Cynthia Moore

Dr. Cynthia Moore


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2017 in JAMA Pediatrics
Verified
Journal Article
Open access
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CMCynthia Moore
Cynthia Moore
JSJ. Erin Staples
J. Erin Staples
WDWilliam B. Dobyns
William B. Dobyns
APAndré Pessoa
André Pessoa
CVCamila Ventura
Camila Ventura
SRSonja A. Rasmussen
Sonja A. Rasmussen
Contracted through the bite of an infected mosquito or through sexual or other modes of transmission, Zika virus (ZIKV) infection can be prenatally passed from mother to fetus.1 The virus was first identified in the region of the Americas in early 2015, when local transmission was reported in Brazil.2 Six months later, a notable increase in the number of infants with congenital microcephaly was observed in northeast Brazil.3,4 Clinical, epidemiologic, and laboratory evidence led investigators to conclude that intrauterine ZIKV infection was a cause of microcephaly and serious brain anomalies.5-7 However, as with other newly recognized teratogens, these features likely represent a portion of a broader spectrum.

6 December 2014 in Current Epidemiology Reports
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Journal Article
Closed access
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STSarah C. Tinker
Sarah C. Tinker
SGSuzanne M Gilboa
Suzanne M Gilboa
JRJennita Reefhui
Jennita Reefhui
MJMary M. Jenkins
Mary M. Jenkins
MSMarcy Schaeffer
Marcy Schaeffer
CMCynthia Moore
Cynthia Moore

2 July 2019 in Birth Defects Research
Verified
Journal Article
Open access
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SOSamantha M. Olson
Samantha M. Olson
ADAugustina Delaney
Augustina Delaney
AJAbbey M. Jones
Abbey M. Jones
CCChristopher P. Carr
Christopher P. Carr
RLRebecca F. Liberman
Rebecca F. Liberman
JCJanet D. Cragan
Janet D. Cragan
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27 June 2022 in The Journal of Pediatrics
Verified
Journal Article
Open access
CMCara T. Mai
Cara T. Mai
JEJane Evans
Jane Evans
CAClinton J. Alverson
Clinton J. Alverson
XYXin Yue
Xin Yue
TFTimothy Flood
Timothy Flood
Russell S. KirbyRussell S. Kirby
Russell S. Kirby
To assess whether the severity of cases of spina bifida changed after the institution of mandatory folic acid fortification in the US. Six active population-based birth defects programs provided data on cases of spina bifida for 1992-1996 (prefortification period) and 1999-2016 (postfortification period). The programs contributed varying years of data. Case information included both a medical record verbatim text description of the spina bifida diagnosis and spina bifida codes (International Classification of Diseases, Clinical Modification, or a modified birth defects surveillance coding system). Comparing the prefortification and postfortification periods, aORs for case severity (upper-level lesions [cervical, thoracic] vs lower-level lesions [lumbar, sacral]) and prevalence ratios (PRs) were estimated. A total of 2593 cases of spina bifida (out of 7 816 062 live births) met the inclusion criteria, including 573 cases from the prefortification period and 2020 cases from the postfortification period. Case severity decreased by 70% (aOR, 0.30; 95% CI, 0.26-0.35) between the fortification periods. The decrease was most pronounced for non-Hispanic White mothers. Overall spina bifida prevalence declined by 23% (PR, 0.77; 95% CI, 0.71-0.85), with similar reductions seen across the early, mid, and recent postfortification periods. A statistically significant decrease in upper-level lesions occurred in the postfortification period compared with the prefortification period (PR, 0.28; 95% CI, 0.22-0.34), whereas the prevalence of lower-level lesions remained relatively similar (PR, 0.94; 95% CI, 0.84-1.05). The severity of spina bifida cases decreased after mandatory folic acid fortification in the US. Further examination is warranted to better understand the potential effect of folic acid on spina bifida severity.

5 May 2021 in Birth Defects Research
Verified
Journal Article
Open access
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HDHelen Dolk
Helen Dolk
ALAminkeng Zawuo Leke
Aminkeng Zawuo Leke
PWPhil Whitfield
Phil Whitfield
RMRebecca Moore
Rebecca Moore
KKKaty Karnell
Katy Karnell
DVDiana Valencia
Diana Valencia
Background: Surveillance programs in low‐ and middle‐income countries (LMICs) have difficulty in obtaining accurate information about congenital anomalies.Methods: As part of the ZikaPLAN project, an International Committee developed an app for the description and coding of congenital anomalies that are externally visible at birth, for use in low resource settings. The “basic” version of the app was designed for a basic clinical setting and to overcome language and terminology barriers by providing diagrams and photos, sourced mainly from international Birth Defects Atlases. The “surveillance” version additionally allows recording of limited pseudonymized data relevant to diagnosis, which can be uploaded to a secure server, and downloaded by the surveillance program data center.Results: The app contains 98 (88 major and 10 minor) externally visible anomalies and 12 syndromes (including congenital Zika syndrome), with definitions and International Classification of Disease v10 ‐based code. It also contains newborn examination videos and links to further resources. The user taps a region of the body, then selects among a range of images to choose the congenital anomaly that best resembles what they observe, with guidance regarding similar congenital anomalies. The “basic” version of the app has been reviewed by experts and made available on the Apple and Google Play stores. Since its launch in November 2019, it has been downloaded in 39 countries. The “surveillance” version is currently being field‐tested.Conclusion: The global birth defects app is a mHealth tool that can help in developing congenital anomaly surveillance in low resource settings to support prevention and care.

Verified
Journal Article
Open access
PDF file
MMMarcela Mercado-Reyes
Marcela Mercado-Reyes
SGSuzanne M Gilboa
Suzanne M Gilboa
DVDiana Valencia
Diana Valencia
MDMarcela Daza
Marcela Daza
VTVan Tong
Van Tong
MMMartha Lucia Ospina Martinez
Martha Lucia Ospina Martinez
Project Vigilancia de Embarazadas con Zika (VEZ), an intensified surveillance of pregnant women with symptoms of the Zika virus disease (ZVD) in Colombia, aimed to evaluate the relationship between symptoms of ZVD during pregnancy and adverse pregnancy, birth, and infant outcomes and early childhood neurodevelopmental outcomes. During May–November 2016, pregnant women in three Colombian cities who were reported with symptoms of ZVD to the national surveillance system, or with symptoms of ZVD visiting participating clinics, were enrolled in Project VEZ. Data from maternal and pediatric (up to two years of age) medical records were abstracted. Available maternal specimens were tested for the presence of the Zika virus ribonucleic acid and/or anti-Zika virus immunoglobulin antibodies. Of 1213 enrolled pregnant women with symptoms of ZVD, 1180 had a known pregnancy outcome. Results of the Zika virus laboratory testing were available for 569 (48.2%) pregnancies with a known pregnancy outcome though testing timing varied and was often distal to the timing of symptoms; 254 (21.5% of the whole cohort; 44.6% of those with testing results) were confirmed or presumptive positive for the Zika virus infection. Of pregnancies with a known outcome, 50 (4.2%) fetuses/infants had Zika-associated brain or eye defects, which included microcephaly at birth. Early childhood adverse neurodevelopmental outcomes were more common among those with Zika-associated birth defects than among those without and more common among those with laboratory evidence of a Zika virus infection compared with the full cohort. The proportion of fetuses/infants with any Zika-associated brain or eye defect was consistent with the proportion seen in other studies. Enhancements to Colombia’s existing national surveillance enabled the assessment of adverse outcomes associated with ZVD in pregnancy.