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dc.contributor.authorDahleh, Munther A.
dc.contributor.authorAdler, Gail K.
dc.contributor.authorKlerman, Elizabeth B.
dc.contributor.authorBrown, Emery N.
dc.contributor.authorFaghih, Rose Taj
dc.date.accessioned2014-04-03T16:55:07Z
dc.date.available2014-04-03T16:55:07Z
dc.date.issued2014-01
dc.date.submitted2013-09
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/85996
dc.description.abstractThe 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[superscript 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.en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH DP1 OD003646)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (0836720)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Office of Emerging Frontiers in Research and Innovation (EFRI-0735956)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0085204en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titleDeconvolution of Serum Cortisol Levels by Using Compressed Sensingen_US
dc.typeArticleen_US
dc.identifier.citationFaghih, Rose T., Munther A. Dahleh, Gail K. Adler, Elizabeth B. Klerman, and Emery N. Brown. “Deconvolution of Serum Cortisol Levels by Using Compressed Sensing.” Edited by Andrew Wolfe. PLoS ONE 9, no. 1 (January 28, 2014): e85204.en_US
dc.contributor.departmentInstitute for Medical Engineering and Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Engineering Systems Divisionen_US
dc.contributor.departmentMassachusetts Institute of Technology. Laboratory for Information and Decision Systemsen_US
dc.contributor.mitauthorFaghih, Rose Tajen_US
dc.contributor.mitauthorDahleh, Munther A.en_US
dc.contributor.mitauthorBrown, Emery N.en_US
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsFaghih, Rose T.; Dahleh, Munther A.; Adler, Gail K.; Klerman, Elizabeth B.; Brown, Emery N.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2668-7819
dc.identifier.orcidhttps://orcid.org/0000-0002-1470-2148
dc.identifier.orcidhttps://orcid.org/0000-0002-9959-8422
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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