Combined treatment with a drug that mimics the action of a gut hormone and basal insulin  is more effective at improving blood sugar control than other anti-diabetic treatments, with similar rates of hypoglycaemia (dangerously low blood sugar levels) and greater weight loss, a systematic review and meta-analysis published in The Lancet shows.
"Achieving normal blood sugar levels in people with type 2 diabetes is compromised by the adverse side effects plaguing currently available treatments. Some anti-diabetic treatments increase risk of hypoglycaemia and weight gain which put patients at increased risk of heart attack and stroke, as well as reducing their quality of life"*, explains Dr Ravi Retnakaran, lead author and endocrinologist at Mount Sinai Hospital, Toronto, Canada.
Glucagon-like peptide-1 (GLP-1) is a hormone that is secreted from the gut after eating. GLP-1 based therapy was recently introduced as a new treatment for patients with type 2 diabetes because of its ability to regulate blood sugar levels and to generate weight loss as opposed to weight gain. Moreover, GLP-1 agonists only stimulate insulin secretion when blood glucose levels are high, without increasing risk of hypoglycaemia. However, their optimal role in the management of type 2 diabetes has yet to be established.
Retnakaran and colleagues identified 2905 studies over 64 years involving basal insulin and/or GLP-1 agonists in adults with type 2 diabetes. The analysis of 15 randomised trials involving more than 4300 participants showed that the combination of basal insulin with a GLP-1 agonist resulted in a 92% greater likelihood of achieving target blood sugar control (A1c of 7% or lower ), with similar rates of hypoglycaemia and an average weight loss of more than 3kg compared with other anti-diabetic treatments. Compared to full basal-bolus insulin regimens , the combined treatment generated modestly better blood sugar control, but had a 33% lower risk of hypoglycaemia and almost 6kg greater weight loss.
According to Dr Retnakaran: "Combining a GLP-1 agonist with basal insulin is a treatment strategy that can achieve the ideal triumvirate of short-term outcomes in diabetes management: optimal glucose control alongside weight loss and a low risk of hypoglycaemic episodes. As such, this combination treatment could improve the management of people with type 2 diabetes."*
Writing in a linked Comment, Dr John Buse, Chief of the Division of Endocrinology at the University of North Carolina School of Medicine in the USA says, "Perhaps the most practical and immediate issue is whether the fixed-dose combinations of a GLP-1 agonist and basal insulin in development will supersede other approaches. This is an unsettled question, but it seems likely that fixed-dose combinations will be welcomed in view of their convenience and efficacy…The major barrier to widespread adoption of these treatments is cost—both GLP-1 agonists and insulin analogues are among the most expensive in diabetes care. One can hope that some incremental cost savings will come with combined products. It has been a 20-year journey, but the combination of GLP-1 agonist and basal insulin has finally arrived as a more powerful and safer alternative to insulin in the management of type 2 diabetes."
Notes to Editors:
 The role of basal insulin, also known as background insulin, is to keep blood glucose at consistent levels during periods of fasting and is taken once or twice a day.
Controlling blood sugar can help prevent small blood vessel (or microvascular) complications that can lead to blindness, kidney failure, and amputations. Blood sugar control is measured using the combination of haemoglobin A1c in the blood, and concentrations less then 7% can substantially reduce the risk of these complications.
 A basal-bolus regimen involves taking a longer acting form of insulin to keep blood glucose levels stable through periods of fasting and separate injections of shorter-acting insulin to prevent rises in blood glucose levels at meal times.
*Quotes direct from author and cannot be found in text of Article.