Electric Fan Use During an Eight-hour Replicated Extreme Heat Event: Sex Differences in Systemic Biomarkers and Thermoregulation

Abstract

Health agencies, including the Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO), recommend different temperature thresholds for electric fan use during heat events. However, these guidelines do not account for the physiological effects of electric fan use on immune and inflammatory responses in males and females. This study evaluated the efficacy of electric fan use in mitigating immune function, inflammation, and organ function during an eight-hour simulated extreme heat event replicating conditions in Hangzhou, China, on the August 3, 2024 (semi-hourly temperature and relative humidity [RH] fluctuations; average temperature: 39.9C & RH: 47.1%). Twenty young adults (10 males and 10 females) underwent three eight-hour trials: (1) no electric fan with limited fluid intake (500mL, Con), (2) electric fan use with limited fluid intake (500mL, Fan) and (3) electric fan use with sufficient fluid intake (3L, Fan+Fluid). Core temperature, cardiovascular responses, plasma electrolytes, stress hormones, inflammatory markers, and organ function biomarkers were assessed. Results showed that Fan+Fluid significantly reduced core temperature, stress hormone levels, inflammatory responses, and organ function biomarkers in both sexes (all p < 0.05). However, females exhibited consistently higher stress hormone levels, inflammatory responses, and organ function markers than males across all trials (all p < 0.05). These findings highlight the benefits of electric fan use in prolonged extreme heat and suggest that females may require more intense cooling interventions due to heightened inflammatory and organ stress responses.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by a NSFC Excellent Young Scientists grant

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

IRB of Xian University of Science and Technology gave the ethical approval for this work

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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