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			 Past studies of the drugs known as glucagon-like peptide-1 receptor 
			agonists - or GLP-1RAs - have found that the medications improve 
			blood sugar control and reduce body weight, but the review's lead 
			author said no research had compared the various versions 
			head-to-head. 
			 
			"The main message is that today several drugs are available for the 
			control of hyperglycemia in type 2 diabetes, as never before," said 
			Dr. Francesco Zaccardi, of the Diabetes Research Center at Leicester 
			General Hospital in the U.K., "Therefore, it is even more important 
			to know differences and similarities among drugs." 
			 
			In type 2 diabetes, the body can’t properly use or make enough of 
			the hormone insulin to convert blood sugar into energy. 
			 
			The drugs compared in the study - three of which are on the market, 
			and two in development - stimulate insulin and have other beneficial 
			effects like slowing digestion, the study team writes in Annals of 
			Internal Medicine. All are taken once a week. 
			
			  
			The American Diabetes Association and the European Association for 
			the Study of Diabetes currently recommend GLP-1RAs as an option for 
			people with type 2 diabetes who have tried other treatments like 
			lifestyle changes and metformin, which is a longstanding oral drug 
			used to improve blood sugar control. 
			 
			For the new study, Zaccardi and colleagues analyzed data from 34 
			trials that included a total of 21,126 participants taking one of 
			the five GLP-1RAs. 
			 
			They found that the drugs performed similarly in reducing blood 
			sugar, as well as heart disease risk factors like high blood 
			pressure, cholesterol and inflammation. The risk of dangerous blood 
			sugar lows known as hypoglycemia was also similar among people 
			taking all five drugs. 
			 
			The medications differed, however, when it came to reducing weight 
			and HbA1c, which is a measure of average blood sugar levels over 
			about three months. 
			 
			Dulaglutide 1.5 milligrams (mg), which is sold as Trulicity by Eli 
			Lilly; once-weekly exenatide, which is sold as Byetta by AstraZeneca; 
			and taspoglutide 20 mg, which is in development by Ipsen and Roche, 
			all performed better on those two points than albiglutide, which is 
			sold as Tanzeum by GlaxoSmithKline and semaglutide, in development 
			by Novo Nordisk. 
			 
			Still, the differences were small. HbA1c is measured in percentages 
			with normal being below 6 percent and 6.5 percent or above being 
			considered diabetes. Zaccardi told Reuters Health in an email that 
			the greatest differences between the drugs were around 0.4 percent 
			for HbA1c and about three pounds of body weight. 
			
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			"The weight loss is instructive because a lot of people hear stories 
			of people losing a lot of weight, but the mean weight loss is 
			modest," said Dr. Sethu Reddy, chief of the Adult Diabetes Section 
			at the Joslin Diabetes Center in Boston. 
			The researchers also found that taspoglutide 20 mg has the highest 
			risk of nausea. And once-weekly exenatide increased heart rate 
			compared with albiglutide and dulaglutide by 1.4 to 3.2 beats per 
			minute. 
			 
			Zaccardi said that few comparisons like this study have been done 
			between similar diabetes drugs, which limits their ability to 
			compare the results to other types of treatments. 
			 
			"I believe that the study underlines the necessity to perform direct 
			comparisons among drugs of the same class to better clarify the pros 
			and cons of each drug," he added. 
			 
			Reddy, who was not involved in the new review, also cautioned that 
			the findings are based on a comparison of existing data from 
			separate studies. 
			 
			"It’s not the 'real deal' so to speak in that there are no trials 
			comparing these drugs to one another," he said. 
			 
			But, Reddy added, the review and new research into GLP-1RAs should 
			give people comfort since it shows the drugs really do work to 
			reduce high blood sugar and other diabetes symptoms. 
			  
			
			  
			 
			"That makes me more comfortable that this therapeutic area is real, 
			and not a flash in the pan and the mechanism is real," he said. 
			 
			SOURCE: http://bit.ly/SQRXAa Annals of Internal Medicine, online 
			December 7, 2015. 
			[© 2015 Thomson Reuters. All rights 
				reserved.] Copyright 2015 Reuters. All rights reserved. This material may not be published, 
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