Evidence map›Paper›PMID 21063759›Full record

ArticleMetabolic brain disease2010

Elevated cerebral glutamate and myo-inositol levels in cognitively normal middle-aged adults with metabolic syndrome.

Andreana P Haley, Mitzi M Gonzales, Takashi Tarumi, Steven C Miles, Katayoon Goudarzi, Hirofumi Tanaka

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolic brain disease, 2010. 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
1.7field-weighted citation impact, top 17% 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, 44 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Andreana P HaleyDepartment of Psychology, The University of Texas at Austin, 1 University Station, A8000, Austin, TX 78712, USA. haley@psy.utexas.edu
Mitzi M Gonzales
Takashi Tarumi
Steven C Miles
Katayoon Goudarzi
Hirofumi Tanaka
The University of Texas at Austin · US

Funding

Variables predictive of self care in well elderlyP30NR005051 · NINR · UNIVERSITY OF TEXAS AUSTIN · PI REW, DONNA LYNN · 1999 to 2008
$3.9M
Resistance Training &Age-Related Arterial StiffeningR01AG020966 · NIA · UNIVERSITY OF WISCONSIN MADISON · PI TANAKA, HIROFUMI · 2003 to 2007
$1.7M
Smoking and exercise on arterial stiffnessF31DA018431 · NIDA · UNIVERSITY OF WISCONSIN MADISON · PI DEVAN, ALLISON ELIZABETH · 2005 to 2007
$145k
NIA NIH HHS AG20966NIDA NIH HHS DA018431NINR NIH HHS P30 NR005051
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a cluster of risk factors associated with significant cardiovascular morbidity and mortality and diminished cognitive function. Given that the cerebral mechanisms mediating the relationship between peripheral metabolic dysfunction and cognitive impairment are unknown, we set out to examine the relationship between diagnosis of metabolic syndrome and cerebral metabolism. Thirteen participants with MetS (aged 48 ± 6 years) and 25 healthy adults (aged 51 ± 6 years) underwent neuropsychological assessment, health screen and proton magnetic resonance spectroscopy ((1)H MRS) examining N-acetyl-aspartate (NAA), myo-inositol (mI), creatine (Cr), choline (Cho), and glutamate (Glu) concentrations in occipitoparietal grey matter. Cerebral metabolite ratios (NAA/Cr, Cho/Cr, mI/Cr, and Glu/Cr) of participants with MetS, defined by the International Diabetes Federation criteria, were compared with controls matched for age, education, cognition, and emotional function. There were no significant differences in global cognitive function, memory, language, and psychomotor performance between the groups. Diagnosis of MetS was associated with significantly higher mI/Cr (F(1,36) = 5.02, p = 0.031) and Glu/Cr ratio (F(1,36) = 4.81, p = 0.035). Even in cognitively normal adults, MetS is related to cerebral metabolic disturbances, a possible indication of early brain vulnerability. Longitudinal studies that begin in mid-life can help validate the use of (1)H MRS markers as indicators of long-term cognitive outcomes.

Indexed as

AdultBrain ChemistryCognition DisordersDisease ProgressionFemaleGlutamic AcidHumansInositolIntelligence TestsLanguageMagnetic Resonance SpectroscopyMaleMemoryMetabolic SyndromeMiddle AgedNeuropsychological TestsGlutamic AcidInositol

Identifiers

PMID21063759
OpenAlexW1984842633

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.