Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course

Psoriasis is a persistent inflammatory skin disorder driven by T cells. The disease is characterized by aberrant keratinocytes (KCs) differentiation, epidermal proliferation, and excessive hyperplasia of veins and arteries. The purpose of the study was to identify the levels of circulating lnc-HULC,...

Full description

Bibliographic Details
Main Authors: Randa Erfan, Olfat G. Shaker, Mahmoud A.F. Khalil, Aya M. AlOrbani, Abeer K. Abu-El-Azayem, Amira Samy, Othman M. Zaki, Haitham Abdelhamid, Reham Fares, Asmaa Mohammed
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2023-09-01
Series:Non-coding RNA Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468054023000252
_version_ 1797791885438222336
author Randa Erfan
Olfat G. Shaker
Mahmoud A.F. Khalil
Aya M. AlOrbani
Abeer K. Abu-El-Azayem
Amira Samy
Othman M. Zaki
Haitham Abdelhamid
Reham Fares
Asmaa Mohammed
author_facet Randa Erfan
Olfat G. Shaker
Mahmoud A.F. Khalil
Aya M. AlOrbani
Abeer K. Abu-El-Azayem
Amira Samy
Othman M. Zaki
Haitham Abdelhamid
Reham Fares
Asmaa Mohammed
author_sort Randa Erfan
collection DOAJ
description Psoriasis is a persistent inflammatory skin disorder driven by T cells. The disease is characterized by aberrant keratinocytes (KCs) differentiation, epidermal proliferation, and excessive hyperplasia of veins and arteries. The purpose of the study was to identify the levels of circulating lnc-HULC, miR-122, and Sirtuin 1 (SIRT-1) in psoriatic patients, evaluate their possible roles as diagnostic biomarkers, and link their levels with the development of metabolic syndrome during psoriasis progression. This study included 176 participants. The subjects were divided into four groups, with 44 participants in each group. All patients have undergone a complete history taking and clinical examination. Laboratory investigations included Low-density lipoprotein (LDL), High-density lipoprotein (HDL), Triglycerides (TG), Fasting blood sugar (FBS), and cholesterol plasma levels. Serum levels of miR-122 and lnc-HULC were examined by qRT-PCR. Serum levels of SIRT-1 were examined by ELISA. The serum concentrations of lnc-HULC and miR-122 were significantly higher in psoriatic participants compared to controls. Psoriatic patients' serum concentrations of SIRT-1 were much lower than those of healthy individuals. There was a negative association between SIRT-1 concentration and BMI, disease duration, PASI score, LDL, and cholesterol levels. The blood levels of lnc-HULC, miR-122, and SIRT-1 in psoriasis patients provide a promising role as diagnostic biomarkers in patients with and without metabolic syndrome.
first_indexed 2024-03-13T02:25:12Z
format Article
id doaj.art-8065a2e07b0242f48a77a5f015c6ec14
institution Directory Open Access Journal
issn 2468-0540
language English
last_indexed 2024-03-13T02:25:12Z
publishDate 2023-09-01
publisher KeAi Communications Co., Ltd.
record_format Article
series Non-coding RNA Research
spelling doaj.art-8065a2e07b0242f48a77a5f015c6ec142023-06-30T04:22:33ZengKeAi Communications Co., Ltd.Non-coding RNA Research2468-05402023-09-0183340349Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease courseRanda Erfan0Olfat G. Shaker1Mahmoud A.F. Khalil2Aya M. AlOrbani3Abeer K. Abu-El-Azayem4Amira Samy5Othman M. Zaki6Haitham Abdelhamid7Reham Fares8Asmaa Mohammed9Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, 12613, Egypt; Corresponding author.Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, 12613, EgyptDepartment of Microbiology and Immunology, Faculty of Pharmacy, Fayoum University, Fayoum, 63514, Egypt; Corresponding author.Department of Dermatology, Faculty of Medicine, Cairo University, 12613, EgyptDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Cairo University, 12613, Cairo, EgyptDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, 12613, Cairo, EgyptDepartment of Clinical Pathology, Faculty of Medicine, Damietta University, Damietta, EgyptPlastic Surgery Center, Haar Restore Klinik, Cairo, 12613, EgyptDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Fayoum University, Fayoum, 63514, EgyptDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Fayoum University, Fayoum, 63514, EgyptPsoriasis is a persistent inflammatory skin disorder driven by T cells. The disease is characterized by aberrant keratinocytes (KCs) differentiation, epidermal proliferation, and excessive hyperplasia of veins and arteries. The purpose of the study was to identify the levels of circulating lnc-HULC, miR-122, and Sirtuin 1 (SIRT-1) in psoriatic patients, evaluate their possible roles as diagnostic biomarkers, and link their levels with the development of metabolic syndrome during psoriasis progression. This study included 176 participants. The subjects were divided into four groups, with 44 participants in each group. All patients have undergone a complete history taking and clinical examination. Laboratory investigations included Low-density lipoprotein (LDL), High-density lipoprotein (HDL), Triglycerides (TG), Fasting blood sugar (FBS), and cholesterol plasma levels. Serum levels of miR-122 and lnc-HULC were examined by qRT-PCR. Serum levels of SIRT-1 were examined by ELISA. The serum concentrations of lnc-HULC and miR-122 were significantly higher in psoriatic participants compared to controls. Psoriatic patients' serum concentrations of SIRT-1 were much lower than those of healthy individuals. There was a negative association between SIRT-1 concentration and BMI, disease duration, PASI score, LDL, and cholesterol levels. The blood levels of lnc-HULC, miR-122, and SIRT-1 in psoriasis patients provide a promising role as diagnostic biomarkers in patients with and without metabolic syndrome.http://www.sciencedirect.com/science/article/pii/S2468054023000252PsoriasisMetabolic syndromeLnc-HULCMiR-122SIRT-1
spellingShingle Randa Erfan
Olfat G. Shaker
Mahmoud A.F. Khalil
Aya M. AlOrbani
Abeer K. Abu-El-Azayem
Amira Samy
Othman M. Zaki
Haitham Abdelhamid
Reham Fares
Asmaa Mohammed
Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
Non-coding RNA Research
Psoriasis
Metabolic syndrome
Lnc-HULC
MiR-122
SIRT-1
title Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
title_full Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
title_fullStr Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
title_full_unstemmed Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
title_short Lnc-HULC, miR-122, and sirtulin-1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
title_sort lnc hulc mir 122 and sirtulin 1 as potential diagnostic biomarkers for psoriasis and their association with the development of metabolic syndrome during the disease course
topic Psoriasis
Metabolic syndrome
Lnc-HULC
MiR-122
SIRT-1
url http://www.sciencedirect.com/science/article/pii/S2468054023000252
work_keys_str_mv AT randaerfan lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT olfatgshaker lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT mahmoudafkhalil lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT ayamalorbani lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT abeerkabuelazayem lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT amirasamy lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT othmanmzaki lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT haithamabdelhamid lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT rehamfares lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse
AT asmaamohammed lnchulcmir122andsirtulin1aspotentialdiagnosticbiomarkersforpsoriasisandtheirassociationwiththedevelopmentofmetabolicsyndromeduringthediseasecourse