Complete blood count, measures of iron status and inflammatory markers in inner-city African Americans with undiagnosed hepatitis C seropositivity

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• 作者：Hilary Ufearo ; Khalid Kambal ; Gladys O. Onojobi ; Mehdi Nouraie ; Charles Agbemabiese ; Sharmin Diaz ; Anita Aggarwal ; Zakari Aliyu ; Robert E. Taylor ; Victor R. Gordeuk
• 关键词：HCV infection ; African American ; CRP ; Iron metabolism
• 刊名：Clinica Chimica Acta
• 出版年：2010
• 出版时间：2 May 2010
• 年：2010
• 卷：411
• 期：9-10
• 页码：653-656
• 全文大小：437 K

文摘

Background

Hepatitis C virus (HCV) infection may be associated with thrombocytopenia and increased iron stores in patients receiving medical care. We aimed to determine how often changes in hematologic, iron metabolic and inflammatory markers occur in individuals with undiagnosed HCV in the community.

Methods

Inner-city African Americans (n = 143) were recruited from the community according to reported ingestion of alcohol. They were divided broadly into those who drank more or less than 56 g alcohol/day as assessed by dietary questionnaire. HCV serology was determined and laboratory values were compared according to HCV seropositivity in analyses that adjusted for alcohol consumption.

Results

The prevalence of HCV seropositivity was 23 % among men and 29 % among women. Levels of hepatocellular enzymes were higher with HCV seropositivity (P < 0.0001) but hemoglobin concentrations, white blood cell and platelet counts and serum ferritin concentrations did not differ. The globulin fraction of the serum protein concentration (P = 0.002) was increased with HCV seropositivity as expected with chronic inflammation. However, erythrocyte sedimentation rate and serum iron and haptoglobin levels did not differ significantly according to HCV status. Furthermore, multivariate analysis revealed that C-reactive protein was decreased and transferrin concentration was increased with both HCV and alcohol consumption (P < 0.014).

Conclusions

Previously undiagnosed HCV seropositivity has little effect on the complete blood count and body iron stores but appears to perturb the response to an inflammatory stimulus, causing reduced rather than increased circulating CRP concentrations and increased rather than decreased transferrin concentrations.