106. The risk, timing and clinical impact of postnatal cytomegalovirus transmission on preterm infants born less than 29 weeks of gestational age: A prospective multicenter cohort study

Abstract Background As the survival rate of extremely preterm infants has increased, postnatal CMV infection (pCMV) has been considered a potential contributor to morbidities in this population. This study aimed to clarify the risk, symptoms, and complications of pCMV. Methods This is a multicenter prospective cohort study of infants born < 29 weeks of postmenstrual age (PMA) with CMV-PCR negative results in urine tests within 2 weeks of birth. Serial viral loads in breast milk and infant blood and urine were monitored every 2 weeks until 36 weeks of PMA. Binding, neutralizing and non-neutralizing functions of maternal serum CMV-specific antibodies, including antibody-dependent cellular cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP), were assessed for the infection risk. Results During the study period from Dec 2021 to Sep 2024, 139 infants were enrolled. Eighty-three (59%) of these infants were born to CMV-seropositive mothers. The infants' gestational age and birth body weight were 26 weeks (IQR 24-27), and 763 g (515-1011), respectively. The prevalence of pCMV by 36 weeks of PMA was 14/139 (10%) overall and 13/83 (16%) in infants born to seropositive mothers. Symptoms associated with pCMV were transient neutropenia (< 1000/µL) (pCMV+ 42% vs. pCMV- 11%, p< 0.01) and acute respiratory exacerbation after 3 weeks of age (31 vs. 11%, p=0.08). Infants with pCMV were born at a lower gestational age (24 vs 25 weeks, p=0.06) and experienced premature rupture of membranes more than 24 hours before birth (58% vs 17%, p=0.01). pCMV was associated with a higher CMV load in maternal milk at 2 weeks (141820 vs 7815 copies/µL, p< 0.01) and 4 weeks (40296 vs 8415 copies/µL, p< 0.04) after birth. In maternal serum, CMV-specific antibody levels were not different, but ADCP activity was lower (85% vs 78%, p=0.01) in the pCMV group. In addition, total serum IgG levels tended to be lower in the pCMV group (245 vs. 340 mg/dL, p=0.07). Conclusion Approximately 16% of extremely preterm infants born to CMV-seropositive mothers develop pCMV by term equivalent age. Risk factors for infection include low maternal ADCP activity, lower gestational age, and premature rupture of membranes more than 24 hours prior to birth. Neutropenia and chronic lung disease may be symptoms of pCMV. Disclosures All Authors: No reported disclosures

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.041
Primary Topic
Cytomegalovirus and herpesvirus research
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article
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article

106. The risk, timing and clinical impact of postnatal cytomegalovirus transmission on preterm infants born less than 29 weeks of gestational age: A prospective multicenter cohort study

Michio SUZUKI, Yoshinori Ito, Yuka Torii, Yoshiaki Sato et al.
Open Forum Infectious Diseases
Cytomegalovirus and herpesvirus research
article

106. The risk, timing and clinical impact of postnatal cytomegalovirus transmission on preterm infants born less than 29 weeks of gestational age: A prospective multicenter cohort study

Michio SUZUKI, Yoshinori Ito, Yuka Torii, Yoshiaki Sato, Keita Takahashi, Takako Suzuki, Ryuichi Tanaka, Y U ichiro Sugiyama, Juri Koizumi, Tetsuo Koshizuka
article en

Abstract

Abstract Background As the survival rate of extremely preterm infants has increased, postnatal CMV infection (pCMV) has been considered a potential contributor to morbidities in this population. This study aimed to clarify the risk, symptoms, and complications of pCMV. Methods This is a multicenter prospective cohort study of infants born < 29 weeks of postmenstrual age (PMA) with CMV-PCR negative results in urine tests within 2 weeks of birth. Serial viral loads in breast milk and infant blood and urine were monitored every 2 weeks until 36 weeks of PMA. Binding, neutralizing and non-neutralizing functions of maternal serum CMV-specific antibodies, including antibody-dependent cellular cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP), were assessed for the infection risk. Results During the study period from Dec 2021 to Sep 2024, 139 infants were enrolled. Eighty-three (59%) of these infants were born to CMV-seropositive mothers. The infants' gestational age and birth body weight were 26 weeks (IQR 24-27), and 763 g (515-1011), respectively. The prevalence of pCMV by 36 weeks of PMA was 14/139 (10%) overall and 13/83 (16%) in infants born to seropositive mothers. Symptoms associated with pCMV were transient neutropenia (< 1000/µL) (pCMV+ 42% vs. pCMV- 11%, p< 0.01) and acute respiratory exacerbation after 3 weeks of age (31 vs. 11%, p=0.08). Infants with pCMV were born at a lower gestational age (24 vs 25 weeks, p=0.06) and experienced premature rupture of membranes more than 24 hours before birth (58% vs 17%, p=0.01). pCMV was associated with a higher CMV load in maternal milk at 2 weeks (141820 vs 7815 copies/µL, p< 0.01) and 4 weeks (40296 vs 8415 copies/µL, p< 0.04) after birth. In maternal serum, CMV-specific antibody levels were not different, but ADCP activity was lower (85% vs 78%, p=0.01) in the pCMV group. In addition, total serum IgG levels tended to be lower in the pCMV group (245 vs. 340 mg/dL, p=0.07). Conclusion Approximately 16% of extremely preterm infants born to CMV-seropositive mothers develop pCMV by term equivalent age. Risk factors for infection include low maternal ADCP activity, lower gestational age, and premature rupture of membranes more than 24 hours prior to birth. Neutropenia and chronic lung disease may be symptoms of pCMV. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 13(Supplement_1)
Aichi Medical University (JP), Gifu Pharmaceutical University (JP), Nagoya University Hospital (JP), Japanese Red Cross Nagoya Daiichi Hospital (JP), Anjo Kosei Hospital (JP), Nagoya University (JP)
Good health and well-being
Openalex Percentile: Top 92%
Cytomegalovirus and herpesvirus research
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