Evidence map›Paper›PMID 19830691›Full record

ArticleInternational journal of cancer2010

The association between birth order, sibship size and glioma development in adulthood.

E Amirian, Michael E Scheurer, Melissa L Bondy

Abstract read
In one paragraph

Article in International journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Observational
  2. Birth Characteristics and Risk of Early-Onset Synovial Sarcoma.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Early life exposures and the risk of adult glioma.European journal of epidemiology · 2013
    Article
  8. 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

3 authors at 2 institutions in 1 country.

E AmirianDepartment of Epidemiology, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Michael E Scheurer
Melissa L Bondy
The University of Texas MD Anderson Cancer Center · USChildren's Cancer Center · US

Funding

CANCER PREVENTION EDUCAT--STUDENT RESEARCH EXPERIENCESR25CA056452 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Shine Chang · 1992 to 2026
$6.9M
MOLECULAR EPIDEMIOLOGY OF GLIOMASR01CA070917 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI BONDY, MELISSA L · 1996 to 2004
$3.0M
Infection and Inflammation in Adult GliomasK07CA131505 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SCHEURER, MICHAEL E. · 2008 to 2012
$784k
NCI NIH HHS K07 CA131505NCI NIH HHS K07CA131505NCI NIH HHS R01 CA070917NCI NIH HHS R01CA070917NCI NIH HHS R25 CA056452NCI NIH HHS R25CA056452
6 · The paper itself

Abstract

The etiology of brain tumors is still largely unknown. Previous research indicates that infectious agents and immunological characteristics may influence adult glioma risk. The purpose of our study was to evaluate the effects of birth order and sibship size (total number of siblings), as indicators of the timing and frequency of early life infections, on adult glioma risk using a population of 489 cases and 540 cancer-free controls from the Harris County Brain Tumor Study. Odds ratios for birth order and sibship size were calculated separately from multivariable logistic regression models, adjusting for sex, family history of cancer, education, and age. Each one-unit increase in birth order confers a 13% decreased risk of glioma development in adulthood (OR = 0.87, 95% CI = 0.79-0.97). However, sibship size was not significantly associated with adult glioma status (OR = 0.97, 95% CI = 0.91-1.04). Our study indicates that individuals who were more likely to develop common childhood infections at an earlier age (those with a higher birth order) may be more protected against developing glioma in adulthood. More biological and epidemiological research is warranted to clarify the exact mechanisms through which the timing of common childhood infections and the course of early life immune development affect gliomagenesis.

Indexed as

Birth OrderSiblingsAdultBrain NeoplasmsChildEducational StatusFamily CharacteristicsFemaleGliomaHumansMaleMedical History TakingMiddle AgedMultivariate AnalysisOdds RatioRegression Analysis

Identifiers

PMID19830691
PMCPMC2847667
OpenAlexW2149315513

What OpenQuestion holds

Textmetadata
LicenceTDM
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.