Evidence map›Paper›PMID 20965155›Full record

Trial reportBrain research2011

Greater endogenous estrogen exposure is associated with longer telomeres in postmenopausal women at risk for cognitive decline.

Jue Lin, Candyce H Kroenke, Elissa Epel, Heather A Kenna, Owen M Wolkowitz, Elizabeth Blackburn, Natalie L Rasgon

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Brain research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 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

7 authors at 2 institutions in 1 country.

Jue LinDepartment of Biochemistry and Biophysics, University of California, San Francisco, CA 94118, USA.
Candyce H Kroenke
Elissa Epel
Heather A Kenna
Owen M Wolkowitz
Elizabeth Blackburn
Natalie L Rasgon
University of California, San Francisco · USStanford University · US

Funding

XOLAIR IN SUBJECTS WITH MODERATE TO SEVERE ATOPIC DERMATITIS WITH FOOD ALLERGYM01RR000070 · NCRR · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 1985 to 2008
$32.4M
Estrogen Use in Protection from Cognitive DeclineR01AG022008 · NIA · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 2003 to 2010
$2.5M
Window of Opportunity of Estrogen Therapy for NeuroprotectionR13AG032903 · NIA · STANFORD UNIVERSITY · PI RASGON, NATALIE L · 2009 to 2009
$25k
NCRR NIH HHS M01 RR000070NCRR NIH HHS M01 RR-00070NIA NIH HHS R01 AG022008NIA NIH HHS R01 AG22008NIA NIH HHS R13 AG032903
6 · The paper itself

Abstract

Longer duration of reproductive years of life and thus greater exposure to endogenous estrogen may be associated with a lower risk of age-related diseases in women. The present study examined the relationship between estimated endogenous estrogen exposure and telomere length (TL) and telomerase activity, two biomarkers of cellular aging, in a sample of postmenopausal women at risk for cognitive decline. Telomere length was measured using a quantitative PCR method and telomerase activity by TRAP (Telomere-Repeats Amplification Protocol) assay in peripheral blood mononuclear cells (PBMCs). Study subjects were 53 postmenopausal women (35 with natural and 18 with surgical menopause) receiving hormone therapy (HT) for at least one year or longer. Length of reproductive years of life, computed as the difference between age at menopause and age at menarche, was used as a proxy of duration of exposure to endogenous estrogen. Length of time on HT was the measure used for duration of exogenous estrogen exposure. We found that longer endogenous estrogen exposure was associated with greater TL (standardized β=0.06, Wald χ(2)=3.7, p=0.04) and with lower telomerase activity (standardized β=-0.09, Wald χ(2)=5.0, p=0.03). Length of reproductive years was also inversely associated with the combination of short TL and high telomerase (OR=0.78, 95% CI: 0.63, 0.97, p=0.02). Length of HT use was not associated with TL or telomerase activity in this study. The results suggest that the endogenous estrogens may be associated with deceleration of cellular aging. This is the first study to examine associations between endogenous estrogens, telomere length and telomerase activity.

Indexed as

AgedCognition DisordersEstrogen Replacement TherapyEstrogensFemaleHumansLongitudinal StudiesMiddle AgedPostmenopauseRisk FactorsTelomereEstrogens

Identifiers

PMID20965155
PMCPMC3057451
OpenAlexW1990822552

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.