Reconsideration of Maternal Serological Testing for Predicting Congenital CMV Infection

• Published in: The Journal of infectious diseases 2024-06, Vol.229 (6), p.1817-1822
• Main Authors: Huang, Yue, Tang, Jiabao, Yu, Huan, Song, Qiaoqiao, Hao, Mengling, Wang, Han, Liu, Junxian, Dong, Yue, Liang, Mufeng, Zhuang, Sijie, Li, Caihong, Wang, Jiangding, Liang, Caihong, Su, Yingying, Li, Tingdong, Wu, Ting, Ge, Shengxiang, Zhang, Jun, Xia, Ningshao
• Format: Article
• Language: English
• Subjects: Adult; Antibodies, Viral - blood; Antibody Affinity; Case-Control Studies; Cohort Studies; Cytomegalovirus - immunology; Cytomegalovirus - isolation & purification; Cytomegalovirus Infections - congenital; Cytomegalovirus Infections - diagnosis; Cytomegalovirus Infections - immunology; Cytomegalovirus Infections - transmission; Cytomegalovirus Infections - urine; DNA, Viral - blood; DNA, Viral - urine; Female; Humans; Immunoglobulin G - blood; Immunoglobulin M - blood; Infant, Newborn; Infectious Disease Transmission, Vertical; Male; Pregnancy; Pregnancy Complications, Infectious - diagnosis; Pregnancy Complications, Infectious - virology; Retrospective Studies; Serologic Tests - methods
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1093/infdis/jiad412

The value of the widely applied maternal cytomegalovirus (CMV) serological testing approach in predicting intrauterine transmission in highly seroprevalent regions remains unknown. A nested case-control study was conducted based on a maternal-child cohort study. Newborns with congenital CMV (cCMV) infection were included, and each of them was matched to 3 newborns without cCMV infection. Retrospective samples were tested for immunoglobulin G (IgG) avidity and immunoglobulin M (IgM) antibodies in maternal serum and CMV DNA in maternal blood and urine to analyze their associations with cCMV infection. Forty-eight newborns with cCMV infection and 144 matched newborns without infection were included in the study. Maternal IgM antibodies and IgG avidity during pregnancy were not statistically associated with intrauterine transmission. The presence of CMV DNAemia indicated a higher risk of cCMV infection, with odds ratio values of 5.7, 6.5, and 13.0 in early, middle, and late pregnancy, respectively. However, the difference in CMV shedding rates in transmitters and nontransmitters was not significant in urine. The value of current maternal CMV serological testing in regions with high seropositivity rates is very limited and should be reconsidered. The detection of DNAemia would be helpful in assessing the risk of intrauterine transmission.