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1                                              BMI at birth was inversely associated with HT; c-BMI fro
2                                              BMI over 25 kg/m(2), diabetes, past and current smoking,
3                                              BMI was classified according to clinical cutoffs.Data fr
4                                              BMI was inversely correlated with the extent of emphysem
5 l, 0.32-0.54] kg/m(2) per A-allele, P<0.001; BMI gene score: 1.05 [95% confidence interval, 0.90-1.20
6 tio, 1.07 [1.02-1.11] per A-allele, P=0.004; BMI gene score, hazard ratio, 1.11 [1.05-1.18] per 1-U i
7 79 (0.58) at 1 year, an improvement of -0.09 BMI z score units (95% CI, -0.13 to -0.05).
8 osure to p,p'-DDE and BMI z-score (beta=0.13 BMI z-score (95% CI: 0.01, 0.25) per log increase of p,p
9 ; nonalcoholic steatohepatitis etiology 24%; BMI 33.3 +/- 3.2 kg/m(2) ; Child A 92%; HVPG >/=10 mm Hg
10   Child weight loss after 6 months was -0.25 BMI z scores in both PBT and FBT.
11 dult BMI (beta = 0.64 (standard error, 0.26) BMI units).
12  1:1 ratio to 1 of 2 groups within each of 3 BMI percentiles: 50th to <70th, 70th to <85th, and 85th
13 bjects were healthy weight [5th through 70th BMI percentiles for age (percentile)], and 50% of subjec
14  score difference: 0.37; 95% CI: 0.04, 0.71; BMI z score difference: 0.35; 95% CI: 0, 0.69), with no
15 [0.42-0.50]; specificity, 0.91 [0.89-0.92]), BMI (performance, 0.22; sensitivity, 0.75 [0.73-0.77]; s
16 e, 46.9 [11.3] years; 16.6% male) achieved a BMI of less than 30 at 1 year after bariatric surgery.
17       To identify predictors for achieving a BMI of less than 30 after bariatric surgery.
18 eight-related morbidity and mortality with a BMI above this threshold.
19  hospital costs were lowest for women with a BMI of 20.0 kg/m(2) to less than 22.5 kg/m(2) ( pound567
20 ildhood SEP was associated with higher adult BMI in both genders, and differences were typically larg
21  was independently related to a higher adult BMI in daughters, particularly for the highest 90th quan
22 nd adulthood is associated with higher adult BMI, but how these associations have changed across time
23 ive policies to reduce inequalities in adult BMI that tackle inequality with respect to both childhoo
24 larly for the highest 90th quantile of adult BMI (beta = 0.64 (standard error, 0.26) BMI units).
25 ize, and childhood growth factors with adult BMI in daughters at midlife using quantile, linear, and
26  fasting insulin (0.00%, -0.06 to 0.07), and BMI (0.11 kg/m(2), -0.09 to 0.30).
27 risk of adult obesity increased with age and BMI, from 1.17 (95% UI, 1.09 to 1.29) for overweight 2-y
28 , previous use of long-term oxygen, age, and BMI.
29      Twelve adults with T2DM and 11 age- and BMI-matched control participants without diabetes underw
30 , healthy non-NAFLD controls (normal ALT and BMI), or indeterminate.
31 ple, we evaluated the association of BMI and BMI change at different ages with ALS risk using uncondi
32 child weight loss (body mass index [BMI] and BMI z score) at 6, 12, and 18 months post treatment.
33  correlations only between beta-carotene and BMI (-0.27), WC (-0.30), and HDL cholesterol (0.31) afte
34 dex (BMI), according to age, sex, cause, and BMI in 195 countries between 1990 and 2015.
35 in HbA1c, triglycerides, HDL cholesterol and BMI in a mixed effects longitudinal analysis model.
36 akly associated with waist circumference and BMI, mostly among women.
37 ationship between H. pylori colonization and BMI/obesity.
38 ssociations between exposure to p,p'-DDE and BMI z-score (beta=0.13 BMI z-score (95% CI: 0.01, 0.25)
39               Baseline HRQoL, depression and BMI should be systematically assessed before starting th
40 e health and suggest that race/ethnicity and BMI play an important role in pregnancy bone health.
41   Results indicate socioeconomic factors and BMI are strong predictors of serum PBDE levels among you
42 odified the relation between the BMI-GRS and BMI among men (EDEN: P-interaction = 0.0001; Fenland: P-
43 , physical and mental health, medication and BMI outcome measures.
44 y relevant association between H. pylori and BMI/obesity.
45 ion between H. pylori genetic risk score and BMI/obesity, nor between BMI or obesity genetic risk sco
46 , and a negative association between t50 and BMI was observed between BMI 12 and 25 kg/m(2) (p = 0.00
47 ely; P < 0.01) but gained more in weight and BMI through 7 mo of age (weight z score difference: 0.37
48  2.8 years), weight (2.8 to 14.5 years), and BMI (2.8 to 8.5 years) compared with the control arm.
49 at 10/11 y) and adulthood (42/43 years), and BMI repeatedly across adulthood, spanning 1966 to 2012.
50 y feeding did not result in more appropriate BMI than traditional spoon-feeding, although children we
51 es of mothers in BMI categories were 2.4% at BMI less than 18.5 (underweight), 61.8% at BMI of 18.5 t
52 BMI of 30 to 34.9 (obesity grade 1), 2.4% at BMI of 35 to 39.9 (obesity grade 2), and 0.8% at BMI 40
53 of 35 to 39.9 (obesity grade 2), and 0.8% at BMI 40 or greater (obesity grade 3).
54 t BMI less than 18.5 (underweight), 61.8% at BMI of 18.5 to 24.9 (normal weight), 24.8% at BMI of 25
55 MI of 18.5 to 24.9 (normal weight), 24.8% at BMI of 25 to 29.9 (overweight), 7.8% at BMI of 30 to 34.
56 % at BMI of 25 to 29.9 (overweight), 7.8% at BMI of 30 to 34.9 (obesity grade 1), 2.4% at BMI of 35 t
57                                      Average BMI at surgery was 13.83 (SD 1.49) and 14 (88%) of the 1
58 ll ages from 7 to 13 years, an above-average BMI z score was positively associated with early ischemi
59            Among children with above-average BMI z scores at age 7 years, a score increase of 0.5 fro
60                  We found that high baseline BMI was associated with a significantly slower rate of f
61 sal hazard ratio for the association between BMI and AF.
62  to infer the direction of causality between BMI and disordered eating in childhood, adolescence, and
63             Significant correlations between BMI and unsaturated fatty acids in intramyocellular lipi
64 etic risk score and BMI/obesity, nor between BMI or obesity genetic risk scores and H. pylori positiv
65 ion between t50 and BMI was observed between BMI 12 and 25 kg/m(2) (p = 0.007).
66  positive dose-response relationship between BMI and current asthma was observed (odds ratios were 0.
67 or excess weight (eg, body mass index [BMI]; BMI z score, measuring the number of standard deviations
68 ither positively or negatively influenced by BMI.
69 at birth was inversely associated with HT; c-BMI from school age to adulthood and c-height from birth
70 nical-community interventions improved child BMI z score and health-related quality of life, as well
71  childhood obesity and improvements in child BMI.
72 k characteristics and higher early childhood BMI.
73                                  The claimed BMI-defined overweight risk paradox may result in part f
74 ording to WHO recommendations, we classified BMI into categories of healthy (20.0-24.9 kg/m(2)), over
75 n at 83 CpGs that replicated across cohorts; BMI-related differential methylation was associated with
76 the highest and lowest fifths were compared, BMI (HR = 1.35, 95%CI: 1.13-1.61; Ptrend < 0.0001), wais
77 s index (BMI) were based on SSB consumption, BMI from the Australian Health Survey 2011-12, and energ
78 obesity, defined as donor body mass index (D-BMI) of 30 kg/m or greater, has been associated with inc
79 ransplant centers establish a threshold of D-BMI of 30 kg/m to decline donor offers for pancreas tran
80                            Associations of D-BMI with pancreas and kidney allograft failure were asse
81    Compared with D-BMI 20 to 25 kg/m, only D-BMI 35 to 50 kg/m was associated with significantly high
82                              Compared with D-BMI 20 to 25 kg/m, only D-BMI 35 to 50 kg/m was associat
83                                 A decreasing BMI from early to middle age and a low BMI in middle age
84 howed increasing levels of FG and decreasing BMI (p < 0.001).
85 plasma from 259 Caucasian women at delivery (BMI 18-55 kg/m(2)).
86  did not modify the effect of post-diagnosis BMI or WHR on the outcomes.
87  association was observed for post-diagnosis BMI or WHR with late recurrence; a U-shaped association
88 creased as grip strength reduced within each BMI category.
89 he prevalence and disease burden of elevated BMI highlights the need for continued focus on surveilla
90                          We sought to extend BMI lifetime by developing an algorithmic technique, imp
91                               Among females, BMI development differed between children with and witho
92 erval (CI), 0.52-0.75] after controlling for BMI and other risk factors.
93   Genome-wide association studies (GWAS) for BMI, waist-to-hip ratio, and other adiposity traits have
94  level of 0.05, 287 loci were identified for BMI and 75 loci for T2D, 23 of which for both traits.
95           The dose-response relationship for BMI with HFpEF risk was also more consistent than with H
96 ypic scores and polygenic profile scores for BMI, HDL cholesterol, low-density lipoprotein cholestero
97 enetic score as an instrumental variable for BMI to assess the causal effect of BMI at age 7 y on dis
98                      By extending functional BMI lifetime, this approach increases the clinical viabi
99 espectively, versus the normal-weight group (BMI 20.0-24.9)).
100 gnificantly greater than that of insulin --&gt; BMI (beta = -0.023, p = 0.207) in childhood, with p < 0.
101 =1604; mean age, 61+/-12 years; 75% men) had BMI measured on admission, and 2-dimensional transthorac
102 nd web-response system, stratified by HbA1c, BMI, region, and estimated glomerular filtration rate.
103            Age, duration of diabetes, HbA1c, BMI, BCVA, and CST had no impact on the ability to achie
104  cases are attributable to diabetes and high BMI.
105 follow-up were also associated with a higher BMI at age 18 years.
106 py), lower RMR (beta = -31 kcal/day), higher BMI (beta = +0.6 kg/m(2)), and higher PFAT (beta = +0.9%
107 confer a lifetime exposure of 5-kg/m2 higher BMI was associated with a lower risk of PD (OR 0.82, 95%
108 oprotein cholesterol in men, and with higher BMI and white blood cell count in women (differences 0.0
109 cts on PD in a manner consistent with higher BMI leading to lower risk of PD.
110  that work stress was associated with higher BMI, waist circumference, waist-hip ratio, alanine trans
111 en with and without asthma, with the highest BMI being seen among females with persistent asthma.
112 .8% in general cognitive ability and 5.4% in BMI in an independent test set, predicting 1.1%, 1.1%, a
113 es to invoke clinically meaningful change in BMI among adult patients with diabetes.
114  18-21 years, BMI at baseline, and change in BMI differed according to genetic risk based on lifetime
115    The primary outcome measure was change in BMI over 5 years.
116 -0.7 to 1.6) at extension week 96; change in BMI was 0.69 (0.56 to 0.81) at extension week 72 and 0.9
117                                   Changes in BMI between baseline and 12 weeks follow-up were assesse
118                  Every 2 kg/m(2) increase in BMI above 20 kg/m(2) was associated with a 7.4% (7.1-7.6
119                The percentages of mothers in BMI categories were 2.4% at BMI less than 18.5 (underwei
120 cant center-level heterogeneity was noted in BMI of accepted donors; the MOR varied from 1.10 for ove
121 t than with HFrEF risk, such that increasing BMI above the normal range (>/=25 kg/m(2)) was associate
122 ugh these studies have shown that increasing BMI is associated with larger increases in body fat cont
123 sults support the conclusion that increasing BMI is causally related to higher prevalence of asthma a
124 sitive effect on lifespan whereas increasing BMI negatively affects lifespan.
125 .4 cm), weight (>5 kg), and body mass index (BMI) (>3.5 kg/m(2)).
126 predictive of having a high body mass index (BMI) and being obese.
127  associated with children's body mass index (BMI) and detailed measures of body composition.
128 sociations between maternal body mass index (BMI) and offspring systemic cardio-metabolic profile are
129 ubstances (PFAS) may affect body mass index (BMI) and other components of cardiometabolic (CM) risk d
130 ons between early pregnancy body mass index (BMI) and rates of cerebral palsy by gestational age and
131 obesity (GPRS-obesity) with body mass index (BMI) and waist circumference (WC) was modified by sleep
132 opometric indices including body mass index (BMI) and waist circumference (WC) were used to determine
133 nation Survey, we regressed body mass index (BMI) and waist-to-height ratios on urinary arsenic conce
134           Diabetes and high body-mass index (BMI) are associated with increased risk of several cance
135  activity (LTPA) and higher body mass index (BMI) are independently associated with risk of heart fai
136  Results were similar using body mass index (BMI) as an anthropometric indicator of nutritional statu
137 were identified as having a body mass index (BMI) at or above the 85th percentile and 2 or more risk
138 ch 31, 2011, in relation to body-mass index (BMI) at recruitment, overall and for categories of healt
139  may be associated with low body mass index (BMI) at the time of diagnosis.
140      Further adjustment for body mass index (BMI) attenuated these associations but remained signific
141  and CDKAL1) overestimated (body mass index (BMI) decreasing) and one (near MTNR1B) underestimated (B
142  in blood pressure (BP) and body mass index (BMI) during childhood and adolescence are sentinels for
143 e frequently and at a lower body mass index (BMI) in Asians than in European populations, the mechani
144                        High body mass index (BMI) is an important contributor to the global burden of
145                             Body mass index (BMI) is used to diagnose obesity in adolescents worldwid
146 1 (1.7) years and mean (SD) body mass index (BMI) of 30.2 (3.5) kg/m(2) in obese and 19.4 (2.2) kg/m(
147 nsplant in individuals with body mass index (BMI) of 40 kg/m or greater.
148 n increases with increasing body mass index (BMI) on recommended calcium intakes.
149  the onset of AN, premorbid body mass index (BMI) spans the entire range from underweight to obese.
150              The total mean body mass index (BMI) was 24.7 +/- 4.2 kg/m(2).
151 estionnaire, and children's body mass index (BMI) was measured.
152                  Changes in body mass index (BMI) were based on SSB consumption, BMI from the Austral
153 n association analyses with body mass index (BMI) were evaluated in the 100 subjects and another inde
154             Paternal age or body mass index (BMI) were not associated with NAFLD in female offspring.
155 re strongly associated than body mass index (BMI) with childhood asthma.
156  examine the association of body mass index (BMI) with FPM/SPM emergence in a representative sample o
157 etermine the association of body mass index (BMI) with mortality and functional outcome in patients w
158                       Lower body-mass index (BMI) z-score and household smoking were strong predictor
159 ip ratio (WHR) adjusted for body mass index (BMI), a measure of abdominal adiposity, with type 2 diab
160  of disease related to high body-mass index (BMI), according to age, sex, cause, and BMI in 195 count
161 d 6 months included weight, body mass index (BMI), body composition, muscle strength, cytokines, comp
162 ified between tiredness and body mass index (BMI), C-reactive protein, high-density lipoprotein (HDL)
163 , reported smoking history, body mass index (BMI), diabetes, HIV, and all other resistance mutations.
164 ve identified >250 loci for body mass index (BMI), implicating pathways related to neuronal biology.
165 The secondary outcomes were body-mass index (BMI), mood, anxiety, affective regulation, and anorexia
166 able fractions for smoking, body-mass index (BMI), physical activity, alcohol intake, type 2 diabetes
167 e statistical analyses were body mass index (BMI), waist circumference (WC), serum adipokines, cytoki
168 h hypertension, and between body mass index (BMI), waist circumference (WC), waist-to-height ratio (W
169 food craving and changes in body mass index (BMI).
170 ing by healthy lifestyle or body mass index (BMI).
171 g food insecurity to a high body mass index (BMI).
172 al homocysteine, and higher body mass index (BMI)] and greater odds of large-vessel cerebral vascular
173                             Body mass index (BMI, calculated as weight in kilograms divided by height
174                 Achieving a body mass index (BMI, calculated as weight in kilograms divided by height
175 re obesity was defined as a body-mass index (BMI, the weight in kilograms divided by the square of th
176 de association to show that body mass index (BMI; a key measure of adiposity) is associated with wide
177 2) for groups with baseline body mass index (BMI; in kg/m(2)) >/=30 and <30, respectively.These findi
178  analysis of variance.Three body mass index (BMI; in kg/m(2)) trajectory patterns were identified and
179 hemoglobin (HbA1c), weight, body mass index (BMI; in kg/m(2)), and LDL cholesterol.
180 lated to weight management [body mass index (BMI; in kg/m(2)), body weight, percentage of body fat, a
181 osity indicators, including body mass index (BMI; in kg/m(2)).
182 re thin at 1 wk postpartum [body mass index (BMI; in kg/m(2)): 22.9 +/- 2.9].
183 ean +/- SD age: 25 +/- 6 y; body mass index (BMI; in kg/m(2)): 23 +/- 2].
184 r groups, being overweight [body mass index (BMI; in kg/m(2)): 25 to <30] is reportedly associated wi
185 tions of breast cancer with body mass index (BMI; weight (kg)/height (m)2) at age 18-21 years, BMI at
186 ing" for height, weight, or body mass index (BMI; weight (kg)/height (m)2) measured concurrently with
187 borhood characteristics and body mass index (BMI; weight (kg)/height (m)2) were assessed from 2000 to
188 on of maternal prepregnancy body mass index (BMI; weight (kg)/height (m)2), gestational weight gain (
189 women or >/= 31 for men and body mass index [BMI] > 25 kg/m(2) ), healthy non-NAFLD controls (normal
190 sure was child weight loss (body mass index [BMI] and BMI z score) at 6, 12, and 18 months post treat
191 ith obesity-related traits (body mass index [BMI] and levels of C-reactive protein [CRP] and leptin).
192 ciations between body size (body mass index [BMI], height, waist circumference, and waist-to-hip rati
193 eight or excess weight (eg, body mass index [BMI]; BMI z score, measuring the number of standard devi
194 akes are associated with unfavorable infancy BMI peak characteristics and higher early childhood BMI.
195 R, we found that variants known to influence BMI had effects on PD in a manner consistent with higher
196 Subjects in North America had higher initial BMIs than those of subjects in Eastern Asia.
197 llow-up studies are warranted to investigate BMI changes over time.
198    Fixed-effects models with a 1-year-lagged BMI were estimated.
199  Secondary outcomes were parent weight loss (BMI), child and parent energy intake, child and parent p
200 asing BMI from early to middle age and a low BMI in middle age may be positively associated with ALS
201             The predictors of MAC-PP are low BMI, NB pattern, and high AFS grade; if these risk facto
202  altered in RRMS patients, especially in low-BMI patients, which may contribute to disease progressio
203                                        Lower BMI in preclinical MCs was significantly associated with
204 e in HbA1c, a 0.55 (95% CI: 0.02, 1.1) lower BMI, a 2.1-kg (95% CI: 1.2-, 2.9-kg) lower weight, and a
205 m those of type 2 diabetes: they had a lower BMI (27.4 kg/m(2) [95% CI 26.7-28.0] vs 32.4 kg/m(2) [32
206 d with smaller waist circumference and lower BMI and body fat percentage.
207 actor profile (higher HDL cholesterol, lower BMI, lower C-reactive protein, lower waist circumference
208                 Older age, white race, lower BMI, IV drug use, lower baseline CD4, HCV coinfection, p
209 tic capacity to digest starch had the lowest BMI, potentially because larger amounts of undigested st
210                   Associations between LTPA, BMI, and risk of overall HF, HFpEF (ejection fraction >/
211 ify dose-response associations between LTPA, BMI, and the risk of different HF subtypes.
212 ated 45% of the association between maternal BMI and rates of cerebral palsy in full-term children wa
213 5%CI -0.11-0.21) per SD increase in maternal BMI (p-value for difference between the two results = 0.
214 5% CI 0.19-0.25) per SD increase in maternal BMI and the pooled MR effect (pooling the 97 variant sco
215                        In newborns, maternal BMI was associated with small (<0.2% per BMI unit (1 kg/
216                             Data on maternal BMI was collected at 15 weeks of gestation, and paternal
217 e association between pre-pregnancy maternal BMI and methylation at over 450,000 sites in newborn blo
218           Our findings suggest that maternal BMI-offspring metabolome associations are likely to be l
219    The pattern of excess risk with a maximum BMI above normal weight was maintained across strata def
220 investigate the relationship between maximum BMI over 16 years and subsequent mortality.
221 hundred fifty children (mean BMI, 26.4; mean BMI z score, 2.0; mean age, 10.4 years; 66.4% girls) and
222          The subgroup of studies with a mean BMI >/=30 exhibited substantially greater lean mass (SMD
223             One hundred fifty children (mean BMI, 26.4; mean BMI z score, 2.0; mean age, 10.4 years;
224                              The lowest mean BMI was observed in the group of participants with a low
225 4 years; 66.4% girls) and their parent (mean BMI, 31.9; mean age, 42.9 years; 87.3% women; and 31% Hi
226      Approximately, 67% were males with mean BMI 26.5 kg/m.
227 umber of standard deviations from the median BMI for age and sex), cardiometabolic outcomes, quality
228 lly reversed by overexpression of PcG member BMI-1, suggesting opposing roles for PEITC and PcG prote
229  crossover study, twelve normoglycaemic men (BMI 25-35 kg/m(2)) underwent four investigational days,
230                           We developed a new BMI that allows arbitrarily fast control and feedback ra
231 little difference in the risk between normal BMI (HR: 3.25; 95% CI: 1.86, 5.65), overweight (HR: 2.50
232    Compared with the reference group (normal BMI and highest handgrip tertile), the risk of all-cause
233 10000 women, compared with women with normal BMI) were 28.8 (95% CI, 12.2-47.2) for underweight women
234  the meta-analyzed estimate between observed BMI and AF (age- and sex-adjusted hazard ratio 1.05 [1.0
235  understand the full genetic architecture of BMI.
236 this sample, we evaluated the association of BMI and BMI change at different ages with ALS risk using
237  years, the cross-lagged path coefficient of BMI --> insulin (beta = 0.326, p < 0.001) was significan
238 iable for BMI to assess the causal effect of BMI at age 7 y on disordered eating patterns at age 13 y
239             We examined the causal effect of BMI on asthma, hay fever, allergic sensitization, serum
240  weight, without any comparable influence of BMI or BSA.
241 here were fairly similar trends in levels of BMI, waist circumference, and skinfold thicknesses in me
242  need for continued focus on surveillance of BMI and identification, implementation, and evaluation o
243 ime with baseline levels and trajectories of BMI and waist circumference over time using linear mixed
244 NT5A interaction may affect the variation of BMI in Han Chinese population.
245 approach increases the clinical viability of BMIs.
246  triglycerides can amplify the FTO impact on BMI.
247 etween AMY1 copy number and starch intake on BMI (P-interaction = 0.007) and body fat percentage (P-i
248 or >9 h daily, the effect of GPRS-obesity on BMI was stronger (beta: 0.60; 95% CI: 0.54, 0.65 and bet
249  and fasting triglycerides with rs9939609 on BMI (p = 0.0005 and p = 5 x 10(-7), respectively).
250 ditional adjustment for concurrent weight or BMI reversed (i.e., to positive) the SGA-adiposity assoc
251 adjustment for concurrent height, weight, or BMI.
252                                          Our BMI paradigm can dissect the contribution of different e
253 dy size which rapidly increases as their own BMI increases.
254 ected at 15 weeks of gestation, and paternal BMI was assessed when the child was 18 months old.
255                 In contrast, higher paternal BMI (P < 0.001), maternal prepregnancy BMI (P < 0.001),
256  present for maternal compared with paternal BMI across these associations; however, there was no str
257 nal BMI was associated with small (<0.2% per BMI unit (1 kg/m2), P < 1.06 x 10-7) methylation variati
258 We found no association between prediagnosis BMI and survival.
259 y correlated with food craving and predicted BMI gains.
260                              Early pregnancy BMI.
261 hibit excessive GWG, both high pre-pregnancy BMI and excessive GWG influence perinatal outcomes.
262 ested the associations between pre-pregnancy BMI or GWG and length of gestation, birthweight, length,
263               However, the role of premorbid BMI in the development of ALS and survival after diagnos
264 ernal BMI (P < 0.001), maternal prepregnancy BMI (P < 0.001), and lower family socioeconomic status (
265 evention of SSI in obese women (prepregnancy BMI >/=30) who had received standard intravenous preoper
266 diabetes diagnosis, systolic blood pressure, BMI, smoking status, estimated glomerular filtration rat
267 rend for prebiotic supplementation to reduce BMI z score to a greater extent than placebo (-3.4%; P =
268 increases transplant eligibility by reducing BMI in kidney transplant candidates, but the effect of s
269  We identified novel and previously reported BMI-related differential methylation at 83 CpGs that rep
270 ncy is positively associated with children's BMI during early childhood and particularly with higher
271                                   Children's BMI, WC, and WHtR were positively associated with their
272  plus coaching group, the adjusted mean (SD) BMI z score was 1.87 (0.56) at baseline and 1.79 (0.58)
273 dard deviation score in body mass index [SDS-BMI]).
274 .A total of 153 participants (means +/- SDs: BMI: 33.3 +/- 4.6; age: 63.8 +/- 6.3 y; 83% women) were
275    One-year changes in age- and sex-specific BMI z score, child health-related quality of life measur
276 atified analyses revealed that the strongest BMI signal originated predominantly from females (chr.
277 t correlate highly with sweat chloride test, BMI, and FEV1% predicted values.
278 olescents as overweight more accurately than BMI z scores and equally as well as updated BMI percenti
279  restraint modified the relation between the BMI-GRS and BMI among men (EDEN: P-interaction = 0.0001;
280 1.42), and 1.87 (95% CI: 1.60, 2.18) for the BMI groups <20.0, 25.0-29.9, and >/=30.0, respectively,
281                                 However, the BMI curves begun to diverge already at 17.8 years before
282 s system to concurrently learn operating the BMI while exploiting the possibility to adapt the availa
283 to a final model explaining FLI best through BMI, waist circumference, and the Lac:Man ratio.
284 % CI -0.1-0.48), but was unlikely related to BMI although the estimate lacked precision.
285 between arsenic concentration in relation to BMI and waist-to-height ratio.
286 ariants across eight cardiometabolic traits (BMI, systolic and diastolic blood pressure, LDL choleste
287 asing) and one (near MTNR1B) underestimated (BMI increasing) associations among 11 type 2 diabetes ri
288                      Obesity and underweight BMI were associated with increased risk of composite adv
289  BMI z scores and equally as well as updated BMI percentiles but is much simpler to use than either b
290  risk of mortality than being normal weight (BMI: 18.5 to <25).
291 struments were significantly associated with BMI (FTO: 0.43 [95% confidence interval, 0.32-0.54] kg/m
292 s2072920 and rs11918967, was associated with BMI after multiple testing corrections (combined P = 2.2
293 roach to discover novel loci associated with BMI and T2D by incorporating the summary statistics from
294 gle-nucleotide polymorphisms associated with BMI from previous genome-wide association studies was co
295 e 2 diabetes alleles will be associated with BMI in sample sizes of >500 000 if the prevalence of tho
296 erfiltering patients and was associated with BMI, waist circumference, blood pressure, heart rate, Hb
297 replaced diabetes and total cholesterol with BMI.
298  also evaluated the association of SNPs with BMI related factors such as sleep duration and quality,
299   Participants were randomly assigned within BMI categories to receive an 18-mo dairy intervention (3
300 weight (kg)/height (m)2) at age 18-21 years, BMI at baseline, and change in BMI differed according to
301 (as a proxy for cognitive ability in youth), BMI, height, systolic blood pressure, coronary artery di

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