Evidence map›Paper›PMID 38829475›Full record

ReviewReviews in endocrine & metabolic disorders2024

Evidence-based definition of hypoprolactinemia in European men aged 40-86 years: the European male ageing study.

Thang S Han, Leen Antonio, György Bartfai, Terence W O'Neill, Margus Punab, Giulia Rastrelli, Mario Maggi, Jolanta Słowikowska-Hilczer, Jos Tournoy, Dirk Vanderschueren and 6 more

Abstract readReview
In one paragraph

Review in Reviews in endocrine & metabolic disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. The relationship between low prolactin and type 2 diabetes.Reviews in endocrine & metabolic disorders · 2024
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Acquired hypoprolactinemia in men, possible phenotype.Reviews in endocrine & metabolic disorders · 2024
    Review
  8. Article
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

16 authors.

Thang S HanInstitute of Cardiovascular Research, Royal Holloway University of London, Egham, TW20 0EX, UK. thang.han@rhul.ac.uk.ORCID 0000-0003-2570-0938
Leen AntonioDepartment of Clinical and Experimental Medicine, Laboratory of Clinical and Experimental Endocrinology, KU Leuven, Leuven, Belgium.ORCID 0000-0002-1079-2860
György BartfaiDepartment of Obstetrics, Gynaecology and Andrology, Albert Szent-Gyorgy Medical University, Szeged, Hungary.ORCID 0009-0005-1782-0720
Terence W O'NeillCentre for Epidemiology Versus Arthritis, Manchester Biomedical Research Centre, The University of Manchester & NIHR, Manchester University NHS Foundation Trust, Manchester, UK.ORCID 0000-0002-8896-4677
Margus PunabAndrology Clinic, Tartu University Hospital, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0001-9601-6311
Giulia RastrelliAndrology, Women's Endocrinology and Gender Incongruence Unit - Careggi Teaching Hospital, Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.ORCID 0000-0002-6164-4278
Mario MaggiEndocrinology Unit - Careggi Teaching Hospital, Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.ORCID 0000-0003-3267-4221
Jolanta Słowikowska-HilczerDepartment of Andrology and Reproductive Endocrinology, Medical University of Łódź, Łódź, Poland.ORCID 0000-0003-3105-1786
Jos TournoyDepartment of Geriatrics, University Hospitals Leuven, Leuven, Belgium.ORCID 0000-0002-0265-9154
Dirk VanderschuerenDepartment of Clinical and Experimental Medicine, Laboratory of Clinical and Experimental Endocrinology, KU Leuven, Leuven, Belgium.ORCID 0000-0003-1395-0104
Michael E J LeanDepartment of Human Nutrition, University of Glasgow, Glasgow, UK.ORCID 0000-0003-2216-0083
Ilpo T HuhtaniemiInstitute of Reproductive and Developmental, Department of Metabolism, Digestion and Reproduction, Imperial College London, Hammersmith Campus, London, UK.ORCID 0000-0001-9092-7886
Frederick C W WuDivision of Endocrinology, Diabetes & Gastroenterology, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0002-7005-4798
Ana I CastroDepartment of Medicine, CIBER de Fisiopatología Obesidad y Nutricion, Instituto Salud Carlos III, , Santiago de Compostela University, Complejo Hospitalario Universitario de Santiago (IDIS), Santiago de Compostela, CB06/03, Spain.ORCID 0000-0002-6314-4445
Marcos C CarreiraDepartment of Medicine, CIBER de Fisiopatología Obesidad y Nutricion, Instituto Salud Carlos III, , Santiago de Compostela University, Complejo Hospitalario Universitario de Santiago (IDIS), Santiago de Compostela, CB06/03, Spain.ORCID 0000-0001-7309-3568
Felipe F CasanuevaDepartment of Medicine, CIBER de Fisiopatología Obesidad y Nutricion, Instituto Salud Carlos III, , Santiago de Compostela University, Complejo Hospitalario Universitario de Santiago (IDIS), Santiago de Compostela, CB06/03, Spain. felipe.casanueva@usc.es.ORCID 0000-0002-9052-8161

Funding

The Commission of the European Communities Fifth Framework Program "Quality of Life and Management of Living Resources" Grant QLK6-CT-2001-00258
6 · The paper itself

Abstract

Empirical evidence for a low normal or reference interval for serum prolactin (PRL) is lacking for men, while the implications of very low PRL levels for human health have never been studied. A clinical state of "PRL deficiency" has not been defined except in relation to lactation. Using data from the European Male Ageing Study (EMAS), we analyzed the distribution of PRL in 3,369 community-dwelling European men, aged 40-80 years at phase-1 and free from acute illnesses. In total, 2,948 and 2,644 PRL samples were collected during phase-1 and phase-2 (3 to 5.7 years later). All samples were analysed in the same centre with the same assay. After excluding individuals with known pituitary diseases, PRL ≥ 35 ng/ml, and PRL-altering drugs including antipsychotic agents, selective serotonin reuptake inhibitors, or dopamine agonists, 5,086 data points (2,845 in phase-1 and 2,241 in phase-2) were available for analysis. The results showed that PRL declined minimally with age (slope = -0.02) and did not correlate with BMI. The positively skewed PRL distribution was log-transformed to a symmetrical distribution (skewness reduced from 13.3 to 0.015). Using two-sigma empirical rule (2[]SD about the mean), a threshold at 2.5% of the lower end of the distribution was shown to correspond to a PRL value of 2.98ng/ml. With reference to individuals with PRL levels of 5-34.9 ng/ml (event rate = 6.3%), the adjusted risk of developing type 2 diabetes increased progressively in those with PRL levels of 3-4.9 ng/ml: event rate = 9.3%, OR (95% CI) 1.59 (0.93-2.71), and more so with PRL levels of 0.3-2.9 ng/ml: event rate = 22.7%, OR 5.45 (1.78-16.62). There was also an increasing trend in prediabetes and diabetes based on fasting blood glucose levels was observed with lower categories of PRL. However, PRL levels were not associated with cancer, cardiovascular diseases, depressive symptoms or mortality. Our findings suggest that a PRL level below 3 ng/ml (64 mlU/l) significantly identifies European men with a clinically-important outcome (of type 2 diabetes), offering a lower reference-value for research and clinical practice.

Indexed as

AgingProlactinAdultAgedAged, 80 and overEuropeHumansMaleMiddle AgedProlactinHealth outcomesHypoprolactinemiaPituitary functionReference valuesType 2 diabetes

Identifiers

PMID38829475
PMCPMC11624245

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Registered trials

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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.