Red cell distribution width (RDW) is associated with cardiovascular disease risk in Crohn's disease

2017 ◽  
Vol 41 (4) ◽  
pp. 490-492 ◽  
Author(s):  
Haider Al Taii ◽  
Zaid Yaqoob ◽  
Sadeer G. Al-Kindi
2016 ◽  
Vol 23 (1) ◽  
pp. 6-12 ◽  
Author(s):  
Ana Maria Oliveira ◽  
Filipe Sousa Cardoso ◽  
Catarina Graça Rodrigues ◽  
Liliana Santos ◽  
Alexandra Martins ◽  
...  

2015 ◽  
Vol 349 (1) ◽  
pp. 42-45 ◽  
Author(s):  
Dong Hu ◽  
Jianan Ren ◽  
Gefei Wang ◽  
Guosheng Gu ◽  
Guanwei Li ◽  
...  

BioFactors ◽  
2019 ◽  
Author(s):  
Seyed M. Parizadeh ◽  
Reza Jafarzadeh‐Esfehani ◽  
Amirhossein Bahreyni ◽  
Maryam Ghandehari ◽  
Mojtaba Shafiee ◽  
...  

2012 ◽  
Vol 44 (3) ◽  
pp. 169-171 ◽  
Author(s):  
Turgay Isik ◽  
Erkan Ayhan ◽  
Ibrahim Halil Tanboga ◽  
Ahmet Kaya ◽  
Enbiya Aksakal ◽  
...  

TH Open ◽  
2018 ◽  
Vol 02 (02) ◽  
pp. e182-e189 ◽  
Author(s):  
Jostein Lappegård ◽  
Trygve Ellingsen ◽  
Kristian Hindberg ◽  
Ellisiv Mathiesen ◽  
Inger Njølstad ◽  
...  

AbstractRed cell distribution width (RDW), a measure of variability in size of circulating erythrocytes, is associated with arterial cardiovascular disease (CVD), but the underlying mechanism remains unclear. We aimed to investigate the impact of chronic inflammation as measured by high-sensitivity C-reactive protein (hs-CRP) on this relationship, and explore whether RDW could be a mediator in the causal pathway between inflammation and arterial CVD. Baseline characteristics, including RDW and hs-CRP, were obtained from 5,765 individuals attending a population-based cohort study. We followed up participants from inclusion in the fourth survey of the Tromsø Study (1994/1995) until December 31, 2012. Multivariable Cox-regression models were used to calculate hazard ratios (HR) with 95% confidence intervals (CI) for incident myocardial infarction (MI) and ischemic stroke across quintiles of hs-CRP and RDW. Subjects with hs-CRP in the highest quintile had 44% higher risk of MI (HR: 1.44, 95% CI: 1.14–1.80), and 64% higher risk of ischemic stroke (HR: 1.64, 95% CI: 1.20–2.24) compared with subjects in the lowest quintile. RDW mediated 7.2% (95% CI: 4.0–30.8%) of the association between hs-CRP and ischemic stroke. Subjects with RDW in the highest quintile had 22% higher risk of MI (HR: 1.22, 95% CI: 0.98–1.54) and 44% higher risk of ischemic stroke (HR: 1.44, 95% CI: 1.06–1.97) compared with subjects in the lowest quintile. These risk estimates were slightly attenuated after adjustments for hs-CRP. Our findings suggest that chronic inflammation is not a primary mechanism underlying the relationship between RDW and arterial CVD.


2021 ◽  
Vol 6 (2) ◽  
pp. 90-104
Author(s):  
Sofi Damjanovska ◽  
Perica Davitkov ◽  
Surya Gopal ◽  
Lenche Kostadinova ◽  
Corrine Kowal ◽  
...  

Background: Hepatitis-C virus (HCV) chronic infection can lead to cirrhosis, hepatocellular carcinoma (HCC), end-stage liver disease, cardiovascular disease (CVD), and mortality. Transient Elastography (TE) is used to non-invasively assess fibrosis. Whether immune monitoring provides additive prognostic value is not established. Increased red-cell distribution width (RDW) and decreased absolute lymphocyte count (ALC) predict mortality in those without liver disease. Whether these relationships remain during HCV infection is unknown.  Materials and Methods: A retrospective cohort of 1,715 single-site VA Liver Clinic patients receiving Transient Elastography (TE) 2014-2019 to evaluate HCV-associated liver damage were evaluated for RDW and ALC in relation to traditional parameters of cardiovascular risk, liver health, development of HCC, and mortality. Results: The cohort was 97% male, 55% African American, 26% with diabetes mellitus, 67% with hypertension, and 66% with tobacco use. After TE, 3% were subsequently diagnosed with HCC, and 12% (n=208) died. Most deaths (n=189) were due to non-liver causes. The TE score associated with prevalent CVD positively correlated with atherosclerotic cardiovascular disease (ASCVD) 10-Year Risk Score, age, RDW, and negatively correlated with ALC. Patients with anisocytosis (RDW above 14%) or lymphopenia (ALC level under 1.2x109/L) had greater subsequent all-cause mortality, even after adjusting for age, TE score, and comorbidities. TE score, and to a modest degree RDW, were associated with subsequent liver-associated mortality, while TE score, RDW, and ALC were each independently associated with non-liver cause of death. Conclusion: Widely available mortality calculators generally require multiple pieces of clinical information. RDW and ALC, parameters collected on a single laboratory test that is commonly performed, prior to HCV therapy may be pragmatic markers of long-term risk of mortality. 


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