Evidence map›Paper›PMID 19155011›Full record

Trial reportAtherosclerosis2009

Changes in remnant and high-density lipoproteins associated with hormone therapy and progression of coronary artery disease in postmenopausal women.

Stefania Lamon-Fava, David M Herrington, David M Reboussin, Michelle Sherman, Katalin Horvath, Ernst J Schaefer, Bela F Asztalos

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Atherosclerosis, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00083824 (Estrogen, HDL, and Coronary Heart Disease in Women), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.3field-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.

NCT00083824 phase2 / phase3completednot on this map

Estrogen, HDL, and Coronary Heart Disease in Women

TypeinterventionalSponsorTufts UniversityRan2004 to 2007Enrolled309ConditionsCardiovascular Diseases, Coronary Disease, Heart Diseases, Coronary ArteriosclerosisArmsEstrogens, Conjugated (USP), Medroxyprogesterone 17-Acetate, Placebo
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 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 3 institutions in 1 country.

Stefania Lamon-FavaLipid Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111, United States. stefania.lamon-fava@tufts.edu
David M Herrington
David M Reboussin
Michelle Sherman
Katalin Horvath
Ernst J Schaefer
Bela F Asztalos
Tufts University · USWake Forest University · USJean Mayer Human Nutrition Research Center on Aging · US

Funding

Estrogen, HDL, and coronary heart disease in womenR01HL070081 · NHLBI · TUFTS UNIVERSITY BOSTON · PI LAMON-FAVA, STEFANIA · 2004 to 2005
$574k
NHLBI NIH HHS R01 HL070081NHLBI NIH HHS R01 HL70081
6 · The paper itself

Abstract

objectiveThis study examined the effect of hormone therapy (HT) on the plasma concentration of remnant lipoprotein cholesterol (RLP-C) and high-density lipoprotein (HDL) subpopulations and the contribution of HT-related changes in these lipoproteins to the progression of coronary heart disease (CHD) in postmenopausal women.

methodsStudy participants were 256 women who completed the Estrogen Replacement and Atherosclerosis (ERA) trial, a placebo-controlled, randomized trial that examined the effects of 3.2 years of conjugated equine estrogen (CEE, 0.625 mg/day) or CEE (0.625 mg/day) plus medroxyprogesterone acetate (MPA, 2.5mg/day) on postmenopausal women with established coronary atherosclerosis. Quantitative coronary angiography and plasma RLP-C and HDL subpopulations were assessed at baseline and at follow-up.

resultsRelative to placebo, both CEE and CEE+MPA caused a significant reduction in plasma RLP-C concentrations and a significant increase in alpha1 and alpha2 HDL subpopulations. However, in the HT-treated subjects, faster progression of coronary atherosclerosis was observed in women who experienced the greatest reductions in RLP-C and in prebeta1 HDL subpopulations.

conclusionsOur data suggest that individual variability in RLP-C and HDL subpopulation response to HT is a predictor of CHD progression. Lipoprotein response to HT may be an indirect marker of susceptibility to other harmful effect of HT in postmenopausal women with established CHD or an indication of formation of dysfunctional lipoproteins.

Indexed as

AgedCholesterolCoronary AngiographyCoronary DiseaseDisease ProgressionEstrogen Replacement TherapyEstrogens, Conjugated (USP)FemaleHormonesHumansLipoproteins, HDLMiddle AgedPlacebosPostmenopauseCholesterolEstrogens, Conjugated (USP)HormonesLipoproteins, HDLPlacebos

Identifiers

PMID19155011
PMCPMC2700198
OpenAlexW2154283203

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.