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. 2021 Mar 25;16(3):e0248801. doi: 10.1371/journal.pone.0248801

The prevalence and demographic features of congenital cytomegalovirus infection in an urban area of East Asia: A population-based study

Tzong-Hann Yang 1,2,3, Hung-Meng Huang 1,4, Wei-Chung Hsu 5, Po-Nien Tsao 6, Tien-Chen Liu 5, Chuan-Jen Hsu 5, Li-Min Huang 6, Chuan-Song Wu 1,7, Shih-Ming Weng 2,8, Chun-Yi Lu 6,*, Chen-Chi Wu 5,9,*
Editor: Kazumichi Fujioka10
PMCID: PMC7993615  PMID: 33765031

Abstract

Congenital cytomegalovirus (cCMV) infection is the leading environmental cause of childhood hearing impairment. However, its significance remains largely undocumented in many regions of the world. The purpose of this study was to investigate the prevalence and clinical features of cCMV infection in East Asia. Neonates born at a municipal hospital in Taipei were prospectively recruited and underwent concurrent hearing and CMV screenings. Those who failed the hearing screening or screened positive for CMV were subjected to a focused audiological and/or virological surveillance. The characteristics of the newborns and their mothers were compared between the CMV-positive and CMV-negative groups. Of the 1,532 newborns who underwent concurrent hearing and CMV screenings, seven (0.46%) were positive for cCMV infection. All seven CMV-positive newborns were asymptomatic at birth, and none of them developed hearing or other symptoms during a follow-up period of 14.4±6.3 months. The mothers of the CMV-positive newborns demonstrated higher gravidity (2.4 ± 1.4 vs. 2.1 ± 1.2) and parity (2.0 ± 1.2 vs. 1.6 ± 0.7) than those in the CMV-negative group; however, the difference did not reach statistical significance. The prevalence of cCMV infection in Taipei newborns was 0.46%, which is slightly lower than that of other populations and that of a previous report in the Taiwanese population. The relatively low prevalence in this study might be attributed to the improved public health system and decreased fertility rate in Taiwan.

Introduction

Sensorineural hearing loss (SNHL) is a common clinical entity in newborns [1,2] and children [3,4]. Pediatric SNHL is an etiologically heterogeneous condition caused by a plethora of genetic [57] and environmental factors [812]. Recent advances in molecular genetics have revolutionized the assessment armamentarium of pediatric SNHL, enabling us to ascertain the etiology in 40–60% of the children with SNHL [13,14]. However, the clinical significance and contribution of the environmental factors that might lead to pediatric SNHL in these children largely remains unclear [8,11,12,15,16].

Among these environmental factors, congenital cytomegalovirus (cCMV) infection is the leading cause of pediatric SNHL [17] and neurodevelopmental disability [18] in developed countries. The importance of identifying cCMV infection as the etiology of SNHL in newborns has become clinically relevant with the availability of oral antiviral agents that may prevent the progression of cCMV-related SNHL [19]. Furthermore, children with cCMV infection are at risk for progressive SNHL that may not be present until several years of age, at a time when the golden period for hearing-loss rehabilitation has passed [2022].

The prevalence and clinical characteristics of cCMV-infected newborns have been reported in several Western series [17,23]. However, there is still a paucity of such reports in East Asia, a populated region with rapid economic development. In the present study, we aimed to investigate the prevalence of cCMV infection in newborns from an urban region of East Asia and the clinical characteristics of cCMV-positive children and their mothers.

Materials and methods

Subject recruitment

From May 2016 to Dec 2018, we prospectively enrolled neonates born at the Taipei City Hospital Fuyou Branch. All newborns underwent hearing screening using automated auditory brainstem response (AABR) testing [24], and saliva swabs were obtained simultaneously for cCMV screening.

For the newborns who screened positive for cCMV, the following variables were recorded: sex, mode of delivery, age at last follow-up, birth weight, maternal age, gestational age, mother’s gravidity and parity, and presence of symptoms/signs at birth, such as newborn hearing screening (NHS) failure or neonatal jaundice, and admission status were recorded.

All infants were of Han Taiwanese ethnicity. Written informed consent was obtained from the parents of all infants. This study was approved by the Research Ethics Committees of Taipei City Hospital and the National Taiwan University Hospital.

CMV screening

CMV screening was performed using a quantitative real-time polymerase chain reaction (PCR) assay with fluorescence resonance energy transfer (FRET) hybridization probes to detect the glycoprotein B of CMV [25]. The lower limit of detection, estimated using a CMV construct, was 10 copies/ml. All positive results were replicated in a second test, and samples that tested positive in both were considered true positives. Positive CMV PCR results were then confirmed by isolating CMV from urine or saliva.

Audiologic and clinical assessments in CMV-positive infants

Infants who tested positive for CMV at birth were subjected to a focused audiologic surveillance, including repeated AABR testing at 1 month, followed by comprehensive audiologic assessments at 3 months, 6 months, and 1 year [25].

These infants also underwent additional clinical evaluations, including complete blood counts, blood biochemistry, brain transfontanellar ultrasonography, abdominal ultrasonography, neurologic assessment, and visual assessment. Virological tests, including the determination of CMV viral loads in the blood using quantitative real-time PCR and the detection of CMV from a culture of bodily fluids (either urine or a throat swab), were performed during every medical examination to monitor viral clearance [25].

Data analyses

The results of the CMV screening were compared to the NHS results. The characteristics of the newborns and their mothers were analyzed according to their sex, mode of delivery, gestational age, birth weight, maternal age at pregnancy, gravidity, and parity. The proportions between the groups were compared using Fisher’s exact test. All analyses were conducted using SAS software, version 9.3 (SAS Institute, Inc., Cary, NC).

Results

During the study period, 3,273 neonates were born at the Taipei City Hospital Fuyou Branch (Fig 1). Of these, the parents of 1,532 neonates agreed to undergo a newborn CMV screening for their children. The CMV screening was positive in seven newborns (0.46%), including one girl and six boys (Table 1). CMV infection was confirmed in all seven newborns by isolation of CMV from saliva and/or urine. All seven CMV-positive newborns passed the NHS. Of the other 1,525 infants who were negative for CMV, 25 (1.6%) failed the initial NHS and three (0.2%) were subsequently confirmed to have unilateral or bilateral SNHL. Among the 1,741 infants who did not undergo CMV screening, 64 (3.7%) failed the initial NHS and 16 (0.9%) were subsequently confirmed to have SNHL. In total, the prevalence of neonatal cCMV infection was 0.46%, with 0.74% for males and 0.14% for females. There was no statistically significant difference in the prevalence between the sexes.

Fig 1. Flow diagram of the recruitment and the outcome of the newborn hearing screening (NHS) and cCMV screening in 3,273 newborns in Taipei, Taiwan.

Fig 1

NTUH denotes National Taiwan University Hospital.

Table 1. Prevalence of cCMV infection in the 1,532 newborns.

cCMV+ cCMV- Total Prevalence P value
Total number 7 1,525 1,532 0.46%
Sex 0.129
 Male 6 805 811 0.74%
 Female 1 721 722 0.14%
Mean age at last follow-up, m 14.4±7.1

The characteristics of the seven CMV-positive newborns are presented in Table 2. The newborns of cases 2 and 3 were given birth by a cesarean section (2/7, 28.6%), while the other five newborns were given birth through a normal spontaneous delivery (5/7, 71.4%).

Table 2. Characteristics of the 7 newborns with cCMV infection.

Case Sex Mode of delivery Age at last follow-up, m Age of mother Gestational age (weeks) Gravidity Parity Birth weight in kg (%) Head girth at birth in cm (%) Hearing level Other symptoms
1 F NSD 19 19 39 1 1 3.50 (50–85) 36 (50–85) normal none
2 M CS lost to follow-up 39 38 2 2 3.14 (15–85) 35 (50–85) NA NA
3 M CS 18 41 38 5 4 3.70 (50–85) 36 (50–85) normal none
4 M NSD lost to follow-up 37 39 2 2 3.90 (50–85) 35.5 (50–85) NA NA
5 M NSD 18 26 34 3 3 3.36 (50–85) 34 (15–50) normal none
6 M NSD 15 51 39 3 1 3.58 (50–85) 36 (50–85) normal none
7 M NSD 2 27 37 1 1 2.78 (3–15) 33 (15–50) normal none

CS, cesarean section; NA, not available; NSD, normal spontaneous delivery.

All seven newborns with cCMV infection were asymptomatic at birth, and none of them were admitted to a neonatal intensive care unit or developed hyperbilirubinemia that required a specific treatment, including phototherapy or plasmapheresis (Table 2). The newborns of cases 2 and 4 were lost to follow-up for unknown reasons. The other five newborns were followed up at the National Taiwan University Hospital for a mean duration of 14.4±6.3 months. None of these five newborns developed hearing or other symptoms during the follow-up period.

Table 3 presents a comparison of the maternal/neonatal characteristics between newborns with and without cCMV infection. The mothers of the CMV-positive neonates had a slightly higher gravidity (2.4 ± 1.4 vs. 2.1 ± 1.2, respectively) and parity (2.0 ± 1.2 vs. 1.6 ± 0.7, respectively) than those whose newborn babies were screened negative for CMV; yet, the difference did not reach statistical significance.

Table 3. Comparison of maternal/neonatal characteristics between subjects with and those without cCMV infection.

Characteristics CMV+(n = 7) CMV-(n = 1,525) P value
Gender (male) 6 (85.7%) 804 (52.7%) .083
Mode of delivery (NSD) 5 (71.4%) 1041 (68.3%) .608
Birth weight (kg) 3.3 ± 0.3 3.1 ± 0.4 .088
Age of mother (y) 34.4 ± 10.9 33.2 ± 4.7 .768
Gestational age (weeks) 38.3 ± 0.8 38.5 ± 1.2 .643
Gravidity 2.4 ± 1.4 2.1 ± 1.2 .509
Parity 2.0 ± 1.2 1.6 ± 0.7 .154
Failed NHS 3 (0.5%) 0 (0%) .986

NHS: Newborn hearing screen; NSD: Normal spontaneous delivery.

Discussion

In this study, we demonstrated that the prevalence of cCMV infection is approximately 0.46% in Taipei, a typical populous city in East Asia. The rate is slightly lower than that in other populations. In developed countries, the prevalence of cCMV infection ranged from 0.58% to 0.70% [17,26,27]. In developing countries, such as Mexico, Nigeria, and Gambia, the prevalence of cCMV infection was higher than that in our study, ranging from 0.9% to 5.4% [2832]. Several factors have been proposed to account for the differences in the prevalence of cCMV infections in newborns between the developed and developing countries, including the testing methods [26], sampling methodology [26], selection bias [26], and seroprevalence rate in the general population [31,3335], and ethnicity [26,36,37].

Noticeably, in a prior study in 1996, the prevalence of cCMV infection in Taiwanese newborns was found to be 1.8% [38]. The significantly lower prevalence in the present study might reflect the improved public health conditions, including better prenatal care in Taiwan over the past two decades. Interestingly, a recent study in China also reported a low cCMV infection prevalence (0.7%, n = 10.933) [33] as compared to that in three other large-scale studies in Portuguese (1.05%, n = 3,600) [34], Brazilian (1.1%, n = 8,047) [35], and Turkish (1.9%, n = 944) [31] populations, although the seroprevalence of CMV is commensurately high among the four populations. The authors attributed the lower cCMV infection in the Chinese population to the lower exposure of pregnant women to young children than in the other populations as a result of China’s unique one-child policy [33]. In our study, we also observed a higher parity number in the mothers with CMV-positive newborns (2.0 ± 1.2) than in those with CMV-negative newborns (1.6 ± 0.7). It is thus likely that the low fertility rate, that is, the number of children a woman is expected to have during her childbearing years, might also contribute to the low cCMV infection rate in the Taiwanese newborns in the present study. Since 2008, one of the lowest fertility rates (0.895–1.27) among any territory in the world has been recorded in the Taiwanese population (https://eng.stat.gov.tw/public/data/dgbas03/bs2/yearbook_eng/y005.pdf).

The screening tool for cCMV infection is also crucial when the prevalence of cCMV infection is determined and compared across populations. It has been demonstrated that real-time PCR assays on saliva samples collected from live-born newborns performed within 2 days from birth, as performed in the present study, enables high sensitivity and specificity for identifying a cCMV infection in newborns [39,40]. In contrast, real-time PCR assay on dry bloodspot samples had a low sensitivity, restraining its value as a screening test for cCMV infection [41]. Our earlier work also showed a lower rate of cCMV infection (0.17%, 3/1,716) in a similar population when PCR on dried blood spot (DBS) specimens was used as a screening method [25].

Of note, although all seven newborns who screened positive for cCMV infection passed the hearing screening at birth and none of them developed a hearing impairment during the follow-up period, a regular and continual check-up on the hearing level and viral status is necessary in these infants, as it has been documented that a certain proportion of infants with asymptomatic cCMV infection might develop a hearing impairment or other sequelae later on, even as late as at the adolescent age [22].

The strength of this study is that all subjects were recruited from a community-based hospital, which offered an unbiased estimation of the representative prevalence of cCMV infection among newborns in Taipei. All the CMV PCR and confirmatory CMV isolation tests were fully supported by research grants and were hence free to parents. This further prevented selection biases brought about by socioeconomic status. The composition of newborns in the present study is different from that recruited from medical centers [26], where the recruitment of subjects could be biased to a study population with a higher risk of disease propensity.

However, some limitations of this study deserve discussion. First, the current study included a sample size of 1,532 newborns and an average follow-up period of 14.4 months. A larger series with a longer follow-up period will possibly disclose the prevalence and clinical outcomes of cCMV infection with greater precision. Second, the notion that low cCMV infection prevalence is associated with low fertility rates needs to be tested in other populations with low fertility rates. Further investigations in other East Asian populations with a low fertility rate, such as the Korean and Japanese populations, are highly expected.

Conclusion

The prevalence of cCMV infection in newborns of Taipei, Taiwan is 0.46%, which is slightly lower than that in other populations and that previously reported in the Taiwanese population. The relatively low prevalence in this study might be attributed to the improved public health and prenatal care system and the decreased fertility rate in Taiwan.

Supporting information

S1 File

(XLSX)

Data Availability

All relevant data are within the paper and its Supporting information files.

Funding Statement

The study was supported by research grants from the National Taiwan University Hospital (107-S3913), Taipei City Government (10501- 62-030), and the Ministry of Science and Technology, Taiwan (107-2622-B-002-008-CC2.

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30 Oct 2020

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The Prevalence and Hearing Outcome of Congenital CMV Infection in an Urban Area of East Asia: Population-based Study

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[Note: HTML markup is below. Please do not edit.]

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Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: No

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The article presents a unique study focused on a locality (Taipei, Taiwan), aiming at a general and comprehensive background of East Asia. No details were given on the choice of the hospital to conduct the research. A more comprehensive study would be needed for the effect of cCMV infection in the population assessment.

The figure needs to improve resolution.

Reviewer #2: "The Prevalence and Hearing Outcome of Congenital CMV Infection in an Urban Area of East Asia: Population-based Study" by Yang et al. is well-written and provides a relatively comprehensive view about Congenital cytomegalovirus prevalence in Taipei, Taiwan. Although the study has limitations already recognized by the authors, this manuscript provide advances in our understanding about the relevance the early identification of cCMV in neonates increasing the quality of life of patients and better follow-up of the public service to these patients telling a nice story. I think it would be suitable for publication in PLoS One after careful revision of English language.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2021 Mar 25;16(3):e0248801. doi: 10.1371/journal.pone.0248801.r002

Author response to Decision Letter 0


18 Jan 2021

PONE-D-20-23918

The Prevalence and Hearing Outcome of Congenital CMV Infection in an Urban Area of East Asia: Population-based Study

PLOS ONE

Dear Dr. Wu,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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Academic Editor

PLOS ONE

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"The study was supported by research grants from the National Taiwan University Hospital (107-S3913), Taipei City Government (10501-62-030), and the Ministry of Science and Technology, Taiwan (107-2622-B-002-008-CC2)."

We note that you have provided funding information that is not currently declared in your Funding Statement. However, funding information should not appear in the Acknowledgments section or other areas of your manuscript. We will only publish funding information present in the Funding Statement section of the online submission form.

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[copy in statement].

Please complete your Competing Interests on the online submission form to state any Competing Interests. If you have no competing interests, please state "The authors have declared that no competing interests exist.", as detailed online in our guide for authors at http://journals.plos.org/plosone/s/submit-now

This information should be included in your cover letter; we will change the online submission form on your behalf.

Please know it is PLOS ONE policy for corresponding authors to declare, on behalf of all authors, all potential competing interests for the purposes of transparency. PLOS defines a competing interest as anything that interferes with, or could reasonably be perceived as interfering with, the full and objective presentation, peer review, editorial decision-making, or publication of research or non-research articles submitted to one of the journals. Competing interests can be financial or non-financial, professional, or personal. Competing interests can arise in relationship to an organization or another person. Please follow this link to our website for more details on competing interests: http://journals.plos.org/plosone/s/competing-interests

4. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: No

Reviewer #2: Yes

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: Yes

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: Yes

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The article presents a unique study focused on a locality (Taipei, Taiwan), aiming at a general and comprehensive background of East Asia. No details were given on the choice of the hospital to conduct the research. A more comprehensive study would be needed for the effect of cCMV infection in the population assessment.

The figure needs to improve resolution.

Reviewer #2: "The Prevalence and Hearing Outcome of Congenital CMV Infection in an Urban Area of East Asia: Population-based Study" by Yang et al. is well-written and provides a relatively comprehensive view about Congenital cytomegalovirus prevalence in Taipei, Taiwan. Although the study has limitations already recognized by the authors, this manuscript provide advances in our understanding about the relevance the early identification of cCMV in neonates increasing the quality of life of patients and better follow-up of the public service to these patients telling a nice story. I think it would be suitable for publication in PLoS One after careful revision of English language.

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Attachment

Submitted filename: Response to reviewers_20201128_YTH1129_1212.docx

Decision Letter 1

Kazumichi Fujioka

8 Mar 2021

The prevalence and demographic features of congenital cytomegalovirus infection in an urban area of East Asia: a population-based study

PONE-D-20-23918R1

Dear Dr. Wu,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Kazumichi Fujioka

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: N/A

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: "The Prevalence and Hearing Outcome of Congenital CMV Infection in an Urban Area of East Asia: Population-based Study" by Yang et al. I had suggested the acceptance of the article by PLoS One after a rigorous review of English, I maintain my decision.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Acceptance letter

Kazumichi Fujioka

16 Mar 2021

PONE-D-20-23918R1

The prevalence and demographic features of congenital cytomegalovirus infection in an urban area of East Asia: a population-based study

Dear Dr. Wu:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Kazumichi Fujioka

Academic Editor

PLOS ONE


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