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1 hip ratio to 1.37 [95% CI: 1.33 to 1.42] for lean body mass).
2 ted in published studies with an increase in lean body mass.
3  secondary to an effect on fat as opposed to lean body mass.
4 lin-like growth factor-1, and enhancement of lean body mass.
5 position by reducing fat mass and increasing lean body mass.
6 6), as measured at our institution and using lean body mass.
7 nsufficient in protein could lead to loss of lean body mass.
8 ose homeostasis, decreased fat and increased lean body mass.
9 ed rate of fatty acid, beta-oxidation, and a lean body mass.
10 no significant difference in percent fat and lean body mass.
11 ic cancer patients for effects on weight and lean body mass.
12 ntake, increased metabolic rate, and loss of lean body mass.
13 f negative energy balance but does not alter lean body mass.
14 re observed in change in lumbar spine BMD or lean body mass.
15  strength and physical skills, and increased lean body mass.
16 sult in low serum protein levels and loss of lean body mass.
17 c response, with protein wasting and loss of lean body mass.
18 ugh BMI does not distinguish between fat and lean body mass.
19 lts in increased fat mass without changes in lean body mass.
20 II) subjects is in excess of the increase in lean body mass.
21 ite and an increase in metabolism of fat and lean body mass.
22  dieting because the latter reduces maternal lean body mass.
23 biquitin-proteasome pathway leads to reduced lean body mass.
24 rences in liver volume and/or differences in lean body mass.
25 s when these measurements were corrected for lean body mass.
26 even of eight women gained body fat and lost lean body mass.
27 d with negative nitrogen balance and loss of lean body mass.
28 ciated with significant increases in BMC and lean body mass.
29 ar VCAN, ADAMTSL3, and IRS1 for appendicular lean body mass.
30  difference in both skeletal muscle mass and lean body mass.
31 se experience weight loss, including loss of lean body mass.
32 anthropometric measures after adjustment for lean body mass.
33 d triglycerides, and decreased proportion of lean body mass.
34  SNS activity, heart rate, blood pressure or lean body mass.
35 t-free mass (-0.6 kg and 2.0 kg; P = 0.036), lean body mass (0.0 kg and 1.9 kg; P = 0.041), and muscl
36  weight (0.8 +/- 2.4 and 0.7 +/- 2.4 kg) and lean body mass (0.3 +/- 1.4 and 0.3 +/- 1.5 kg) did not
37 .1 +/- 0.3 v +2.3 +/- 0.7 kg; P =.002/0.04); lean body mass (+0.8 +/- 0.2 v -0.4 +/- 0.3 kg; P =.02/0
38  CI -2.9 to -0.7, p = 0.0016), and increased lean body mass (1.5 kg, 95% CI 0.9-2.1, p < 0.001).
39 0.28 +/- 0.02 to 0.20 +/- 0.02 mmol FFA x kg lean body mass(-1) x h(-1); P < 0.002), as did the rate
40  overall lean body mass increased (change in lean body mass, 2.1 kg [CI, 1.3 to 2.9]) (P < 0.001), an
41 n body mass, 25 g glucose, 1 mmol glycine/kg lean body mass + 25 g glucose, or water only, given in r
42 iod after the ingestion of 1 mmol glycine/kg lean body mass, 25 g glucose, 1 mmol glycine/kg lean bod
43 ease +/- SD, 1.6 +/- 3.7 kg [P < 0.001]) and lean body mass (3.0 +/- 3.0 kg [P < 0.001]), accompanied
44 8 [13.6] vs 57.3 [7.2] g; p=0.0152) and less lean body mass (450.1 [9.6] vs 491.9 [11.7] g; p=0.0120)
45 the testosterone analog oxandrolone improves lean body mass accretion and bone mineral content and th
46 ntral fat, prevented bone loss, and improved lean body mass accretion.
47                                          For lean body mass-adjusted SUV(peak), the wCVs appeared sim
48 ed to test whether LY increases appendicular lean body mass (aLBM) and improves physical performance
49 r if the processes that adapt kidney mass to lean body mass also mediate renal hypertrophy following
50 s associated with breathing difficulties and lean body mass, although EDCs concentrations were low.
51 trophy subjects after routine adjustment for lean body mass and after adjustment for each organ-tissu
52  both patients with CF and control subjects, lean body mass and arm muscle area significantly correla
53 (P = 0.011 for body weight and P < 0.001 for lean body mass and body fat).
54 ng myostatin, can prevent or restore loss of lean body mass and body weight in simian immunodeficienc
55                                              Lean body mass and bone mineral content did not change.
56                                              Lean body mass and bone mineral density at the hip decre
57 h factor therapy had significantly increased lean body mass and decreased fat mass by 6 weeks, but th
58         The significant (P<.05) increases in lean body mass and decreases in fat mass were also not d
59  oxidation was significantly correlated with lean body mass and diet.
60 et-supplemented uremic mice, which lost both lean body mass and fat mass and had an increase in basal
61                                        Their lean body mass and fat mass were 39.4 +/- 2.7 kg and 16.
62 oducing national reference distributions for lean body mass and fat mass, however, is currently limit
63 , elderly and young participants matched for lean body mass and fat mass.
64 KE group compared to PF after adjustment for lean body mass and fat-mass ( P = 0.001 and 0.007, respe
65 nome-wide association studies for whole body lean body mass and find five novel genetic loci to be si
66 B11, VCAN, ADAMTSL3, IRS1, and FTO for total lean body mass and for three single-nucleotide polymorph
67 n of healthy body weight and preservation of lean body mass and functional ability with age.
68 eight gain or loss women were likely to lose lean body mass and gain fat mass during treatment for br
69 efficacy endpoints were the median change in lean body mass and handgrip strength over 12 weeks and w
70 ologic testosterone administration increases lean body mass and improves quality of life among androg
71  an anabolic steroid that attenuates loss of lean body mass and improves wound healing in burn patien
72 ) individuals from 33 cohorts for whole body lean body mass and in 45,090 (42,360 of European ancestr
73         The peri(-/-) animals have a greater lean body mass and increased metabolic rate but they als
74  are particularly susceptible to the loss of lean body mass and its attendant increased morbidity and
75 ines was found to have beneficial effects on lean body mass and leg power in elderly men.
76 body proteolysis suggesting that the loss of lean body mass and muscle wasting in insulinopenia is re
77 tion in whom preservation and restoration of lean body mass and neuromuscular function are crucial.
78 ange since 25 years of age, body mass index, lean body mass and percent body fat, and nonspine fractu
79 ptive glomerular changes driven by increased lean body mass and potential direct nephrotoxic effects
80 al energy expenditure, reductions in fat and lean body mass and prevention from diet-induced obesity.
81 els for the purposes of increasing strength, lean body mass and sexual performance.
82 , and was a composite of stable or increased lean body mass and stability or improvement in two of th
83 ome characterized by the progressive loss of lean body mass and systemic inflammation.
84 d increased serum levels of WISP2, increased lean body mass and whole body energy expenditure, hyperp
85  finding does not appear to be a function of lean body mass and, although modified by certain patient
86 astating effects of the loss of body weight, lean body mass, and adipose tissue were recognized as co
87                                      Weight, lean body mass, and body surface area in the denominator
88 ection and after normalizing to body weight, lean body mass, and body surface area, and simplified me
89                            Weight; body fat, lean body mass, and bone mineral content (measured by du
90 ical impedance-derived measures of fat mass, lean body mass, and fat percentage.
91                               Cellular mass, lean body mass, and fat were assessed "directly" by tota
92 ratory fitness, functional task performance, lean body mass, and fatigue, with inconsistent effects o
93 9%) increased food intake, body weight gain, lean body mass, and gastrocnemius muscle mass as compare
94 elated peptide, resist tumor-induced loss of lean body mass, and maintain normal circadian activity p
95  density (BMD), mental health score, fat and lean body mass, and safety outcomes, i.e., fractures, fa
96 t with growth hormone increases body weight, lean body mass, and treadmill work output and appears to
97     Low values of serum proteins and loss of lean body mass are commonly found in patients with chron
98  to the profound catabolic state and loss of lean body mass associated with the AIDS wasting syndrome
99  16/17 y; with percentage fat and percentage lean body mass at age 16/17 y; and with a metabolic synd
100 1)) after adjustment for age, sex, race, and lean body mass (beta=1.29; false discovery rate q=5.3x10
101  body fat mass without altering food intake, lean body mass, body temperature, or biochemical and hae
102                         Oxandrolone improved lean body mass, bone mineral content and muscle strength
103 ere burn, oxandrolone significantly improves lean body mass, bone mineral content, and muscle strengt
104                              Height, weight, lean body mass, bone mineral content, cardiac function,
105         GH treatment increased femur BMD and lean body mass but decreased the % fat measured by DXA i
106 improved if adjusted by body surface area or lean body mass but was improved if adjusted by height (r
107 n affected energy expenditure and storage of lean body mass, but not body fat storage.
108           Anamorelin significantly increased lean body mass, but not handgrip, strength in patients w
109 ith baseline, significant increases in total lean body mass by day 113 or end of study were noted in
110                          Primary outcome was lean body mass by dual-energy x-ray absorptiometry over
111                                          The lean body mass (by dual-energy X-ray absorptiometry) inc
112 ion, percentage body fat, visceral fat mass, lean body mass, cardiopulmonary fitness, physical activi
113  (TNF) and IL-1, induce anorexia and loss of lean body mass, common manifestations of acute and chron
114 enic compounds with undoubted effects on the lean body mass compartment.
115 fication of proteins which determine fat and lean body mass composition is critical to better underst
116 dations during energy deficit (ED) preserves lean body mass, concerns have been raised regarding the
117 n have greater clearance of ethanol per unit lean body mass, confirming previous oral alcohol adminis
118                                              Lean body mass, consisting mostly of skeletal muscle, is
119 methods including percentage change in SUVs, lean body mass-corrected (SUL) SULpeak, SULmax, and tota
120                                              Lean body mass correction of the SUVmax did not change a
121 ated with height, total or central body fat, lean body mass, current smoking, physical activity, or c
122  placebo, weight (increase, 0.1 +/- 3.1 kg), lean body mass (decrease, 0.1 +/- 2.0 kg), and body fat
123 s. males: -0.05+/-0.007%) and an increase in lean body mass (Delta females: 5+/-4% vs. Delta males: -
124                                              Lean body mass determined by DXA was highly correlated w
125 ice; however, the fat mass was decreased and lean body mass did not change.
126 yielded similar results, and adjustments for lean body mass did not substantially alter the findings.
127                 Prior to and after bed rest, lean body mass (dual-energy X-ray absorptiometry) and qu
128                          Conclusions: Higher lean body mass during childhood and adolescence is consi
129 es skeletal muscle hypertrophy and increases lean body mass, effects not previously reported with sma
130 morphisms were significantly associated with lean body mass either genome wide (p < 5 x 10(-8)) or su
131                                     Juvenile lean body mass, estimated using urinary creatinine excre
132 male Panx1(Deltaot) mice exhibited increased lean body mass, even though pannexin levels in skeletal
133 thermore, NBI-12i-treated uremic mice gained lean body mass, fat mass, and had a lower basal metaboli
134     The primary endpoint was change in total lean body mass from baseline, assessed by dual-energy x-
135 duced a microbiota-dependent augmentation of lean body mass gain, changed bone morphology, and altere
136 ry taxa in recipient animals correlated with lean body mass gain; liver, muscle, and brain metabolism
137                                  At 6 weeks, lean body mass had increased and total fat mass had decr
138                                     Although lean body mass has a high heritability, studies evaluati
139                                      Fat and lean body mass have important implications for health an
140 s were body mass index, body fat percentage, lean body mass, high-density lipoprotein cholesterol, lo
141 ation remained substantial when adjusted for lean body mass (highest HR: 1.05 [95% CI: 1.01 to 1.10]
142 accumulate relatively more body fat and less lean body mass, ie, muscle and bone.
143 ood and skeletal muscle ammonia, increase in lean body mass, improved grip strength, higher skeletal
144  week, which will promote the maintenance of lean body mass, improvements in muscular strength and en
145 ely correlated to body weight, fat mass, and lean body mass in adolescent, perimenopausal, and elderl
146 n II (AngII) could contribute to the loss of lean body mass in chronic kidney disease, but the mechan
147 dy weight, muscle mass, muscle strength, and lean body mass in HIV-infected men with weight loss and
148 rotein supplement did not increase weight or lean body mass in HIV-positive subjects who were eating
149 nds, significantly increases strength and/or lean body mass in humans by increasing testosterone leve
150 ate with inflammation and predict changes in lean body mass in patients with CKD, and activation of t
151 body mass increased in the PRO group whereas lean body mass in the CON group remained stable during t
152 n greater relative increases in both fat and lean body mass in the undernourished rats when compared
153  -2.1 kg [95% CI, -2.8 to -1.35] and overall lean body mass increased (change in lean body mass, 2.1
154 (from 31.9% +/- 6.5% to 28.3% +/- 7.0%), and lean body mass increased (from 59.0 +/- 8.5 kg to 61.5 +
155                                              Lean body mass increased at a steeper rate in males (P<0
156                                      Average lean body mass increased by 2.3 kg (P = .004) and 2.6 kg
157                               Over 12 weeks, lean body mass increased in 38 patients in the anamoreli
158                                              Lean body mass increased in growth hormone recipients co
159                               Over 12 weeks, lean body mass increased in patients assigned to anamore
160                                              Lean body mass increased in the PRO group whereas lean b
161                                              Lean body mass increased significantly in patients given
162                   The adjustment of PkVO2 to lean body mass increases the prognostic value of cardiop
163                                        Seven lean (body mass index < 25 kg/m(2)), young, sedentary IR
164 sk associated with SHBG rs6259 was found for lean (body mass index <23) postmenopausal minor allele c
165                                          Ten lean (body mass index, 19-25 kg/m(2)), healthy Caucasian
166 eference curves for fat mass index (FMI) and lean body mass index (LBMI) and evaluate the effects of
167                                       Higher lean body mass index trajectories were associated with h
168 ase in both sexes (e.g., boys in the highest lean body mass index trajectory had on average a 0.62 L
169       Methods: Sex-specific body mass index, lean body mass index, and fat mass index trajectories we
170           Both men and women were remarkably lean: body mass index = 21.3 (3.6) and 23.0 (5.2) kg/m2,
171                                              Lean body mass is an important predictor of survival and
172                                      Loss of lean body mass is common in patients with acute or chron
173 l anabolic strategies to reverse the loss of lean body mass is of critical importance to increase sur
174 dence suggests that growth hormone increases lean body mass, it may not improve strength; in addition
175 (body mass index, body fat (%), weight (kg), lean body mass (kg), and fat mass (kg)) were significant
176 % +/- 0.007 nmol/100 mL leg/min) and loss of lean body mass (LBM) (-4.1% +/- 1.9%); P < 0.05.
177 s for estimation of total body fat (TBF) and lean body mass (LBM) (n = 10,525) were followed for 13.6
178 stration to elderly individuals can increase lean body mass (LBM) and decrease fat, but interactive e
179                          It is not clear how lean body mass (LBM) and fat mass (FM) compare in their
180 e associations of early nutrition with adult lean body mass (LBM) and muscle strength in a birth coho
181 ) was assessed by hyperinsulinemic clamp and lean body mass (LBM) and total body fat were assessed by
182 rolled RCT was powered on a 5% difference in lean body mass (LBM) at 1 month.
183 omputerized scheme that evaluates whole-body lean body mass (LBM) based on CT data from limited-whole
184 ined the effect of body mass index (BMI) and lean body mass (LBM) depletion on handgrip (HG) force an
185 rther aim was to estimate a patient-specific lean body mass (LBM) from these MR-AC data.
186                                              Lean body mass (LBM) is a complex trait for human health
187          Primary outcomes included change in lean body mass (LBM) measured by dual-energy x-ray absor
188                           A profound loss of lean body mass (LBM) occurred in both groups during the
189 lness of creatinine excretion as an index of lean body mass (LBM) or muscle mass in healthy men and w
190                                 Repletion of lean body mass (LBM) that patients lose in human immunod
191 dependent contributions of fat mass (FM) and lean body mass (LBM) to body weight, which vary accordin
192 al status on serum ferritin, after change in lean body mass (LBM) was controlled for, were evaluated
193 ne-third of that of 18 AL (P < 0.001), while lean body mass (LBM) was unchanged.
194  +/- 2, 17 +/- 2, and 22 +/- 2 pmol x kg(-1) lean body mass (LBM) x min(-1) (P < 0.05, days 5 and 10
195 ion of EE by either total body mass (TBM) or lean body mass (LBM), 2) compared the independent contri
196 ine, p < 0.01); after adjustment for age and lean body mass (LBM), DES excretion in rapid decliners w
197 ptake lean body mass (SUL), calculated using lean body mass (LBM), is essential for the semiquantific
198 e during an energy deficit helps to preserve lean body mass (LBM), particularly when combined with ex
199                                              Lean body mass (LBM), skeletal muscle index (SMI), and f
200      Control patients lost 8 +/- 1% of their lean body mass (LBM), whereas oxandrolone-treated patien
201 take at the RDA or a high amount [1.1 g . kg lean body mass (LBM)-1 . d-1 or >2.1 g . kg LBM-1 . d-1,
202 ith HIV lipodystrophy [33.2 +/- 0.27 kcal/kg lean body mass (LBM)] than for both HIV-infected and hea
203 able content of the diet with the percentage lean body mass (%LBM) or change in %LBM in older subject
204 tandardized uptake value (SUV) normalized by lean body mass ([LBM] SUL) is becoming a popular metric
205 iometry-assessed body composition (including lean body mass [LBM], appendicular lean mass [ALM], and
206 ngs provide new insight into the genetics of lean body mass.Lean body mass is a highly heritable trai
207 severity score, lower body mass index, lower lean body mass, less participation in organized sports,
208 ate and contribute to disrupted homeostasis, lean body mass loss, and deteriorated performance in ind
209  in the tumor-bearing mice and reverse their lean body mass loss.
210                              When indexed to lean body mass, LV growth in the II subjects was abolish
211 milligrams of glucose uptake per kilogram of lean body mass (M(lbm)) per minute).
212 mal glucose tolerance and 12 age-, sex-, and lean body mass-matched healthy control subjects underwen
213        Differences in bone density and trunk lean body mass may account for some of these measured di
214                         In addition, greater lean body mass may be a cause.
215          Group 3 had the greatest changes in lean body mass (mean +/- SE, 3.2 +/- 0.59 kg; P < 0.001)
216                                      Fat and lean body mass measured by dual-energy x-ray absorptiome
217                   The use of <19 ml O2/kg of lean body mass/min as a cutoff in PkVO2 should be used f
218 owed that a nodal standardized uptake value (lean body mass) more than 1.8 had a positive predictive
219   Secondary clinical end points were weight, lean body mass, muscle mass, exercise functional capacit
220 onstrated progressive decreases in body fat, lean body mass, muscle power, and nitrogen balance and a
221 n = 38,292) and appendicular (arms and legs) lean body mass (n = 28,330) measured using dual energy X
222  [95% CI, 165-289 kcal/d]) and body protein (lean body mass) (normal protein diet: 2.87 kg [95% CI, 2
223       The highest correlation between Ki and lean body mass-normalized SUV was found for the interval
224                Consistent with the increased lean body mass of s/s animals, locomotor activity and ac
225                     To determine whether the lean body mass of well-nourished women was mobilized to
226 ssed by the change in SUVpeak, normalized to lean body mass, of the most (18)F-FDG-avid lesion (PERCI
227 h the highest average SUL [SUV normalized to lean body mass]) of up to 5 lesions according to PERCIST
228 h as the "constant" hydration coefficient of lean body mass or the "constant" density of fat-free mas
229 ixel value in the numerator and with weight, lean body mass, or body surface area in the denominator.
230        Water, 25 g glucose, 1 mmol lysine/kg lean body mass, or lysine plus glucose was given on sepa
231 mble chronic inflammatory disease [decreased lean body mass, osteopenia, low-grade anemia, decreased
232 n excess of maternal nitrogen in the form of lean body mass over that deposited in the fetus and the
233 ificantly increased skeletal muscle mass and lean body mass over time.
234 o eat (P = 0.356; SED: 3.7), preservation of lean body mass (P = 0.334; SED: 0.2), and loss of percen
235 ic rate (PCR), transferrin, cholesterol, and lean body mass per height.
236 5.4 [SE 4.0] vs 60.6 [7.2] micromoles per kg lean body mass per min; p=0.023) owing to a reduction in
237 -SD] change, 1.5 +/- 2.1 mg of glucose/kg of lean body mass per minute vs. -0.4 +/- 1.6 mg/kg per min
238 2(+/-) and ROCK2(+/KD) mouse models showed a lean body mass phenotype during aging, associated with i
239  adjusted model (which included age, age(2), lean body mass, pulse rate, pulse pressure, hormone-repl
240 ), which was attenuated after adjustment for lean body mass (r = 0.25, P = 0.08).
241 tively correlated with the change in percent lean body mass (r = 0.32; P = .003) and the change in th
242 related closely with body size, particularly lean body mass (r=.69, P<.0001) and systolic (r=.35, P<.
243 eater antecedent weight loss and a lower fat/lean body mass ratio.
244 on can be explained solely by a reduction in lean body mass remains controversial.
245 = 0.60 for SUV normalized to body weight and lean body mass, respectively), most likely because of de
246 nintentional loss of body weight and loss of lean body mass (sarcopenia).
247 nt feeding and fat mass after adjustment for lean body mass, sex, birth weight, maternal obesity, rac
248                                              Lean body mass significantly increased in the GHRH group
249                                 Body weight, lean body mass, SIV titers, and somatometric measurement
250                            SUV corrected for lean body mass (SUL and SULpeak) were obtained.
251 mum standardized uptake values corrected for lean body mass (SUL(max)) on (18)F-FDG PET predicted pat
252 gnificant decrease in SUV(max) corrected for lean body mass (SUL(max)) on images obtained after MSG a
253                      SUV(max) normalized for lean body mass (SUL(max)) was measured at the primary tu
254                  Maximum SUVs normalized for lean body mass (SUL(max)) were measured in all scans.
255 02) [standardized uptake value corrected for lean body mass (SUL) = 5.42 +/- 2.77, 8.04 +/-3.25 and 1
256 e value calculated on the basis of predicted lean body mass (SUL) on these images, and we calculated
257 ed uptake value (SUV) corrected by predicted lean body mass (SUL) was calculated and compared.
258     Standardized uptake values corrected for lean body mass (SUL) were determined for several normal
259                      The standardized uptake lean body mass (SUL), calculated using lean body mass (L
260 RCIST5 (analyzing the peak SUV normalized by lean body mass [SUL(peak)] of 1 or up to 5 lesions), imP
261 mum standardized uptake values corrected for lean body mass (SULmax) on [(18)F]fluorodeoxyglucose pos
262 ts; SUV normalized to body weight (SUV(BW)), lean body mass (SUV(LBM)), whole blood (SUV(WB)), parent
263 ke, standardized uptake value normalized for lean body mass (SUV-lean) was measured 1 h after FDG inj
264  weight (SUVbw), ideal body weight (SUVibw), lean body mass (SUVlbm), and body surface area (SUVbsa)
265     The standard uptake value normalized for lean body mass (SUVlean) in tumors was measured 50-60 mi
266                          The mean values for lean body mass, Tanner stage, height-for-age Z score and
267 d patients, leading to a progressive loss of lean body mass that was not prevented by nutritional sup
268                   To further keep erosion of lean body mass to a minimum, administration of anabolic
269 ain further insight into the relation of the lean body mass to REE and to better understand differenc
270           SURs calculated with weight versus lean body mass versus body surface area in the denominat
271 t of the 9 measures left the association for lean body mass virtually unchanged (lowest HR: 1.33 [95%
272                         SUVmax corrected for lean body mass was 0.4-12.1 (mean +/- SD, 2.1 +/- 2.0).
273                                              Lean body mass was 42% greater in men than in women.
274 stic was associated with BMD loss, but lower lean body mass was associated with greater BMD loss at b
275  were not affected; whereas no difference in lean body mass was detected in male mice.
276  However, after developing HF, loss of total lean body mass was disproportionate; men with HF lost 65
277                                    Change in lean body mass was greater in those treated with growth
278                                              Lean body mass was maintained in women who exclusively b
279                                2) Erosion of lean body mass was not attenuated by increased caloric b
280 +/-0.6) and fat mass (FM: -2.3+/-1.5), while lean body mass was preserved (LBM: 0.0+/-0.7).
281                                              Lean body mass was preserved throughout lactation in wel
282 y) subjects from 25 cohorts for appendicular lean body mass was successful for five single-nucleotide
283                                              Lean body mass was the predominant anthropometric risk f
284     Chronic MFP dosing for 25 days increased lean body mass, weight gain, and bone mineral density si
285 nation rate and liver volume per kilogram of lean body mass were 33% and 38% higher in women than in
286 vity levels, energy expenditure (Vo(2)), and lean body mass were all better sustained with age in rat
287             Standardized uptake values using lean body mass were determined over areas of interest.
288 fferent between groups at year 2; weight and lean body mass were greater at years 4 and 6, and fat ma
289                  By year 4, weight, BMI, and lean body mass were greater in the high-risk than in the
290 lute measures (total fat, abdominal fat, and lean body mass) were secondary outcomes.
291 eostatic responses allowing them to maintain lean body mass when dietary protein intake is restricted
292 compensatory mechanisms designed to conserve lean body mass when dietary protein intake is restricted
293 explanation for death after the depletion of lean body mass when some body fat is still available to
294 scle protein net balance and preservation of lean body mass, which are associated with shortened hosp
295    30 patients were assessable for change in lean body mass, which increased by a mean of 1.02 kg (SD
296 rexia, negative nitrogen balance and loss of lean body mass will ensue.
297 tion, the association between higher BMI and lean body mass with natriuretic peptides may be mediated
298                              Change in total lean body mass within the placebo group (median 0.02 kg,
299 e of enobosarm might lead to improvements in lean body mass, without the toxic effects associated wit
300 stment of peak oxygen consumption (PkVO2) to lean body mass would yield a more accurate discriminator

 
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