Ongphiphadhanakul B, Puavilai G, Rajatanavin R
Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 1996 Sep;79(9):563-7.
Thyroid hormone stimulates both osteoblast and osteoclast. However, the effect on osteoclast exceeds that of osteoblast resulting in a decrease in bone mass. TSH-suppressive doses of levothyroxine (L-T4) with otherwise normal thyroid function, so-called subclinical hyperthyroidism, has been reported to cause a reduction in bone mass. However, the sites of bone loss vary among studies. Moreover, the effect of menopausal status on thyroid-hormone-induced bone loss is inconclusive. Ethnic and geographical differences may modify the skeletal response to thyroid hormone. In the present study, we looked at the effect of TSH-suppressive doses of L-T4 on bone mineral density (BMD) in Thai pre- and post-menopausal women. Subjects consisted of 27 Thai females aged between 23-79 years. Eighteen were premenopausal and nine were postmenopausal. All were attending the Thyroid Clinic at Ramathibodi Hospital and had been on at least 150 micrograms/day of L-T4 for the treatment of nodular thyroid diseases for more than 2 years with at least one TSH value during the follow-up period in the suppressive range. None of the subjects had a previous history of Graves' disease. BMD was determined by dual-energy X-ray absorptiometry. Data of 54 age-matched healthy controls were used for comparison. BMD values were converted to Z-scores before analyses. Data were expressed as mean +/- SEM. Compared to controls, postmenopausal women on long-term L-T4 had decreased BMD at anteroposterior spine (-0.69 +/- 0.20 vs 0.05 +/- 0.17, P < 0.01), femoral neck (-0.61 +/- 0.35 vs 0.18 +/- 0.24, P < 0.05), femoral trochanter (-0.64 +/- 0.37 vs 0.13 +/- 0.22, P < 0.05) but not at Ward's triangle. In contrast to the findings in postmenopausal women. there was no significant difference of BMD compared to controls in premenopausal women at the lumbar spine, Ward's femoral neck or femoral trochanter. We conclude that Thai postmenopausal women on long-term TSH-suppressive doses of L-T4 have reduced BMD at various skeletal sites which may increase fracture risks. TSH-suppressive doses of thyroid hormone should only be prescribed when appropriate and no longer than necessary to minimize this adverse effect of excessive doses of thyroid hormone on bone.
甲状腺激素可同时刺激成骨细胞和破骨细胞。然而,其对破骨细胞的作用超过成骨细胞,导致骨量减少。据报道,在甲状腺功能其他方面正常的情况下,使用促甲状腺激素抑制剂量的左甲状腺素(L-T4),即所谓的亚临床甲状腺功能亢进,会导致骨量减少。然而,不同研究中骨质流失的部位有所不同。此外,绝经状态对甲状腺激素诱导的骨质流失的影响尚无定论。种族和地域差异可能会改变骨骼对甲状腺激素的反应。在本研究中,我们观察了促甲状腺激素抑制剂量的L-T4对泰国绝经前和绝经后女性骨密度(BMD)的影响。研究对象为27名年龄在23至79岁之间的泰国女性。其中18名是绝经前女性,9名是绝经后女性。所有患者均在拉玛蒂博迪医院甲状腺诊所就诊,因结节性甲状腺疾病接受至少150微克/天的L-T4治疗超过2年,且随访期间至少有一次促甲状腺激素值处于抑制范围内。所有受试者既往均无格雷夫斯病病史。通过双能X线吸收法测定骨密度。使用54名年龄匹配的健康对照者的数据进行比较。在分析前将骨密度值转换为Z评分。数据以平均值±标准误表示。与对照组相比,长期服用L-T4的绝经后女性在腰椎前后位(-0.69±0.20 vs 0.05±0.17,P<0.01)、股骨颈(-0.61±0.35 vs 0.18±0.24,P<0.05)、股骨转子(-0.64±0.37 vs 0.13±0.22,P<0.05)处的骨密度降低,但在沃德三角区未降低。与绝经后女性的研究结果相反,绝经前女性在腰椎、沃德股骨颈或股骨转子处的骨密度与对照组相比无显著差异。我们得出结论,长期服用促甲状腺激素抑制剂量L-T4的泰国绝经后女性在多个骨骼部位的骨密度降低,这可能会增加骨折风险。甲状腺激素的促甲状腺激素抑制剂量仅应在适当的时候使用,且使用时间不应超过必要时间,以尽量减少甲状腺激素过量对骨骼的这种不良影响。