Evidence map›Paper›PMID 42281425›Full record

ArticleJournal of diabetes investigation2026

Sudomotor dysfunction in people with type 1 diabetes with and without clinical peripheral neuropathy: A study from Pune, India.

Rohan Shah, Rishikesh Behere, Aboli Bhalerao, Sanat Phatak, Alma Baptist, Chinmay S Marathe, Chittaranjan S Yajnik

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Article in Journal of diabetes investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Rohan ShahDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.
Rishikesh BehereDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.
Aboli BhaleraoDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.
Sanat PhatakDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.
Alma BaptistDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.
Chinmay S MaratheFaculty of Health and Medical Sciences, Adelaide University, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-8086-2449
Chittaranjan S YajnikDiabetes Unit, King Edward Memorial Hospital Research Centre, Pune, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsIt is appreciated that current screening tools for diabetic peripheral neuropathy (DPN) often fail to detect early disease. Sudomotor (sweat gland) dysfunction, among the earliest manifestations of DPN, can be measured objectively by the SUDOSCAN® device. We compared SUDOSCAN® with conventional validated screening (Michigan Neuropathy Screening Instrument or MNSI) in type 1 diabetes (T1D).

methodsT1D participants (n = 264, 46.2% male, mean age 26.3 years, mean diabetes duration 13.2 years) enrolled in the prospective PICTURE study (Diabetes Unit, KEM Hospital, Pune, India) underwent simultaneous assessments for sudomotor dysfunction (electrochemical skin conductance ESC <60 μS indicating dysfunction) and DPN (MNSI) and were classified as: (a) MNSI abnormal ('clinical DPN'), (b) MNSI normal, but ESC <60 ('subclinical DPN) and (c) Both normal ('no neuropathy').

resultsSudomotor dysfunction was more common than clinical DPN (46.2 vs 22.3%) with a sensitivity of 72.8% and specificity of 61.4% for detecting clinical DPN. Those with sudomotor dysfunction (ESC <60 μS) were 4.3 times more likely to have clinical DPN compared with participants without sudomotor dysfunction (ESC ≥60 μS). Among participants with normal MNSI (i.e., without clinical DPN), subclinical DPN was detected in 38.5% and was associated with younger age, shorter duration of diabetes, anemia, vitamin D deficiency, and microvascular complications.

conclusionSudomotor testing is an objective and sensitive method for DPN screening in T1D, aiding early detection.

Indexed as

Diabetes Mellitus, Type 1Diabetic NeuropathiesSweat GlandsAdultFemaleGalvanic Skin ResponseHumansIndiaMaleMiddle AgedPrognosisProspective StudiesYoung AdultSudomotor dysfunctionSUDOSCANType 1 diabetes

Identifiers

PMID42281425
PMCPMC13398954

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