Evidence map›Paper›PMID 35474467›Full record

ArticleClinical endocrinology2023

Sex difference in patients with controlled acromegaly-A multicentre survey.

Jakob Dal, Christian Rosendal, Jesper Karmisholt, Ulla Feldt-Rasmussen, Marianne S Andersen, Marianne Klose, Claus Feltoft, Ansgar Heck, Eigil H Nielsen, Jens O L Jørgensen

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Clinical endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. The acromegaly patient experience: burden of treatment and quality of life.The Journal of clinical endocrinology and metabolism · 2026
    Review
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  10. Review
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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

10 authors at 7 institutions in 2 countries.

Jakob DalDepartment of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.ORCID 0000-0002-0610-7867
Christian RosendalDepartment of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.
Jesper KarmisholtDepartment of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.ORCID 0000-0001-6026-5834
Ulla Feldt-RasmussenDepartment of Endocrinology and Metabolism, National University Hospital Rigshospitalet, Copenhagen, Denmark.
Marianne S AndersenDepartment of Endocrinology, Odense University Hospital, Odense, Denmark.
Marianne KloseDepartment of Endocrinology and Metabolism, National University Hospital Rigshospitalet, Copenhagen, Denmark.
Claus FeltoftDepartment of Endocrinology, Herlev University Hospital, Herlev, Denmark.
Ansgar HeckSection of Specialized Endocrinology, Oslo University Hospital and Faculty of Medicine, University of Oslo, Oslo, Norway.
Eigil H NielsenDepartment of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.
Jens O L JørgensenDepartment of Endocrinology, Aarhus University Hospital, Aarhus C, Denmark.
Aalborg University Hospital · DKAarhus University Hospital · DKHerlev Hospital · DKOdense University Hospital · DKOslo University Hospital · NORigshospitalet · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveActive acromegaly is subject to sex differences in growth hormone (GH) and Insulin like growth factor 1 (IGF-I) patterns as well as clinical features but whether this also pertains to controlled disease is unclear.

designIn a cross-sectional, multi-centre study, 84 patients with acromegaly (F = 43, M = 41), who were considered controlled after surgery alone (n = 23) or during continued somatostatin receptor ligand (SRL) treatment (n = 61), were examined.

methodsSerum concentrations of GH, insulin, glucose and free fatty acid (FFA) were measured during an oral glucose tolerance test (OGTT) together with baseline serum IGF-I and completion of two HR-Qol questionnaires (acromegaly quality of life questionnaire [AcroQol] and Patient-assessed Acromegaly Symptom Questionnaire [PASQ]).

resultsThe mean age at the time of the study was 57 (±1.1) years and the majority of females (were postmenopausal. Females had significantly higher fasting GH but comparable IGF-I standard deviation scores (SDS). Using fasting GH < 1.0 µg/L as cut off, disease control was less prevalent in females (F: 56% vs. M: 83%, p = .007) whereas a comparable figure was observed using IGF-I SDS < 2 (F:79% vs. M:76%, p = .71). Compared with males, female patients showed impaired AcroQol physical score (p = .05), higher fasting FFA (p = .03) and insulin concentrations during the OGTT (p = .04).

conclusionIn patients with acromegaly considered controlled, postmenopausal females exhibited higher GH levels than males despite comparable IGF-I levels, which also translated into impaired metabolic health and well-being. Our findings point to the relevance of including GH measurements in the assessment of disease control and suggest that disease-specific sex differences prevail after treatment.

Indexed as

Insulin-Like Growth Factor ISex CharacteristicsCross-Sectional StudiesFemaleHumansInsulinMaleQuality of LifeInsulinInsulin-Like Growth Factor IacromegalyageFFAGHIGF-Iinsulinpituitary adenomaquality of lifesex

Identifiers

PMID35474467
PMCPMC10083986
OpenAlexW4224943709

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.