Validation of whole-body magnetic resonance spectroscopy as a tool to assess murine body composition

被引:42
作者
Mystkowski, P
Shankland, E
Schreyer, SA
LeBouef, RC
Schwartz, RS
Cummings, DE
Kushmerick, M
Schwartz, MW
机构
[1] Univ Washington, Harborview Med Ctr, Div Endocrinol Metab, Dept Internal Med, Seattle, WA 98104 USA
[2] VA Puget Sound Hlth Care Syst, Seattle, WA USA
[3] Univ Washington, Dept Pathobiol & Nutr, Seattle, WA 98195 USA
[4] VA Puget Sound Hlth Care Syst, Seattle, WA USA
[5] Univ Washington, Dept Radiol, Seattle, WA 98195 USA
[6] Univ Colorado, Hlth Sci Ctr, Dept Internal Med, Denver, CO USA
关键词
proton spectroscopy; obesity; body composition; mice;
D O I
10.1038/sj.ijo.0801231
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE: To evaluate proton magnetic resonance spectroscopy (MRS) as a tool for the non-invasive assessment of murine body composition. DESIGN: Twenty C57/BL6 male mice with a wide range of body adiposities underwent both pre- and post-mortem whole-body MRS to assess body composition. MRS measures were compared to the results obtained by chemical carcass analysis, the current 'gold standard' for determination of body composition. MEASUREMENTS: Areas under the curve (AUC) for lipid and water peaks of whole body MRS spectra (AUC(lipid) and AUC(H2O), respectively) were used to determine percentages of body fat (%FAT(MRS)) and fat free mass by MRS (%FFMMRS) Total body fat, total body water, fat free mass, and total lean mass were determined by chloroform/methanol extraction of lipid from dessicated whole carcass and compared to MRS measures (%FAT(MRS), %FFMMRS, AUC(lipid), and AUC(H2O)) The variability of the MRS technique was assessed by determining the coefficients of variation (COV) associated with %FAT(MRS), AUC(lipid), and AUC(H2O) for mice of three different adiposities. RESULTS: %FAT(MRS) in live mice was highly correlated with body fat percentage (r = 0.994, P < 0.001) and total body fat (r = 0.980, P < 0.001) derived from chemical carcass analysis over a broad range of adiposities (7-48% body fat content by carcass analysis). There was no difference in %FAT(MRS) measured pre- vs post-mortem (r = 1.00, P < 0.001). AUC(lipid) was highly correlated with chemically derived total fat mass (r = 0.996, P < 0.001) and body fat percentage (r = 0.981, P < 0.001), while %FFMMRS was strongly correlated to chemical determinations of percentage body water (r = 0.994, P < 0.001), percentage fat free mass (r = 0.993, P < 0.001), and percentage lean mass (r = 0.792, P < 0.001). AUC(H2O) was strongly associated with carcass analysis determinations of total body water (r = 0.964, P < 0.001), total fat free mass (r = 0.953, P < 0.001), and total lean mass (r = 0.89, P < 0.001). In mice of 6%, 12%, and 43% body fat, COVs determined for %FAT(MRS) and AUC(lipid) were less than 10%. The COVs for AUC(H2O) were less than 2%. CONCLUSIONS: MRS provides precise, accurate, rapid, and non-invasive measures of body fat, body water, fat free mass, and lean mass in living mice with a broad range of adiposities.
引用
收藏
页码:719 / 724
页数:6
相关论文
共 22 条
[11]  
NAGY TR, 1999, OBES RES S, V7, pS27
[12]   BIOLOGICAL H-1-NMR SPECTROSCOPY [J].
PETROFF, OAC .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1988, 90 (02) :249-260
[13]   Measurement of body composition: Applications in hormone research [J].
Pierson, RN ;
Wang, J ;
Thornton, JC .
HORMONE RESEARCH, 1997, 48 :56-62
[14]   ESTIMATION OF BODY-FAT IN NORMAL AND OBESE MICE [J].
ROGERS, P ;
WEBB, GP .
BRITISH JOURNAL OF NUTRITION, 1980, 43 (01) :83-93
[15]   ADIPOSE-TISSUE VOLUME MEASURED BY MAGNETIC-RESONANCE-IMAGING AND COMPUTERIZED-TOMOGRAPHY IN RATS [J].
ROSS, R ;
LEGER, L ;
GUARDO, R ;
DEGUISE, J ;
PIKE, BG .
JOURNAL OF APPLIED PHYSIOLOGY, 1991, 70 (05) :2164-2172
[16]  
STEIN DT, 1995, INT J OBESITY, V19, P804
[17]   A frameshift mutation in human MC4R is associated with a dominant form of obesity [J].
Vaisse, C ;
Clement, K ;
Guy-Grand, B ;
Froguel, P .
NATURE GENETICS, 1998, 20 (02) :113-114
[18]  
WEIGLE DS, 1997, SCI MED MAY, P38
[19]   Nuclear magnetic resonance spectroscopy of skeletal muscle and muscle proteins [J].
Yamada, T ;
Sugi, H .
JAPANESE JOURNAL OF PHYSIOLOGY, 1996, 46 (03) :201-213
[20]  
YOSHIKAWA K, 1980, PHYSIOL CHEM PHYS M, V12, P515