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. 2023 Jun 7;14:3280. doi: 10.1038/s41467-023-38383-y

Fig. 3. CFHR5 concentration is associated with VTE in 5 independent studies.

Fig. 3

Plasma samples were generated as part of: (a) the Swedish VEBIOS ER or (b) the Swedish DFW-VTE study, both of which recruited patients presenting with suspected VTE. Samples were drawn pre- treatment, and cases and controls were identified based on confirmed or ruled out diagnosis. c The French FARIVE study recruited patients with confirmed acute VTE, with controls recruited from hospital patients treated for non-VTE causes. Samples were drawn within 1 week from diagnosis, during initiation of treatment (d) The Swedish VEBIOS Coagulation or (e), Spanish RETROVE study recruited cases from patients who had a prior first time VTE, sampled post-treatment (6–12 months anticoagulants), with healthy controls recruited from the general population. CFHR5 concentration was measured in the respective samples using a dual binder assay. Case and control groups was compared using a linear model adjusting for age and sex (3a–e). ***p < 0.001, ****p < 0.0001. OR (1 SD) = Odds ratio for 1 standard deviation elevation. CI confidence interval. All dot plots are represented as median value with 95% CI. Source data are provided as a Source Data file.