Saliva Polymerase-Chain-Reaction Assay for Cytomegalovirus Screening in Newborns

被引:346
作者
Boppana, Suresh B. [1 ,2 ]
Ross, Shannon A. [1 ]
Shimamura, Masako [1 ]
Palmer, April L. [5 ]
Ahmed, Amina [6 ]
Michaels, Marian G. [7 ,8 ]
Sanchez, Pablo J. [9 ]
Bernstein, David I. [10 ,11 ]
Tolan, Robert W., Jr. [12 ,13 ]
Novak, Zdenek [1 ]
Chowdhury, Nazma [1 ]
Britt, William J. [1 ,2 ,3 ]
Fowler, Karen B. [1 ,4 ]
机构
[1] Univ Alabama Birmingham, Dept Pediat, Birmingham, AL 35233 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35233 USA
[3] Univ Alabama Birmingham, Dept Neurobiol, Birmingham, AL 35233 USA
[4] Univ Alabama Birmingham, Dept Epidemiol & Int Hlth, Birmingham, AL 35233 USA
[5] Univ Mississippi, Med Ctr, Dept Pediat, Jackson, MS 39216 USA
[6] Carolinas Med Ctr, Dept Pediat, Charlotte, NC 28203 USA
[7] Univ Pittsburgh, Dept Pediat, Pittsburgh, PA 15260 USA
[8] Childrens Hosp Pittsburgh, Pittsburgh, PA 15213 USA
[9] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[10] Univ Cincinnati, Cincinnati, OH USA
[11] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[12] St Peters Univ Hosp, New Brunswick, NJ USA
[13] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
关键词
DRIED BLOOD SPOTS; SENSORINEURAL HEARING-LOSS; CONGENITAL CMV INFECTION; DNA DETECTION; LIKELIHOOD RATIOS; FILTER-PAPER; CHILDREN; TRANSMISSION; VIRUS; URINE;
D O I
10.1056/NEJMoa1006561
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Congenital cytomegalovirus (CMV) infection is an important cause of hearing loss, and most infants at risk for CMV-associated hearing loss are not identified early in life because of failure to test for the infection. The standard assay for newborn CMV screening is rapid culture performed on saliva specimens obtained at birth, but this assay cannot be automated. Two alternatives - real-time polymerase-chain-reaction (PCR)-based testing of a liquid-saliva or dried-saliva specimen obtained at birth - have been developed. Methods In our prospective, multicenter screening study of newborns, we compared real-time PCR assays of liquid-saliva and dried-saliva specimens with rapid culture of saliva specimens obtained at birth. Results A total of 177 of 34,989 infants (0.5%; 95% confidence interval [CI], 0.4 to 0.6) were positive for CMV, according to at least one of the three methods. Of 17,662 newborns screened with the use of the liquid-saliva PCR assay, 17,569 were negative for CMV, and the remaining 85 infants (0.5%; 95% CI, 0.4 to 0.6) had positive results on both culture and PCR assay. The sensitivity and specificity of the liquid-saliva PCR assay were 100% (95% CI, 95.8 to 100) and 99.9% (95% CI, 99.9 to 100), respectively, and the positive and negative predictive values were 91.4% (95% CI, 83.8 to 96.2) and 100% (95% CI, 99.9 to 100), respectively. Of 17,327 newborns screened by means of the dried-saliva PCR assay, 74 were positive for CMV, whereas 76 (0.4%; 95% CI, 0.3 to 0.5) were found to be CMV-positive on rapid culture. Sensitivity and specificity of the dried-saliva PCR assay were 97.4% (95% CI, 90.8 to 99.7) and 99.9% (95% CI, 99.9 to 100), respectively. The positive and negative predictive values were 90.2% (95% CI, 81.7 to 95.7) and 99.9% (95% CI, 99.9 to 100), respectively. Conclusions Real-time PCR assays of both liquid-and dried-saliva specimens showed high sensitivity and specificity for detecting CMV infection and should be considered potential screening tools for CMV in newborns. (Funded by the National Institute on Deafness and Other Communication Disorders.)
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收藏
页码:2111 / 2118
页数:8
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