Investigation of skeletal muscle quantity and quality in end-stage renal disease

被引:84
作者
Cheema, Birinder [1 ,3 ]
Abas, Haifa [1 ]
Smith, Benjamin [1 ]
O'Sullivan, Anthony J. [4 ]
Chan, Maria [5 ]
Patwardhan, Aditi [8 ]
Kelly, John [6 ]
Gillin, Adrian [7 ]
Pang, Glen [5 ]
Lloyd, Brad [1 ]
Berger, Klaus [10 ]
Baune, Bernhard T. [9 ]
Singh, Maria Fiatarone [1 ,2 ,11 ]
机构
[1] Univ Sydney, Exercise Hlth & Performance Res Grp, Sydney, NSW 2006, Australia
[2] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[3] Univ Western Sydney, Sch Biomed & Hlth Sci, Sydney, NSW, Australia
[4] Univ New S Wales, Dept Med, Sydney, NSW, Australia
[5] St George Hosp, Dept Nutr & Dietet, Sydney, NSW, Australia
[6] St George Hosp, Dept Renal Med, Sydney, NSW, Australia
[7] Royal Prince Alfred Hosp, Dept Renal Med, Sydney, NSW, Australia
[8] Royal Prince Alfred Hosp, Dept Nutr & Dietet, Sydney, NSW, Australia
[9] James Cook Univ, Sch Med & Dent, Douglas, Qld, Australia
[10] Univ Munster, Inst Epidemiol & Social Med, Munster, Germany
[11] Tufts Univ, Hebrew SeniorLife & Jean Mayer USDA Human Nutr Ct, Boston, MA 02111 USA
基金
英国医学研究理事会;
关键词
attenuation; cytokines; diabetes; insulin resistance; obesity; quality of life; CHRONIC-HEMODIALYSIS PATIENTS; TYPE-2; DIABETES-MELLITUS; INSULIN-RESISTANCE; CONTROLLED-TRIAL; KIDNEY-DISEASE; CARDIOVASCULAR MORTALITY; PROGRESSIVE EXERCISE; CALORIC RESTRICTION; PHYSICAL-ACTIVITY; BODY-COMPOSITION;
D O I
10.1111/j.1440-1797.2009.01261.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Aim: A more precise understanding of the aetiology and sequelae of muscle wasting in end-stage renal disease (ESRD) is required for the development of effective interventions to target this pathology. Methods: We investigated 49 patients with ESRD (62.6 +/- 14.2 years, 0.3-16.7 years on haemodialysis). Thigh muscle cross-sectional area (CSA), intramuscular lipid and intermuscular adipose tissue (IMAT) were measured via computed tomography as indices of muscle quantity (i.e. CSA) and quality (i.e. intramuscular lipid and IMAT). Additional health and clinical measures were investigated to determine associations with these variables. Results: Age, energy intake, disease burden, pro-inflammatory cytokines, nutritional status, strength and functioning were related to muscle quantity and quality. Potential aetiological factors entered into forward stepwise regression models indicated that hypoalbuminaemia and lower body mass index accounted significantly and independently for 32% of the variance in muscle CSA (r = 0.56, P < 0.001), while older age and interleukin-8 accounted for 41% of the variance in intramuscular lipid (r = 0.64, P < 0.001) and body mass index accounted for 45% of the variance in IMAT (r = 0.67, P < 0.001). Stepwise regression models revealed that intramuscular lipid was independently predictive of habitual gait velocity and 6 min walk distance, while CSA was independently predictive of maximal isometric strength (P < 0.05). Conclusion: Ageing, poor nutritional status and elevated interleukin-8 are factors potentially contributing to the loss of muscle quality and quantity in ESRD. These deficits can predict functional impairments, with intramuscular lipid accumulation most closely related to decline of submaximal musculoskeletal performance (walking), and low muscle CSA most closely related to decline of maximal performance (peak isometric strength).
引用
收藏
页码:454 / 463
页数:10
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