NEW YORK, Sept. 30, 2019 /PRNewswire/ -- Increasing levels of a simplified version of "good" cholesterol reversed disease in the blood vessels of mice with diabetes, a new study finds.
Published online in the journal Circulation on September 30, the study results revolve around atherosclerosis, a condition where high levels
Led by researchers from NYU School of Medicine, this study provides the "first direct evidence" that raising levels of a simple, functional version of good cholesterol – the HDL protein shuttle that pulls cholesterol out of cells – reversed the progression of atherosclerosis in mice with diabetes.
The results, say the study authors, reflect the emerging view that HDL's ability to extract cholesterol from cells reduces inflammation, the immune reaction in which cells rush to injury sites. Part of the natural process that repairs damaged tissues, inflammation worsens disease in the wrong place (e.g. plaques).
"Our study results argue that raising levels of functional good cholesterol addresses inflammatory roots of atherosclerosis driven by cholesterol buildup beyond what existing drugs can achieve," says study senior author Edward Fisher, MD, PhD, the Leon H. Charney Professor of Cardiovascular Medicine at NYU Langone Health. "Good cholesterol is back as therapeutic target because we now understand its biology well enough to change it in ways that lower disease risk."
Treatments for atherosclerosis for decades have focused on lowering blood levels of LDL or "bad cholesterol," a second shuttle that delivers molecules of cholesterol from the diet (and from the liver) to the body's cells, including those in vessel walls. But the ability of treatments that lower LDL cholesterol to reduce heart attack risk is limited, and especially in adults with diabetes, who are twice as likely to die from heart disease or stroke as people without diabetes, according to the American Heart Association.
To reduce disease risk not addressed by lowering bad cholesterol, the field designed drugs that raised levels of the "good" cholesterol (HDL) shuttle that carts cholesterol from blood vessel walls to the liver for expulsion from the body. The two mechanisms should work together, but much anticipated HDL-raising drugs (e.g. cholesteryl ester transfer protein inhibitors) failed in 2016 clinical trials to reduce the risk of heart attacks beyond what could be accomplished by cholesterol lowering.
Faced with these limits, researchers looked more closely at the roles in atherosclerosis and diabetes of inflammation. Part of this shift was the realization that old measures for how a given "HDL-raising drug" countered disease – like how much of the HDL shuttle was in a person's bloodstream – needed to be replaced. The new measure, says Fisher, should be how well a person's HDL can pull cholesterol out of cells (total cholesterol efflux), because it better captures the inflammatory part of the disease process.
The new measure builds on the discovery that signaling proteins and fats related to high blood sugar attach to, lower the number of, and disable HDL – which is composed of a protein called apolipoprotein A-I (apoA-I) linked to phospholipids. This lowers supplies of the shuttle capable of achieving cholesterol efflux, termed "functional HDL."
In sets of experiments, the current study authors raised functional HDL levels in diabetic mice by increasing the amounts apoA-I present, either by genetic engineering or direct injection. They found that the increase in functional HDL stopped cholesterol-driven immune cell multiplication (proliferation) in bone marrow, reduced inflammation in immune cells in plaques by half, and enhanced the reversal of atherosclerotic disease processes (regression) by 30 percent in mice already treated to lower their bad cholesterol.
Finally, the study results also show that increased HDL levels kept another set of immune cells called neutrophils from giving off webs of fibers that increase inflammation and blot clot formation in atherosclerosis, further blocking blood flow.
"For the study we built our own version of the HDL particle, called reconstituted HDL, which promises to become the basis for new kinds of functional HDL treatments that finally reduce the residual risk for cardiovascular disease not addressed currently," says first author Tessa Barrett, PhD, research assistant professor in the Department of Medicine at NYU School of Medicine.
Along with Fisher and Barrett, study authors from the Division of Cardiology at the NYU School of Medicine were Emilie Distel, Michael Garshick, Yoscar Ogando; along with Jiyuan Hu in the Division of Biostatistics, Jeffrey Berger in the Divisions of Cardiology and Hematology, and Ira Goldberg, in the Division of Endocrinology, Diabetes, and Metabolism. Also study authors were Andrew Murphy in the Division of Immunometabolism at Baker Heart and Diabetes Institute in Melbourne, Australia; Jianhua Liu in the Department of Surgery at Mount Sinai School of Medicine, and Tomas Vaisar and Jay Heinecke, in the Division of Metabolism, Endocrinology, and Nutrition at the University of Washington School of Medicine in Seattle.
Funding for the study was provided by National Institute of Health grants R01 DK095684, R01 HL117226, R01 2 HL084312, PO1 HL092969, P01HL131481, and R01 HL114978; American Heart Association grants 18CDA34110203AHA, and 18CDA34080540), and by National Health and Medical Research Council (Australia) grants APP1083138, APP1106154, as well as a National Heart Foundation (Australia) 100440).
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SOURCE NYU School of Medicine