenopausal and perimenopausal bone resorption may also be due to increased secretion of gonadotropic hormone in circulation [34,35] and decreased secretion of inhibin B [15], as the levels of gonadotropic hormone are increased greatly and levels of estrogen are slightly decreased or BAP bone-specific alkaline phosphatase, OC osteocalcin, sNTX serum cross-linked N-terminal telopeptides of type I collagen (NTX), sCTX serum C-terminal telopeptides of type I collagen (CTX), uNTX urinary NTX, uCTX urinary CTX, uDPD urinary deoxypyridinoline a P=0.001 normal. In view of the relationship between serum FSH and LH and bone turnover indicators, measuring bone turnover indicators and FSH simultaneously is more effective in the screening and prediction of osteoporosis in perimenopausal women [40].…”
Section: Discussionmentioning
confidence: 99%
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“…Subsequently, the confirmation of these actions in human cells provided further evidence that changes in ovarian inhibins might directly influence bone turnover via changes in cell differentiation [97]. Clinical studies in peri-menopausal women that measured serum circulating levels of steroids, inhibins and FSH confirmed that decrease in inhibin levels across the menopausal transition is associated with increasing bone turnover as well as with bone mass regardless of changes in steroids or FSH levels [95,97,98] (Fig. 4).…”
Section: Inhibins and Its Role In Tumourigenesismentioning
confidence: 83%
“…We have demonstrated direct suppressive effects of inhibins on osteoblasts and osteoclasts in mice and humans [21,22]. Clinical studies in women across the menopause transition demonstrate that decreases in inhibins are good predictors of increases in bone turnover markers in premenopausal, perimenopausal, and postmenopausal women, independent of both FSH and estradiol [22,26]. These findings also support the hypothesis that changes in inhibins drive the bone loss associated with onset of menopause, and suggest that like the pituitary, the skeleton is an inhibin target organ.…”
Section: Inhibins/activinsmentioning
confidence: 88%