1 Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Johns Hopkins University School of Medicine , Baltimore, Maryland.
2 Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health , Baltimore, Maryland.
Thyroid. 2017 Nov;27(11):1370-1377. doi: 10.1089/thy.2017.0211. Epub 2017 Oct 13.
Average thyrotropin (TSH) levels are known to be higher in older adults when measured in cross-sectional populations. Possible etiologies include differential survival, neutral aging changes, or increased disease prevalence at older ages. This study aimed to elucidate the mechanisms underlying changing thyroid function during aging, and to determine the association of changes with survival, by analyzing the individual thyroid axis over time.
Individual patterns of changing TSH and free thyroxine (fT4) were determined in 640 participants in the Baltimore Longitudinal Study of Aging who had at least three measures of serum TSH and fT4, not on medications, over an average of seven years of follow-up. Participants with changing phenotypes were identified based on quintiles for both slopes. Those with alterations in primary thyroid gland function demonstrated intact negative feedback (rising TSH with declining fT4 or declining TSH with rising fT4). Other participants had a parallel rise or fall of TSH and fT4 levels, consistent with pituitary dysfunction. Predictors of phenotype were analyzed by logistic regression. Differential survival between thyroid aging phenotypes was analyzed using multivariate Cox regression.
While the majority of participants at all ages had stable thyroid function, changes were more common among older adults, with 32.3% of those aged >80 years but only 9.5% of those aged <60 years demonstrating thyroid function changes in the highest and lowest quintiles. Regression to the mean accounts for some of the changes, for example increased baseline TSH was associated with a falling TSH pattern (odds ratio = 1.4 [confidence interval 1.1-1.7] per 1 mIU/L). Importantly, changing thyroid function in either the upper or lower quintiles of slope for TSH and fT4 was associated with increased risk of death compared to stable thyroid status (hazard ratio = 5.4 [confidence interval 3.1-9.5]).
Changing thyroid hormone function is increasingly common at older ages and is associated with decreased survival. Nonetheless, the tendency for abnormal thyroid function tests to resolve, along with altered pituitary responsiveness underlying some TSH elevations, suggests that an elevated TSH level should be not assumed to represent subclinical hypothyroidism in older adults. Thus, caution is appropriate when determining the need for thyroid hormone supplements in older adults.
在横断面人群中,已知老年人的平均促甲状腺激素(TSH)水平较高。可能的病因包括生存差异、中性衰老变化或老年时疾病患病率增加。本研究旨在通过分析随时间变化的个体甲状腺轴,阐明衰老过程中甲状腺功能变化的潜在机制,并确定变化与生存的关联。
在巴尔的摩纵向衰老研究中,640 名参与者至少有三次血清 TSH 和游离甲状腺素(fT4)测量值,且在平均 7 年的随访期间未服用任何药物。根据 TSH 和 fT4 斜率的五分位数确定改变 TSH 和 fT4 模式的个体。那些表现出原发性甲状腺功能改变的个体表现出完整的负反馈(随着 fT4 的下降而 TSH 升高,或随着 fT4 的升高而 TSH 下降)。其他参与者的 TSH 和 fT4 水平平行升高或下降,与垂体功能障碍一致。通过逻辑回归分析表型的预测因素。使用多变量 Cox 回归分析甲状腺老化表型之间的差异生存。
虽然所有年龄段的大多数参与者都有稳定的甲状腺功能,但随着年龄的增长,变化更为常见,80 岁以上的参与者中 32.3%,而 60 岁以下的参与者中只有 9.5%表现出甲状腺功能在最高和最低五分位数的变化。均值回归解释了部分变化,例如基础 TSH 增加与 TSH 模式下降相关(每增加 1mIU/L,比值比=1.4[置信区间 1.1-1.7])。重要的是,与稳定的甲状腺状态相比,TSH 和 fT4 斜率的上或下五分位的甲状腺功能变化与死亡风险增加相关(危险比=5.4[置信区间 3.1-9.5])。
随着年龄的增长,改变甲状腺激素功能变得越来越常见,并且与生存降低相关。尽管如此,异常甲状腺功能测试趋于缓解,以及一些 TSH 升高背后的垂体反应改变,表明在老年人中,升高的 TSH 水平不应被假定为亚临床甲状腺功能减退。因此,在确定是否需要为老年人补充甲状腺激素时应保持谨慎。