Chronic Iodine Excess and Aging Synergistically Impact Thyrotropin Elevation: A Prospective 20-Year Follow-Up Study in China.

IF 6.7 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Thyroid Pub Date : 2026-04-01 Epub Date: 2026-03-10 DOI:10.1177/10507256261427353
Xiaotong Gao, Weiping Li, Qingling Gu, Yushu Li, Yongze Li, Haoyu Wang, Xiaochun Teng, Di Teng, Shuangning Ding, Weiping Teng, Zhongyan Shan
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引用次数: 0

Abstract

Background: Chronic iodine excess is associated with increased serum thyrotropin (TSH) levels. We assessed the independent and interactive effects of iodine-excess transition outcomes and aging on TSH levels over 20-year follow-up.

Methods: The original prospective cohort study started in 1999 and focused on three communities in North China (n = 1176). Based on the iodine status transition over the 20-year period, the euthyroid participants were categorized into groups according to urinary iodine concentrations (UIC): continuous iodine sufficiency (UIC 100-299 μg/L) (SI-SI, n = 261), from iodine excess (UIC >299 μg/L) to iodine deficiency (UIC <100 μg/L) (EI-DI, n = 145), from iodine excess to iodine sufficiency (EI-SI, n = 530), and continuous iodine excess (EI-EI, n = 240), respectively.

Results: During 1999-2004, the baseline median TSH levels were positively associated with the initial UIC levels. After 20 years, for participants with negative thyroid antibodies, the three iodine-excess groups all exhibited elevated median TSH levels (SI-SI 1.81 mU/L vs. EI-DI 2.19 mU/L vs. EI-SI 2.08 mU/L vs. EI-EI 2.01 mU/L), an increased prevalence of mild subclinical hypothyroidism (SCH) with TSH <10.0 mU/L (SI-SI 5.3% vs. EI-DI 11.2% vs. EI-SI 12.3% vs. EI-EI 9.4%) and reduced central thyroid hormone sensitivity compared with the SI-SI group (p < 0.05). However, the EI-EI group had the lowest TSH rising degree (SI-SI 0.32 mU/L [24.57%] vs. EI-DI 0.47 mU/L [24.56%] vs. EI-SI 0.45 mU/L [37.52%] vs. EI-EI 0.21 mU/L [14.18%], p < 0.05). Repeated-measures analysis revealed that aging was primarily related to a stable increase in TSH. Iodine-excess transition outcomes were also associated. Furthermore, a significant interaction effect existed between aging and different iodine-excess transition outcomes, modulating the TSH rising degree. Alleviation of iodine excess promoted aging-related TSH elevation, whereas persistent iodine excess suppressed aging-related TSH elevation. However, among participants with positive thyroid antibodies, no significant interaction effect above was observed. By comparison, there was a greater prevalence of SCH, especially an obvious high prevalence of severe SCH under persistent iodine excess.

Conclusions: Elevated TSH levels induced by chronic iodine excess cannot be downregulated by reducing iodine intake. In nonautoimmune contexts, an interaction effect between iodine status and aging synergistically modulates the TSH rising degree. Iodine excess contributes to mild SCH and is correlated with high baseline TSH levels.

慢性碘过量和衰老协同影响促甲状腺激素升高:中国一项前瞻性20年随访研究。
背景:慢性碘过量与血清促甲状腺素(TSH)水平升高有关。在20年的随访中,我们评估了碘过量过渡结果和衰老对TSH水平的独立和相互作用影响。方法:最初的前瞻性队列研究始于1999年,集中在华北地区的三个社区(n = 1176)。根据20年期间的碘状态转变,甲状腺功能正常的参与者根据尿碘浓度(UIC)分为连续碘充足(UIC 100-299 μg/L) (SI-SI, n = 261),从碘过量(UIC >299 μg/L)到碘缺乏(UIC n = 145),从碘过量到碘充足(EI-SI, n = 530)和连续碘过量(EI-EI, n = 240)。结果:1999-2004年期间,基线TSH中位数水平与初始UIC水平呈正相关。20年后,对于甲状腺抗体阴性的参与者,三个碘过量组均表现出TSH水平中位数升高(SI-SI 1.81 mU/L vs. EI-DI 2.19 mU/L vs. EI-SI 2.08 mU/L vs. EI-EI 2.01 mU/L),轻度亚临床甲状腺功能减退(SCH)患病率增加,TSH p < 0.05)。EI-EI组TSH升高程度最低(SI-SI为0.32 mU/L [24.57%], EI-DI为0.47 mU/L [24.56%], EI-SI为0.45 mU/L [37.52%], EI-EI为0.21 mU/L [14.18%], p < 0.05)。重复测量分析显示,衰老主要与TSH的稳定增加有关。碘过量过渡结果也相关。此外,衰老与不同的碘过量过渡结果之间存在显著的交互作用,调节TSH上升程度。缓解碘过量促进衰老相关的TSH升高,而持续碘过量抑制衰老相关的TSH升高。然而,在甲状腺抗体阳性的参与者中,没有观察到上述显著的相互作用。相比之下,SCH的患病率更高,特别是在持续碘过量的情况下,严重SCH的患病率明显较高。结论:慢性碘过量引起的TSH水平升高不能通过减少碘摄入量来下调。在非自身免疫环境下,碘状态和衰老之间的相互作用协同调节TSH升高程度。碘过量导致轻度SCH,并与高基线TSH水平相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Thyroid
Thyroid 医学-内分泌学与代谢
CiteScore
12.30
自引率
6.10%
发文量
195
审稿时长
6 months
期刊介绍: This authoritative journal program, including the monthly flagship journal Thyroid, Clinical Thyroidology® (monthly), and VideoEndocrinology™ (quarterly), delivers in-depth coverage on topics from clinical application and primary care, to the latest advances in diagnostic imaging and surgical techniques and technologies, designed to optimize patient care and outcomes. Thyroid is the leading, peer-reviewed resource for original articles, patient-focused reports, and translational research on thyroid cancer and all thyroid related diseases. The Journal delivers the latest findings on topics from primary care to clinical application, and is the exclusive source for the authoritative and updated American Thyroid Association (ATA) Guidelines for Managing Thyroid Disease.
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