Franklyn J, Betteridge J, Holder R, Daykin J, Lilley J, Sheppard M
Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, UK.
Clin Endocrinol (Oxf). 1994 Oct;41(4):425-32. doi: 10.1111/j.1365-2265.1994.tb02572.x.
The results of studies examining the influence of T4 therapy upon bone mineral density (BMD) are conflicting. This conflict may, in part, reflect inclusion of patients with varying thyroid disorders. We have therefore examined the influence of preceding thyroid history and T4 therapy on BMD.
Case-control studies of patients on long-term T4 therapy who have or have not previously received radioiodine treatment for thyrotoxicosis, as well as previously thyrotoxic patients who have not required T4 replacement.
Twenty-seven premenopausal and 60 postmenopausal females with a past history of thyrotoxicosis and subsequent T4 treated hypothyroidism (group 1), 39 post-menopausal females with a past history of radioiodine treated thyrotoxicosis not receiving T4 (group 2) and 22 post-menopausal females with primary hypothyroidism on T4 (group 3). Female controls individually matched to patients by age and menopausal status.
BMD measured by dual-energy X-ray absorptiometry. Serum biochemistry and tests of thyroid function.
No significant differences were found in femoral or lumbar spine BMD measurements between premenopausal patients and controls in group 1 or between group 2 patients and controls. Measurements of BMD at all sites were lower in post-menopausal patients in groups 1 and 2 than in controls; when allowance was made for differences in BMD due to body mass index by analysis of variance, significant reductions in femoral trochanter BMD (3.9%, P < 0.05) and lumbar spine (5.6-8.5%, P < 0.01) BMD results were found in post-menopausal females in group 1 and reductions in femoral trochanter (3.9%, P < 0.01), Ward's triangle (5.6%, P < 0.05) and lumbar spine (8.5%, P < 0.01) BMD results in group 2. Separate analysis of BMD results of those with normal or reduced serum TSH did not affect outcome. BMD measurements were not significantly correlated with duration of T4 therapy, T4 dose, or serum free T4 or TSH in any patient group.
Thyroxine therapy alone does not represent a significant risk factor for loss of bone mineral density but there is a risk of bone loss in post-menopausal (but not premenopausal) females with a previous history of thyrotoxicosis treated with radioiodine.
研究甲状腺素(T4)治疗对骨密度(BMD)影响的结果相互矛盾。这种矛盾可能部分反映了纳入了患有不同甲状腺疾病的患者。因此,我们研究了既往甲状腺病史和T4治疗对骨密度的影响。
对长期接受T4治疗、既往有或无放射性碘治疗甲状腺毒症的患者,以及既往有甲状腺毒症但无需T4替代治疗的患者进行病例对照研究。
27名绝经前和60名绝经后有甲状腺毒症病史且随后接受T4治疗的甲状腺功能减退女性(第1组),39名有放射性碘治疗甲状腺毒症病史且未接受T4治疗的绝经后女性(第2组),以及22名接受T4治疗的原发性甲状腺功能减退的绝经后女性(第3组)。女性对照按年龄和绝经状态与患者个体匹配。
采用双能X线吸收法测量骨密度。检测血清生化指标和甲状腺功能。
第1组绝经前患者与对照组之间或第2组患者与对照组之间,股骨或腰椎骨密度测量无显著差异。第1组和第2组绝经后患者所有部位的骨密度测量值均低于对照组;通过方差分析校正因体重指数导致的骨密度差异后,发现第1组绝经后女性股骨转子骨密度显著降低(3.9%,P<0.05),腰椎骨密度降低(5.6 - 8.5%,P<0.01);第2组股骨转子骨密度降低(3.9%,P<0.01)、沃德三角区骨密度降低(5.6%,P<0.05)和腰椎骨密度降低(8.5%,P<0.01)。对血清促甲状腺激素(TSH)正常或降低的患者的骨密度结果进行单独分析,不影响结果。在任何患者组中,骨密度测量值与T4治疗持续时间、T4剂量、血清游离T4或TSH均无显著相关性。
单独使用甲状腺素治疗并非骨密度降低的显著危险因素,但既往有放射性碘治疗甲状腺毒症病史的绝经后(而非绝经前)女性存在骨质流失风险。