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DOI 10.3390/biomedicines12081627

Медицинская библиотека · Biomedicines · 2024

Early Cerebral Microvasculature Impairment and Increased Body Mass Index in Patients with Psoriasis.

Piec Katarzyna, Marek-Józefowicz Luiza, Nadolska Katarzyna, Lemanowicz Adam, Serafin Zbigniew, Kozera Grzegorz

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Аннотация

Psoriasis induces systemic atherosclerosis, but its impact on cerebrovascular function remains unclear. However, stroke prevention must be considered in psoriasis, as it is commonly comorbid with classic cardiovascular risk factors. Thus, the aim of the study is to assess cerebral microvasculature function and its confounders in patients with psoriasis. The study protocol included cerebral autoregulation assessment with measurements of vasomotor reactivity reserve (VMRr) on the middle cerebral arteries with the use of a Transcranial Doppler (TCD) in 50 patients with psoriasis without cerebrovascular events (46; 21-74 years) and 26 healthy controls (41; 29-58 years). Analyses of VMRr relationships with the psoriasis course, comorbidities, inflammatory markers and intima-media thickness (IMT) were performed. The study showed that VMRr was lower (64% vs. 76%, p = 0.001), and the IMT was higher (0.65 vs. 0.52 mm, p = 0.001) in patients compared to controls. The patients were also characterized by a higher body mass index (BMI) and a higher level of Il-6 than the controls (29.14 vs. 25.76 kg/m2, p = 0.004 and 585 vs. 204 pg/mL, p < 0.001, respectively), but only BMI was independently impacting VMRr reduction (p = 0.02). In conclusion, early cerebral microvasculature dysfunction may occur in patients with psoriasis, and its extent is associated with an increase in BMI. Thus, body mass reduction should be strongly recommended for stroke prophylaxis in patients with psoriasis.

Для цитирования: Piec Katarzyna, Marek-Józefowicz Luiza, Nadolska Katarzyna, Lemanowicz Adam, Serafin Zbigniew, Kozera Grzegorz. Early Cerebral Microvasculature Impairment and Increased Body Mass Index in Patients with Psoriasis.. Biomedicines. 2024. DOI: 10.3390/biomedicines12081627.
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