* Department of Pediatrics, Nagoya University Graduate School of
Medicine
Maternity and Perinatal Care Center, Nagoya University Hospital
Department of Pediatric Cardiology and Neonatology, Ogaki Municipal Hospital ¶ Department of Neonatology, Nagoya First Red Cross Hospital || Department of Nursing, Nagoya University School of Health Science,
Nagoya, Japan
Objective. Preterm infants are at greater risk of symptomaticcytomegalovirus (CMV) infection than term infants. Breast milk
is the main source of perinatal CMV infections. This study evaluated
the kinetics of CMV load in breast milk and the rate of postnatalCMV
transmission via breast milk from mothers to their preterminfants.
Methods. This was a prospective study of 30 mothers and their43 preterm infants. The infants either had a gestational ageof
<34 weeks or weighed <2000 g at birth. Breast milk,serum, and urine
samples were collected every 2 weeks untildischarge, and screened
for CMV infection using a real-timePCR assay. Most of the breast
milk had been preserved at -20°Cbefore feeding to the preterm
infants.
Results. Twenty-four mothers (24 of 30, 80%), who had 34 preterminfants, were CMV immunoglobulin G positive. Twenty-one (87.5%)
of the 24 seropositive mothers, who had 30 preterm infants,had
detectable CMV deoxyribonucleic acid (DNA) in breast milkduring the
study period. Most breast milk became positive forCMV DNA 2 weeks
after delivery. Viral DNA copy numbers increaseduntil they peaked at
4 to 6 weeks. Afterward, the CMV DNA copynumbers decreased. Of the
30 infants who were fed CMV DNA-positivebreast milk, CMV infection
was confirmed in 3 infants. However,they had no clinical symptoms of
CMV infection.
Conclusions. Despite the high rate of CMV DNA in breast milk,symptomatic infections in the preterm infants did not occur.
These results might be associated with the method of breastmilk
preservation and the population we studied. CMV infections
transmitted via breast milk feeding did not have much impacton
preterm infants in our institutes.
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