Short-term weight loss reverses obesity-induced microvascular endothelial dysfunction
Obesity is one of the major risk factors for cardiovascular diseases and its prevalence is increasing in all age groups, with the biggest impact observed in middle-aged and older adults. A critical mechanism by which obesity promotes vascular pathologies in these patients involves impairment of endo...
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creator | Csipo, Tamas Fulop, Gabor A. Lipecz, Agnes Tarantini, Stefano Kiss, Tamas Balasubramanian, Priya Csiszar, Anna Ungvari, Zoltan Yabluchanskiy, Andriy |
description | Obesity is one of the major risk factors for cardiovascular diseases and its prevalence is increasing in all age groups, with the biggest impact observed in middle-aged and older adults. A critical mechanism by which obesity promotes vascular pathologies in these patients involves impairment of endothelial function. While endothelial dysfunction in large vessels promotes atherogenesis, obesity-induced microvascular endothelial dysfunction impairs organ perfusion and thereby is causally related to the pathogenesis of ischemic heart disease, chronic kidney disease, intermittent claudication, exercise intolerance, and exacerbates cognitive decline in aging. Reduction of weight via calorie-based diet and exercise in animal models of obesity results in significant improvement of endothelial function both in large vessels and in the microcirculation, primarily due to attenuation of oxidative stress and inflammation. Clinical data on the protective effects of weight loss on endothelial function is limited to studies of flow-mediated dilation assessed in brachial arteries. Currently, there is no guideline on testing the effects of different weight management strategies on microvascular endothelial function in obese patients. Here, we provide proof-of-concept that weight loss-induced improvement of microvascular endothelial function can be reliably assessed in the setting of a geriatric outpatient clinic using a fast, reproducible, non-invasive method: laser speckle contrast imaging-based measurement of endothelium-dependent microvascular responses during post-occlusive reactive hyperemia tests. Our study also provides initial evidence that short-term weight loss induced by consumption of a low-carbohydrate low-calorie diet can reverse microvascular endothelial dysfunction associated with obesity. |
doi_str_mv | 10.1007/s11357-018-0028-9 |
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A critical mechanism by which obesity promotes vascular pathologies in these patients involves impairment of endothelial function. While endothelial dysfunction in large vessels promotes atherogenesis, obesity-induced microvascular endothelial dysfunction impairs organ perfusion and thereby is causally related to the pathogenesis of ischemic heart disease, chronic kidney disease, intermittent claudication, exercise intolerance, and exacerbates cognitive decline in aging. Reduction of weight via calorie-based diet and exercise in animal models of obesity results in significant improvement of endothelial function both in large vessels and in the microcirculation, primarily due to attenuation of oxidative stress and inflammation. Clinical data on the protective effects of weight loss on endothelial function is limited to studies of flow-mediated dilation assessed in brachial arteries. Currently, there is no guideline on testing the effects of different weight management strategies on microvascular endothelial function in obese patients. Here, we provide proof-of-concept that weight loss-induced improvement of microvascular endothelial function can be reliably assessed in the setting of a geriatric outpatient clinic using a fast, reproducible, non-invasive method: laser speckle contrast imaging-based measurement of endothelium-dependent microvascular responses during post-occlusive reactive hyperemia tests. Our study also provides initial evidence that short-term weight loss induced by consumption of a low-carbohydrate low-calorie diet can reverse microvascular endothelial dysfunction associated with obesity.</description><identifier>ISSN: 2509-2715</identifier><identifier>EISSN: 2509-2723</identifier><identifier>DOI: 10.1007/s11357-018-0028-9</identifier><identifier>PMID: 29916025</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Aging ; Animal models ; Arteries ; Atherogenesis ; Biomedical and Life Sciences ; Body weight loss ; Cardiovascular diseases ; Cell Biology ; Cognitive ability ; Coronary artery disease ; Endothelium ; Geriatrics/Gerontology ; Heart diseases ; Hyperemia ; Hypocaloric diet ; Intolerance ; Ischemia ; Life Sciences ; Low carbohydrate diet ; Low density lipoprotein ; Microvasculature ; Molecular Medicine ; Nutrient deficiency ; Obesity ; Original ; Original Article ; Oxidative stress ; Perfusion ; Risk factors ; Weight control</subject><ispartof>GeroScience, 2018-06, Vol.40 (3), p.337-346</ispartof><rights>American Aging Association 2018</rights><rights>GeroScience is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-2b7a090b3b1d9f33b2f60da8afa34ec9d8f3fd2f65d70d346b885aa04f461d373</citedby><cites>FETCH-LOGICAL-c470t-2b7a090b3b1d9f33b2f60da8afa34ec9d8f3fd2f65d70d346b885aa04f461d373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060194/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060194/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,41493,42562,51324,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29916025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Csipo, Tamas</creatorcontrib><creatorcontrib>Fulop, Gabor A.</creatorcontrib><creatorcontrib>Lipecz, Agnes</creatorcontrib><creatorcontrib>Tarantini, Stefano</creatorcontrib><creatorcontrib>Kiss, Tamas</creatorcontrib><creatorcontrib>Balasubramanian, Priya</creatorcontrib><creatorcontrib>Csiszar, Anna</creatorcontrib><creatorcontrib>Ungvari, Zoltan</creatorcontrib><creatorcontrib>Yabluchanskiy, Andriy</creatorcontrib><title>Short-term weight loss reverses obesity-induced microvascular endothelial dysfunction</title><title>GeroScience</title><addtitle>GeroScience</addtitle><addtitle>Geroscience</addtitle><description>Obesity is one of the major risk factors for cardiovascular diseases and its prevalence is increasing in all age groups, with the biggest impact observed in middle-aged and older adults. A critical mechanism by which obesity promotes vascular pathologies in these patients involves impairment of endothelial function. While endothelial dysfunction in large vessels promotes atherogenesis, obesity-induced microvascular endothelial dysfunction impairs organ perfusion and thereby is causally related to the pathogenesis of ischemic heart disease, chronic kidney disease, intermittent claudication, exercise intolerance, and exacerbates cognitive decline in aging. Reduction of weight via calorie-based diet and exercise in animal models of obesity results in significant improvement of endothelial function both in large vessels and in the microcirculation, primarily due to attenuation of oxidative stress and inflammation. Clinical data on the protective effects of weight loss on endothelial function is limited to studies of flow-mediated dilation assessed in brachial arteries. Currently, there is no guideline on testing the effects of different weight management strategies on microvascular endothelial function in obese patients. Here, we provide proof-of-concept that weight loss-induced improvement of microvascular endothelial function can be reliably assessed in the setting of a geriatric outpatient clinic using a fast, reproducible, non-invasive method: laser speckle contrast imaging-based measurement of endothelium-dependent microvascular responses during post-occlusive reactive hyperemia tests. Our study also provides initial evidence that short-term weight loss induced by consumption of a low-carbohydrate low-calorie diet can reverse microvascular endothelial dysfunction associated with obesity.</description><subject>Aging</subject><subject>Animal models</subject><subject>Arteries</subject><subject>Atherogenesis</subject><subject>Biomedical and Life Sciences</subject><subject>Body weight loss</subject><subject>Cardiovascular diseases</subject><subject>Cell Biology</subject><subject>Cognitive ability</subject><subject>Coronary artery disease</subject><subject>Endothelium</subject><subject>Geriatrics/Gerontology</subject><subject>Heart diseases</subject><subject>Hyperemia</subject><subject>Hypocaloric diet</subject><subject>Intolerance</subject><subject>Ischemia</subject><subject>Life Sciences</subject><subject>Low carbohydrate diet</subject><subject>Low density lipoprotein</subject><subject>Microvasculature</subject><subject>Molecular Medicine</subject><subject>Nutrient 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subjects | Aging Animal models Arteries Atherogenesis Biomedical and Life Sciences Body weight loss Cardiovascular diseases Cell Biology Cognitive ability Coronary artery disease Endothelium Geriatrics/Gerontology Heart diseases Hyperemia Hypocaloric diet Intolerance Ischemia Life Sciences Low carbohydrate diet Low density lipoprotein Microvasculature Molecular Medicine Nutrient deficiency Obesity Original Original Article Oxidative stress Perfusion Risk factors Weight control |
title | Short-term weight loss reverses obesity-induced microvascular endothelial dysfunction |
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