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OBJECTIVE: The chronic pain syndromes (CPS) include syndromes such as chronic widespread pain (CWP), dry eye disease (DED) and irritable bowel syndrome (IBS). Highly prevalent and lacking pathognomonic biomarkers, the CPS are known to cluster in individuals in part due to their genetic overlap, but patient diagnosis can be difficult. The success of quantitative sensory testing (QST) and inflammatory biomarkers as phenotyping tools in conditions such as painful neuropathies warrant their investigation in CPS. We aimed to examine whether individual QST modalities and candidate inflammatory markers were associated with CWP, DED or IBS in a large, highly phenotyped population sample. DESIGN: Cross-sectional study. SETTING: Community-dwelling cohort. PARTICIPANTS: Twins from the TwinsUK cohort PRIMARY AND SECONDARY OUTCOME MEASURES: We compared 10 QST modalities, measured in participants with and without a CWP diagnosis between 2007 and 2012. We investigated whether inflammatory markers measured by Olink were associated with CWP, including interleukin-6 (IL-6), IL-8, IL-10, monocyte chemoattractant protein-1 and tumour necrosis factor. All analyses were repeated in DED and IBS with correction for multiple testing. RESULTS: In N=3022 twins (95.8% women), no association was identified between individual QST modalities and CPS diagnoses (CWP, DED and IBS). Analyses of candidate inflammatory marker levels and CPS diagnoses in n=1368 twins also failed to meet statistical significance. CONCLUSION: Our findings in a large population cohort suggest a lack of true association between singular QST modalities or candidate inflammatory markers and CPS.

Original publication

DOI

10.1136/bmjopen-2024-085814

Type

Journal article

Journal

BMJ Open

Publication Date

03/09/2024

Volume

14

Keywords

Chronic Pain, Cross-Sectional Studies, Dry Eye Syndromes, EPIDEMIOLOGIC STUDIES, Irritable Bowel Syndrome, Humans, Cross-Sectional Studies, Male, Female, Chronic Pain, Middle Aged, Irritable Bowel Syndrome, Adult, Dry Eye Syndromes, Aged, Biomarkers, Interleukin-6, Interleukin-8, Tumor Necrosis Factor-alpha, Chemokine CCL2, United Kingdom, Interleukin-10, Pain Measurement