Literature DB >> 28511747

Red Blood Cell Distribution Width is a Reliable Marker of Inflammation in Plaque Psoriasis.

Sibel Doğan1, Nilgün Atakan.   

Abstract

Psoriasis is a systemic inflammatory disease accepted as an independent risk factor for cardiovascular diseases (CVD). Elevated levels and correlation of red cell distribution width (RDW) with inflammatory markers has recently been shown in studies investigating CVD risk and prognosis in rheumatoid arthritis and ankylosing spondylitis. The aim of this study was to evaluate levels and correlation of RDW with inflammatory markers in patients with plaque psoriasis. Data including demographics, disease severity indices, laboratory parameters, and bioelectrical impedance analysis was collected from medical charts of patients who were diagnosed with plaque psoriasis at the Hacettepe University Department of Dermatology between March 2014 and August 2015. Patients were evaluated for major CVD risk factors defined by international guidelines. 199 patients with psoriasis and 73 volunteers were included. Patients had statistically significant higher values of metabolic age, visceral fat rating, body-mass index (BMI), red blood cells (RBC), white blood cells (WBC), red blood cell distribution width (RDW), alanine aminotransferase (ALT), uric acid, low-density lipoprotein (LDL), and C-reactive protein (CRP) (p=0.044, p=0.047,p=0.029, p= 0.005, p=0.02, p<0,01, p=0.001, p=0,016, p=0,014, p<0.01). A statistically significant relationship and positive correlation between RDW and CRP levels was found in the patient group (p=0.01, r=0.396). Patients without major CVD risk factors (n=79) had significantly higher values of RDW, LDL, and CRP (p=0.01, p=0.031, p=0.03, respectively). Patients with psoriasis who had one or more CVD risk factors (n=120) had significantly higher values of BMI, RDW, thrombocytes, ALT, and CRP (p=0.038, p=0.01, p=0.017, p=0.02, p=0.01, respectively). RDW, which is elevated as well as CRP, reflects the systemic inflammatory burden and can be used for prediction of CVD in psoriasis. In fact, patients with psoriasis who do not have any major CVD risk factors still have high levels of CRP and RDW, supporting the hypothesis that psoriatic inflammation itself can simultaneously cause CRP and RDW elevation. Coexistence of CVD risk factors is associated with ALT elevation since additional CVD risk factors may predict psoriatic comorbidities such as non-alcoholic fatty liver disease.

Entities:  

Year:  2017        PMID: 28511747

Source DB:  PubMed          Journal:  Acta Dermatovenerol Croat        ISSN: 1330-027X            Impact factor:   1.256


  11 in total

Review 1.  The association between platelet indices and presence and severity of psoriasis: a systematic review and meta-analysis.

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2.  Welch-weighted Egger regression reduces false positives due to correlated pleiotropy in Mendelian randomization.

Authors:  Brielin C Brown; David A Knowles
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3.  Increased red blood cell distribution width in patients with plaque psoriasis.

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7.  Psoriasis and Psoriatic Arthritis Cardiovascular Disease Endotypes Identified by Red Blood Cell Distribution Width and Mean Platelet Volume.

Authors:  Rosalynn Rz Conic; Giovanni Damiani; Kory P Schrom; Amy E Ramser; Chunlei Zheng; Rong Xu; Thomas S McCormick; Kevin D Cooper
Journal:  J Clin Med       Date:  2020-01-09       Impact factor: 4.241

8.  Comparison of mean platelet volume (MPV) and red blood cell distribution width (RDW) between psoriasis patients and controls: A systematic review and meta-analysis.

Authors:  Ping Yi; Jiao Jiang; Zheyu Wang; Xing Wang; Mingming Zhao; Haijing Wu; Yan Ding
Journal:  PLoS One       Date:  2022-02-25       Impact factor: 3.240

9.  Updated Evidence of the Association Between Elevated Serum Uric Acid Level and Psoriasis.

Authors:  Ying Zhang; Liu Liu; Xiaoying Sun; Hongjin Li; Yifei Wang; Min Zhou; Liang Hua; Bin Li; Xin Li
Journal:  Front Med (Lausanne)       Date:  2021-06-29

10.  Evaluation of Erythroid Disturbance and Thiol-Disulphide Homeostasis in Patients with Psoriasis.

Authors:  Suzan Demir Pektas; Gokhan Pektas; Kursad Tosun; Gursoy Dogan; Salim Neselioglu; Ozcan Erel
Journal:  Biomed Res Int       Date:  2018-06-05       Impact factor: 3.411

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