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Biomedical subjects

Hugh Montgomery

Publications and source records attributed to Hugh Montgomery.

4 recordsLinked to original sources

Transdermal 17β-Estradiol for the Treatment of COVID-19: Protocol of an Early Terminated Phase 2 Randomized Controlled Trial.

BACKGROUND: Early epidemiological studies suggested that pre- and postmenopausal women receiving estrogen therapy were less likely to develop severe disease or die from COVID-19 infection. Potential mechanisms include estrogen-mediated immunomodulation and 17β-estradiol-induced downregulation of angiotensin-converting enzyme type 2 (ACE2), the cellular receptor for SARS-CoV-2. OBJECTIVE: This study aimed to evaluate the feasibility, safety, and preliminary efficacy of transdermal 17β-estradiol as an adjunctive treatment for COVID-19 in men and postmenopausal women. METHODS: We designed and conducted a randomized controlled trial comparing 17β-estradiol transdermal gel plus standard care with standard care alone in adults with confirmed COVID-19. Initial ethics and funding approvals were obtained in March 2021. Owing to changes in the epidemiology of COVID-19 in Qatar and revisions to national quarantine policies, protocol amendments were required before recruitment commenced in February 2022. The treatment duration was reduced from 10 to 7 days due to changes in national quarantine guidelines. Recruitment and follow-up were conducted between February 2022 and June 2022. RESULTS: Recruitment was substantially lower than anticipated because widespread COVID-19 vaccination, declining disease severity, and revised national quarantine policies markedly reduced the number of eligible hospitalized patients. Consequently, the planned sample size was not achieved, and the study was terminated in June 2022. A total of 29 men with mild COVID-19 were enrolled, with 44.8% (n=13) randomized to standard care and 55.2% (n=16) to transdermal 17β-estradiol plus standard care. The intervention was well tolerated, with no adverse safety signals or thromboembolic events reported. CONCLUSIONS: Although the study was underpowered to assess efficacy because recruitment targets were not achieved, it showed that transdermal 17β-estradiol was well tolerated, with no major safety concerns among enrolled participants. The experience also provided important operational lessons for conducting clinical trials during rapidly evolving pandemics. Adequately powered studies are required to determine whether transdermal estrogen has therapeutic potential against COVID-19, other ACE2-mediated coronavirus infections, or potentially other severe viral illnesses.

Humans↗

Analysis of gene-environment interactions by "stressing-the-genotype" studies: the angiotensin converting enzyme and exercise-induced left ventricular hypertrophy as an example.

The human angiotensin converting enzyme (ACE) gene contains a length polymorphism consisting of the presence (insertion, I) or absence (deletion, D) of a 287 base pair "Alu" repeat sequence in intron 16, with the D allele being associated with higher ACE levels than the I allele in plasma and in tissues. We have carried out several studies to examine the relationship between this polymorphism and cardiovascular health, and have examined the hypothesis that if renin-angiotensin systems regulate left ventricular (LV) growth, individuals of DD genotype might show a greater hypertrophic response than those of II genotype. A strategy was used involving screening over 1200 male military recruits to select only subjects homozygous for the I or D allele for the expensive and time-consuming but extremely accurate method of LV mass determination by magnetic resonance imaging. LV dimensions and mass were compared at the start and end of a 10-week physical training period. LV mass increased with training by 8.4 g overall (p < 0.0001), but with DD men showing roughly 3 fold greater growth than II men (p < 0.001). When indexed to lean body mass, LV growth in II subjects was essentially negligible whilst remaining significant in DD subjects (-0.022 vs +0.131 g/kg respectively, p = 0.0009). Although the precise molecular mechanism of this effect remains to be elucidated it clearly demonstrates the importance of the ACE-renin-angiotensin system in determining LV dimensions in situations of high cardiac demand, which may also be important in pathology such as hypertension and heart failure. The use of these "stress-the-genotype" approaches to explore gene-environment interactions are likely to be the key to understanding the causes determining both coronary artery disease and other multi-factorial disorders.

Angiotensin-Converting Enzyme Inhibitors↗