Evidence map›Paper›PMID 22371332›Full record

ArticleBirth defects research. Part A, Clinical and molecular teratology2012

Is maternal parity an independent risk factor for birth defects?

Hao T Duong, Adrienne T Hoyt, Suzan L Carmichael, Suzanne M Gilboa, Mark A Canfield, Amy Case, Melanie L McNeese, Dorothy Kim Waller, National Birth Defects Prevention Study

Abstract read
In one paragraph

Article in Birth defects research. Part A, Clinical and molecular teratology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
8.5field-weighted citation impact, top 2% of its field
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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Risk factors and demographics for microtia in South America: a case-control analysis.Birth defects research. Part A, Clinical and molecular teratology · 2013
    Trial
  4. Article
  5. Maternal Risk Factors for Omphalocele.Fetal diagnosis and therapy · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Epidemiology of Birth Defects in Eastern China and the Associated Risk Factors.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

9 authors at 4 institutions in 1 country.

Hao T DuongThe University of Texas, Houston Health Science Center, School of Public Health, USA.
Adrienne T Hoyt
Suzan L Carmichael
Suzanne M Gilboa
Mark A Canfield
Amy Case
Melanie L McNeese
Dorothy Kim Waller
National Birth Defects Prevention Study
Texas Department of State Health Services · USThe University of Texas Health Science Center at Houston · USNational Center on Birth Defects and Developmental Disabilities · USStanford University · US

Funding

Texas Center for Birth Defects Research and PreventionU01DD000494 · DD · TEXAS STATE DEPT OF HEALTH SERVICES · PI CANFIELD, MARK A · 2009 to 2013
$3.9M
Intramural CDC HHS CC999999NCBDD CDC HHS 5U01DD000494NCBDD CDC HHS U01 DD000494
6 · The paper itself

Abstract

backgroundAlthough associations between maternal parity and birth defects have been observed previously, few studies have focused on the possibility that parity is an independent risk factor for birth defects. We investigated the relation between levels of parity and a range of birth defects, adjusting each defect group for the same covariates.

methodsWe included infants who had an estimated delivery date between 1997 and 2007 and participated in the National Birth Defects Prevention Study, a multisite case-control study. Cases included infants or fetuses belonging to 38 phenotypes of birth defects (n = 17,908), and controls included infants who were unaffected by a major birth defect (n = 7173). Odds ratios (ORs) were adjusted for 12 covariates using logistic regression.

resultsCompared with primiparous mothers, nulliparous mothers were more likely to have infants with amniotic band sequence, hydrocephaly, esophageal atresia, hypospadias, limb reduction deficiencies, diaphragmatic hernia, omphalocele, gastroschisis, tetralogy of Fallot, and septal cardiac defects, with significant ORs (1.2 to 2.3). Compared with primiparous mothers, multiparous mothers had a significantly increased risk of omphalocele, with an OR of 1.5, but had significantly decreased risk of hypospadias and limb reduction deficiencies, with ORs of 0.77 and 0.77.

conclusionsNulliparity was associated with an increased risk of specific phenotypes of birth defects. Most of the phenotypes associated with nulliparity in this study were consistent with those identified by previous studies. Research into biologic or environmental factors that are associated with nulliparity may be helpful in explaining some or all of these associations.

Indexed as

ParityAdultCase-Control StudiesCongenital AbnormalitiesFemaleHeart Defects, CongenitalHernia, UmbilicalHumansOdds RatioPhenotypePregnancyPregnancy ComplicationsRisk FactorsYoung Adult

Identifiers

PMID22371332
PMCPMC4476024
OpenAlexW2116033384

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.