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Published on: July 9, 2014
Prevalence and determinants of cytomegalovirus infection in pre-school children
Timothy P O'Brien1, John M D Thompson, Peter N Black
1Departments of Paediatrics, University of Auckland, Private Bag 92019, Auckland, New Zealand.
Insights
The seroprevalence of cytomegalovirus (CMV) infection in New Zealand preschoolers is 32.8%, with significant ethnic variations. No clear determinants like socioeconomic status or daycare were identified.
Area of Science:
- Pediatric infectious diseases
- Epidemiology
- Immunology
Background:
- Cytomegalovirus (CMV) is a common viral infection with potential health implications in early childhood.
- Understanding CMV seroprevalence is crucial for public health strategies in developed nations.
Purpose of the Study:
- To determine the seroprevalence of cytomegalovirus (CMV) infection among 3.5-year-old children in New Zealand.
- To identify factors associated with CMV seropositivity in this population.
Main Methods:
- A cohort of 1714 children, enrolled at birth, was followed until 3.5 years of age.
- Blood samples from 530 children were analyzed for CMV-specific immunoglobulin using enzyme-linked immunosorbent assay (ELISA).
Main Results:
- The overall weighted seroprevalence of CMV was 32.8% (95% CI 27.4-38.1%).
- Significant ethnic disparities in seroprevalence were observed, with Maori (68.0%) and Pacific (74.5%) children showing higher rates.
- No association was found between CMV seropositivity and socioeconomic factors, number of siblings, daycare attendance, maternal smoking, or breastfeeding.
Conclusions:
- CMV seroprevalence in New Zealand preschoolers is comparable to other developed countries.
- Marked ethnic differences in CMV seroprevalence exist but are not explained by the investigated socioeconomic or environmental factors.
Aim:
The aim of this study is to measure the seroprevalence of cytomegalovirus (CMV) infection in 3.5-year-old children, and identify the determinants of seropositivity.
Methods:
A total of 1714 children were enrolled at birth. Approximately half were small for gestational age and half were appropriate for gestational age. Information on the children was collected at birth, 1 year and 3.5 years. At 3.5 years blood was collected and tested for CMV-specific immunoglobulin by an enzyme-linked immunosorbent assay in 530 children.
Results:
The weighted seroprevalence of CMV was 32.8% (95% confidence interval (CI) 27.4-38.1%). The seroprevalence of CMV varied markedly by ethnicity (European: 26.5% (95% CI 20.9-32.2%); Maori: 68.0% (44.0-92.0%); Pacific: 74.5% (56.3-92.6%); Indian: 50.0% (20.2-79.8%); Chinese: 47.2% (10.8-83.5%); Other: 21.9% (0.0-52.7%); P < 0.001). Socio-economic factors, number of siblings, day care centres attendance, maternal smoking, breastfeeding and other factors examined were not related to CMV seropositivity.
Conclusions:
The seroprevalence of CMV in New Zealand pre-school children is similar to that reported from other developed countries. The finding of marked ethnic differences is unexplained by socio-economic factors, or other factors that were examined.
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