School of Health and Population Sciences, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B152TT, United Kingdom.
J Clin Endocrinol Metab. 2010 Aug;95(8):3623-32. doi: 10.1210/jc.2009-2571. Epub 2010 May 25.
Subclinical hypothyroidism (SCH) and cognitive dysfunction are both common in the elderly and have been linked. It is important to determine whether T4 replacement therapy in SCH confers cognitive benefit.
Our objective was to determine whether administration of T4 replacement to achieve biochemical euthyroidism in subjects with SCH improves cognitive function.
We conducted a double-blind placebo-controlled randomized controlled trial in the context of United Kingdom primary care.
Ninety-four subjects aged 65 yr and over (57 females, 37 males) with SCH were recruited from a population of 147 identified by screening.
T4 or placebo was given at an initial dosage of one tablet of either placebo or 25 microg T4 per day for 12 months. Thyroid function tests were performed at 8-weekly intervals with dosage adjusted in one-tablet increments to achieve TSH within the reference range for subjects in treatment arm. Fifty-two subjects received T4 (31 females, 21 males; mean age 73.5 yr, range 65-94 yr); 42 subjects received placebo (26 females, 16 males; mean age 74.2 yr, 66-84 yr).
Mini-Mental State Examination, Middlesex Elderly Assessment of Mental State (covering orientation, learning, memory, numeracy, perception, attention, and language skills), and Trail-Making A and B were administered.
Eighty-two percent and 84% in the T4 group achieved euthyroidism at 6- and 12-month intervals, respectively. Cognitive function scores at baseline and 6 and 12 months were as follows: Mini-Mental State Examination T4 group, 28.26, 28.9, and 28.28, and placebo group, 28.17, 27.82, and 28.25 [not significant (NS)]; Middlesex Elderly Assessment of Mental State T4 group, 11.72, 11.67, and 11.78, and placebo group, 11.21, 11.47, and 11.44 (NS); Trail-Making A T4 group, 45.72, 47.65, and 44.52, and placebo group, 50.29, 49.00, and 46.97 (NS); and Trail-Making B T4 group, 110.57, 106.61, and 96.67, and placebo group, 131.46, 119.13, and 108.38 (NS). Linear mixed-model analysis demonstrated no significant changes in any of the measures of cognitive function over time and no between-group difference in cognitive scores at 6 and 12 months.
This RCT provides no evidence for treating elderly subjects with SCH with T4 replacement therapy to improve cognitive function.
亚临床甲状腺功能减退症(SCH)和认知功能障碍在老年人中都很常见,并且已经相关联。重要的是要确定 SCH 患者中 T4 替代治疗是否能带来认知益处。
我们的目的是确定给予 T4 替代治疗以实现 SCH 患者的生化正常甲状腺功能是否能改善认知功能。
我们在英国初级保健的背景下进行了一项双盲安慰剂对照随机对照试验。
从通过筛查确定的 147 名患者中招募了 94 名年龄在 65 岁及以上的 SCH 患者(57 名女性,37 名男性)。
T4 或安慰剂以每天一片安慰剂或 25 微克 T4 的初始剂量给予 12 个月。每隔 8 周进行一次甲状腺功能检查,并根据需要增加剂量,使 TSH 在治疗组患者的参考范围内。52 名患者接受 T4(31 名女性,21 名男性;平均年龄 73.5 岁,范围 65-94 岁);42 名患者接受安慰剂(26 名女性,16 名男性;平均年龄 74.2 岁,66-84 岁)。
简易精神状态检查、米德尔塞克斯老年认知状态评估(涵盖定向、学习、记忆、算术、知觉、注意力和语言技能)和 Trail-Making A 和 B。
分别有 82%和 84%的 T4 组患者在 6 个月和 12 个月时达到甲状腺功能正常。基线和 6 个月和 12 个月时的认知功能评分如下:简易精神状态检查 T4 组,28.26、28.9 和 28.28,安慰剂组,28.17、27.82 和 28.25[无显著差异(NS)];米德尔塞克斯老年认知状态评估 T4 组,11.72、11.67 和 11.78,安慰剂组,11.21、11.47 和 11.44(NS);Trail-Making A T4 组,45.72、47.65 和 44.52,安慰剂组,50.29、49.00 和 46.97(NS);Trail-Making B T4 组,110.57、106.61 和 96.67,安慰剂组,131.46、119.13 和 108.38(NS)。线性混合模型分析显示,认知功能的任何指标在时间上均无显著变化,6 个月和 12 个月时认知评分无组间差异。
这项 RCT 没有提供证据表明用 T4 替代治疗治疗老年 SCH 患者可以改善认知功能。