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Deconvolution of Serum Cortisol Levels by Using Compressed Sensing

The pulsatile release of cortisol from the adrenal glands is controlled by a hierarchical system that involves corticotropin releasing hormone (CRH) from the hypothalamus, adrenocorticotropin hormone (ACTH) from the pituitary, and cortisol from the adrenal glands. Determining the number, timing, and...

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Autores principales: Faghih, Rose T., Dahleh, Munther A., Adler, Gail K., Klerman, Elizabeth B., Brown, Emery N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904842/
https://www.ncbi.nlm.nih.gov/pubmed/24489656
http://dx.doi.org/10.1371/journal.pone.0085204
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author Faghih, Rose T.
Dahleh, Munther A.
Adler, Gail K.
Klerman, Elizabeth B.
Brown, Emery N.
author_facet Faghih, Rose T.
Dahleh, Munther A.
Adler, Gail K.
Klerman, Elizabeth B.
Brown, Emery N.
author_sort Faghih, Rose T.
collection PubMed
description The pulsatile release of cortisol from the adrenal glands is controlled by a hierarchical system that involves corticotropin releasing hormone (CRH) from the hypothalamus, adrenocorticotropin hormone (ACTH) from the pituitary, and cortisol from the adrenal glands. Determining the number, timing, and amplitude of the cortisol secretory events and recovering the infusion and clearance rates from serial measurements of serum cortisol levels is a challenging problem. Despite many years of work on this problem, a complete satisfactory solution has been elusive. We formulate this question as a non-convex optimization problem, and solve it using a coordinate descent algorithm that has a principled combination of (i) compressed sensing for recovering the amplitude and timing of the secretory events, and (ii) generalized cross validation for choosing the regularization parameter. Using only the observed serum cortisol levels, we model cortisol secretion from the adrenal glands using a second-order linear differential equation with pulsatile inputs that represent cortisol pulses released in response to pulses of ACTH. Using our algorithm and the assumption that the number of pulses is between 15 to 22 pulses over 24 hours, we successfully deconvolve both simulated datasets and actual 24-hr serum cortisol datasets sampled every 10 minutes from 10 healthy women. Assuming a one-minute resolution for the secretory events, we obtain physiologically plausible timings and amplitudes of each cortisol secretory event with R (2) above 0.92. Identification of the amplitude and timing of pulsatile hormone release allows (i) quantifying of normal and abnormal secretion patterns towards the goal of understanding pathological neuroendocrine states, and (ii) potentially designing optimal approaches for treating hormonal disorders.
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spelling pubmed-39048422014-01-31 Deconvolution of Serum Cortisol Levels by Using Compressed Sensing Faghih, Rose T. Dahleh, Munther A. Adler, Gail K. Klerman, Elizabeth B. Brown, Emery N. PLoS One Research Article The pulsatile release of cortisol from the adrenal glands is controlled by a hierarchical system that involves corticotropin releasing hormone (CRH) from the hypothalamus, adrenocorticotropin hormone (ACTH) from the pituitary, and cortisol from the adrenal glands. Determining the number, timing, and amplitude of the cortisol secretory events and recovering the infusion and clearance rates from serial measurements of serum cortisol levels is a challenging problem. Despite many years of work on this problem, a complete satisfactory solution has been elusive. We formulate this question as a non-convex optimization problem, and solve it using a coordinate descent algorithm that has a principled combination of (i) compressed sensing for recovering the amplitude and timing of the secretory events, and (ii) generalized cross validation for choosing the regularization parameter. Using only the observed serum cortisol levels, we model cortisol secretion from the adrenal glands using a second-order linear differential equation with pulsatile inputs that represent cortisol pulses released in response to pulses of ACTH. Using our algorithm and the assumption that the number of pulses is between 15 to 22 pulses over 24 hours, we successfully deconvolve both simulated datasets and actual 24-hr serum cortisol datasets sampled every 10 minutes from 10 healthy women. Assuming a one-minute resolution for the secretory events, we obtain physiologically plausible timings and amplitudes of each cortisol secretory event with R (2) above 0.92. Identification of the amplitude and timing of pulsatile hormone release allows (i) quantifying of normal and abnormal secretion patterns towards the goal of understanding pathological neuroendocrine states, and (ii) potentially designing optimal approaches for treating hormonal disorders. Public Library of Science 2014-01-28 /pmc/articles/PMC3904842/ /pubmed/24489656 http://dx.doi.org/10.1371/journal.pone.0085204 Text en © 2014 Faghih et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Faghih, Rose T.
Dahleh, Munther A.
Adler, Gail K.
Klerman, Elizabeth B.
Brown, Emery N.
Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title_full Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title_fullStr Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title_full_unstemmed Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title_short Deconvolution of Serum Cortisol Levels by Using Compressed Sensing
title_sort deconvolution of serum cortisol levels by using compressed sensing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904842/
https://www.ncbi.nlm.nih.gov/pubmed/24489656
http://dx.doi.org/10.1371/journal.pone.0085204
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