Abstract

Objectives: To evaluate the prevalence of cytomegalovirus (CMV) infection in preterm infants with cholestasis.Study design: Preterm infants (<37 weeks gestational age) with cholestasis were tested for CMV DNA using Taqman PCR in blood cells from sedimented whole blood, plasma, and urine. Infants were regarded as positive for CMV if any sample was tested positive. Their mothers were tested for CMV serostatus simultaneously. A control group of non-cholestatic preterm infants, and their mothers, were tested at a similar age.Results: A total of 69 preterm infants with a median gestational age of 26 weeks and 5 days were included, 45 cholestatic and 24 non-cholestatic. Of the cholestatic infants, 31/45 (69%) were CMV positive vs. 3/24 (13%) of the non-cholestatic infants (p < 0.001). Cholestatic infants were equally preterm as the non-cholestatic ones, but were more severely ill. After adjusting for the risk factors necrotizing enterocolitis, prolonged parenteral nutrition, and gestational age, being CMV positive remained significantly associated with cholestasis in a multivariable logistic regression model. Characteristics of CMV-positive and -negative cholestatic infants showed differences only for necrotizing enterocolitis, occurring in 55% (17/31) of CMV positive vs. 21% (3/14) of CMV negative (p = 0.054), and mortality. Eight cholestatic CMV-positive infants died (26%) vs. none of the CMV-negative infants (p = 0.044).Conclusions: CMV DNA was detected in two out of three cholestatic preterm infants, by far more often than in the non-cholestatic control group. Cholestasis with simultaneous detection of CMV DNA may be associated with increased mortality.

Highlights

  • MATERIALS AND METHODSHuman cytomegalovirus (CMV) infection is among the most common viral infections in neonates [1]

  • A total of 69 infants were included in the study, with a median gestational age of 26 weeks and 5 days and birth weight 0.845 kg

  • Nine infants in the cholestasis group and four in the noncholestasis group were from duplex pregnancies

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Summary

Introduction

MATERIALS AND METHODSHuman cytomegalovirus (CMV) infection is among the most common viral infections in neonates [1]. The outcome of a congenital infection may vary from asymptomatic to multiple severe symptoms and present with low birth weight, microcephaly, liver disease with jaundice, retinitis, hearing and vision loss, and developmental and motor delays [2, 3]. In a meta-analysis, the prevalence of congenital CMV infection (cCMV) was estimated to 0.64%, with higher prevalence in low-income countries, and 11% were estimated to be symptomatic [3]. Kadambari et al found an increase in hospital diagnoses of cCMV infections in England over the last decades, presumably due to improved diagnostics. They found that a substantial burden of disease lay among the preterm infants in neonatal wards [4]

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