Genetics of Exertional Heat Illness: Revealing New Associations and Expanding Heterogeneity

• Published in: International journal of molecular sciences 2024-10, Vol.25 (20), p.11269
• Main Authors: Sambuughin, Nyamkhishig, Mungunsukh, Ognoon, Klein, Michael G, Ren, Mingqiang, Bedocs, Peter, Kazman, Josh B, Cofer, Kristen, Friel, Liam P, McNally, Beth, Kwon, Kyung, Haigney, Mark C, Leggit, Jeffrey C, Pazgier, Marzena, Deuster, Patricia A, O'Connor, Francis G
• Format: Article
• Language: English
• Subjects: Adult; Amino acids; Cardiac function; Disease; Diseases; Environmental risk; Exome Sequencing; Fainting; Female; Fever; Genes; Genetic aspects; Genetic Predisposition to Disease; Health aspects; Health risk assessment; Heat; Heat Stress Disorders - genetics; Humans; Hyperthermia; Hypotheses; Kinases; Male; Metabolism; Middle Aged; Military personnel; Musculoskeletal system; Physical Exertion; Risk factors; Ryanodine Receptor Calcium Release Channel - genetics; TRPM Cation Channels - genetics
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms252011269

Environmental heat stress represents a pervasive threat to warfighters, athletes, and occupational workers, impacting performance and increasing the risk of injury. Exertional heat illness (EHI) is a spectrum of clinical disorders of increasing severity. While frequently predictable, EHI can occur unexpectedly and may be followed by long-term comorbidities, including cardiovascular dysfunction and exercise intolerance. The objective of this study was to assess genetic factors contributing to EHI. Whole-exome sequencing was performed in a cohort of 53 cases diagnosed with EHI. Rare variants in prioritized gene sets were analyzed and classified per published guidelines. Clinically significant pathogenic and potentially pathogenic variants were identified in 30.2% of the study cohort. Variants were found in 14 genes, including the previously known and genes and 12 other genes ( , , , , , and genes for mitochondrial disorders) reported here for the first time in EHI. Supporting structural and functional studies of the p.Arg905Trp variant show that it impairs the thermal sensitivity of the TRPM4 channel, revealing a potentially new molecular mechanism contributing to EHI susceptibility. Our study demonstrates associations between EHI and genes implicated in muscle disorders, cardiomyopathies, thermoregulation, and oxidative phosphorylation deficiencies. These results expand the genetic heterogeneity of EHI and shed light on its molecular pathogenesis.