Case––control study of the association between select HLA genes and anti-erythropoietin antibody-positive pure red-cell aplasia. (February 2008)
- Record Type:
- Journal Article
- Title:
- Case––control study of the association between select HLA genes and anti-erythropoietin antibody-positive pure red-cell aplasia. (February 2008)
- Main Title:
- Case––control study of the association between select HLA genes and anti-erythropoietin antibody-positive pure red-cell aplasia
- Authors:
- Fijal, Bonnie
Ricci, Deborah
Vercammen, Els
Palmer, Peter A
Fotiou, Fotis
Fife, Daniel
Lindholm, Anders
Broderick, Erin
Francke, Stephan
Wu, Xiaodong
Colaianne, James
Cohen, Nadine - Abstract:
- Aims: Antibody (Ab)-positive pure red-cell aplasia (PRCA) is a very rare but serious adverse event associated with recombinant human erythropoietin treatment (4.1 reports per 100, 000 patient-years) in which patients produce antibodies to recombinant and endogenous erythropoietin, halting red blood cell production. In a previous case series, four Thai subjects with chronic kidney disease and Ab-positive PRCA were reported to have the HLA-DRB1*9 allele. To confirm a possible association of HLA-DRB1*9 and Ab-positive PRCA, we performed a pharmacogenomic analysis using subjects from an earlier case––control study of risk factors associated with Ab-positive PRCA, which had been performed using subjects from Europe or Canada. The primary goal of the analysis was to test the association between HLA-DRB1*9 and Ab-positive PRCA. A secondary goal was to perform an exploratory analysis in order to identify additional HLA alleles potentially associated with Ab-positive PRCA.Patients & Methods: Subjects were taken from a case––control study of Ab-positive PRCA in chronic kidney disease patients treated in Europe or Canada. Ab-positive PRCA cases (n = 24) were matched to controls (n = 81) by timing of treatment exposure and, when possible, by location.Results: The allele frequency of HLA-DRB1*9 was 12.5% in cases vs 1.2% in controls (p = 0.002). The frequency of the HLA-DRB1*9 /other genotype was 25.0% in cases vs 2.5% in controls (p = 0.004; OR: 10.8 [95% CI: 2.2––53.7]).Aims: Antibody (Ab)-positive pure red-cell aplasia (PRCA) is a very rare but serious adverse event associated with recombinant human erythropoietin treatment (4.1 reports per 100, 000 patient-years) in which patients produce antibodies to recombinant and endogenous erythropoietin, halting red blood cell production. In a previous case series, four Thai subjects with chronic kidney disease and Ab-positive PRCA were reported to have the HLA-DRB1*9 allele. To confirm a possible association of HLA-DRB1*9 and Ab-positive PRCA, we performed a pharmacogenomic analysis using subjects from an earlier case––control study of risk factors associated with Ab-positive PRCA, which had been performed using subjects from Europe or Canada. The primary goal of the analysis was to test the association between HLA-DRB1*9 and Ab-positive PRCA. A secondary goal was to perform an exploratory analysis in order to identify additional HLA alleles potentially associated with Ab-positive PRCA.Patients & Methods: Subjects were taken from a case––control study of Ab-positive PRCA in chronic kidney disease patients treated in Europe or Canada. Ab-positive PRCA cases (n = 24) were matched to controls (n = 81) by timing of treatment exposure and, when possible, by location.Results: The allele frequency of HLA-DRB1*9 was 12.5% in cases vs 1.2% in controls (p = 0.002). The frequency of the HLA-DRB1*9 /other genotype was 25.0% in cases vs 2.5% in controls (p = 0.004; OR: 10.8 [95% CI: 2.2––53.7]). Within the exploratory analysis, six additional HLA alleles ( HLA-A*25, HLA-B*53, HLA-C*12, HLA-DQB1*3, HLA-DQB1*6 and HLA-DRB1*4 ) were also found to be associated with Ab-positive PRCA.Conclusion: This study confirmed that HLA-DRB1*9 occurs at a significantly higher frequency in Ab-positive PRCA cases than in controls; however, within this sample set, carrying the *9 allele was neither necessary nor sufficient to cause Ab-positive PRCA. … (more)
- Is Part Of:
- Pharmacogenomics. Volume 9:Number 2(2008)
- Journal:
- Pharmacogenomics
- Issue:
- Volume 9:Number 2(2008)
- Issue Display:
- Volume 9, Issue 2 (2008)
- Year:
- 2008
- Volume:
- 9
- Issue:
- 2
- Issue Sort Value:
- 2008-0009-0002-0000
- Page Start:
- 157
- Page End:
- 167
- Publication Date:
- 2008-02
- Subjects:
- Ab-positive PRCA -- anemia -- Eprex®® -- erythropoetin -- immunogenicity -- pharmacogenomics -- recombinant protein
Pharmacogenomics -- Periodicals
615.1 - Journal URLs:
- http://www.futuremedicine.com/loi/pgs ↗
http://www.futuremedicine.com/ ↗ - DOI:
- 10.2217/14622416.9.2.157 ↗
- Languages:
- English
- ISSNs:
- 1462-2416
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6446.249500
British Library DSC - BLDSS-3PM
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