Reconsideration of Maternal Serological Testing for Predicting Congenital CMV Infection

Author:

Huang Yue12,Tang Jiabao12,Yu Huan2,Song Qiaoqiao2,Hao Mengling2,Wang Han2,Liu Junxian12,Dong Yue12,Liang Mufeng12,Zhuang Sijie12,Li Caihong3,Wang Jiangding4,Liang Caihong5,Su Yingying12,Li Tingdong12,Wu Ting12,Ge Shengxiang12,Zhang Jun12ORCID,Xia Ningshao12ORCID

Affiliation:

1. State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Department of Laboratory Medicine, School of Public Health, Xiamen University , Xiamen, Fujian , China

2. National Institute of Diagnostics and Vaccine Development in Infectious Diseases, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Collaborative Innovation Center of Biologic Products, National Innovation Platform for Industry-Education Integration in Vaccine Research, NMPA Key Laboratory for Research and Evaluation of Infectious Disease Diagnostic Technology, the Research Unit of Frontier Technology of Structural Vaccinology of Chinese Academy of Medical Sciences, Xiamen University , Xiamen, Fujian , China

3. Xinmi Maternal and Child Health Hospital , Xinmi, Henan , China

4. Jiaxian Maternal and Child Health Hospital , Jiaxian, Henan , China

5. Zhongmu Maternal and Child Health Hospital , Zhongmu, Henan , China

Abstract

Abstract Background The value of the widely applied maternal cytomegalovirus (CMV) serological testing approach in predicting intrauterine transmission in highly seroprevalent regions remains unknown. Methods 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. Results 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. Conclusions 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.

Funder

National Natural Science Foundation of China

Science and Technology Key Project of

Fujian Province

Fujian Provincial Health Commission

Fundamental Research Funds for the Central Universities

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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