接受左甲状腺素治疗的绝经前甲状腺功能减退症女性是否需要进行骨状况监测?

Clinical medicine insights. Women's health Pub Date : 2015-03-15 eCollection Date: 2015-01-01 DOI:10.4137/CMWH.S22114
Ruby P Babu, Alap Christy, Anupama Hegde, Poornima Manjrekar, Vivian D'Souza
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摘要

背景:据报道,抑制剂量的左甲状腺素疗法会降低女性的骨矿物质密度(BMD)。有关接受替代疗法的绝经前甲减妇女骨质变化的数据十分有限。因此,本研究采用骨标记物和 BMD 来评估该群体的骨质变化:这项基于医院的病例对照研究包括 75 名年龄在 30-45 岁之间的绝经前妇女。根据受试者的甲状腺功能和病史将其分为三组:25 名甲状腺功能正常、25 名新诊断为甲状腺功能减退和 25 名服用 100-200 μg 左甲状腺素至少 5 年的甲状腺功能减退妇女。通过估算血浆骨钙素、血清钙和磷,以及通过定量超声波检查测量 BMD,对各组间的骨骼变化进行生化评估和比较。统计分析采用方差分析、Tukey 检验和 IBM SPSS 统计 20 的皮尔逊相关性:结果:长期接受左甲状腺素治疗的患者的血浆骨钙素、血清钙和血清磷水平明显高于新诊断的甲状腺功能减退妇女和甲状腺功能正常组。治疗组妇女的 BMD 显示出明确的骨质疏松特征(T 评分:-2.26 ± 0.5),而新诊断的妇女和甲状腺功能正常的妇女的 BMD 则在正常范围内。骨钙素水平与 T 评分之间存在明显的相关性:结论:长期接受左甲状腺素治疗的甲状腺机能减退妇女显示出骨转换增加和吸收性变化增加的迹象,但并非真正的骨质疏松症。因此,对服用左甲状腺素超过5年的患者进行骨质状况评估可能非常重要。
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Do premenopausal hypothyroid women on levothyroxine therapy need bone status monitoring?

Background: Suppressive doses of levothyroxine therapy are reported to reduce bone mineral density (BMD) in women. Data on bone changes in premenopausal hypothyroid women with replacement therapy are limited. Hence, this study was undertaken to evaluate bone changes in this group using bone markers and BMD.

Materials and methods: A hospital-based case-control study including 75 premenopausal women aged 30-45 years was conducted. The subjects were categorized based on their thyroid function and history into three groups of 25 euthyroid, 25 newly diagnosed hypothyroid, and 25 hypothyroid women on 100-200 μg of levothyroxine for a minimum of 5 years. The bone changes were evaluated and compared among the groups biochemically by estimating their plasma osteocalcin and serum calcium and phosphorus and radiologically by measuring their BMD by quantitative ultrasonography. Statistical analysis was conducted by using analysis of variance, Tukey's test, and Pearson's correlation using IBM SPSS Statistics 20.

Results: Levels of plasma osteocalcin, serum calcium, and serum phosphorus in patients on long-term levothyroxine therapy were significantly higher than those in newly diagnosed hypothyroid women and in the euthyroid group. BMD showed definite features of osteopenia (T-score: -2.26 ± 0.5) among the women in the treatment group, while it was well within the normal range in the newly diagnosed and euthyroid women. A significant correlation was found between the osteocalcin levels and T-score.

Conclusion: Hypothyroid women on long-term levothyroxine therapy showed signs of increased bone turnover and increased resorptive changes, though not frank osteoporosis. Hence, it may be important to evaluate the bone status of patients on levothyroxine for >5 years.

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