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Author Notes:

Correspondence: Laura Cousino Klein; lcklein@psu.edu

Authors’ contributions: KNW developed the hypotheses and data analytic strategy, analyzed the data and drafted the manuscript.

LCK and EJC designed the experiment and obtained funding.

JU and LMD provided crucial clinical and scientific endocrine and thyroid functioning expertise.

JU and LCK assisted with data analytic strategies.

LMD provided funding and conducted FT4 and FT3 assays.

JMB and CAW assisted with running the experiment, as well as TSH and cortisol assays.

All authors made intellectual revisions to the entire manuscript, edited all sections of the manuscript and approved this version of the submitted manuscript.

Acknowledgements: We thank Michele M. Stine, our research assistants in the Biobehavioral Health Studies Lab, and the GCRC nursing staff for assistance with data collection, and Rick Ball for guidance on the biological assays.

We also thank the Core Endocrine Laboratory at the Penn State Hershey Medical Center for performing the free T3 and free T4 measurements.

Disclosures: The authors have no competing interests to declare.

Subjects:

Research Funding:

This work was supported by a grant from the National Science Foundation (SBR 9905157), a seed grant from the College of Health and Human Development at Penn State (223 15 3605), and Penn State’s General Clinical Research Center (NIH grant M01-RR-10732).

Elevated thyroid stimulating hormone is associated with elevated cortisol in healthy young men and women

Tools:

Journal Title:

Thyroid Research

Volume:

Volume 5, Number 13

Publisher:

, Pages 1-6

Type of Work:

Article | Final Publisher PDF

Abstract:

Background Recent attention has been given to subclinical hypothyroidism, defined as an elevation of TSH (4.5-10 uIU/L) with T4 and T3 levels still within the normal range. Controversy exists about the proper lower limit of TSH that defines patients in the subclinical hypothyroidism range and about if/when subclinical hypothyroidism should be treated. Additional data are needed to examine the relationship between markers of thyroid function in the subclinical hypothyroidism range, biomarkers of health and ultimately health outcomes. Objective We aimed to assess the relationship between serum TSH levels in the 0.5-10 uIU/L range and serum cortisol in a cohort of healthy young men and women without clinical evidence of hypothyroidism. Based on data in frank hypothyroidism, we hypothesized that serum TSH levels would be positively correlated with serum cortisol levels, suggesting derangement of the cortisol axis even in subclinical hypothyroidism. Methods We conducted a cross sectional study in 54 healthy, young (mean 20.98 +/− 0.37 yrs) men (19) and women (35). Lab sessions took place at 1300 hrs where blood was drawn via indwelling catheter for later assessment of basal serum TSH, free T3, free T4, and cortisol levels. Results All but 1 participant had free T3 levels within the normal reference intervals; free T4 levels for all participants were within the normal reference intervals. Linear regression modeling revealed that TSH levels in the 0.5-10 uIU/L were significantly and positively correlated with cortisol levels. This positive TSH-cortisol relationship was maintained below the accepted 4.5 uIU/L subclinical hypothyroid cutoff. Separate regression analyses conducted by systematically dropping the TSH cutoff by 0.50 uIU/L revealed that the TSH-cortisol relationship was maintained for TSH levels (uIU/L) ≤4.0, ≤3.5, ≤3.0, and ≤2.5 but not ≤2.0. Linear regression modeling did not reveal a relationship between free T3 or free T4 levels and cortisol levels. Conclusions Results suggest a positive relationship between TSH and cortisol in apparently healthy young individuals. In as much as this relationship may herald a pathologic disorder, these preliminary results suggest that TSH levels > 2.0 uIU/L may be abnormal. Future research should address this hypothesis further, for instance through an intervention study.

Copyright information:

© 2012 Walter et al.; licensee BioMed Central Ltd.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 2.0 Generic License (http://creativecommons.org/licenses/by/2.0/).

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