Evidence map›Paper›PMID 17194198›Full record

SynthesisPLoS medicine2006

Angiotensin-converting enzyme I/D polymorphism and preeclampsia risk: evidence of small-study bias.

Norma C Serrano, Luis A Díaz, Maria C Páez, Clara M Mesa, Rodrigo Cifuentes, Alvaro Monterrosa, Adriana González, Liam Smeeth, Aroon D Hingorani, Juan P Casas

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS medicine, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 6 pooled it
2.7field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 6 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Three polymorphisms of renin-angiotensin system and preeclampsia risk.Journal of assisted reproduction and genetics · 2020
    Pooled it
  2. Association Between Gene Polymorphisms on Chromosome 1 and Susceptibility to Pre-Eclampsia: An Updated Meta-Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Pooled it
  3. Pooled it
  4. GSTP1 Ala114Val polymorphism and colorectal cancer risk: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
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  18. Does angiotensin-converting enzyme polymorphism have association with symptomatic benign prostatic hyperplasia?Indian journal of urology : IJU : journal of the Urological Society of India · 2010
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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

10 authors at 7 institutions in 3 countries.

Norma C SerranoUniversidad Autónoma de Bucaramanga, Bucaramanga, Colombia. nserrano@unab.edu.co
Luis A Díaz
Maria C Páez
Clara M Mesa
Rodrigo Cifuentes
Alvaro Monterrosa
Adriana González
Liam Smeeth
Aroon D Hingorani
Juan P Casas
University of London · GBBritish Heart Foundation · GBIndustrial University of Santander · COInstituto de Investigaciones en Ciencias de la Salud · ARUniversidad Autónoma de Bucaramanga · COUniversidad del Valle · COUniversity of Cartagena · CO

Funding

Medical Research Council G108/492
6 · The paper itself

Abstract

backgroundInappropriate activation of the renin-angiotensin system may play a part in the development of preeclampsia. An insertion/deletion polymorphism within the angiotensin-I converting enzyme gene (ACE-I/D) has shown to be reliably associated with differences in angiotensin-converting enzyme (ACE) activity. However, previous studies of the ACE-I/D variant and preeclampsia have been individually underpowered to detect plausible genotypic risks. METHODS AND

findingsA prospective case-control study was conducted in 1,711 unrelated young pregnant women (665 preeclamptic and 1,046 healthy pregnant controls) recruited from five Colombian cities. Maternal blood was obtained to genotype for the ACE-I/D polymorphism. Crude and adjusted odds ratio (OR) and 95% confidence interval (CI) using logistic regression models were obtained to evaluate the strength of the association between ACE-I/D variant and preeclampsia risk. A meta-analysis was then undertaken of all published studies to February 2006 evaluating the ACE-I/D variant in preeclampsia. An additive model (per-D-allele) revealed a null association between the ACE-I/D variant and preeclampsia risk (crude OR = 0.95 [95% CI, 0.81-1.10]) in the new case-control study. Similar results were obtained after adjusting for confounders (adjusted per-allele OR = 0.90 [95% CI, 0.77-1.06]) and using other genetic models of inheritance. A meta-analysis (2,596 cases and 3,828 controls from 22 studies) showed a per-allele OR of 1.26 (95% CI, 1.07-1.49). An analysis stratified by study size showed an attenuated OR toward the null as study size increased.

conclusionsIt is highly likely that the observed small nominal increase in risk of preeclampsia associated with the ACE D-allele is due to small-study bias, similar to that observed in cardiovascular disease. Reliable assessment of the origins of preeclampsia using a genetic approach may require the establishment of a collaborating consortium to generate a dataset of adequate size.

Indexed as

BiasCase-Control StudiesColombiaFemaleGenotypeHumansLogistic ModelsMolecular Sequence DataMultivariate AnalysisPeptidyl-Dipeptidase APolymorphism, GeneticPre-EclampsiaPregnancyProspective StudiesRenin-Angiotensin SystemPeptidyl-Dipeptidase A

Identifiers

PMID17194198
PMCPMC1716194
OpenAlexW1963733189

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.