Evidence map›Paper›PMID 35277952›Full record

ArticleBirth defects research2023

Patterns of multiple congenital anomalies in the National Birth Defect Prevention Study: Challenges and insights.

Meredith M Howley, Eva Williford, A J Agopian, Angela E Lin, Lorenzo D Botto, Christopher M Cunniff, Paul A Romitti, Eirini Nestoridi, Marilyn L Browne, National Birth Defects Prevention Study

Abstract read
In one paragraph

Article in Birth defects research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Systematic method for classifying multiple congenital anomaly cases in electronic health records.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Patterns of co-occurring birth defects in children with anotia and microtia.American journal of medical genetics. Part A · 2023
    Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Meredith M HowleyBirth Defects Registry, New York State Department of Health, Albany, New York, USA.ORCID https://orcid.org/0000-0002-8420-5040
Eva WillifordBirth Defects Registry, New York State Department of Health, Albany, New York, USA.
A J AgopianDepartment of Epidemiology, Human Genetics, and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-5874-4155
Angela E LinMedical Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, Massachusetts, USA.
Lorenzo D BottoDivision of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
Christopher M CunniffDivision of Medical Genetics, Department of Pediatrics, Weill Cornell Medical College, New York, New York, USA.
Paul A RomittiDepartment of Epidemiology, University of Iowa, Iowa City, Iowa, USA.ORCID https://orcid.org/0000-0001-5393-9984
Eirini NestoridiCenter for Birth Defects Research and Prevention, Massachusetts Department of Public Health, Boston, Massachusetts, USA.
Marilyn L BrowneBirth Defects Registry, New York State Department of Health, Albany, New York, USA.
National Birth Defects Prevention Study

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
BD-STEPS II (Birth Defects Study To Evaluate Pregnancy exposures) - Core (Component A) & Steps Stillbirth (Component B)U01DD001224 · DD · MASSACHUSETTS STATE DEPT OF PUB HEALTH · PI MITCHELL, ALLEN A, YAZDY, MAHSA M · 2018 to 2022
$6.5M
New York Center for Birth Defects Research and PreventionU01DD000487 · DD · NYSDOH/HEALTH RESEARCH, INC. · PI BROWNE, MARILYN L. · 2009 to 2013
$3.8M
New York State BD-STEPSU01DD001032 · DD · CENTER OF ENVIRONMENTAL HEALTH · PI BROWNE, MARILYN L. · 2013 to 2017
$3.5M
A multidisciplinary approach for identifying and characterizing novel congenital malformation syndromesR01HD093660 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI AGOPIAN, A.J., LUPO, PHILIP · 2018 to 2022
$2.0M
CDC HHS FOA #DD09-001CDC HHS FOA #DD13-003CDC HHS NOFO #DD18-001CDC HHS PA #02081CDC HHS PA #96043EPA EP-D-18-001HSRD VA CDP 13-003NCBDD CDC HHS U01 DD000487NCBDD CDC HHS U01 DD001032NCBDD CDC HHS U01 DD001224NCBDD CDC HHS U01 DD001227NICHD NIH HHS R01 HD093660NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

backgroundAbout 20%-30% of children with birth defects have multiple major birth defects in more than one organ system, often referred to as multiple congenital anomalies (MCAs). Evaluating the patterns of MCAs can provide clues to the underlying causes, pathogenic mechanisms, and developmental pathways. We sought to explore selected patterns of MCAs within the National Birth Defects Prevention Study (NBDPS), a population-based, case-control study that excluded cases attributed to known chromosomal or single-gene abnormalities.

methodsWe defined MCAs as having two or more NBDPS-eligible birth defects and calculated the adjusted observed-to-expected ratio for all observed MCA patterns using co-occurring defect analysis.

resultsOf the 50,186 case infants eligible for NBDPS, 2,734 (3.7%) had at least two eligible birth defects. We observed 209 distinct 2-way combinations of birth defects, 297 distinct 3-way combinations, 179 distinct 4-way combinations, and 69 distinct 5-way combinations. Sacral agenesis had the largest proportion of cases with MCAs (70%), whereas gastroschisis had the lowest (3%). Among the cases with MCAs, 63% had a heart defect, 23% had an oral cleft, and 21% had anorectal atresia/stenosis. Of the patterns with adjusted observed-to-expected ratios in the top 20%, most were consistent with the known associations or syndromes, including VATER/VACTERL association and CHARGE syndrome.

conclusionsMost but not all patterns that had the highest adjusted observed-to-expected ratios were instances of known syndromes or associations. These findings highlight the importance of considering birth defect combinations that suggest syndromic patterns in the absence of a formal syndromic diagnosis. New approaches for screening for sequences and associations, and VATER/VACTERL in particular, in surveillance systems with limited resources for manual review may be valuable for improving surveillance system quality. The observed MCA patterns within NBDPS may help focus future genetic studies by generating case groups of higher yield.

Indexed as

Abnormalities, MultipleGastroschisisHeart Defects, CongenitalNervous System MalformationsCase-Control StudiesChildHumansInfantco-occurrencemultiple birth defectsmultiple congenital anomaliesobserved-to-expected ratio

Identifiers

PMID35277952
PMCPMC9464263

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.