Lisa Klous

Dr. Lisa Klous

Vrije Universiteit Amsterdam
orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 December 2020 in European Journal of Applied Physiology
Verified
Journal Article
Open access
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LKLisa Klous
Lisa Klous
CRCornelis Johannes de Ruiter
Cornelis Johannes de Ruiter
SSS. Scherrer
S. Scherrer
NGNicola Gerrett
Nicola Gerrett
HDHein A.M. Daanen
Hein A.M. Daanen
Purpose: To reduce the need for invasive and expensive measures of human biomarkers, sweat is becoming increasingly popular in use as an alternative to blood. Therefore, the (in)dependency of blood and sweat composition has to be explored.Methods: In an environmental chamber (33 °C, 65% relative humidity; RH), 12 participants completed three subsequent 20-min cycling stages to elicit three different local sweat rates (LSR) while aiming to limit changes in blood composition: at 60% of their maximum heart rate (HRmax), 70% HRmaxand 80% HRmax, with 5 min of seated-rest in between. Sweat was collected from the arm and back during each stage and post-exercise. Blood was drawn from a superficial antecubital vein in the middle of each stage. Concentrations of sodium, chloride, potassium, ammonia, lactate and glucose were determined in blood plasma and sweat.Results: With increasing exercise intensity, LSR, sweat sodium, chloride and glucose concentrations increased (P ≤ 0.026), while simultaneously limited changes in blood composition were elicited for these components (P ≥ 0.093). Sweat potassium, lactate and ammonia concentrations decreased (P ≤ 0.006), while blood potassium decreased (P = 0.003), and blood ammonia and lactate concentrations increased with higher exercise intensities (P = 0.005;P = 0.007, respectively). The vast majority of correlations between blood and sweat parameters were non-significant (P > 0.05), with few exceptions.Conclusion: The data suggest that sweat composition is at least partly independent of blood composition. This has important consequences when targeting sweat as non-invasive alternative for blood measurements.

1 October 2020 in Journal of Thermal Biology
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Journal Article
Open access
LKLisa Klous
Lisa Klous
CRCornelis De Ruiter
Cornelis De Ruiter
PAPuck Alkemade
Puck Alkemade
HDHein A.M. Daanen
Hein A.M. Daanen
NGNicola Gerrett
Nicola Gerrett
The purpose of this study was to determine local sweat rate (LSR) and sweat composition during heat acclimation (HA). For ten consecutive days of HA, eight participants cycled in 33 °C and 65% relative humidity at an intensity such that a rectal temperature of 38.5 °C was reached within ~40 min, followed by a 60-min clamp of this rectal temperature (i.e., controlled hyperthermia). Four participants extended HA by a 28-day decay period and five consecutive days of heat re-acclimation (HRA) using controlled hyperthermia. Sweat from the upper arm and upper back was collected three times during each heat exposure session. LSR and sweat sodium, chloride, lactate, and potassium concentrations were determined. Relative to HA day 1, LSR was increased at the final day of HA (day 10) (arm: +58%, P < 0.001; back: +36%, P < 0.05). Concentrations of sodium, chloride, and lactate significantly (P < 0.05) decreased to ~60% at HA day 10 compared to day 1 on the arm and back. Potassium concentration did not significantly differ on HA day 10 compared to day 1 (arm: +11%, P > 0.05; back: +8%, P > 0.05). The induction patterns of the sudomotor adaptations were different. Whilst LSR increased from HA day 8 on the arm and from HA day 7 on the back, sodium and chloride conservation already occurred from HA day 3 on both skin sites. Lastly, the sweat lactate reduction occurred from HA day 6 on the arm and back. Initial evidence is provided that adaptations were partly conserved after decay (28 days) and that a 5-day HRA may be sufficient to restore HA adaptations. In conclusion, ten days of exercise-induced HA using controlled hyperthermia led to increases in LSR and concomitant reductions of sweat sodium, chloride, and lactate concentrations, whilst potassium concentrations remained relatively constant.

11 October 2020 in Temperature
Verified
Journal Article
Open access
LKLisa Klous
Lisa Klous
CRCornelis Johannes de Ruiter
Cornelis Johannes de Ruiter
PAPuck Alkemade
Puck Alkemade
HDHein A.M. Daanen
Hein A.M. Daanen
NGNicola Gerrett
Nicola Gerrett
The purpose of this study was to investigate local sweat rate (LSR) and sweat composition before and after active or passive heat re-acclimation (HRA). Fifteen participants completed four standardized heat stress tests (HST): before and after ten days of controlled hyperthermia (CH) heat acclimation (HA), and before and after five days of HRA. Each HST consisted of 35 min of cycling at 1.5W·kg−1 body mass (33°C and 65% relative humidity), followed by a graded exercise test. For HRA, participants were re-exposed to either CH (CH-CH, n = 6), hot water immersion (water temperature ~40°C for 40 min; CH-HWI, n = 5) or control (CH-CON, n = 4). LSR, sweat sodium, chloride, lactate and potassium concentrations were determined on the arm and back. LSR increased following HA (arm +18%; back +41%, P ≤  0.03) and HRA (CH-CH: arm +31%; back +45%; CH-HWI: arm +65%; back +49%; CH-CON arm +11%; back +11%, P ≤ 0.021). Sweat sodium, chloride and lactate decreased following HA (arm 25–34; back 21–27%, P < 0.001) and HRA (CH-CH: arm 26–54%; back 20–43%; CH-HWI: arm 9–49%; back 13–29%; CH-CON: arm 1–3%, back 2–5%, P < 0.001). LSR increases on both skin sites were larger in CH-CH and CH-HWI than CH-CON (P ≤ 0.010), but CH-CH and CH-HWI were not different (P ≥ 0.148). Sweat sodium and chloride conservation was larger in CH-CH than CH-HWI and CH-CON on the arm and back, whilst CH-HWI and CH-CON were not different (P ≥ 0.265). These results suggest that active HRA leads to similar increases in LSR, but more conservation of sweat sodium and chloride than passive HRA. Abbreviations: ANOVA: Analysis of variance; ATP: Adenosine triphosphate; BSA (m2): Body surface area; CH: Controlled hyperthermia; CH-CH: Heat re-acclimation by controlled hyperthermia; CH-CON: Control group (no heat re-acclimation); CH-HWI: Heat re-acclimation by hot water immersion; CV (%): Coefficient of variation; dt (min): Duration of a stimulus; F: Female; GEE: Generalized estimating equations; HA: Heat acclimation; HRA : Heat re-acclimation; HST: Heat stress test; LSR (mg·cm−2·min−1) : Local sweat rate; LOD (mmol·L−1): Limit of detection; M: Male; mx (mg): Mass of x; RH (%): Relative humidity; RT: Recreationally trained; SA (cm2): Surface area; t (min): Time; T: Trained; Tsk (°C): Skin temperature; Tre (°C): Rectal temperature; USG : Urine specific gravity; VO2peak (mL·kg−1·min−1): Peak oxygen uptake; WBSL (L): Whole-body sweat loss; WBSR (L·h−1): Whole-body sweat rate

16 September 2020 in Animals
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Journal Article
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LKLisa Klous
Lisa Klous
ESEsther Siegers
Esther Siegers
JBJan van Den Broek
Jan van Den Broek
MFMireille Folkerts
Mireille Folkerts
NGNicola Gerrett
Nicola Gerrett
Carolien C.B.M. MunstersCarolien C.B.M. Munsters
Carolien C.B.M. Munsters
In this study, we examined the effects of pre-cooling on thermophysiological responses in horses exercising in moderate environmental conditions (average wet bulb globe temperature: 18.5 ± 3.8 °C). Ten international eventing horses performed moderate intensity canter training on two separate days, and were either pre-cooled with cold-water rinsing (5–9 °C for 8 ± 3 min; cooling) or were not pre-cooled (control). We determined velocity (V), heart rate (HR), rectal temperature (Tre,), shoulder and rump skin temperature (Tshoulder and Trump), plasma lactate concentration (LA), gross sweat loss (GSL), and local sweat rate (LSR), as well as sweat sodium, chloride and potassium concentrations. The effect of pre-cooling on Tre was dependent on time; after 20 min of exercise the effect was the largest (estimate: 0.990, 95% likelihood confidence intervals (95% CI): 0.987, 0.993) compared to the control condition, resulting in a lower median Tre of 0.3 °C. Skin temperature was also affected by pre-cooling compared to the control condition (Tshoulder: −3.30 °C, 95% CI: −3.739, −2.867; Trump: −2.31 °C, 95% CI: −2.661, −1.967). V, HR, LA, GSL, LSR and sweat composition were not affected by pre-cooling. In conclusion, pre-cooling by cold-water rinsing could increase the margin for heat storage, allowing a longer exercise time before a critical Tre is reached and, therefore, could potentially improve equine welfare during competition.

15 January 2021 in Temperature
Verified
Journal Article
Open access
LKLisa Klous
Lisa Klous
MFMireille Folkerts
Mireille Folkerts
HDHein A.M. Daanen
Hein A.M. Daanen
NGNicola Gerrett
Nicola Gerrett
Due to time and logistical constraints sweat samples cannot always be analyzed immediately. The purpose of this study was to investigate the effect of storage temperature and duration on sweat electrolyte and metabolite concentrations. Twelve participants cycled for 60 min at 40 W.m−2 in 33°C and 65% RH. Using the absorbent patch technique, six sweat samples were collected from the posterior torso. Sweat from the six samples was mixed, divided again over six samples and placed in sealed vials. Sweat sodium, chloride, potassium, ammonia, lactate and urea concentrations in one sample were determined immediately. Two samples were stored at room temperature (~25°C, 42% RH) for 7 and 28 days respectively. The remaining samples were frozen at −20°C for 1 h, 7 or 28 days respectively before analysis. Sweat sodium, chloride, potassium and urea concentrations were not affected by storage temperature and duration. Sweat lactate decreased (−1.8 ± 1.8 mmol.L−1, P = 0.007) and ammonia concentrations increased (5.1 ± 3.9 mmol.L−1, P = 0.017) after storage for 28 days at 25°C only. The storage temperature and duration did not affect sodium, chloride, potassium and urea concentrations. However, sweat samples should not be stored for longer than 7 days at 25°C to obtain reliable sweat lactate and ammonia concentrations. When samples are frozen at −20°C, the storage duration could be extended to 28 days for these components.

23 October 2024 in Temperature
Verified
Journal Article
Open access
LKLisa Klous
Lisa Klous
HTHilde Teien
Hilde Teien
SHSarah Hollis
Sarah Hollis
KLKoen Levels
Koen Levels
ABAppie Boonstra
Appie Boonstra
BKBoris Kingma
Boris Kingma
Military cold weather operations (CWOs) introduce a range of challenges, including extreme temperatures, strong winds, difficult terrain, and exposure to snow, ice, and water. Personnel undertaking these missions face a heightened risk of cold weather injury (CWI), such as hypothermia, freezing cold injuries, and non-freezing cold injuries. The risk of these injuries is influenced by various factors, including age, sex, and body composition. To ensure optimal and safe performance in CWOs, it is crucial to implement effective preventive measures against CWI. This article emphasizes the most pertinent strategies for CWI prevention in CWOs. Initially, it is important to assess individual vulnerability to CWI. Education and training on CWI prevention should be provided before deployment in CWOs. During CWOs, attention should be given to crucial behaviors such as using a proper layered clothing system, recognizing the risks associated with prolonged stationary periods in cold conditions, consuming adequate calories, and staying hydrated. Additionally, environmental monitoring using tools like the windchill index and regular checks on physical status are essential. Although monitoring by itself does not prevent CWI, it can prompt necessary behavioral adjustments. Education and behavioral modifications are central to preventing CWI. Given the limited research on CWI prevention in military settings, despite the frequent occurrence of these injuries, there is a pressing need for further studies to evaluate effective preventive strategies within this specific operational framework.