Evie van der Spoel, Saskia Cornet, Ana Zutinic, Bart Ballieux, P Eline Slagboom, Hanno Pijl, Diana van Heemst
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Changes in hormone concentration profiles relative to baseline were determined for 4 and 5 days respectively.</p><p><strong>Results: </strong>IGF-1 increased with a maximum of 6.3% (SEM=1.6%, P=0.002) in the rhTSH challenge and 8.8% (SEM=1.6%, P<0.001) in the T3 challenge, while LH (19.3% (SEM=6.6%, P=0.048)), testosterone (13.8% (SEM=4.7%, P=0.048)), and SHBG (11.8% (SEM=3.5%, P=0.02)) increased significantly in the T3 challenge only. Moreover, prolactin significantly decreased in both rhTSH and T3 challenges (-8.8% (SEM=3.4%, P=0.048) and -12.0% (3.3%, P=0.004) respectively) as did cortisol (-14.8% (SEM=3.6%, P<0.001) and -15.6% (SEM=3.5%, P<0.001)). There was no significant interaction with type of challenge, sex, or familial longevity, except for prolactin in the rhTSH challenge (P=0.004) which decreased significantly in men only.</p><p><strong>Conclusions: </strong>Upon modulation of thyroid status, changes were observed in IGF-1, prolactin, and cortisol. In the T3 challenge, LH, testosterone, and SHBG increased in men. Observed changes are hypothesized to be driven by (f)T3.</p>","PeriodicalId":19117,"journal":{"name":"Neuroendocrinology","volume":" ","pages":"1-22"},"PeriodicalIF":3.2000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of thyroid status modulation on pituitary and peripheral hormone concentrations in healthy older subjects.\",\"authors\":\"Evie van der Spoel, Saskia Cornet, Ana Zutinic, Bart Ballieux, P Eline Slagboom, Hanno Pijl, Diana van Heemst\",\"doi\":\"10.1159/000542832\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Depending on age, sex, and familial longevity, alterations in thyroid status occur frequently, and often co-occur with differences in other hormonal axes. However, studies that explore the effects of thyroid status modulation on other hormonal axes remain scarce. We aim to determine the effects of thyroid status modulation on prolactin, IGF-1, cortisol, LH, testosterone, and SHBG levels. We also explored whether effects differed depending on type of challenge, sex, and familial longevity.</p><p><strong>Methods: </strong>Data was gathered from two single-arm challenge studies comprising an intramuscular injection of 0.1 mg recombinant human (rh)TSH (N=29) or 100 µg T3 orally (N=27) in healthy older individuals. Changes in hormone concentration profiles relative to baseline were determined for 4 and 5 days respectively.</p><p><strong>Results: </strong>IGF-1 increased with a maximum of 6.3% (SEM=1.6%, P=0.002) in the rhTSH challenge and 8.8% (SEM=1.6%, P<0.001) in the T3 challenge, while LH (19.3% (SEM=6.6%, P=0.048)), testosterone (13.8% (SEM=4.7%, P=0.048)), and SHBG (11.8% (SEM=3.5%, P=0.02)) increased significantly in the T3 challenge only. Moreover, prolactin significantly decreased in both rhTSH and T3 challenges (-8.8% (SEM=3.4%, P=0.048) and -12.0% (3.3%, P=0.004) respectively) as did cortisol (-14.8% (SEM=3.6%, P<0.001) and -15.6% (SEM=3.5%, P<0.001)). There was no significant interaction with type of challenge, sex, or familial longevity, except for prolactin in the rhTSH challenge (P=0.004) which decreased significantly in men only.</p><p><strong>Conclusions: </strong>Upon modulation of thyroid status, changes were observed in IGF-1, prolactin, and cortisol. In the T3 challenge, LH, testosterone, and SHBG increased in men. 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引用次数: 0
摘要
简介:根据年龄、性别和家族寿命的不同,甲状腺状态的改变经常发生,并且经常与其他激素轴的差异同时发生。然而,探讨甲状腺状态调节对其他激素轴的影响的研究仍然很少。我们的目的是确定甲状腺状态调节对催乳素、IGF-1、皮质醇、LH、睾酮和SHBG水平的影响。我们还探讨了影响是否因挑战类型、性别和家族寿命而异。方法:数据来自两项单臂挑战研究,包括在健康老年人中肌肉注射0.1 mg重组人(rh)TSH (N=29)或口服100µg T3 (N=27)。激素浓度曲线相对于基线的变化分别测定了4天和5天。结果:在rhTSH刺激下,IGF-1最高升高6.3% (SEM=1.6%, P=0.002), 8.8% (SEM=1.6%, P)。结论:调节甲状腺状态后,IGF-1、催乳素和皮质醇发生变化。在T3挑战中,男性的LH、睾酮和SHBG增加。假设观测到的变化是由(f)T3驱动的。
Effect of thyroid status modulation on pituitary and peripheral hormone concentrations in healthy older subjects.
Introduction: Depending on age, sex, and familial longevity, alterations in thyroid status occur frequently, and often co-occur with differences in other hormonal axes. However, studies that explore the effects of thyroid status modulation on other hormonal axes remain scarce. We aim to determine the effects of thyroid status modulation on prolactin, IGF-1, cortisol, LH, testosterone, and SHBG levels. We also explored whether effects differed depending on type of challenge, sex, and familial longevity.
Methods: Data was gathered from two single-arm challenge studies comprising an intramuscular injection of 0.1 mg recombinant human (rh)TSH (N=29) or 100 µg T3 orally (N=27) in healthy older individuals. Changes in hormone concentration profiles relative to baseline were determined for 4 and 5 days respectively.
Results: IGF-1 increased with a maximum of 6.3% (SEM=1.6%, P=0.002) in the rhTSH challenge and 8.8% (SEM=1.6%, P<0.001) in the T3 challenge, while LH (19.3% (SEM=6.6%, P=0.048)), testosterone (13.8% (SEM=4.7%, P=0.048)), and SHBG (11.8% (SEM=3.5%, P=0.02)) increased significantly in the T3 challenge only. Moreover, prolactin significantly decreased in both rhTSH and T3 challenges (-8.8% (SEM=3.4%, P=0.048) and -12.0% (3.3%, P=0.004) respectively) as did cortisol (-14.8% (SEM=3.6%, P<0.001) and -15.6% (SEM=3.5%, P<0.001)). There was no significant interaction with type of challenge, sex, or familial longevity, except for prolactin in the rhTSH challenge (P=0.004) which decreased significantly in men only.
Conclusions: Upon modulation of thyroid status, changes were observed in IGF-1, prolactin, and cortisol. In the T3 challenge, LH, testosterone, and SHBG increased in men. Observed changes are hypothesized to be driven by (f)T3.
期刊介绍:
''Neuroendocrinology'' publishes papers reporting original research in basic and clinical neuroendocrinology. The journal explores the complex interactions between neuronal networks and endocrine glands (in some instances also immunecells) in both central and peripheral nervous systems. Original contributions cover all aspects of the field, from molecular and cellular neuroendocrinology, physiology, pharmacology, and the neuroanatomy of neuroendocrine systems to neuroendocrine correlates of behaviour, clinical neuroendocrinology and neuroendocrine cancers. Readers also benefit from reviews by noted experts, which highlight especially active areas of current research, and special focus editions of topical interest.