甲状腺功能亢进症、甲状腺功能减退症、促甲状腺激素与痴呆症风险:2011-2012 年国家健康调查(NHANES)和孟德尔随机分析的结果。

IF 4.1 2区 医学 Q2 GERIATRICS & GERONTOLOGY Frontiers in Aging Neuroscience Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fnagi.2024.1456525
Xixi Sheng, Jixiang Gao, Kunfei Chen, Xuzhen Zhu, Yu Wang
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引用次数: 0

摘要

导言:随着全球老龄化的加剧,痴呆症给社会和经济带来了沉重的负担,但目前诊断痴呆症的方法仍然有限,而且还没有针对痴呆症病因的更好疗法。本研究旨在探讨甲状腺疾病、促甲状腺激素(TSH)浓度、游离四碘甲状腺原氨酸(FT4)浓度与认知功能之间的关系:本研究利用2011-2012年美国国家健康与营养调查(NHANES)中的认知功能和甲状腺数据,采用加权逻辑回归和受限立方样条法(RCS)评估了不同组别的促甲状腺激素(TSH)和游离四碘甲状腺原氨酸(FT4)浓度与认知功能之间的关系,然后采用双样本孟德尔随机法(MR)评估了甲状腺功能亢进、甲状腺功能减退、TSH和FT4浓度与痴呆之间的因果关系:我们对2011-2012年NHANES数据的分析表明,与TSH浓度高的人相比,TSH浓度低的人的阿尔茨海默病单词表注册联盟1(CERAD1)和CERAD.delay.recall得分更高;与FT4浓度高的人相比,FT4浓度低的人的CERAD3和动物流畅性测试得分更高。我们的研究结果还显示,血清促甲状腺激素和 FT4 浓度与动物流畅性测试之间存在非线性关系。TSH 浓度在 1.703 至 3.145 mIU/L 范围内与动物流畅度测试呈正相关,而超出此范围则与动物流畅度测试呈负相关。在 FT4 浓度拐点(0.849 纳克/升)左侧,FT4 浓度与动物流畅度测试呈正相关,而在拐点右侧则呈负相关。磁共振分析结果进一步表明,甲状腺功能亢进症的遗传易感性可能与痴呆症和血管性痴呆症(VaD)的风险降低有关。相反,甲状腺功能减退症的遗传易感性似乎与痴呆症和血管性痴呆症的风险增加有关。此外,TSH浓度升高的遗传易感性可能与阿尔茨海默病(AD)风险的增加有关:本研究提供的证据表明,TSH 和 FT4 浓度与认知功能之间存在非线性关系,甲状腺功能亢进会降低痴呆症和 VaD 的风险,甲状腺功能减退会增加痴呆症和 VaD 的风险,而血清 TSH 浓度升高会增加 AD 的风险。此外,通过评估痴呆症高危人群的甲状腺功能,优先考虑早期检测、诊断和治疗也是至关重要的。这一策略有可能大大有助于预防和减缓痴呆症的进展。
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Hyperthyroidism, hypothyroidism, thyroid stimulating hormone, and dementia risk: results from the NHANES 2011-2012 and Mendelian randomization analysis.

Introduction: As the world ages, dementia places a heavy burden on society and the economy, but current methods of diagnosing dementia are still limited and there are no better therapies that target the causes of dementia. The purpose of this work is to explore the relationship between thyroid disease, thyroid stimulating hormone (TSH) concentrations, free tetraiodothyronine (FT4) concentrations and cognitive function.

Methods: This study utilized cognitive function and thyroid data from the 2011-2012 National Health and Nutrition Examination Survey (NHANES) to assess the relationship between different groups of TSH and FT4 concentrations and cognitive function using weighted logistic regression and restricted cubic spline (RCS), and then used two-sample Mendelian Randomization (MR) to assess the causal relationship between hyperthyroidism, hypothyroidism, TSH and FT4 concentrations with dementia.

Results: Our analysis of the 2011-2012 NHANES data showed that the individuals with low TSH concentrations had higher Alzheimer's Disease Word List Registry Consortium1 (CERAD1) and CERAD.delay.recall scores than individuals with high TSH concentrations, and individuals with low FT4 concentrations had higher CERAD3 and Animal Fluency Test scores than individuals with high FT4 concentrations. Our results also showed a non-linear relationship between serum TSH and FT4 concentrations and the Animal Fluency Test. The TSH concentrations within the range of 1.703 to 3.145 mIU/L exhibit a positive correlation with Animal Fluency Test, whereas concentrations outside this range are negatively correlated with Animal Fluency Test. The FT4 concentrations exhibited a positive correlation with Animal Fluency Test to the left of the FT4 concentrations inflection point (0.849 ng/L), whereas to the right of this inflection point, correlation was negative. MR analysis results further indicate that genetic predisposition to hyperthyroidism may be associated with a reduced risk of dementia and vascular dementia(VaD). Conversely, genetic predisposition to hypothyroidism appears to be linked with an increased risk of dementia and VaD. Additionally, genetic predisposition to elevated TSH concentrations may be correlated with a heightened risk of risk of Alzheimer's disease (AD).

Conclusion: This study provides evidence of a nonlinear relationship between TSH and FT4 concentrations and cognitive function, with hyperthyroidism decreasing the risk of dementia and VaD, hypothyroidism increasing the risk of dementia and VaD, and elevated serum TSH concentrations increasing the risk of AD. Furthermore, prioritizing early detection, diagnosis, and treatment through the assessment of thyroid function in individuals at high risk for developing dementia is of paramount importance. This strategy has the potential to significantly contribute to the prevention and deceleration of dementia progression.

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来源期刊
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience GERIATRICS & GERONTOLOGY-NEUROSCIENCES
CiteScore
6.30
自引率
8.30%
发文量
1426
期刊介绍: Frontiers in Aging Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the mechanisms of Central Nervous System aging and age-related neural diseases. Specialty Chief Editor Thomas Wisniewski at the New York University School of Medicine is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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