# Genetic overlap between multi-site chronic pain and cognition: a large-scale genome-wide cross-trait analysis

## TL;DR

This study explores the genetic links between chronic pain and cognitive traits, finding a negative genetic correlation and identifying shared genetic loci.

## Contribution

The study reveals a significant negative genetic correlation between chronic pain and cognitive functions, and identifies pleiotropic loci using genome-wide analysis.

## Key findings

- A significant negative genetic correlation was found between chronic pain and intelligence (rg = −0.11, p = 7.77 × 10−64).
- CPASSOC identified 150 pleiotropic loci, with 20 loci showing pleiotropic effects at the same genomic position.
- LCV analysis found no causal relationship between chronic pain and cognitive traits.

## Abstract

Different studies have consistently demonstrated a positive correlation between chronic pain and cognitive changes. This study aimed to explore the genetic factors underlying the relationship between chronic pain and cognitive traits, and to investigate whether an inherent causal connection exists between them.

The genetic contributions of chronic multi-site pain and eight cognitive traits were investigated based on Genome-wide association studies (GWAS) data. Linkage disequilibrium score regression (LDSC) was employed to assess the genetic correlations between each pair of traits. The shared genetic components of these traits were investigated by identifying single nucleotide polymorphisms (SNPs) with pleiotropic effects using the Cross Phenotype Association (CPASSOC) method. Furthermore, enrichment analysis and transcriptome-wide association studies (TWAS) were performed to characterize the significant associations between genetic traits. The latent causal variable model (LCV) was employed to explore the potential causal relationship between both traits.

A significant negative genetic correlation was found between chronic pain and several cognitive functions, particularly intelligence (rg = −0. 11, p = 7.77 × 10−64). CPASSOC identified 150 pleiotropic loci. A co-localization analysis was conducted, which identified 20 loci exhibiting pleiotropic effects at the same genomic position. The LCV analysis indicated no causal relationship between both traits.

The present work contributed to an enhanced understanding of the complex genetic interplay between cognitive function and chronic pain.