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A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity

BACKGROUND: Studies investigating cognitive dysfunction in psoriatic patients remain inconclusive. OBJECTIVE: To investigate the risk of cognitive decline in plaque‐type psoriasis patients. METHODS: Serum neurofilament light chain (NFL) and tau protein concentrations in 45 patients with plaque‐type...

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Autores principales: Okan, Gokhan, Baki, Adile Merve, Yorulmaz, Eda, Doğru‐Abbasoğlu, Semra, Vural, Pervin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843295/
https://www.ncbi.nlm.nih.gov/pubmed/32896023
http://dx.doi.org/10.1002/jcla.23564
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author Okan, Gokhan
Baki, Adile Merve
Yorulmaz, Eda
Doğru‐Abbasoğlu, Semra
Vural, Pervin
author_facet Okan, Gokhan
Baki, Adile Merve
Yorulmaz, Eda
Doğru‐Abbasoğlu, Semra
Vural, Pervin
author_sort Okan, Gokhan
collection PubMed
description BACKGROUND: Studies investigating cognitive dysfunction in psoriatic patients remain inconclusive. OBJECTIVE: To investigate the risk of cognitive decline in plaque‐type psoriasis patients. METHODS: Serum neurofilament light chain (NFL) and tau protein concentrations in 45 patients with plaque‐type psoriasis and forty‐five healthy controls were measured by enzyme‐linked immunosorbent assay (ELISA). RESULTS: Mean homeostasis model assessment (HOMA‐IR) values (6.82 vs 3.25) and serum levels of insulin (28.19 vs 15.71), NFL (5.74 vs 1.98), and tau (348.17 vs 207.30) in patients with psoriasis were found to be significantly higher than those of in healthy controls. There was a significant positive correlation between NFL and tau (r = .257, P = .015). There was significant correlation between NFL, tau and PASI (r = .310, P = .040) and (r = .383, P = .010), respectively. Significant correlations between NFL and insulin, TC, HDL‐C, TG, VLDL‐C, and BMI were found. NFL (9.38 vs 3.08) and tau (439.28 vs 281.58) concentrations and PASI values (23.94 vs 14.18) in patients with disease onset before 40 years were significantly higher than that of the patients with disease onset after 40 years. C‐reactive protein (CRP) was significantly correlated with BMI (r = .449, P < .001), LDL‐C (r = .240, P = .026), TG (r = .244, P = .024), and VLDL‐C (r = .241, P = .025) in patients with psoriasis. CONCLUSIONS: Increased serum NFL and tau protein levels and the presence of positive correlations between NFL, tau protein and PASI score show cognitive decline risk may be higher in moderate‐to‐severe psoriasis.
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spelling pubmed-78432952021-02-02 A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity Okan, Gokhan Baki, Adile Merve Yorulmaz, Eda Doğru‐Abbasoğlu, Semra Vural, Pervin J Clin Lab Anal Research Articles BACKGROUND: Studies investigating cognitive dysfunction in psoriatic patients remain inconclusive. OBJECTIVE: To investigate the risk of cognitive decline in plaque‐type psoriasis patients. METHODS: Serum neurofilament light chain (NFL) and tau protein concentrations in 45 patients with plaque‐type psoriasis and forty‐five healthy controls were measured by enzyme‐linked immunosorbent assay (ELISA). RESULTS: Mean homeostasis model assessment (HOMA‐IR) values (6.82 vs 3.25) and serum levels of insulin (28.19 vs 15.71), NFL (5.74 vs 1.98), and tau (348.17 vs 207.30) in patients with psoriasis were found to be significantly higher than those of in healthy controls. There was a significant positive correlation between NFL and tau (r = .257, P = .015). There was significant correlation between NFL, tau and PASI (r = .310, P = .040) and (r = .383, P = .010), respectively. Significant correlations between NFL and insulin, TC, HDL‐C, TG, VLDL‐C, and BMI were found. NFL (9.38 vs 3.08) and tau (439.28 vs 281.58) concentrations and PASI values (23.94 vs 14.18) in patients with disease onset before 40 years were significantly higher than that of the patients with disease onset after 40 years. C‐reactive protein (CRP) was significantly correlated with BMI (r = .449, P < .001), LDL‐C (r = .240, P = .026), TG (r = .244, P = .024), and VLDL‐C (r = .241, P = .025) in patients with psoriasis. CONCLUSIONS: Increased serum NFL and tau protein levels and the presence of positive correlations between NFL, tau protein and PASI score show cognitive decline risk may be higher in moderate‐to‐severe psoriasis. John Wiley and Sons Inc. 2020-09-08 /pmc/articles/PMC7843295/ /pubmed/32896023 http://dx.doi.org/10.1002/jcla.23564 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Okan, Gokhan
Baki, Adile Merve
Yorulmaz, Eda
Doğru‐Abbasoğlu, Semra
Vural, Pervin
A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title_full A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title_fullStr A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title_full_unstemmed A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title_short A preliminary study about neurofilament light chain and tau protein levels in psoriasis: Correlation with disease severity
title_sort preliminary study about neurofilament light chain and tau protein levels in psoriasis: correlation with disease severity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843295/
https://www.ncbi.nlm.nih.gov/pubmed/32896023
http://dx.doi.org/10.1002/jcla.23564
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