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Stephen C. Bain

Researcher at Swansea University

Publications -  276
Citations -  14044

Stephen C. Bain is an academic researcher from Swansea University. The author has contributed to research in topics: Diabetes mellitus & Type 2 diabetes. The author has an hindex of 48, co-authored 250 publications receiving 11362 citations. Previous affiliations of Stephen C. Bain include Morriston Hospital & Abertawe Bro Morgannwg University Health Board.

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Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.

TL;DR: In patients with type 2 diabetes who were at high cardiovascular risk, the rate of cardiovascular death, nonfatal myocardial infarction, orNonfatal stroke was significantly lower among patients receiving semaglutide than among those receiving placebo, an outcome that confirmed the noninferiority of semag lutide.
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Angiotensin-receptor blockade versus converting-enzyme inhibition in type 2 diabetes and nephropathy.

TL;DR: Telmisartan is not inferior to enalapril in providing long-term renoprotection in persons with type 2 diabetes and early nephropathy, and these findings support the clinical equivalence of angiotensin II-receptor blockers and ACE inhibitors in people with conditions that place them at high risk for cardiovascular events.
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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

TL;DR: In this article, the authors described linkage and association of type 1 diabetes to the CTLA-4 gene (cytotoxic T lymphocyte associated-4) on chromosome 2q33 (designated IDDM12), which is a strong candidate gene for T cell mediated autoimmune disease because it encodes a T cell receptor that mediates T cell apoptosis and is a vital negative regulator of T cell activation.
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3 years of liraglutide versus placebo for type 2 diabetes risk reduction and weight management in individuals with prediabetes: a randomised, double-blind trial

Carel W. le Roux, +200 more
- 08 Apr 2017 - 
TL;DR: Liraglutide 3·0 mg might provide health benefits in terms of reduced risk of diabetes in individuals with obesity and prediabetes in this trial, with the limitation that withdrawn individuals were not followed up after discontinuation.
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A search for type 1 diabetes susceptibility genes in families from the United Kingdom

TL;DR: A genome-wide scan of 93 affected sibpair families from the UK indicated a similar genetic basis for human type 1 diabetes, with the major genetic component at the MHC locus (IDDM1) explaining 34% of the familial clustering of the disease.