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Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states
Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states
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Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states
Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states

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Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states
Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states
Journal Article

Detection rate, demographic associations and clinical implications of anti-C1q antibody elevations across diverse disease states

2025
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Overview
BackgroundAnti-C1q autoantibodies can disrupt normal complement function, contributing to the formation of pathogenic immune complexes and end-organ damage. Although their role in SLE is well-established, their detection rate and clinical relevance across a broader spectrum of diseases remain insufficiently characterised. This study aimed to investigate the distribution of abnormal anti-C1q levels in the population and examine their associations with age, sex and specific clinical subtypes.MethodsThis retrospective study included patients who underwent anti-C1q testing at our hospital between September 2020 and September 2023. The primary outcome was the detection rate of abnormal anti-C1q levels (>10 U/mL) categorised by patient sex, age and disease diagnosis. One-way and two-way fixed-effect models were used to assess associations between odds of abnormal antibody levels and demographic factors. Multivariate logistic regression was performed to identify disease-specific correlates.ResultsAmong 15 363 patients (median (IQR) age, 38 (28–53) years; 79.02% female; 52.19% aged <40 years) representing 67 distinct diagnoses, 7.88% showed abnormal anti-C1q levels. Female sex and younger age showed higher median anti-C1q levels and a greater proportion of abnormal results. SLE subtypes showed the highest detection rate of abnormal anti-C1q levels, with SLE without severe complications (853 of 3760, 22.69%) and lupus nephritis (88 of 294, 29.93%) being the most obvious. Lupus haematological and encephalopathic manifestations were associated with elevated antibody levels. Additionally, autoimmune cirrhosis (7 of 59, 11.86%) and systemic sclerosis (19 of 165, 11.52%) also showed high detection rates of abnormal anti-C1q levels. Both univariate and multivariate analyses indicated that male sex and younger age were significantly associated with increased odds of abnormal anti-C1q levels.ConclusionElevations in anti-C1q levels extend beyond SLE and are influenced by both demographic factors and specific disease phenotypes. Male sex and younger age emerged as significant predictors of abnormal anti-C1q status. Our findings underscore the potential utility of anti-C1q testing for improving diagnostic precision and risk stratification across a wide range of clinical conditions.