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Hyperhidrosis

Bones, Joints, Muscles and Skin · NLM MeSH · updated 2026-11-04 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

Excessive sweating.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (830 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Hyperidrosis.

Where it fits in the MeSH classification

Broader topics
Sweat Gland Diseases
Narrower topics
Sweating, Gustatory

Research landscape

PubMed indexes 4,353 records tagged with the MeSH heading “Hyperhidrosis” (counts retrieved 2026-11-04). 634 of them (14.6%) were published from 2020 onward, and the busiest period so far is through 1999 with 1,312 records.

Reviews account for 534 records (12.3%) and meta-analyses for 46. Randomized controlled trials number 197 (4.5%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 1,312 records; 2000-2009: 1,219 records; 2010-2019: 1,188 records; 2020 onward: 634 records1,312through 19991,2192000-20091,1882010-20196342020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 19991,312
2000-20091,219
2010-20191,188
2020 onward634
Share of records by publication typeReviews: 12.3 percent; Meta-analyses: 1.1 percent; Randomized controlled trials: 4.5 percentReviews12.3% (534)Meta-analyses1.1% (46)Randomized controlled trials4.5% (197)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 4,353 PubMed records
TypeRecordsShare
Reviews53412.3%
Meta-analyses461.1%
Randomized controlled trials1974.5%

Method: PubMed query "Hyperhidrosis"[MeSH Terms] with publication-type and date filters, retrieved 2026-11-04.

Reading the evidence in bones, joints, muscles and skin

Joint, bone, muscle and skin conditions are often judged by pain scores, function questionnaires, imaging or photographs, and symptoms can fluctuate, so placebo response and natural improvement matter. Imaging changes are common in people without symptoms. Nothing on this page is advice about treatment. Check how outcomes were measured, whether the comparison group received a placebo or usual care, and how long the benefit lasted.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Hyperhidrosis Prevalence and Demographical Characteristics in Dermatology Outpatients in Shanghai and Vancouver
Liu Y, Bahar R, Kalia S, Huang RY, Phillips A, Su M, et al.
2016Research article
Design not recorded in structured metadata
49cc by
PMID 27105064 · DOI · PMC4841532
CRLF1 and CLCF1 in Development, Health and Disease
Crisponi L, Buers I, Rutsch F
2022Review article
Design not recorded in structured metadata
47cc by
PMID 35055176 · DOI · PMC8780587
Efficacy and safety of botulinum toxin type A for treatment of Frey's syndrome: evidence from 22 published articles
Xie S, Wang K, Xu T, Guo XS, Shan XF, Cai ZG
2015Meta-analysis
Design not recorded in structured metadata
26cc by
PMID 26310612 · DOI · PMC4673990
A neurocutaneous NaV1.8 channelopathy underlies a genetic subtype of primary idiopathic hyperhidrosis
Yamauchi S, Vander Cruyssen J, Cervellera M, Wohler E, De Waele J, Lammens M, et al.
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42467787 · DOI · PMC13378580

Hyperhidrosis Prevalence and Demographical Characteristics in Dermatology Outpatients in Shanghai and Vancouver [1]

Research article Liu Y, Bahar R, Kalia S, Huang RY, Phillips A, Su M, et al. · · 2016 · cited 49 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundThere is a wide variation in the reported prevalence of primary hyperhidrosis in the literature.
Closing excerpt
However, certain specific HH subtypes can show great variations according to ethnicity, age, body mass index and sex.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (343 words)

BackgroundThere is a wide variation in the reported prevalence of primary hyperhidrosis in the literature. Further, it is unknown if primary hyperhidrosis is a lifelong condition, or if demographical factors influence hyperhidrosis prevalence.ObjectivesThis study aims to examine the prevalence of hyperhidrosis in multiple ethnic groups from two ethnically diverse cities and to determine if the prevalence of primary hyperhidrosis changes according to age, gender, ethnicity, body mass index, and geographical locations.MethodsIn total, 1010 consecutive subjects attending dermatology outpatient clinics in Shanghai Skin Disease Hospital and 1018 subjects in Skin Care Center of Vancouver General Hospital were invited to fill out a questionnaire on their presenting concerns, demographical information, and sweating symptoms. The subjects were then classified to have primary hyperhidrosis using the criteria of International Hyperhidrosis Society, late-onset hyperhidrosis, or no-hyperhidrosis. The prevalence of primary HH and late-onset HH was calculated for the entire study population and in subgroups stratified according to age of examination, sex, ethnicity, presenting diagnosis, body mass index, and specific study cities. Multivariate logistic regression analyses were performed to assess the impact of these factors on HH prevalence.ResultsThe prevalence of primary hyperhidrosis is very similar in Shanghai and in Vancouver, at 14.5% and 12.3% respectively. In addition, 4.0% of subjects in Shanghai and 4.4% subjects in Vancouver suffer from late-onset HH. Primary HH has highest prevalence in those younger than 30 years of age, decreasing dramatically in later years. Caucasian subjects are at least 2.5 times more likely to develop axillary hyperhidrosis compared to Chinese subjects. Obesity does not have much influence on primary HH presentation, although it does increase significantly the development of late-onset HH. Finally, there is no major difference of hyperhidrosis between Chinese subjects in Shanghai and Vancouver.LimitationsThe data were gathered according to patients' self-reports only and the sample size was relatively small in some groups after stratification for gender, ethnicity and age.ConclusionPrevalence of primary HH and late-onset HH is similar in dermatology outpatients independent of geographical locations. However, certain specific HH subtypes can show great variations according to ethnicity, age, body mass index and sex.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 27105064 · DOI · PMC4841532

CRLF1 and CLCF1 in Development, Health and Disease [2]

Review article Crisponi L, Buers I, Rutsch F · · 2022 · cited 47 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Cytokines and their receptors have a vital function in regulating various processes such as immune function, inflammation, haematopoiesis, cell growth and differentiation.
Closing excerpt
In this review, we highlight the role of the soluble type I cytokine receptor CRLF1 (cytokine receptor-like factor-1) and the Interleukin (IL)-6 cytokine CLCF1 (cardiotrophin-like cytokine factor 1) during development in physiological and pathological conditions with particular emphasis on Crisponi/cold-induced sweating syndrome (CS/CISS) and discuss new insights, challenges and possibilities arising from recent studies.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (108 words)

Cytokines and their receptors have a vital function in regulating various processes such as immune function, inflammation, haematopoiesis, cell growth and differentiation. The interaction between a cytokine and its specific receptor triggers intracellular signalling cascades that lead to altered gene expression in the target cell and consequent changes in its proliferation, differentiation, or activation. In this review, we highlight the role of the soluble type I cytokine receptor CRLF1 (cytokine receptor-like factor-1) and the Interleukin (IL)-6 cytokine CLCF1 (cardiotrophin-like cytokine factor 1) during development in physiological and pathological conditions with particular emphasis on Crisponi/cold-induced sweating syndrome (CS/CISS) and discuss new insights, challenges and possibilities arising from recent studies.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 35055176 · DOI · PMC8780587

Efficacy and safety of botulinum toxin type A for treatment of Frey's syndrome: evidence from 22 published articles [3]

Meta-analysis Xie S, Wang K, Xu T, Guo XS, Shan XF, Cai ZG · · 2015 · cited 26 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Frey's syndrome (FS) is an unavoidable sequela following the surgery of the parotid gland.
Closing excerpt
However, owing to lack of strong evidence, future studies with well-designed inclusion criteria and multicenter randomized controlled trials are needed to give more credible evidence, if possible.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (236 words)

Frey's syndrome (FS) is an unavoidable sequela following the surgery of the parotid gland. Although several treatment methods are available, their efficacy is short term or accompanied by unacceptable complications. In the past two decades, botulinum toxin type A (BTXA) has been widely used to treat FS. Although several systematic reviews have been reported recently, they were conflicting and with obvious deficiencies. Thus, we performed an objectively systematic review to determine whether BTXA is an effective and safe treatment for FS. A literature retrieval covering PubMed, Web of Science, Ovid, Embase and Cochrane library was performed on 16 January, 2015. Proportion meta-analysis and corresponding 95% confidence interval (CI) were performed to evaluate the efficacy and safety of BXTA in treatment of FS. A total of 499 records were retrieved and 22 articles with 23 studies were included after scrutiny by two independent authors. Statistical analyses regarding the effective rate, incidence of complications were used to estimate the efficacy and safety of BTXA. Our results suggested that the effective rate of BTXA for treatment of FS is 98.5% (95% CI = 0.971-0.994) and the incidence of complication is 3.6% (95% CI = 0.017-0.061). In conclusion, our study supports that BTXA produces meaningful benefits on the treatment of patients with FS. However, owing to lack of strong evidence, future studies with well-designed inclusion criteria and multicenter randomized controlled trials are needed to give more credible evidence, if possible.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 26310612 · DOI · PMC4673990

A neurocutaneous NaV1.8 channelopathy underlies a genetic subtype of primary idiopathic hyperhidrosis [4]

Research article Yamauchi S, Vander Cruyssen J, Cervellera M, Wohler E, De Waele J, Lammens M, et al. · · 2026

Abstract reading summary — source excerpts
Opening excerpt
Primary idiopathic hyperhidrosis (PIH) is a poorly understood disorder characterized by excessive sweating.
Closing excerpt
Together, these findings define a targetable neurocutaneous channelopathy underlying a subset of PIH and support a model in which excessive sweating arises from either gland-intrinsic dysfunction or altered sympathetic drive, motivating stratified therapeutic approaches.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (143 words)

Primary idiopathic hyperhidrosis (PIH) is a poorly understood disorder characterized by excessive sweating. We identify a genetically defined subset of PIH associated with rare coding changes in voltage-gated Na+ (NaV) channels. Whole-exome sequencing of hereditary PIH families revealed gene-level enrichment within the NaV channel family, with SCN10A (NaV1.8) most strongly implicated. A knock-in mouse carrying the clinically observed NaV1.8p.R14L substitution recapitulated excessive sweating. NaV1.8 was detected in a subset of postganglionic neurons in thoracic sympathetic ganglia in humans and mice, where p.R14L produced a gain-of-function profile that enhanced cholinergic responsiveness. Excessive sweating in mutant mice was reversible with NaV channel inhibition, including clinically used agents and a NaV1.8-preferential compound. Together, these findings define a targetable neurocutaneous channelopathy underlying a subset of PIH and support a model in which excessive sweating arises from either gland-intrinsic dysfunction or altered sympathetic drive, motivating stratified therapeutic approaches.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42467787 · DOI · PMC13378580

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Biology of sweat glands and their disorders. II. Disorders of sweat gland function [5]
    Sato K, Kang WH, Saga K, Sato KT · J Am Acad Dermatol · 1989 · cited 173 times (Europe PMC)
  • Research article Focal hyperhidrosis: diagnosis and management [6]
    Haider A, Solish N · CMAJ · 2005 · cited 137 times (Europe PMC)
  • Research article The etiology, diagnosis, and management of hyperhidrosis: A comprehensive review: Therapeutic options [7]
    Nawrocki S, Cha J · J Am Acad Dermatol · 2019 · cited 111 times (Europe PMC)
  • Research article Drug-induced hyperhidrosis and hypohidrosis: incidence, prevention and management [8]
    Cheshire WP, Fealey RD · Drug Saf · 2008 · cited 99 times (Europe PMC)
  • Research article The etiology, diagnosis, and management of hyperhidrosis: A comprehensive review: Etiology and clinical work-up [9]
    Nawrocki S, Cha J · J Am Acad Dermatol · 2019 · cited 90 times (Europe PMC)
  • Research article Treatment of hyperhidrosis [10]
    Stolman LP · Dermatol Clin · 1998 · cited 85 times (Europe PMC)

References

  1. Liu Y, Bahar R, Kalia S, Huang RY, Phillips A, Su M, et al.. Hyperhidrosis Prevalence and Demographical Characteristics in Dermatology Outpatients in Shanghai and Vancouver. . 2016. PMID 27105064 · DOI · PMC4841532
  2. Crisponi L, Buers I, Rutsch F. CRLF1 and CLCF1 in Development, Health and Disease. . 2022. PMID 35055176 · DOI · PMC8780587
  3. Xie S, Wang K, Xu T, Guo XS, Shan XF, Cai ZG. Efficacy and safety of botulinum toxin type A for treatment of Frey's syndrome: evidence from 22 published articles. . 2015. PMID 26310612 · DOI · PMC4673990
  4. Yamauchi S, Vander Cruyssen J, Cervellera M, Wohler E, De Waele J, Lammens M, et al.. A neurocutaneous NaV1.8 channelopathy underlies a genetic subtype of primary idiopathic hyperhidrosis. . 2026. PMID 42467787 · DOI · PMC13378580
  5. Sato K, Kang WH, Saga K, Sato KT. Biology of sweat glands and their disorders. II. Disorders of sweat gland function. J Am Acad Dermatol. 1989. PMID 2654213 · DOI
  6. Haider A, Solish N. Focal hyperhidrosis: diagnosis and management. CMAJ. 2005. PMID 15632408 · DOI · PMC543948
  7. Nawrocki S, Cha J. The etiology, diagnosis, and management of hyperhidrosis: A comprehensive review: Therapeutic options. J Am Acad Dermatol. 2019. PMID 30710603 · DOI
  8. Cheshire WP, Fealey RD. Drug-induced hyperhidrosis and hypohidrosis: incidence, prevention and management. Drug Saf. 2008. PMID 18217788 · DOI
  9. Nawrocki S, Cha J. The etiology, diagnosis, and management of hyperhidrosis: A comprehensive review: Etiology and clinical work-up. J Am Acad Dermatol. 2019. PMID 30710604 · DOI
  10. Stolman LP. Treatment of hyperhidrosis. Dermatol Clin. 1998. PMID 9891696 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-11-04; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-11-04.

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At a glance

4,353
PubMed records on this heading
15%
published since 2020
534
review articles
197
randomized trials
10
verified references below

Counts come from PubMed on 2026-11-04; they show how much has been written, not how strong the evidence is.

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