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February 19, 2026Journal of Neurology Neurosurgery & Psychiatry0 citations

Genetic susceptibility to heat identifies rare neurological diseases at particular risk from climate change impacts

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RBRavishankara BellampalliEpilepsy Research UKJMJames D. MillsRutgers, The State University of New JerseyAVAngeliki VakrinouEpilepsy Research UK

Key Points

  • Examine the impact of genetic susceptibility to heat on rare neurological diseases and associated phenotypes.
  • Conducted a literature review to curate genetic variants with temperature-dependent effects.
  • Analyzed the occurrence of calortypic variants in a rare disease cohort from the Genomics England programme.
  • Performed transcriptomic analysis in astrocyte models with varying temperature exposures.
  • Identified 159 calortypic variants across 65 genes linked to temperature-sensitive disease phenotypes.
  • Found that 66.7% of these variants were associated with disease phenotypes, particularly in neurological disorders.
  • Documented temperature-related phenotypes in 8 participants, with 6 having previously identified disease-causing variants.

Abstract

Background Climate change is one of the greatest contemporary challenges to human health, undermining human health through multiple mechanisms. Among relatively understudied mechanisms are those related to individual genomic variation. We aimed to examine this possibility. Methods Through a defined, agnostic literature review-based approach, we curated human genetic variants with functionally characterised temperature-dependent effects: we call these ‘calortypic variants’, some of which are linked to temperature-sensitive disease phenotypes. Next, we examined their occurrence in whole-genome sequenced rare disease cohort and analysed their associated phenotypes. Finally, we performed transcriptomic analysis in astrocyte models to examine the impact of short-term exposure to elevated ambient temperature. Results A set of 159 calortypic variants across 65 calortypic genes was identified; most (66.7%) calortypic variants caused temperature-sensitive disease phenotypes, and 44.7% were found in neurological and neurodevelopmental diseases. Calortypic variants were also found in 300/39 834 participants recruited to the Genomics England (GEL) 100 000 Genomes rare disease programme. Temperature-related phenotypes were documented in eight GEL participants; in 6/8 participants (two probands and four of their relatives), calortypic variants had already been identified as the disease-causing variant. Gene expression changes across human astrocyte transcriptomes studied under different temperature exposures prominently featured genes related to extracellular matrix maintenance, inflammation, immune response and energy metabolism, all processes that feature in various neurological diseases. Conclusions Genetic variation may generate latent phenotypes that manifest only at elevated ambient temperatures, with some neurological disease groups being highlighted. This is an exploratory study. Identifying more calortypic variants will help uncover the full spectrum of human genetic vulnerability to climate change impacts.

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Cite This Study

Bellampalli et al. (2026) studied this question.

synapsesocial.com/papers/6996a7a5ecb39a600b3ed7e5https://doi.org/10.1136/jnnp-2025-337077
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