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Complex differences in infection rates between ethnic groups in Scotland: a retrospective, national census-linked cohort study of 1.65 million cases.

Authors :
Gruer, L D
Cézard, G I
Wallace, L A
Hutchinson, S J
Douglas, A F
Buchanan, D
Katikireddi, S V
Millard, A D
Goldberg, D J
Sheikh, A
Bhopal, R S
Source :
Journal of Public Health; Mar2022, Vol. 44 Issue 1, p60-69, 10p
Publication Year :
2022

Abstract

Background Ethnicity can influence susceptibility to infection, as COVID-19 has shown. Few countries have systematically investigated ethnic variations in infection. Methods We linked the Scotland 2001 Census, including ethnic group, to national databases of hospitalizations/deaths and serological diagnoses of bloodborne viruses for 2001–2013. We calculated age-adjusted rate ratios (RRs) in 12 ethnic groups for all infections combined, 15 infection categories, and human immunodeficiency virus (HIV), hepatitis B (HBV) and hepatitis C (HCV) viruses. Results We analysed over 1.65 million infection-related hospitalisations/deaths. Compared with White Scottish, RRs for all infections combined were 0.8 or lower for Other White British, Other White and Chinese males and females, and 1.2–1.4 for Pakistani and African males and females. Adjustment for socioeconomic status or birthplace had little effect. RRs for specific infection categories followed similar patterns with striking exceptions. For HIV, RRs were 136 in African females and 14 in males; for HBV, 125 in Chinese females and 59 in males, 55 in African females and 24 in males; and for HCV, 2.3–3.1 in Pakistanis and Africans. Conclusions Ethnic differences were found in overall rates and many infection categories, suggesting multiple causative pathways. We recommend census linkage as a powerful method for studying the disproportionate impact of COVID-19. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17413842
Volume :
44
Issue :
1
Database :
Complementary Index
Journal :
Journal of Public Health
Publication Type :
Academic Journal
Accession number :
155649293
Full Text :
https://doi.org/10.1093/pubmed/fdaa267