Characterization of Cortisol Dysregulation in Fibromyalgia and Chronic Fatigue Syndromes: A State-Space Approach
Abstract
OBJECTIVE: Fibromyalgia syndrome (FMS) and chronic fatigue syndrome (CFS) are complicated medical disorders, with little known etiologies. The purpose of this research is to characterize FMS and CFS by studying the variations in cortisol secretion patterns, timings, amplitudes, the number of underlying pulses, as well as infusion and clearance rates of cortisol. METHODS: Using a physiological state-space model with plausible constraints, we estimate the hormonal secretory events and the physiological system parameters (i.e., infusion and clearance rates). RESULTS: Our results show that the clearance rate of cortisol is lower in FMS patients as compared to their matched healthy individuals based on a simplified cortisol secretion model. Moreover, the number, magnitude, and energy of hormonal secretory events are lower in FMS patients. During early morning hours, the magnitude and energy of the hormonal secretory events are higher in CFS patients. CONCLUSION: Due to lower cortisol clearance rate, there is a higher accumulation of cortisol in FMS patients as compared to their matched healthy subjects. As the FMS patient accumulates higher cortisol residues, internal inhibitory feedback regulates the hormonal secretory events. Therefore, the FMS patients show a lower number, magnitude, and energy of hormonal secretory events. Though CFS patients have the same number of secretory events, they secrete lower quantities during early morning hours. When we compare the results for CFS patients against FMS patients, we observe different cortisol alteration patterns. SIGNIFICANCE: Characterizing CFS and FMS based on the cortisol alteration will help us to develop novel methods for treating these disorders.
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The proposed architecture has been previously verified for cortisol in healthy subjects and in patients with chronic fatigue and fibromyalgia syndromes.
“The proposed architecture has been previously verified for cortisol in healthy subjects and also on patients suffering from chronic fatigue and fibromyalgia syndromes (32–34).”
From Sparse System Identification of Leptin Dynamics in Women With Obesity (2022) · cites this paper as [32]
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2020 Index IEEE Transactions on Biomedical Engineering Vol. 67
(2020) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2020.3048339
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- Authors
- Pednekar, D. D., Amin, M. R., Azgomi, H. F., Aschbacher, K., Crofford, L. J., & Faghih, R. T.
- Affiliations
- University of Houston (US)
- University of California, San Francisco (US)
- Vanderbilt University (US)
- Venue
- IEEE Transactions on Biomedical Engineering
- Published
- 2020-11
- Volume
- 67
- Issue
- 11
- Pages
- 3163-3172
- ISSN
- 0018-9294 (ISSN-L)
- 1558-2531
- OpenAlex
- W3009154718
- Cited by
- 27
- References
- 45
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 8 · 2022: 5 · 2021: 3 · 2020: 2
- FWCI
- 3.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- IEEE Transactions on Biomedical Engineering (publishedVersion)
- PubMed (publishedVersion)
- Funders
- NSF (1755780)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Fibromyalgia and Chronic Fatigue Syndrome Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Keywords
- fibromyalgia, chronic fatigue syndrome, cortisol secretion, state-space model, circadian rhythm, hypothalamic-pituitary-adrenal axis
- MeSH terms
- Fibromyalgia, Humans, Hydrocortisone, Fatigue Syndrome, Chronic
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