2019
DOI: 10.1089/thy.2018.0259
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Thyrotoxicosis Involves β2-Adrenoceptor Signaling to Negatively Affect Microarchitecture and Biomechanical Properties of the Femur

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Cited by 6 publications
(4 citation statements)
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“…Osteocalcin has been proposed as a biomarker for OA detection and monitoring. Its biologic function is considered to be related to the inhibition of bone matrix mineralization [35,36]. In addition, multiple cross-sectional studies have found that FT3/FT4, TSHI, and TT4RI are significantly correlated with chronic kidney disease (CKD), non-alcoholic fatty liver disease (NAFLD), and coronary artery disease (CAD) [37][38][39].…”
Section: Discussionmentioning
confidence: 99%
“…Osteocalcin has been proposed as a biomarker for OA detection and monitoring. Its biologic function is considered to be related to the inhibition of bone matrix mineralization [35,36]. In addition, multiple cross-sectional studies have found that FT3/FT4, TSHI, and TT4RI are significantly correlated with chronic kidney disease (CKD), non-alcoholic fatty liver disease (NAFLD), and coronary artery disease (CAD) [37][38][39].…”
Section: Discussionmentioning
confidence: 99%
“…The impact on osteoblasts is demonstrated by stimulating the expression of osteocalcin and promoting bone formation, facilitating osteoblast differentiation, suppressing osteoblast proliferation, and contributing to the maintenance of bone mass. The effect on osteoclasts is evidenced by an increase in tartrate-resistant acid phosphatase (TRAP) expression and the promotion of osteoclastogenesis, facilitating the differentiation of osteoclasts and aiding in the preservation of bone density ( 103–105 ).…”
Section: Iodine and Kashin-beck Diseasementioning
confidence: 99%
“…Osteoclasts are derived from hematopoietic progenitors and promote bone resorption ( 49 ). Studies showed that T3 increased the RANKL/OPG ratio in the femur in wild-type mice but not in β2-adrenergic receptor (AR) -/- mice, indicated that T3 activated osteoclasts function through the β2-AR pathway in bone ( 50 ). In addition, thyrotoxicosis impaired bone mineral density (BMD) in WT mice, and the stimulative effect to bone resorption was more stronger than bone formation ( 51 ), however, BMD was not significantly decreased in response to the supraphysiological dose of T3 in α2A/C-AR double knockout mice, suggesting that α2-AR mediated T3-induced bone resorption ( 52 ).…”
Section: Effects Of Ths On Bonementioning
confidence: 99%