Evidence map›Paper›PMID 20488256›Full record

ArticleBiochimica et biophysica acta2010

Allopregnanolone levels are reduced in temporal cortex in patients with Alzheimer's disease compared to cognitively intact control subjects.

Jennifer C Naylor, Jason D Kilts, Christine M Hulette, David C Steffens, Dan G Blazer, John F Ervin, Jennifer L Strauss, Trina B Allen, Mark W Massing, Victoria M Payne and 3 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Biochimica et biophysica acta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 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

13 authors at 4 institutions in 1 country.

Jennifer C NaylorVA Mid-Atlantic Mental Illness, Research and Clinical Center (MIRECC), Durham, NC, USA.
Jason D Kilts
Christine M Hulette
David C Steffens
Dan G Blazer
John F Ervin
Jennifer L Strauss
Trina B Allen
Mark W Massing
Victoria M Payne
Nagy A Youssef
Lawrence J Shampine
Christine E Marx
Duke University Hospital · USDuke Medical Center · USDurham VA Health Care System · USDurham VA Medical Center · US

Funding

TASTE AND SMELL MEASUREMENTS OF PATIENTS AT RISK FOR ALZHEIMER'S DISEASEP50AG005128 · NIA · DUKE UNIVERSITY · PI WELSH-BOHMER, KATHLEEN ANNE · 1985 to 2005
$11.2M
NEUROPATHOLOGY COREP30AG028377 · NIA · DUKE UNIVERSITY · PI WELSH-BOHMER, KATHLEEN ANNE · 2006 to 2011
$9.6M
Neurosteroids and SchizophreniaK23MH065080 · NIMH · DUKE UNIVERSITY · PI MARX, CHRISTINE E · 2001 to 2005
$856k
NIA NIH HHS P30 AG028377NIA NIH HHS P50 AG005128NIA NIH HHS P50 AG05128NIMH NIH HHS K23 MH065080NIMH NIH HHS K23 MH 65080
6 · The paper itself

Abstract

The neurosteroid allopregnanolone has pronounced neuroprotective actions, increases myelination, and enhances neurogenesis. Evidence suggests that allopregnanolone dysregulation may play a role in the pathophysiology of Alzheimer's disease (AD) and other neurodegenerative disorders. Our prior data demonstrate that allopregnanolone is reduced in prefrontal cortex in male patients with AD compared to male cognitively intact control subjects, and inversely correlated with neuropathological disease stage (Braak and Braak). We therefore determined if allopregnanolone levels are also reduced in AD patients compared to control subjects in temporal cortex, utilizing a larger set of samples from both male and female patients. In addition, we investigated if neurosteroids are altered in subjects who are APOE4 allele carriers. Allopregnanolone, dehydroepiandrosterone (DHEA), and pregnenolone levels were determined in temporal cortex postmortem samples by gas chromatography/mass spectrometry, preceded by high performance liquid chromatography (40 subjects with AD/41 cognitively intact control subjects). Allopregnanolone levels are reduced in temporal cortex in patients with AD (median 2.68 ng/g, n=40) compared to control subjects (median 5.64 ng/g, n=41), Mann-Whitney p=0.0002, and inversely correlated with Braak and Braak neuropathological disease stage (Spearman r=-0.38, p=0.0004). DHEA and pregnenolone are increased in patients with AD compared to control subjects. Patients carrying an APOE4 allele demonstrate reduced allopregnanolone levels in temporal cortex (Mann-Whitney p=0.04). In summary, our findings indicate that neurosteroids are altered in temporal cortex in patients with AD and related to neuropathological disease stage. In addition, the APOE4 allele is associated with reduced allopregnanolone levels. Neurosteroids may be relevant to the neurobiology and therapeutics of AD.

Indexed as

AdultAgedAged, 80 and overAllelesAlzheimer DiseaseApolipoprotein E4Case-Control StudiesCerebral CortexChromatography, High Pressure LiquidCognitionFemaleGas Chromatography-Mass SpectrometryHumansMaleMiddle AgedModels, BiologicalApolipoprotein E4Pregnanolone

Identifiers

PMID20488256
PMCPMC2907131
OpenAlexW2042429529

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.