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      Steroid Metabolome Analysis in Disorders of Adrenal Steroid Biosynthesis and Metabolism

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          Abstract

          Steroid biosynthesis and metabolism are reflected by the serum steroid metabolome and, in even more detail, by the 24-hour urine steroid metabolome, which can provide unique insights into alterations of steroid flow and output indicative of underlying conditions. Mass spectrometry–based steroid metabolome profiling has allowed for the identification of unique multisteroid signatures associated with disorders of steroid biosynthesis and metabolism that can be used for personalized approaches to diagnosis, differential diagnosis, and prognostic prediction. Additionally, steroid metabolome analysis has been used successfully as a discovery tool, for the identification of novel steroidogenic disorders and pathways as well as revealing insights into the pathophysiology of adrenal disease. Increased availability and technological advances in mass spectrometry–based methodologies have refocused attention on steroid metabolome profiling and facilitated the development of high-throughput steroid profiling methods soon to reach clinical practice. Furthermore, steroid metabolomics, the combination of mass spectrometry–based steroid analysis with machine learning–based approaches, has facilitated the development of powerful customized diagnostic approaches. In this review, we provide a comprehensive up-to-date overview of the utility of steroid metabolome analysis for the diagnosis and management of inborn disorders of steroidogenesis and autonomous adrenal steroid excess in the context of adrenal tumors.

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          The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline.

          To develop clinical practice guidelines for the management of patients with primary aldosteronism.
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            Adrenocortical carcinoma.

            Adrenocortical carcinoma (ACC) is a rare endocrine malignancy, often with an unfavorable prognosis. Here we summarize the knowledge about diagnosis, epidemiology, pathophysiology, and therapy of ACC. Over recent years, multidisciplinary clinics have formed and the first international treatment trials have been conducted. This review focuses on evidence gained from recent basic science and clinical research and provides perspectives from the experience of a large multidisciplinary clinic dedicated to the care of patients with ACC.
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              K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.

              Endocrine tumors such as aldosterone-producing adrenal adenomas (APAs), a cause of severe hypertension, feature constitutive hormone production and unrestrained cell proliferation; the mechanisms linking these events are unknown. We identify two recurrent somatic mutations in and near the selectivity filter of the potassium (K(+)) channel KCNJ5 that are present in 8 of 22 human APAs studied. Both produce increased sodium (Na(+)) conductance and cell depolarization, which in adrenal glomerulosa cells produces calcium (Ca(2+)) entry, the signal for aldosterone production and cell proliferation. Similarly, we identify an inherited KCNJ5 mutation that produces increased Na(+) conductance in a Mendelian form of severe aldosteronism and massive bilateral adrenal hyperplasia. These findings explain pathogenesis in a subset of patients with severe hypertension and implicate loss of K(+) channel selectivity in constitutive cell proliferation and hormone production.
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                Author and article information

                Journal
                Endocr Rev
                Endocr. Rev
                edrv
                Endocrine Reviews
                Endocrine Society (Washington, DC )
                0163-769X
                1945-7189
                December 2019
                11 July 2019
                11 July 2019
                : 40
                : 6
                : 1605-1625
                Affiliations
                [1 ] Department of Biochemistry, Stellenbosch University , Stellenbosch, South Africa
                [2 ] Institute of Metabolism and Systems Research, University of Birmingham , Birmingham, United Kingdom
                [3 ] Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners , Birmingham, United Kingdom
                [4 ] Department of Paediatric Endocrinology and Diabetes, Birmingham Women’s and Children’s Hospital NHS Foundation Trust , Birmingham, United Kingdom
                [5 ] Department of Endocrinology, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust , Birmingham, United Kingdom
                [6 ] NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust and University of Birmingham , Birmingham, United Kingdom
                [7 ] UCSF Benioff Children’s Hospital Oakland Research Institute , Oakland, California
                Author notes
                Correspondence and Reprint Requests:  Wiebke Arlt, MD, DSc, Institute of Metabolism and Systems Research, Medical School IBR Tower, Room 236, University of Birmingham, Birmingham B15 2TT, United Kingdom. E-mail: w.arlt@ 123456bham.ac.uk .

                W.A. and C.H.L.S. are joint senior authors.

                Author information
                http://orcid.org/0000-0003-1669-6383
                http://orcid.org/0000-0001-8540-4861
                http://orcid.org/0000-0002-2731-577X
                http://orcid.org/0000-0002-4906-8239
                http://orcid.org/0000-0002-4821-0336
                http://orcid.org/0000-0002-8280-703X
                http://orcid.org/0000-0002-0708-2999
                http://orcid.org/0000-0002-5835-5643
                http://orcid.org/0000-0001-9181-3995
                http://orcid.org/0000-0001-5106-9719
                Article
                201800262
                10.1210/er.2018-00262
                6858476
                31294783
                92e93e10-3724-4dcd-8717-8bf245faeb73
                Copyright © 2019 Endocrine Society

                This article has been published under the terms of the Creative Commons Attribution License (CC BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s).

                History
                : 02 November 2018
                : 04 June 2019
                Page count
                Pages: 21
                Funding
                Funded by: Wellcome Trust 10.13039/100010269
                Award ID: WT209492/Z/17/Z
                Award ID: WT101671AIA
                Funded by: Medical Research Council 10.13039/501100000265
                Award ID: G1001964
                Award ID: MR/R017913/1
                Funded by: Diabetes UK 10.13039/501100000361
                Award ID: 18/0005782
                Funded by: Academy of Medical Sciences UK
                Award ID: NAF004\1002
                Categories
                Reviews
                Adrenal

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