Jump to content

Edit filter log

Details for log entry 2672154

13:29, 7 May 2010: 77.89.162.226 (talk) triggered filter 135, performing the action "edit" on Sarcopenia. Actions taken: Tag; Filter description: Repeating characters (examine)

Changes made in edit



Extreme muscle loss is often a result of both diminishing [[anabolic]] signals, such as [[growth hormone]] and [[testosterone]], and promotion of [[catabolic]] signals, such as pro-inflammatory [[cytokines]].{{Citation needed|date=January 2010}}
Extreme muscle loss is often a result of both diminishing [[anabolic]] signals, such as [[growth hormone]] and [[testosterone]], and promotion of [[catabolic]] signals, such as pro-inflammatory [[cytokines]].{{Citation needed|date=January 2010}}
TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN IS A TWAT!!!!!!!!!


==Sarcopenia as a public-health problem==
==Sarcopenia as a public-health problem==

Action parameters

VariableValue
Name of the user account (user_name)
'77.89.162.226'
Page ID (page_id)
3108990
Page namespace (page_namespace)
0
Page title without namespace (page_title)
'Sarcopenia'
Full page title (page_prefixedtitle)
'Sarcopenia'
Action (action)
'edit'
Edit summary/reason (summary)
'/* Loss of anabolic signals */ '
Whether or not the edit is marked as minor (no longer in use) (minor_edit)
false
Old page wikitext, before the edit (old_wikitext)
'{{Update|date=October 2009}} '''Sarcopenia''' (from the Greek meaning "poverty of flesh") is the degenerative loss of [[skeletal muscle]] mass and strength associated with [[aging]]. Sarcopenia is a component of the [[Frailty syndrome]]. 0.5-1% of loss per year after the age of 25 {{tocright}} ==Markers of sarcopenia== Sarcopenia is characterized first by a decrease in the size of the [[muscle]], which causes weakness and frailty. However, this loss of muscle mass may be caused by different cellular mechanisms than those that cause [[muscle atrophy]]. For example, during sarcopenia, there is a replacement of muscle fibres with [[fat]] and an increase in [[fibrosis]]. == Benefit of exercise== [[Exercise]] and increases in activity have been shown to be beneficial in settings of sarcopenia; exercise even in the very old can increase strength and muscle function. Lack of exercise is currently thought to be a significant risk factor, increasing the likelihood of sarcopenia.<ref>{{cite journal |author=Abate M, Di Iorio A, Di Renzo D, Paganelli R, Saggini R, Abate G |title=Frailty in the elderly: the physical dimension |journal=Eura Medicophys |volume=43 |issue=3 |pages=407–15 |year=2007 |month=September |pmid=17117147 |doi= |url=http://www.minervamedica.it/index2.t?show=R33Y2007N03A0407}}</ref> Not only muscle but the entire musculoskeletal system of muscle, neuromuscular responsiveness, endocrine function, vasocapillary access, tendon, joint, ligament, and bone, depends on regular and lifelong exercise to maintain integrity. The slow attenuation, atrophy, or loss of muscle tissue that medical professionals sometimes describe as sarcopenia (literally, "flesh loss') is currently thought to be the result of cumulative loss of musculoskeletal strength and mass associated with chronic absence of exercise of sufficient intensity or volume. However, even highly trained athletes experience the effects of sarcopenia. It is interesting to note that athletic speed and strength records are generally set by individuals no older than 30 years of age, although some powerlifters and other strength athletes continue to set records into their 50s.{{Citation needed|date=October 2009}} == Fiber-type changes in sarcopenia== Simple [[circumference]] does not provide enough data to determine whether or not an individual is suffering from severe sarcopenia. Sarcopenia is also marked by a decrease in the circumference of distinct types of [[muscle fiber]]s. Skeletal muscle has different fiber-types, which are characterized by expression of distinct [[myosin]] variants. During sarcopenia, there is a decrease in "type 2" fiber circumference ([[Muscle fiber#Type II|Type II]]), but not nearly as much "type I" fiber circumference ([[muscle fiber#Type I|Type I]]). However, we lose both type I and type II muscle fibers (muscle cells) equally as we age (contrary to popular belief that we lose type II more rapidly).{{Citation needed|date=January 2010}} ==Loss of satellite cell function== [[Satellite cells]] are small mononuclear cells that abut the muscle fiber. [[Satellite cell]]s are normally activated upon injury or exercise. These cells then differentiate and fuse into the muscle fiber, helping to maintain its function. One theory is that sarcopenia, is in part casued by a failure in satellite cell activation.{{Citation needed|date=January 2010}} Therefore, the ability to repair damaged muscles or respond to nutritional signals is impaired. ==Loss of anabolic signals== Extreme muscle loss is often a result of both diminishing [[anabolic]] signals, such as [[growth hormone]] and [[testosterone]], and promotion of [[catabolic]] signals, such as pro-inflammatory [[cytokines]].{{Citation needed|date=January 2010}} ==Sarcopenia as a public-health problem== Due to the lessened physical activity and increased [[longevity]] of industrialized populations, sarcopenia is emerging as a major health concern. Sarcopenia may progress to the extent that an older person may lose his or her ability to live independently. Furthermore, sarcopenia is an important independent predictor of disability in population-based studies, linked to poor balance, gait speed, falls, and fractures. Sarcopenia can be thought of as a muscular analog of [[osteoporosis]], which is loss of bone, also caused by inactivity and counteracted by exercise. The combination of [[osteoporosis]] and sarcopenia results in the significant frailty often seen in the elderly population. == Natural history == Strength losses with ageing for men and women are relatively similar. They are greater for lower than upper extremity muscles. Maximum attainable strength peaks in mid-twenties and declines thereafter. The decline is precipitous after 65 years of age, though few longitudinal studies exist on this topic. A direct assessment of the effects of sarcopenia, even in extremely physically fit individuals, can be seen in the age-related decline in [[Masters athletics (track and field)]] world records of muscle-intensive sports, such as weight lifting. No substance-free, proven Olympic weight-lifting record has been set by any athlete of either sex or any weight class above the age of 31. ((''However, in the non-Olympic sport of powerlifting, many world records in several weight divisions have been accomplished by athletes well into their forties, purportedly, "verified" by the [[International Powerlifting Federation]] to have been accomplished drug-free. However, that this certification carries any weight is doubtful considering that even in highly supervised events such as the Olympics, drug cheating invariably occurs (some of which is detected right away, much of it is not). Furthermore, casting doubt on any records set outside the traditional Olympic athletic system, drug cheating is rampant in professional sports that do not perform random drug testing (e.g. baseball).'')) == Diagnosis == Consensus on clinical diagnosis of sarcopenia has quickly developed over the last decade around the working definition proposed in 1998 by Baumgartner et al. <ref>{{cite journal |author=Baumgartner RN, Koehler KM, Gallagher D, ''et al.'' |title=Epidemiology of sarcopenia among the elderly in New Mexico |journal=Am. J. Epidemiol. |volume=147 |issue=8 |pages=755–63 |year=1998 |month=April |pmid=9554417 |doi= |url=http://aje.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=9554417}}</ref>, which uses a measure of lean body mass as determined by [[Dual energy X-ray absorptiometry]] (DEXA) compared to a normal reference population. His working definition uses a cut point of 2 standard deviations below the mean of lean mass for gender specific healthy young adults. This methodology is attractive for definitive diagnosis in clinical settings as well for several reasons. Primarily, emerging research shows it is predictive of negative outcomes and it is also a method familiar to most clinicians. This later point is especially true for those that treat the geriatric population, given its similarity to the 1996 [[World Health Organization]] (WHO) methodology for definitive diagnosis of [[osteoporosis]], which also uses DEXA, but uses a measure of lean mass rather than bone mineral density (BMD). DEXA is widely used already in clinical settings in develop countries to identify and monitor severity of osteoporosis. And the degree of sarcopenia can be measured using DEXA in patients being evaluated for osteoporosis, at the same time with the same scan, with no added cost or radiation exposure to the patient. Since Baumgartner’s working definition first appeared, some several consensus groups have refined the definition, including the recent joint effort of the European Society on Clinician Nutrition and Metabolism (ESPEN) Special Interest Groups (SIG) on geriatric nutrition and on [[cachexia]]-[[anorexia]] in chronic wasting diseases. Their consensus definition is: <b>1) A low muscle mass, >2 standard deviations below that mean measured in young adults (aged 18–39 years in the 3rd NHANES population) of the same sex and ethnic background, and 2) Low gait speed (e.g. a walking speed below 0.8 m/s in the 4-m walking test). However, it can be replaced by one of the well-established functional tests utilized locally as being part of the comprehensive geriatric assessment.</b><ref>{{cite journal |author= Muscaritoli M, Anker S, Argilés J, ''et al.'' |title= Consensus definition of sarcopenia, cachexia and pre-cachexia: Joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics” |journal= Clinical Nutrition | year=2010 |doi=10.1016/j.clnu.2009.12.004 |url=http://linkinghub.elsevier.com/retrieve/pii/S0261561409002428}}</ref> There remains many opportunities for further refinement of reference populations by ethic groups, and to further correlate of the degrees of severity of sarcopenia to overt declines in functional performance (preferably using verified functional tests), as well as incidence of hospitalization admissions, morbidity and mortality. Work toward this objective has already begun, and the body of research to date clearly points toward severe sarcopenia is predicative of negative outcomes, similar to what already been shown to exist with the [[Frailty syndrome]], as defined by the criteria set forth in 2001 by Fried et al. <ref>{{cite journal |author= Fried LP, Tangen CM, Walston J, ''et al.'' |title= Frailty in Older Adults: Evidence for a Phenotype. |journal= J Gerontol A Biol Sci Med Sci. |year=2001|url= http://www.ncbi.nlm.nih.gov/pubmed/11253156}}</ref> == Management == Primary management of sarcopenia is through the application of a graded exercise program, across both cardiovascular and strength domains, dosed in such a way as to provoke beneficial adaptation without overloading the weakened body.<ref>{{cite journal |author=Taaffe DR |title=Sarcopenia--exercise as a treatment strategy |journal=Aust Fam Physician |volume=35 |issue=3 |pages=130–4 |year=2006 |month=March |pmid=16525526 |doi= |url=http://www.racgp.org.au/afp/200603/3608}}</ref> Possible therapeutic strategies include use of testosterone or anabolic steroids, though long term use of these agents is controversial in men given concerns of prostate symptoms, and essentially contraindicated in women, given concerns of virilization. Other approved medications have been shown to have little to no effect in this setting, including agents such DHEA and human growth hormone. New therapies in clinical development hold great promise in this area, including the Selective Androgen Receptor Modulators (SARMs), as evidenced by recent studies. Nonsteriodal SARMs are of particular interest, given they exhibit significant selectivity between the anabolic effects of testosterone on muscle, but apparently with little to no androgenic effects such as prostate stimulation in men or virilization in women. Nutritional evaluation may also be indicated if malnutrition is suspected, or current nutritional intake is insufficient to maintain adequate total body mass, although increased exercise also increases appetite. Physical activity incorporating resistance training is probably the most effective measure to prevent and treat sarcopenia. An extract from the plant Ginkgo biloba (EGb 761) was shown to reduce the muscle loss in a rat model of sarcopenia (Bidon ''et al''., 2009)<ref>{{cite journal |author=Bidon C, Lachuer J, Molgó J, Wierinckx A, de la Porte S, et al. |year=2009 |title=The Extract of Ginkgo biloba EGb 761 Reactivates a Juvenile Profile in the Skeletal Muscle of Sarcopenic Rats by Transcriptional Reprogramming. |journal=PLoS ONE 4(11): |url=http://www.plosone.org/article/info:doi%2F10.1371%2Fjournal.pone.0007998 |doi=doi:10.1371/journal.pone.0007998}}</ref>. ==See also== * [[Sarcopenic obesity]] == References == {{reflist}} *{{cite journal |author=Roubenoff R |title=Physical activity, inflammation, and muscle loss |journal=Nutr. Rev. |volume=65 |issue=12 Pt 2 |pages=S208–12 |year=2007 |month=December |pmid=18240550 |doi= 10.1111/j.1753-4887.2007.tb00364.x|url=http://openurl.ingenta.com/content/nlm?genre=article&issn=0029-6643&volume=65&issue=12%20Pt%202&spage=S208&aulast=Roubenoff}} *{{cite journal |author=Lynch GS |title=Tackling Australia's future health problems: developing strategies to combat sarcopenia—age-related muscle wasting and weakness |journal=Intern Med J |volume=34 |issue=5 |pages=294–6 |year=2004 |month=May |pmid=15151679 |doi=10.1111/j.1444-0903.2004.00568.x |url=}} *{{cite journal |author=Edström E, Ulfhake B |title=Sarcopenia is not due to lack of regenerative drive in senescent skeletal muscle |journal=Aging Cell |volume=4 |issue=2 |pages=65–77 |year=2005 |month=April |pmid=15771610 |doi=10.1111/j.1474-9728.2005.00145.x |url=}} *{{cite journal |author=Fujita S, Volpi E |title=Amino acids and muscle loss with aging |journal=J. Nutr. |volume=136 |issue=1 Suppl |pages=277S–80S |year=2006 |month=January |pmid=16365098 |doi= |url=http://jn.nutrition.org/cgi/pmidlookup?view=long&pmid=16365098}} *{{cite journal |last=Visser |first=Marjolein |authorlink= |coauthors=Deeg D, Lips P |year=2003 |month= |title=Low vitamin D and high parathyroid hormone levels as determinants of loss of muscle strength and muscle mass (sarcopenia) |journal=J. Clin. Endocrinol. Metab. |volume=88 |issue=12 |pages=5766–5772 |id= |url=http://cat.inist.fr/?aModele=afficheN&cpsidt=15356420 |accessdate= 2007-11-06 |quote=|doi=10.1210/jc.2003-030604|pmid=14671166 }} [[Category:Aging-associated diseases]] [[Category:Geriatrics]] [[Category:Rehabilitation medicine]] [[de:Sarkopenie]] [[es:Sarcopenia]] [[fr:Sarcopénie]] [[it:Sarcopenia]] [[pt:Sarcopenia]]'
New page wikitext, after the edit (new_wikitext)
'{{Update|date=October 2009}} '''Sarcopenia''' (from the Greek meaning "poverty of flesh") is the degenerative loss of [[skeletal muscle]] mass and strength associated with [[aging]]. Sarcopenia is a component of the [[Frailty syndrome]]. 0.5-1% of loss per year after the age of 25 {{tocright}} ==Markers of sarcopenia== Sarcopenia is characterized first by a decrease in the size of the [[muscle]], which causes weakness and frailty. However, this loss of muscle mass may be caused by different cellular mechanisms than those that cause [[muscle atrophy]]. For example, during sarcopenia, there is a replacement of muscle fibres with [[fat]] and an increase in [[fibrosis]]. == Benefit of exercise== [[Exercise]] and increases in activity have been shown to be beneficial in settings of sarcopenia; exercise even in the very old can increase strength and muscle function. Lack of exercise is currently thought to be a significant risk factor, increasing the likelihood of sarcopenia.<ref>{{cite journal |author=Abate M, Di Iorio A, Di Renzo D, Paganelli R, Saggini R, Abate G |title=Frailty in the elderly: the physical dimension |journal=Eura Medicophys |volume=43 |issue=3 |pages=407–15 |year=2007 |month=September |pmid=17117147 |doi= |url=http://www.minervamedica.it/index2.t?show=R33Y2007N03A0407}}</ref> Not only muscle but the entire musculoskeletal system of muscle, neuromuscular responsiveness, endocrine function, vasocapillary access, tendon, joint, ligament, and bone, depends on regular and lifelong exercise to maintain integrity. The slow attenuation, atrophy, or loss of muscle tissue that medical professionals sometimes describe as sarcopenia (literally, "flesh loss') is currently thought to be the result of cumulative loss of musculoskeletal strength and mass associated with chronic absence of exercise of sufficient intensity or volume. However, even highly trained athletes experience the effects of sarcopenia. It is interesting to note that athletic speed and strength records are generally set by individuals no older than 30 years of age, although some powerlifters and other strength athletes continue to set records into their 50s.{{Citation needed|date=October 2009}} == Fiber-type changes in sarcopenia== Simple [[circumference]] does not provide enough data to determine whether or not an individual is suffering from severe sarcopenia. Sarcopenia is also marked by a decrease in the circumference of distinct types of [[muscle fiber]]s. Skeletal muscle has different fiber-types, which are characterized by expression of distinct [[myosin]] variants. During sarcopenia, there is a decrease in "type 2" fiber circumference ([[Muscle fiber#Type II|Type II]]), but not nearly as much "type I" fiber circumference ([[muscle fiber#Type I|Type I]]). However, we lose both type I and type II muscle fibers (muscle cells) equally as we age (contrary to popular belief that we lose type II more rapidly).{{Citation needed|date=January 2010}} ==Loss of satellite cell function== [[Satellite cells]] are small mononuclear cells that abut the muscle fiber. [[Satellite cell]]s are normally activated upon injury or exercise. These cells then differentiate and fuse into the muscle fiber, helping to maintain its function. One theory is that sarcopenia, is in part casued by a failure in satellite cell activation.{{Citation needed|date=January 2010}} Therefore, the ability to repair damaged muscles or respond to nutritional signals is impaired. ==Loss of anabolic signals== Extreme muscle loss is often a result of both diminishing [[anabolic]] signals, such as [[growth hormone]] and [[testosterone]], and promotion of [[catabolic]] signals, such as pro-inflammatory [[cytokines]].{{Citation needed|date=January 2010}} TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN TOM MARSDEN IS A TWAT!!!!!!!!! ==Sarcopenia as a public-health problem== Due to the lessened physical activity and increased [[longevity]] of industrialized populations, sarcopenia is emerging as a major health concern. Sarcopenia may progress to the extent that an older person may lose his or her ability to live independently. Furthermore, sarcopenia is an important independent predictor of disability in population-based studies, linked to poor balance, gait speed, falls, and fractures. Sarcopenia can be thought of as a muscular analog of [[osteoporosis]], which is loss of bone, also caused by inactivity and counteracted by exercise. The combination of [[osteoporosis]] and sarcopenia results in the significant frailty often seen in the elderly population. == Natural history == Strength losses with ageing for men and women are relatively similar. They are greater for lower than upper extremity muscles. Maximum attainable strength peaks in mid-twenties and declines thereafter. The decline is precipitous after 65 years of age, though few longitudinal studies exist on this topic. A direct assessment of the effects of sarcopenia, even in extremely physically fit individuals, can be seen in the age-related decline in [[Masters athletics (track and field)]] world records of muscle-intensive sports, such as weight lifting. No substance-free, proven Olympic weight-lifting record has been set by any athlete of either sex or any weight class above the age of 31. ((''However, in the non-Olympic sport of powerlifting, many world records in several weight divisions have been accomplished by athletes well into their forties, purportedly, "verified" by the [[International Powerlifting Federation]] to have been accomplished drug-free. However, that this certification carries any weight is doubtful considering that even in highly supervised events such as the Olympics, drug cheating invariably occurs (some of which is detected right away, much of it is not). Furthermore, casting doubt on any records set outside the traditional Olympic athletic system, drug cheating is rampant in professional sports that do not perform random drug testing (e.g. baseball).'')) == Diagnosis == Consensus on clinical diagnosis of sarcopenia has quickly developed over the last decade around the working definition proposed in 1998 by Baumgartner et al. <ref>{{cite journal |author=Baumgartner RN, Koehler KM, Gallagher D, ''et al.'' |title=Epidemiology of sarcopenia among the elderly in New Mexico |journal=Am. J. Epidemiol. |volume=147 |issue=8 |pages=755–63 |year=1998 |month=April |pmid=9554417 |doi= |url=http://aje.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=9554417}}</ref>, which uses a measure of lean body mass as determined by [[Dual energy X-ray absorptiometry]] (DEXA) compared to a normal reference population. His working definition uses a cut point of 2 standard deviations below the mean of lean mass for gender specific healthy young adults. This methodology is attractive for definitive diagnosis in clinical settings as well for several reasons. Primarily, emerging research shows it is predictive of negative outcomes and it is also a method familiar to most clinicians. This later point is especially true for those that treat the geriatric population, given its similarity to the 1996 [[World Health Organization]] (WHO) methodology for definitive diagnosis of [[osteoporosis]], which also uses DEXA, but uses a measure of lean mass rather than bone mineral density (BMD). DEXA is widely used already in clinical settings in develop countries to identify and monitor severity of osteoporosis. And the degree of sarcopenia can be measured using DEXA in patients being evaluated for osteoporosis, at the same time with the same scan, with no added cost or radiation exposure to the patient. Since Baumgartner’s working definition first appeared, some several consensus groups have refined the definition, including the recent joint effort of the European Society on Clinician Nutrition and Metabolism (ESPEN) Special Interest Groups (SIG) on geriatric nutrition and on [[cachexia]]-[[anorexia]] in chronic wasting diseases. Their consensus definition is: <b>1) A low muscle mass, >2 standard deviations below that mean measured in young adults (aged 18–39 years in the 3rd NHANES population) of the same sex and ethnic background, and 2) Low gait speed (e.g. a walking speed below 0.8 m/s in the 4-m walking test). However, it can be replaced by one of the well-established functional tests utilized locally as being part of the comprehensive geriatric assessment.</b><ref>{{cite journal |author= Muscaritoli M, Anker S, Argilés J, ''et al.'' |title= Consensus definition of sarcopenia, cachexia and pre-cachexia: Joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics” |journal= Clinical Nutrition | year=2010 |doi=10.1016/j.clnu.2009.12.004 |url=http://linkinghub.elsevier.com/retrieve/pii/S0261561409002428}}</ref> There remains many opportunities for further refinement of reference populations by ethic groups, and to further correlate of the degrees of severity of sarcopenia to overt declines in functional performance (preferably using verified functional tests), as well as incidence of hospitalization admissions, morbidity and mortality. Work toward this objective has already begun, and the body of research to date clearly points toward severe sarcopenia is predicative of negative outcomes, similar to what already been shown to exist with the [[Frailty syndrome]], as defined by the criteria set forth in 2001 by Fried et al. <ref>{{cite journal |author= Fried LP, Tangen CM, Walston J, ''et al.'' |title= Frailty in Older Adults: Evidence for a Phenotype. |journal= J Gerontol A Biol Sci Med Sci. |year=2001|url= http://www.ncbi.nlm.nih.gov/pubmed/11253156}}</ref> == Management == Primary management of sarcopenia is through the application of a graded exercise program, across both cardiovascular and strength domains, dosed in such a way as to provoke beneficial adaptation without overloading the weakened body.<ref>{{cite journal |author=Taaffe DR |title=Sarcopenia--exercise as a treatment strategy |journal=Aust Fam Physician |volume=35 |issue=3 |pages=130–4 |year=2006 |month=March |pmid=16525526 |doi= |url=http://www.racgp.org.au/afp/200603/3608}}</ref> Possible therapeutic strategies include use of testosterone or anabolic steroids, though long term use of these agents is controversial in men given concerns of prostate symptoms, and essentially contraindicated in women, given concerns of virilization. Other approved medications have been shown to have little to no effect in this setting, including agents such DHEA and human growth hormone. New therapies in clinical development hold great promise in this area, including the Selective Androgen Receptor Modulators (SARMs), as evidenced by recent studies. Nonsteriodal SARMs are of particular interest, given they exhibit significant selectivity between the anabolic effects of testosterone on muscle, but apparently with little to no androgenic effects such as prostate stimulation in men or virilization in women. Nutritional evaluation may also be indicated if malnutrition is suspected, or current nutritional intake is insufficient to maintain adequate total body mass, although increased exercise also increases appetite. Physical activity incorporating resistance training is probably the most effective measure to prevent and treat sarcopenia. An extract from the plant Ginkgo biloba (EGb 761) was shown to reduce the muscle loss in a rat model of sarcopenia (Bidon ''et al''., 2009)<ref>{{cite journal |author=Bidon C, Lachuer J, Molgó J, Wierinckx A, de la Porte S, et al. |year=2009 |title=The Extract of Ginkgo biloba EGb 761 Reactivates a Juvenile Profile in the Skeletal Muscle of Sarcopenic Rats by Transcriptional Reprogramming. |journal=PLoS ONE 4(11): |url=http://www.plosone.org/article/info:doi%2F10.1371%2Fjournal.pone.0007998 |doi=doi:10.1371/journal.pone.0007998}}</ref>. ==See also== * [[Sarcopenic obesity]] == References == {{reflist}} *{{cite journal |author=Roubenoff R |title=Physical activity, inflammation, and muscle loss |journal=Nutr. Rev. |volume=65 |issue=12 Pt 2 |pages=S208–12 |year=2007 |month=December |pmid=18240550 |doi= 10.1111/j.1753-4887.2007.tb00364.x|url=http://openurl.ingenta.com/content/nlm?genre=article&issn=0029-6643&volume=65&issue=12%20Pt%202&spage=S208&aulast=Roubenoff}} *{{cite journal |author=Lynch GS |title=Tackling Australia's future health problems: developing strategies to combat sarcopenia—age-related muscle wasting and weakness |journal=Intern Med J |volume=34 |issue=5 |pages=294–6 |year=2004 |month=May |pmid=15151679 |doi=10.1111/j.1444-0903.2004.00568.x |url=}} *{{cite journal |author=Edström E, Ulfhake B |title=Sarcopenia is not due to lack of regenerative drive in senescent skeletal muscle |journal=Aging Cell |volume=4 |issue=2 |pages=65–77 |year=2005 |month=April |pmid=15771610 |doi=10.1111/j.1474-9728.2005.00145.x |url=}} *{{cite journal |author=Fujita S, Volpi E |title=Amino acids and muscle loss with aging |journal=J. Nutr. |volume=136 |issue=1 Suppl |pages=277S–80S |year=2006 |month=January |pmid=16365098 |doi= |url=http://jn.nutrition.org/cgi/pmidlookup?view=long&pmid=16365098}} *{{cite journal |last=Visser |first=Marjolein |authorlink= |coauthors=Deeg D, Lips P |year=2003 |month= |title=Low vitamin D and high parathyroid hormone levels as determinants of loss of muscle strength and muscle mass (sarcopenia) |journal=J. Clin. Endocrinol. Metab. |volume=88 |issue=12 |pages=5766–5772 |id= |url=http://cat.inist.fr/?aModele=afficheN&cpsidt=15356420 |accessdate= 2007-11-06 |quote=|doi=10.1210/jc.2003-030604|pmid=14671166 }} [[Category:Aging-associated diseases]] [[Category:Geriatrics]] [[Category:Rehabilitation medicine]] [[de:Sarkopenie]] [[es:Sarcopenia]] [[fr:Sarcopénie]] [[it:Sarcopenia]] [[pt:Sarcopenia]]'
Whether or not the change was made through a Tor exit node (tor_exit_node)
0
Unix timestamp of change (timestamp)
1273238940