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Effects of testosterone and sex hormone binding globulin on lung function in males and females: a multivariable Mendelian Randomisation study.
van der Plaat, Diana A; Lenoir, Alexandra; Dharmage, Shyamali; Potts, James; Gómez Real, Francisco; Shaheen, Seif O; Jarvis, Debbie; Minelli, Cosetta; Leynaert, Bénédicte.
Affiliation
  • van der Plaat DA; National Heart and Lung Institute (NHLI), Imperial College London, London, UK d.van-der-plaat@imperial.ac.uk.
  • Lenoir A; Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Dharmage S; Gesundheitsamt Fürstenfeldbruck, Fürstenfeldbruck, Switzerland.
  • Potts J; Allergy and Lung Health Unit, The University of Melbourne School of Population and Global Health, Melbourne, Victoria, Australia.
  • Gómez Real F; National Heart and Lung Institute (NHLI), Imperial College London, London, UK.
  • Shaheen SO; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Jarvis D; Department of Gynecology and Obstetrics, Haukeland University Hospital, Bergen, Norway.
  • Minelli C; Wolfson Institute of Population Health, Queen Mary University of London, Barts and The London School of Medicine and Dentistry, London, London, UK.
  • Leynaert B; National Heart and Lung Institute (NHLI), Imperial College London, London, UK.
Thorax ; 79(6): 564-572, 2024 May 20.
Article in En | MEDLINE | ID: mdl-38418196
ABSTRACT

BACKGROUND:

Observational studies suggest that total testosterone (TT) and sex hormone-binding globulin (SHBG) may have beneficial effects on lung function, but these findings might be spurious due to confounding and reverse causation. We addressed these limitations by using multivariable Mendelian randomisation (MVMR) to investigate the independent causal effects of TT and SHBG on lung function.

METHODS:

We first identified genetic instruments by performing genome-wide association analyses of TT and SHBG in the large UK Biobank, separately in males and females. We then assessed the independent effects of TT and SHBG on forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC) and FEV1/FVC using one-sample MVMR. We addressed pleiotropy, which could bias MVMR, using several methods that account for it. We performed subgroup MVMR analyses by obesity, physical activity and menopausal status, and assessed associations between TT and SHBG with lung function decline. Finally, we compared the MVMR results with those of observational analyses in the UK Biobank.

FINDINGS:

In the MVMR analyses, there was evidence of pleiotropy, but results were consistent when accounting for it. We found a strong beneficial effect of TT on FVC and FEV1 in both males and females, but a moderate detrimental effect of SHBG on FEV1 and FEV1/FVC in males only. Subgroup analyses suggested stronger effects of TT among obese and older males. The observational analyses, in line with previous studies, agreed with MRMV for TT, but not for SHBG.

INTERPRETATION:

These findings suggest that testosterone improves lung function in males and females, while SHBG has an opposite independent effect in males.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Testosterone / Sex Hormone-Binding Globulin / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Thorax Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Testosterone / Sex Hormone-Binding Globulin / Genome-Wide Association Study / Mendelian Randomization Analysis Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Thorax Year: 2024 Document type: Article Affiliation country:
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