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Aims: This study done in subjects with an initial normal glucose tolerance (NGT) was to assess the ability of EZSCAN, a new device developed to evaluate sudomotor function, to predict future abnormalities in glucose tolerance. Methods: South Asian (Indian) subjects (n= 69, 48% male, mean age 42 ± 9 years, mean BMI 28 ± 5 kg/m 2 ) diagnosed as NGT with a previous oral glucose tolerance test (OGTT, T0) underwent a frequently sampled OGTT (FSOGTT), 8 months later (T8). At both times EZSCAN tests were done. Using the AUC glucose and AUC insulin measured by the FSOGTT, subjects were categorised as normal, high AUC insulin or isolated high AUC glucose . Odds ratio (OR) for having high AUC insulin or isolated high AUC glucose vs normal was computed by logistic regression analysis using EZSCAN risk classification at T0 as independent variable ( 65%=high risk). Results: At T8, 11 and 5 subjects developed impaired glucose tolerance and diabetes respectively. OR of having high AUC insulin or isolated high AUC glucose in the different risk groups was 6.19 (CI 95% 1.50 – 25.48, p = 0.0116) for high risk vs no risk and 3.0 (CI 95% 0.98 – 9.19, p = 0.0545) for intermediate risk vs no risk. Sensitivity of EZSCAN for early detection of these abnormalities in glucose tolerance was 77% while it was 14% for fasting plasma glucose and 66% for HbA 1C . Conclusions: Assessment of sudomotor function by EZSCAN, a sensitive method when compared with the con - ventional methods may be very useful to identify and manage subjects at risk for developing glucose intolerance.

Small fiber neuropathy is a dysfunction caused by diseases such as type II diabetes and cystic fibrosis. Nowadays, it is possible to analyze neuropathy with SudoscanTM technology (Impeto Medical Inc.) which provides a rapid and non-invasive early diagnosis. This technology is based on measurements of the electrochemical conductance of the skin viathe imposition of low amplitude voltages between electrodes applied to the skin and measuring the low current generated. The output measurement is related to the sweat composition associated to glands innervations and their permeability to chloride and proton ions [1]. The results obtained with this in vivo technology show a typical anode current response (curve J-E) with a significant offset and a linear part. The characteristic shape of the J-E graph easily indicates the type of disease and its progress [2]. To have a deeper understanding of the mechanisms occurring at electrodes and optimize the sensitivity of the instrument, in vitro experiments were performed in mimetic electrolytic solutions of sweat. Preliminary in vitro experiments led to same shapes than in vivo but with larger current densities (≈ 50 times greater than those obtained in vivo). This phenomenon is probably due to the high resistivity of a human body and the difference of the electrodes system between in vitro and in vivo measurements. For these reasons, it was necessary to modify in vitro conditions to get similar current densities and mimic realistically in vivo conditions. To this end, major modifications in the in vitro system were realized: (i) Concerning the in vitro configuration: the electrodes arrangement was changed and 3 identical electrodes were used leading to a decrease in the current densities by a factor of 10 (ii) To simulate the body resistance and, consequently, to decrease the current densities in vitro, the electrolyte composition was optimized by increasing its viscosity to reduce the flux of chloride ions to the electrode surface. The new composition allowed to reach current densities close to those obtained in vivo [3]. The aim of this work was to find the optimized electrolyte, mimicking sweat in terms of composition and the resistance of the human body under in vitroconditions. Then, the goal was to go deeper in the knowledge on the mechanism governing the electrode response to sweat. For this, linear voltammetry and electrochemical impedance spectroscopy were implemented to study the influence of sweat components such as pH, chloride concentration, buffer and carbonate concentration on a nickel model electrode [4]. Finally, different stainless steel electrodes were tested. Such electrodes are required because they are not allergenic and less expensive than nickel, but they need to be sensible to ions detection in sweat, with reproducible results allowing the early detection of diseases. References: [1] A. Calmet, H. Ayoub, V. Lair, and S. Griveau, Actual. Chim., vol. 390, pp. 48–49, 2014. [2] P. Brunswick and N. Bocquet, “Système d’analyse électrophysiologique,” 0753461. [3] A. Calmet, K. Khalfallah, H. Ayoub, V. Lair, S. Griveau, P. Brunswick, F. Bedioui, and M. Cassir, Electrochim. Acta, vol. 140, pp. 37–41, Sep. 2014. [4] H. Ayoub , S. Griveau, V. Lair, P. Brunswick, M. Cassir, and F. Bedioui, Electroanalysis, vol. 22, no. 21, pp. 2483–2490, Nov. 2010.