Homocysteine Is a Marker of Increased Cardio-Cerebrovascular Disease Risk in Psoriatic Patients, but It Does Not Reflect the Effect of Biological Therapy in the Longitudinal Observation

Author:

Baloghova Janette1ORCID,Feketeova Eva2ORCID,Kolarcik Peter3ORCID

Affiliation:

1. Department of Dermatovenerology, Faculty of Medicine, P.J. Šafárik University and Louis Pasteur University Hospital, 04011 Košice, Slovakia

2. Department of Neurology, Faculty of Medicine, P.J. Šafárik University and Louis Pasteur University Hospital, 04011 Košice, Slovakia

3. Department of Health Psychology and Research Methodology, Faculty of Medicine, P.J. Šafárik University, 04011 Košice, Slovakia

Abstract

Background. Psoriasis is linked to atherosclerosis. Homocysteine (HCYS) has been identified as a marker of increased risk of cardio-cerebrovascular diseases (CCVD) in population. Objective. The aim of the study was to determine whether elevated HCYS serves as a marker of increased CCVD in psoriasis and whether biological therapy for long-term monitoring influences HCYS levels. Methods. Clinical data, laboratory tests, and comorbid diagnoses were summarized for the two groups of patients based on entrance HCYS levels. Patients (n = 76) were included in the follow-up gradually over a period of 5 years. Results. The psoriatic patients with normal (54%) and elevated (46%) HCYS before biological treatment did not vary in clinical data, laboratory tests, treatment, and comorbid diagnoses apart from CCVD. Elevated HCYS group showed a four-fold excess of CCVD (OR 4.2, 95%CI 1.21–4.86, p = 0.024 ). HCYS levels in the longitudinal observation did not vary. Conclusion. An increased CCVD risk, independent of other risk factors, is present in psoriatic patients with elevated HCYS. The HCYS level was not influenced by biological therapy in longitudinal observation. Further studies are needed to explore if elevated HCYS could serve as a marker of increased CCVD in any stage of psoriasis and if it should be included in classical screening strategies.

Funder

VEGA

Publisher

Hindawi Limited

Subject

General Medicine

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