Evidence map›Paper›PMID 18615541›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2009

Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression.

Christel M Middeldorp, Patrick F Sullivan, Naomi R Wray, Jouke-Jan Hottenga, Eco J C de Geus, Mireille van den Berg, Grant W Montgomery, Will L Coventry, Dixie J Statham, Gavin Andrews and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Genetics Factors in Major Depression Disease.Frontiers in psychiatry · 2018
    Review
  6. Review
  7. Article
  8. Article
  9. An examination of TOR1A variants in recurrent major depression.International journal of molecular epidemiology and genetics · 2012
    Article
  10. Review
  11. Article
  12. Review
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

13 authors at 7 institutions in 3 countries.

Christel M MiddeldorpDepartment of Biological Psychology, VU University, Amsterdam, The Netherlands. cm.middeldorp@psy.vu.nl
Patrick F Sullivan
Naomi R Wray
Jouke-Jan Hottenga
Eco J C de Geus
Mireille van den Berg
Grant W Montgomery
Will L Coventry
Dixie J Statham
Gavin Andrews
P Eline Slagboom
Dorret I Boomsma
Nicholas G Martin
QIMR Berghofer Medical Research Institute · AUAmsterdam UMC Location VUmc · NLLeiden University Medical Center · NLNetherlands Organisation for Health Research and Development · NLSt Vincent's Hospital Sydney · AUUniversity of New England · AUUniversity of North Carolina at Chapel Hill · US

Funding

Genetic Epideniologic Models of Alcohol AbuseR37AA007728 · NIAAA · WASHINGTON UNIVERSITY · PI HEATH, ANDREW C. · 1998 to 2007
$2.2M
PERSISTENCE &CHANGE IN DRINKING HABITS: TWIN STUDYR01AA007535 · NIAAA · WASHINGTON UNIVERSITY · PI HEATH, ANDREW C. · 1989 to 1996
–
NATURAL HISTORY OF ALCOHOL USE &ABUSE--GENETIC MODELSR01AA007728 · NIAAA · WASHINGTON UNIVERSITY · PI HEATH, ANDREW C. · 1988 to 1998
–
GENE MAPPING FOR QUANTITATIVE TRAITSR01HL055976 · NHLBI · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI VOGLER, GEORGE P · 1995 to 1998
–
NHLBI NIH HHS R01 HL055976NHLBI NIH HHS R01 HL55976NIAAA NIH HHS AA07728NIAAA NIH HHS R01 AA007535NIAAA NIH HHS R01 AA007728NIAAA NIH HHS R37 AA007728
6 · The paper itself

Abstract

It is well established that major depressive disorder (MDD) is partly heritable. We present a genome-wide linkage study aiming to find regions on the genome that influence the vulnerability for MDD. Our sample consists of 110 Australian and 23 Dutch pedigrees with two or more siblings affected with MDD (total N = 278). Linkage analysis was carried out in MERLIN. Three regions showed suggestive linkage signals. The highest LOD-score of 2.1 was found on chromosome 17 at 52.6 cM along with LOD scores of 1.9 and 1.7 on chromosome 8 at 2.7 cM and chromosome 2 at 90.6 cM, respectively. The result on chromosome 8 seems most promising as two previous studies also found linkage in this region, once suggestive and once significant. The linkage peak on chromosome 17 harbors the serotonin transporter gene. In the Australian and Dutch sample, the serotonin transporter length polymorphism did not show evidence for association, thus other genes in this region or other polymorphisms in the serotonin transporter gene might be associated with MDD. Further replication is needed to establish the relevance of our linkage finding on chromosome 2.

Indexed as

Chromosomes, Human, Pair 17Chromosomes, Human, Pair 2Chromosomes, Human, Pair 8Genetic LinkageAdultAllelesAustraliaDNAFemaleGene FrequencyGenetic MarkersGenetic Predisposition to DiseaseHumansInterviews as TopicMajor Depressive DisorderMaleDNAGenetic Markers

Identifiers

PMID18615541
PMCPMC2784956
OpenAlexW2145192862

What OpenQuestion holds

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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.