Evidence map›Paper›PMID 37522858›Full record

ArticleEndocrine connections2023

Effects of aromatase inhibitor therapy on adiposity and cardiometabolic health in postmenopausal women: a controlled cohort extension study.

Yee-Ming M Cheung, Rudolf Hoermann, Karen Van, Damian Wu, Jenny Healy, Bella Halim, Manjri Raval, Maria McGill, Ali Al-Fiadh, Michael Chao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Endocrine connections, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 58% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

14 authors at 4 institutions in 2 countries.

Yee-Ming M CheungDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.ORCID 0000-0003-3875-5698
Rudolf HoermannDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Karen VanDepartment of Endocrinology, Austin Health, Melbourne, Australia.
Damian WuDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Jenny HealyDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Bella HalimDepartment of Endocrinology, Austin Health, Melbourne, Australia.
Manjri RavalDepartment of Endocrinology, Austin Health, Melbourne, Australia.
Maria McGillDepartment of Radiology, Austin Health, Melbourne, Australia.
Ali Al-FiadhDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Michael ChaoOlivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne, Australia.
Shane WhiteOlivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne, Australia.
Belinda YeoOlivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne, Australia.
Jeffrey D ZajacDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Mathis GrossmannDepartment of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
The University of Melbourne · AUAustin Health · AUOlivia Newton-John Cancer Wellness & Research Centre · AUNorthwell Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We previously demonstrated that 12 months of aromatase inhibitor (AI) treatment was not associated with a difference in body composition or other markers of cardiometabolic health when compared to controls. Here we report on the pre-planned extension of the study. The pre-specified primary hypothesis was that AI therapy for 24 months would lead to increased visceral adipose tissue (VAT) area when compared to controls. Methods: We completed a 12-month extension to our prospective 12-month cohort study of 52 women commencing AI treatment (median age 64.5 years) and 52 women with breast pathology not requiring endocrine therapy (63.5 years). Our primary outcome of interest was VAT area. Secondary and exploratory outcomes included other measures of body composition, hepatic steatosis, measures of atherosclerosis and vascular reactivity. Using mixed models and the addition of a fourth time point, we increased the number of study observations by 79 and were able to rigorously determine the treatment effect. Results: Among study completers (AI = 39, controls = 40), VAT area was comparable between groups over 24 months, the mean-adjusted difference was -1.54 cm2 (95% CI: -14.9; 11.9, P = 0.79). Both groups demonstrated parallel and continuous increases in VAT area over the observation period that did not diverge or change between groups. No statistically significant difference in our secondary and exploratory outcomes was observed between groups. Conclusions: While these findings provide reassurance that short-to-medium-term exposure to AI therapy is not associated with metabolically adverse changes when compared to controls, risk evolution should be less focussed on the AI-associated effect and more on the general development of cardiovascular risk over time.

Indexed as

aromatase inhibitorbreast cancercardiometabolic riskvisceral adipose tissuevisceral fat

Identifiers

PMID37522858
PMCPMC10503251
OpenAlexW4385406929

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.