The Duffy-null genotype and risk of infection. (22nd September 2020)
- Record Type:
- Journal Article
- Title:
- The Duffy-null genotype and risk of infection. (22nd September 2020)
- Main Title:
- The Duffy-null genotype and risk of infection
- Authors:
- Legge, Sophie E
Christensen, Rune H
Petersen, Liselotte
Pardiñas, Antonio F
Bracher-Smith, Matthew
Knapper, Steven
Bybjerg-Grauholm, Jonas
Baekvad-Hansen, Marie
Hougaard, David M
Werge, Thomas
Nordentoft, Merete
Mortensen, Preben Bo
Owen, Michael J
O'Donovan, Michael C
Benros, Michael E
Walters, James T R - Abstract:
- Abstract: Many medical treatments, from oncology to psychiatry, can lower white blood cell counts and thus access to these treatments can be restricted to individuals with normal levels of white blood cells, principally in order to minimize risk of serious infection. This adversely affects individuals of African or Middle Eastern ancestries who have on average a reduced number of circulating white blood cells, because of the Duffy-null (CC) genotype at rs2814778 in the ACKR1 gene. Here, we investigate whether the Duffy-null genotype is associated with the risk of infection using the UK Biobank sample and the iPSYCH Danish case-cohort study, two population-based samples from different countries and age ranges. We found that a high proportion of those with the Duffy-null genotype (21%) had a neutrophil count below the threshold often used as a cut-off for access to relevant treatments, compared with 1% of those with the TC/TT genotype. In addition we found that despite its strong association with lower average neutrophil counts, the Duffy-null genotype was not associated with an increased risk of infection, viral or bacterial. These results have widespread implications for the clinical treatment of individuals of African ancestry and indicate that neutrophil thresholds to access treatments could be lowered in individuals with the Duffy-null genotype without an increased risk of infection.
- Is Part Of:
- Human molecular genetics. Volume 29:Number 20(2020)
- Journal:
- Human molecular genetics
- Issue:
- Volume 29:Number 20(2020)
- Issue Display:
- Volume 29, Issue 20 (2020)
- Year:
- 2020
- Volume:
- 29
- Issue:
- 20
- Issue Sort Value:
- 2020-0029-0020-0000
- Page Start:
- 3341
- Page End:
- 3349
- Publication Date:
- 2020-09-22
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddaa208 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21684.xml