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      Prognosis after steroid pulse therapy and seasonal effect in acquired idiopathic generalized anhidrosis

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          Abstract

          Acquired idiopathic generalized anhidrosis is a rare disease with unknown etiology. Sudden loss of sweating function adversely affects young patients’ quality of life. Although systemic corticosteroid therapy is the most frequently reported treatment for the disease, its effectiveness is controversial because of the risk of recurrence. To assist clinical decision‐making regarding whether to use steroids, we investigated the treatment responsiveness and recurrence rates in patients undergoing steroid pulse therapy and explored factors affecting these rates. We retrospectively collected data of 124 patients who received steroid pulse therapy to calculate the rate of responsiveness to the therapy. We also conducted a time‐to‐event analysis in a cohort of 57 patients who responded to steroid pulse therapy to estimate the recurrence rate after the therapy. As a result, the response and recurrence rates were 73% and 48%, respectively. Recurrence occurred within 1 year in most patients. The overall effectiveness of steroid pulse therapy was estimated to be 57% considering the recurrence rate. A delay from onset to treatment and younger age appeared to be negative factors for effectiveness. Moreover, we found a significant seasonal effect on both treatment and recurrence: autumn was the worst season for acquired idiopathic generalized anhidrosis in Japan. Our study revealed that steroid pulse therapy can be expected to be effective in half of treated patients. We recommend starting the therapy promptly after the diagnosis; however, it is also worth considering the season for treatment planning.

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          Most cited references23

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Long-term Systemic Corticosteroid Exposure: A Systematic Literature Review

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              Idiopathic pure sudomotor failure: anhidrosis due to deficits in cholinergic transmission.

              Acquired idiopathic generalized anhidrosis (AIGA) represents a heterogeneous clinical syndrome including sudomotor neuropathy and failure of the sweat glands. However, most AIGA cases comprise idiopathic pure sudomotor failure (IPSF), a distinct subgroup without sudomotor neuropathy or sweat gland failure. Eight patients with IPSF (mean +/- SD age 20 +/- 5 years) were assessed by thermoregulatory and pilocarpine-induced sweating tests, as well as emotional sweating using sudorometer (4 cases), microneurography of skin sympathetic nerve activity (2 cases), and skin biopsies from the forearm or axilla (3 cases). Clinical features of IPSF comprise early onset; acute or sudden onset; concomitant sharp pain or cholinergic urticaria over the entire body; lack of autonomic dysfunction other than generalized anhidrosis; elevated serum IgE levels; and marked response to steroid. Sudomotor function testing revealed complete absence of thermoregulatory sweating, but well-preserved emotional sweating; pilocarpine did not induce sweating, and microneurography revealed that bursts of skin sympathetic nerve activity were not decreased; and skin biopsy displayed no morphologic abnormalities in sweat glands. The first two findings suggest lesions on the postsynaptic side of the nerve-sweat gland junction. The lesions in IPSF may be in the muscarinic cholinergic receptors of sweat glands. Allergic mechanisms are probably involved in its pathophysiology.
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                Author and article information

                Contributors
                3064derm@tmd.ac.jp
                Journal
                J Dermatol
                J Dermatol
                10.1111/(ISSN)1346-8138
                JDE
                The Journal of Dermatology
                John Wiley and Sons Inc. (Hoboken )
                0385-2407
                1346-8138
                04 November 2020
                March 2021
                : 48
                : 3 ( doiID: 10.1111/jde.v48.3 )
                : 271-278
                Affiliations
                [ 1 ] Department of Dermatology Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Tokyo Japan
                [ 2 ] Department of Maxillofacial Surgery Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Tokyo Japan
                [ 3 ] Department of Dermatology Aichi Medical University School of Medicine Nagakute Japan
                [ 4 ] Department of Neurology Saitama Medical University Moroyama Japan
                Author notes
                [*] [* ] Correspondence: Hiroo Yokozeki, M.D., Ph.D., Department of Dermatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1‐5‐45 Yushima, Bunkyo‐ku, Tokyo 113‐8510, Japan. Email: 3064derm@ 123456tmd.ac.jp

                [*]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-5869-2017
                https://orcid.org/0000-0002-1092-1159
                https://orcid.org/0000-0002-5773-9485
                Article
                JDE15666
                10.1111/1346-8138.15666
                7984388
                33146891
                a26639e6-1c3f-4bd0-984d-8808341baacc
                © 2020 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 July 2020
                : 28 September 2020
                Page count
                Figures: 3, Tables: 3, Pages: 8, Words: 6296
                Funding
                Funded by: Japan Agency for Medical Research and Development , open-funder-registry 10.13039/100009619;
                Award ID: JP20ek0109435
                Funded by: Health and Labour Sciences Research Grants
                Award ID: 19FC1009
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                March 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.0 mode:remove_FC converted:22.03.2021

                cohort studies,hypohidrosis,sweat glands,temperature,urticaria

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