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SHBG, free testosterone, and type 2 diabetes risk in middle-aged African men: a longitudinal study
Biomedical Research Innovation Platform, South African Medical Research Council, Cape Town, South Africa.
Riverland Academy of Clinical Excellence, Riverland Mallee Coorong Local Health Network, South Australia Health, SA, Berri, Australia; South African Medical Research Council, WITS Developmental Pathways for Health Research Unit, Department of Paediatrics, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa; Health through Physical Activity, Lifestyle and Sport Research Centre, FIMS International Collaborating Centre of Sports Medicine, Division of Physiological Sciences, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa.
Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa.
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2024 (English)In: Journal of the Endocrine Society, E-ISSN 2472-1972, Vol. 8, no 8, article id bvae129Article in journal (Refereed) Published
Abstract [en]

Objectives: To investigate longitudinal changes in SHBG and free testosterone (free T) levels among Black middle-aged African men, with and without coexistent HIV, and explore associations with incident dysglycaemia and measures of glucose metabolism.

Design: This longitudinal study enrolled 407 Black South African middle-aged men, comprising primarily 322 men living without HIV (MLWOH) and 85 men living with HIV (MLWH), with normal fasting glucose at enrollment. Follow-up assessments were conducted after 3.1 ± 1.5 years.

Methods: At baseline and follow-up, SHBG, albumin, and total testosterone were measured and free T was calculated. An oral glucose tolerance test at follow-up determined dysglycaemia (impaired fasting glucose, impaired glucose tolerance, type 2 diabetes) and glucose metabolism parameters including insulin sensitivity (Matsuda index), insulin resistance (homeostasis model assessment of insulin resistance), and beta(β)cell function (disposition index). The primary analysis focussed on MLWOH, with a subanalysis on MLWH to explore whether associations in MLWOH differed from MLWH.

Results: The prevalence of dysglycaemia at follow-up was 17% (n = 55) in MLWOH. Higher baseline SHBG was associated with a lower risk of incident dysglycaemia (odds ratio 0.966; 95% confidence interval 0.945-0.987) and positively associated with insulin sensitivity (β = 0.124, P < .001) and β-cell function (β = 0.194, P = .001) at follow-up. Free T did not predict dysglycaemia. In MLWH, dysglycaemia prevalence at follow-up was 12% (n = 10). Neither baseline SHBG nor free T were associated with incident dysglycaemia and glucose metabolism parameters in MLWH.

Conclusion: SHBG levels predict the development of dysglycaemia in middle-aged African men but do not exhibit the same predictive value in MLWH.

Place, publisher, year, edition, pages
Endocrine Society, 2024. Vol. 8, no 8, article id bvae129
Keywords [en]
Africa, dysglycaemia, free testosterone, sex hormone-binding globulin, type 2 diabetes
National Category
Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:umu:diva-228334DOI: 10.1210/jendso/bvae129ISI: 001276871400001PubMedID: 39055720Scopus ID: 2-s2.0-85199780181OAI: oai:DiVA.org:umu-228334DiVA, id: diva2:1887865
Available from: 2024-08-09 Created: 2024-08-09 Last updated: 2025-04-24Bibliographically approved

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Olsson, Tommy

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