Sarcopenia and Cardiovascular Diseases
Sarcopenia is the loss of muscle strength, mass, and function, which is often exacerbated by chronic comorbidities including cardiovascular diseases, chronic kidney disease, and cancer. Sarcopenia is associated with faster progression of cardiovascular diseases and higher risk of mortality, falls, a...
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| Vydané v: | Circulation (New York, N.Y.) Ročník 147; číslo 20; s. 1534 |
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| Hlavní autori: | , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
United States
16.05.2023
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| Predmet: | |
| ISSN: | 1524-4539, 1524-4539 |
| On-line prístup: | Zistit podrobnosti o prístupe |
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| Abstract | Sarcopenia is the loss of muscle strength, mass, and function, which is often exacerbated by chronic comorbidities including cardiovascular diseases, chronic kidney disease, and cancer. Sarcopenia is associated with faster progression of cardiovascular diseases and higher risk of mortality, falls, and reduced quality of life, particularly among older adults. Although the pathophysiologic mechanisms are complex, the broad underlying cause of sarcopenia includes an imbalance between anabolic and catabolic muscle homeostasis with or without neuronal degeneration. The intrinsic molecular mechanisms of aging, chronic illness, malnutrition, and immobility are associated with the development of sarcopenia. Screening and testing for sarcopenia may be particularly important among those with chronic disease states. Early recognition of sarcopenia is important because it can provide an opportunity for interventions to reverse or delay the progression of muscle disorder, which may ultimately impact cardiovascular outcomes. Relying on body mass index is not useful for screening because many patients will have sarcopenic obesity, a particularly important phenotype among older cardiac patients. In this review, we aimed to: (1) provide a definition of sarcopenia within the context of muscle wasting disorders; (2) summarize the associations between sarcopenia and different cardiovascular diseases; (3) highlight an approach for a diagnostic evaluation; (4) discuss management strategies for sarcopenia; and (5) outline key gaps in knowledge with implications for the future of the field. |
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| AbstractList | Sarcopenia is the loss of muscle strength, mass, and function, which is often exacerbated by chronic comorbidities including cardiovascular diseases, chronic kidney disease, and cancer. Sarcopenia is associated with faster progression of cardiovascular diseases and higher risk of mortality, falls, and reduced quality of life, particularly among older adults. Although the pathophysiologic mechanisms are complex, the broad underlying cause of sarcopenia includes an imbalance between anabolic and catabolic muscle homeostasis with or without neuronal degeneration. The intrinsic molecular mechanisms of aging, chronic illness, malnutrition, and immobility are associated with the development of sarcopenia. Screening and testing for sarcopenia may be particularly important among those with chronic disease states. Early recognition of sarcopenia is important because it can provide an opportunity for interventions to reverse or delay the progression of muscle disorder, which may ultimately impact cardiovascular outcomes. Relying on body mass index is not useful for screening because many patients will have sarcopenic obesity, a particularly important phenotype among older cardiac patients. In this review, we aimed to: (1) provide a definition of sarcopenia within the context of muscle wasting disorders; (2) summarize the associations between sarcopenia and different cardiovascular diseases; (3) highlight an approach for a diagnostic evaluation; (4) discuss management strategies for sarcopenia; and (5) outline key gaps in knowledge with implications for the future of the field.Sarcopenia is the loss of muscle strength, mass, and function, which is often exacerbated by chronic comorbidities including cardiovascular diseases, chronic kidney disease, and cancer. Sarcopenia is associated with faster progression of cardiovascular diseases and higher risk of mortality, falls, and reduced quality of life, particularly among older adults. Although the pathophysiologic mechanisms are complex, the broad underlying cause of sarcopenia includes an imbalance between anabolic and catabolic muscle homeostasis with or without neuronal degeneration. The intrinsic molecular mechanisms of aging, chronic illness, malnutrition, and immobility are associated with the development of sarcopenia. Screening and testing for sarcopenia may be particularly important among those with chronic disease states. Early recognition of sarcopenia is important because it can provide an opportunity for interventions to reverse or delay the progression of muscle disorder, which may ultimately impact cardiovascular outcomes. Relying on body mass index is not useful for screening because many patients will have sarcopenic obesity, a particularly important phenotype among older cardiac patients. In this review, we aimed to: (1) provide a definition of sarcopenia within the context of muscle wasting disorders; (2) summarize the associations between sarcopenia and different cardiovascular diseases; (3) highlight an approach for a diagnostic evaluation; (4) discuss management strategies for sarcopenia; and (5) outline key gaps in knowledge with implications for the future of the field. Sarcopenia is the loss of muscle strength, mass, and function, which is often exacerbated by chronic comorbidities including cardiovascular diseases, chronic kidney disease, and cancer. Sarcopenia is associated with faster progression of cardiovascular diseases and higher risk of mortality, falls, and reduced quality of life, particularly among older adults. Although the pathophysiologic mechanisms are complex, the broad underlying cause of sarcopenia includes an imbalance between anabolic and catabolic muscle homeostasis with or without neuronal degeneration. The intrinsic molecular mechanisms of aging, chronic illness, malnutrition, and immobility are associated with the development of sarcopenia. Screening and testing for sarcopenia may be particularly important among those with chronic disease states. Early recognition of sarcopenia is important because it can provide an opportunity for interventions to reverse or delay the progression of muscle disorder, which may ultimately impact cardiovascular outcomes. Relying on body mass index is not useful for screening because many patients will have sarcopenic obesity, a particularly important phenotype among older cardiac patients. In this review, we aimed to: (1) provide a definition of sarcopenia within the context of muscle wasting disorders; (2) summarize the associations between sarcopenia and different cardiovascular diseases; (3) highlight an approach for a diagnostic evaluation; (4) discuss management strategies for sarcopenia; and (5) outline key gaps in knowledge with implications for the future of the field. |
| Author | Batchelor, Wayne B Krishnaswami, Ashok Gerstenblith, Gary Goyal, Parag Forman, Daniel E Rich, Michael W Alfaraidhy, Maha Kumar, Manish Alexander, Karen P Cawthon, Peggy Damluji, Abdulla A Rohant, Namit N AlHajri, Noora deFilippi, Christopher R Bahrainy, Samira Al Malouf, Christina Ji Kwak, Min Kirkpatrick, James |
| Author_xml | – sequence: 1 givenname: Abdulla A orcidid: 0000-0002-8774-6416 surname: Damluji fullname: Damluji, Abdulla A organization: Johns Hopkins University School of Medicine, Baltimore, MD (A.A.D., M.A., G.G.) – sequence: 2 givenname: Maha orcidid: 0000-0003-3096-3222 surname: Alfaraidhy fullname: Alfaraidhy, Maha organization: Johns Hopkins University School of Medicine, Baltimore, MD (A.A.D., M.A., G.G.) – sequence: 3 givenname: Noora surname: AlHajri fullname: AlHajri, Noora organization: Cleveland Clinic, Abu Dhabi, United Arab Emirates (N.A.) – sequence: 4 givenname: Namit N surname: Rohant fullname: Rohant, Namit N organization: University of Arizona, Tucson (N.N.R., P.G.) – sequence: 5 givenname: Manish surname: Kumar fullname: Kumar, Manish organization: University of Connecticut, Hartford (M.K.) – sequence: 6 givenname: Christina surname: Al Malouf fullname: Al Malouf, Christina organization: Weill Cornell Medicine, New York, NY (C.A.M.) – sequence: 7 givenname: Samira orcidid: 0000-0003-2724-426X surname: Bahrainy fullname: Bahrainy, Samira organization: University of Washington, Seattle (S.B., J.K.) – sequence: 8 givenname: Min orcidid: 0000-0003-2778-3984 surname: Ji Kwak fullname: Ji Kwak, Min organization: University of Texas, Houston (M.J.K.) – sequence: 9 givenname: Wayne B orcidid: 0000-0002-3016-1150 surname: Batchelor fullname: Batchelor, Wayne B organization: Inova Center of Outcomes Research, Inova Heart and Vascular Institute, Falls Church, VA (A.A.D., W.B.B., C.R.D.) – sequence: 10 givenname: Daniel E orcidid: 0000-0002-5697-2189 surname: Forman fullname: Forman, Daniel E organization: University of Pittsburgh and the Pittsburgh Geriatric Research Education and Clinical Center, PA (D.E.F.) – sequence: 11 givenname: Michael W surname: Rich fullname: Rich, Michael W organization: Washington University, St Louis, MO (M.W.R.) – sequence: 12 givenname: James surname: Kirkpatrick fullname: Kirkpatrick, James organization: University of Washington, Seattle (S.B., J.K.) – sequence: 13 givenname: Ashok surname: Krishnaswami fullname: Krishnaswami, Ashok organization: Kaiser Permanente, San Jose, CA (A.K.) – sequence: 14 givenname: Karen P orcidid: 0000-0003-4418-1424 surname: Alexander fullname: Alexander, Karen P organization: Duke Clinical Research Institute, Duke University, Durham, NC (K.P.A.) – sequence: 15 givenname: Gary orcidid: 0000-0001-6046-6812 surname: Gerstenblith fullname: Gerstenblith, Gary organization: Johns Hopkins University School of Medicine, Baltimore, MD (A.A.D., M.A., G.G.) – sequence: 16 givenname: Peggy surname: Cawthon fullname: Cawthon, Peggy organization: University of California San Francisco (P.C.) – sequence: 17 givenname: Christopher R orcidid: 0000-0002-0660-4943 surname: deFilippi fullname: deFilippi, Christopher R organization: Inova Center of Outcomes Research, Inova Heart and Vascular Institute, Falls Church, VA (A.A.D., W.B.B., C.R.D.) – sequence: 18 givenname: Parag orcidid: 0000-0001-7474-3737 surname: Goyal fullname: Goyal, Parag organization: University of Arizona, Tucson (N.N.R., P.G.) |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37186680$$D View this record in MEDLINE/PubMed |
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| Keywords | older adults cardiovascular diseases body mass index sarcopenia |
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