Evidence map›Paper›PMID 22703619›Full record

ArticlePsychiatry research2012

AGTR1 gene variation: association with depression and frontotemporal morphology.

Warren D Taylor, Sophiya Benjamin, Douglas R McQuoid, Martha E Payne, Ranga R Krishnan, James R MacFall, Allison Ashley-Koch

Open access · greenAbstract read
In one paragraph

Article in Psychiatry research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Ang II-mediated effects on BBB integrity in psychiatric and neurological disorders.Progress in neuro-psychopharmacology & biological psychiatry · 2026
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  7. Strategies for dementia prevention: latest evidence and implications.Therapeutic advances in chronic disease · 2017
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  12. LRRC4 haplotypes are associated with pituitary adenoma in a Chinese population.Medical oncology (Northwood, London, England) · 2014
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  13. 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

7 authors at 3 institutions in 2 countries.

Warren D TaylorDepartment of Psychiatry, Duke University Medical Center, Durham, NC 27710, USA. warren.taylor@duke.edu
Sophiya Benjamin
Douglas R McQuoid
Martha E Payne
Ranga R Krishnan
James R MacFall
Allison Ashley-Koch
Duke Medical Center · USCenter for Human Genetics · USDuke University · US

Funding

Recruitment and Assessment Core Patient RecruitmentP50MH060451 · NIMH · DUKE UNIVERSITY · PI MCCARTHY, GREGORY E · 2001 to 2010
$22.3M
Vascular Depression: Longitudinal ChangesR01MH078216 · NIMH · DUKE UNIVERSITY · PI TAYLOR, WARREN D · 2007 to 2010
$1.4M
NIMH NIH HHS P50 MH060451NIMH NIH HHS R01 MH078216
6 · The paper itself

Abstract

The renin-angiotensin system (RAS) is implicated in the response to physiological and psychosocial stressors, but its role in stress-related psychiatric disorders is poorly understood. We examined if variation in AGTR1, the gene coding for the type 1 angiotensin II receptor (AT(1)R), is associated with a diagnosis of depression and differences in white matter hyperintensities and frontotemporal brain volumes. Participants comprised 257 depressed and 116 nondepressed elderly Caucasian subjects who completed clinical assessments and provided blood samples for genotyping. We used a haplotype-tagging single nucleotide polymorphism (htSNP) analysis to test for variation in AGTR1. For measurement of hyperintense lesions, 1.5 Tesla magnetic resonance imaging (MRI) data were available on 33 subjects. For measurements of the hippocampus and dorsolateral prefrontal cortex (dlPFC), 3 Tesla MRI data were available on 70 subjects. Two htSNPs exhibited statistically significant frequency differences between diagnostic cohorts: rs10935724 and rs12721331. Although hyperintense lesion volume did not significantly differ by any htSNP, dlPFC and hippocampus volume differed significantly for several htSNPs. Intriguingly, for those htSNPs differing significantly for both dlPFC and hippocampus volume, the variant associated with smaller dlPFC volume was associated with larger hippocampal volume. This supports the idea that genetic variation in AGTR1 is associated with depression and differences in frontotemporal morphology.

Indexed as

AgedAged, 80 and overFemaleFrontal LobeGene FrequencyGenetic Association StudiesGenotypeHumansImage Processing, Computer-AssistedLogistic ModelsMagnetic Resonance ImagingMajor Depressive DisorderMaleMental Status ScheduleMiddle AgedPolymorphism, Single NucleotideAGTR1 protein, humanReceptor, Angiotensin, Type 1

Identifiers

PMID22703619
PMCPMC3398195
OpenAlexW2063468701

What OpenQuestion holds

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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.