Why the study?
Familial Mediterranean fever may cause endothelial dysfunction and arterial stiffness, but differences according to colchicine response required evaluation.
Does colchicine resistance (requiring anti-IL-1 therapy) associate with increased arterial stiffness and nocturnal hypertension in pediatric patients with FMF?
Does colchicine resistance (requiring anti-IL-1 therapy) associate with increased arterial stiffness and nocturnal hypertension in pediatric patients with FMF?
Arterial stiffness and nocturnal hypertension are more pronounced in colchicine-resistant pediatric FMF patients requiring anti-IL-1 therapy, likely due to subclinical inflammation.
Chronic subclinical inflammation may increase arterial stiffness in pediatric FMF; leaves open whether colchicine optimization reduces long-term CV risk.
Familial Mediterranean fever (FMF) is an autoinflammatory disease which may cause endothelial dysfunction and arterial stiffness. In this study, we evaluated patients with FMF in terms of arterial stiffness indicators and investigated whether there was any difference according to colchicine response. This is a single-center, prospective, case-control study conducted on pediatric patients with FMF. Patients were categorized into 2 groups: patients on colchicine monotherapy (group 1) and patients who used anti-interleukin-1 (IL-1) plus colchicine (group 2). Patient age, mutations in the MEFV gene, overall duration of treatments, and general characteristics of symptoms were recorded. Laboratory values in an attack-free period were noted. Pulse wave velocity (PWV) was measured in all patients. Erythrocyte sedimentation rate and C-reactive protein, nocturnal hypertension, and PWV were higher in group 2. Arterial stiffness develops due to subclinical inflammation in patients with FMF. It is more pronounced in colchicine-resistant patients.
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Leventoğlu et al. (2023) studied this question.
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