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Efficacy Evaluated in Maternal Screening for Congenital CMV

By Labmedica International staff writers
Posted on 31 Jul 2017
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Image: Transmission electron microscopic (TEM) depicts numbers of cytomegalovirus (CMV) virions that were present in a tissue sample (Photo courtesy of Sylvia Whitfield).
Image: Transmission electron microscopic (TEM) depicts numbers of cytomegalovirus (CMV) virions that were present in a tissue sample (Photo courtesy of Sylvia Whitfield).
Researchers have evaluated for the first time the efficacy of maternal universal screening using cytomegalovirus (CMV) IgG avidity tests for congenital CMV infection, and they have also identified problematic issues with the current maternal CMV screening methods.

Senior author Prof. Hideto Yamada, of the Graduate School of Medicine at Kobe University (Japan), and colleagues conducted the study. The risk of CMV transmission to the fetus is highest for mothers who were infected by the virus for the first time during pregnancy (primary infection), but the results of this study showed that a number of mothers with infected fetuses were already infected before pregnancy (non-primary infection). Current screening methods, which only aim to identify women with primary infection during pregnancy, may be overlooking these cases.

Recently, the neurological complications caused by congenital CMV infection in affected infants have been successfully treated with antiviral agents, but early diagnosis of congenital infection is vital for this treatment to be effective. To identify primary CMV infection, maternal blood tests for CMV-specific immunoglobulin (Ig) M antibodies (CMV IgM) are widely used. However, CMV IgM tests can remain positive for years after primary infection, so a positive result for CMV IgM does not always indicate primary infection during pregnancy. A CMV IgG avidity test is also used for identifying a recent infection.

This study aimed to determine the effectiveness of CMV IgG avidity tests as a maternal universal screening for congenital CMV infection. The research group enrolled 2,193 pregnant women. They carried out CMV IgG antibody (CMV IgG) tests before 22 gestational weeks (GW). If the tests were negative, women were told how to avoid CMV infection, and tested for CMV IgG again in 34-36 GW. If they tested positive for CMV IgG in the second tests, they were considered to have primary infection during pregnancy.

For women who tested positive for CMV IgG, they carried out CMV IgG avidity tests. When the avidity index was 45% or less, they added CMV IgM tests, and if the avidity index was less than 35% and/or CMV IgM was positive, the women were considered to have primary infection during pregnancy. If their avidity index was over 45%, this was judged as chronic infection (infection before pregnancy).

They also measured CMV IgM in the stored serum samples in order to compare the efficacy of maternal screening using avidity tests with that using CMV IgM tests.

Of the 2,193 subjects, 10 infants had congenital CMV infection. A total of 93 women were judged as having primary CMV infection during pregnancy. Among these subjects, 3 gave birth to infants with congenital infection. On the other hand, among the 1,287 people judged as having non-primary infection, there were 7 cases of congenital infection. Screening using avidity testing had the same level of diagnostic accuracy as screening using CMV IgM.

These results suggest that standard maternal screening methods likely miss many cases of congenital CMV. In order to identify all infants with congenital CMV infection upon birth, a change in strategy in needed. For example including use PCR to test for CMV in urine samples from all newborns. The researchers plan to develop a more comprehensive screening method for congenital CMV infection, enabling early detection and treatment.

The study, by Tanimura K et al, was published July 20, 2017, in the journal Clinical Infectious Diseases.

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