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1 1.20; P = 0.063; CI 95% 0.99 to 1.45 in the adjusted model).
2 ivers (1.07, 1.02-1.13; p=0.007 in the fully-adjusted model).
3 nterval: 1.11, 1.82, P = 8.0 x 10(-9), fully-adjusted model).
4 vascular death and total mortality (in fully adjusted models).
5 0.229] log-ISI per unit, P = 0.001 in fully adjusted models).
6 ratio [adjOR] 1.72, 95% CI 1.47-2.01) in the adjusted model.
7 nd mortality remained significant in a fully adjusted model.
8 t significant predictors of diary use in the adjusted model.
9 al, 2.23-5.21) to be diagnosed with AS in an adjusted model.
10 comes were compared between the groups in an adjusted model.
11 Similar results were found in the adjusted model.
12 rderline statistical significance in a fully adjusted model.
13 e latter was attenuated in the multivariable-adjusted model.
14 st quartile (<200 pg/mL) in the age- and sex-adjusted model.
15 tive predictor of having a GOCD in the fully adjusted model.
16 ant increases at all capillary levels in the adjusted model.
17 with increased PTSD symptoms (p = 0.009) in adjusted models.
18 lusion of functional status into SRTR's risk-adjusted models.
19 when surveillance was removed from otherwise adjusted models.
20 d statistically significant in multivariable adjusted models.
21 % confidence interval]: 1.52 [1.07-2.16]) in adjusted models.
22 egression analysis in age- and multivariable-adjusted models.
23 e and Sequential Organ Failure Assessment in adjusted models.
24 k was associated with stroke in age- and sex-adjusted models.
25 HR, 1.55; 95% CI, 1.04-2.32 in multivariable adjusted models.
26 wed statistically significant changes in the adjusted models.
27 al dismissal patients in unadjusted and risk-adjusted models.
28 with the lowest variation in body weight in adjusted models.
29 ntly associated with depression in the fully adjusted models.
30 I<16.0, 2.53; 95% CI, 1.26-5.07) in mutually adjusted models.
31 ardiac troponin I (hs-cTnI) were included in adjusted models.
32 ow-up period were examined in unadjusted and adjusted models.
33 ts and the general population in demographic-adjusted models.
34 other types of cancer based on results from adjusted models.
35 d with the lowest quartiles in multivariable adjusted models.
36 cancer risk in unadjusted and multivariable-adjusted models.
37 h LTL in either basic or confounder/mediator-adjusted models.
38 g/mL; odds ratio 1.80; 95% CI, 1.21-2.68) in adjusted models.
39 ficantly associated with 30-day mortality in adjusted models.
40 were associated with a lower risk of CRC in adjusted models.
41 ociation between H2RA use and incident HF in adjusted models.
42 8) tertiles based on traditional risk factor-adjusted models.
43 ted with all-cause or CVD mortality in fully adjusted models.
44 ed with peak Vo2 levels at baseline in fully adjusted models.
45 found in risk of lung cancer death in fully adjusted models.
46 enza A(H1N1)pdm09 infection was estimated in adjusted models.
47 idney transplantation in both unadjusted and adjusted models.
48 g and higher prepregnancy body mass index in adjusted models.
49 - 0.6, 3.8) higher fasting glucose in fully adjusted models.
50 ed logistic regression analysis in crude and adjusted models.
51 ression (HR, 1.11; 95% CI, 1.00-1.24) in the adjusted models.
52 rd ratio, 1.48 [95% CI, 1.01-2.18]) in fully adjusted models.
53 s of systolic blood pressure in multivariate-adjusted models.
54 g NP levels was assessed using multivariable-adjusted models.
55 0.62, 0.86; P-trend < 0.01) in multivariable adjusted models.
56 ptide) levels were examined in multivariable-adjusted models.
57 d rhinorrhea were associated with BoV RTI in adjusted models.
58 8, 1.25; P-trend < 0.0001) insomnia in fully adjusted models.
59 the subgroup analysis of ever smokers and in adjusted models.
60 nts undergoing EVT in unadjusted and in risk-adjusted models.
61 ntly associated with depression in the fully adjusted models.
62 roduct with mortality was found in the fully adjusted models.
63 io test (LRT) chi2(2) = 7.1, p = 0.03; fully adjusted model].
64 MSSP was associated with hip fracture in the adjusted model (-0.24 hospitalizations for hip fracture
65 es, and no difference was found in the fully adjusted model (-0.39; 95% CI, -1.24 to 0.45; P = .36).
68 r tanning was associated with sunburn in the adjusted model: 82.3% (95% CI, 77.9%-86.0%) of indoor ta
88 0.70, 95%CI 0.50-0.98, p = 0.037) or a fully adjusted model (AOR = 0.69, 95%CI 0.50-0.97, p = 0.033).
96 sity and breast cancer risk were observed in adjusted models (body mass index (BMI): Odds ratio (OR)
99 ificantly associated with incident HF in age-adjusted models, but not after multivariable adjustment.
100 wer on mother hands in the sanitation arm in adjusted models, but these associations were not signifi
102 d incremental value for psoriasis in a fully adjusted model (chi2 = 4.48, P = .03) in predicting coro
112 yr) were associated with ARDS (P < 0.01) in adjusted models, despite exposure levels largely below U
127 surrogacy for the surrogate covariate in the adjusted model for all-cause mortality: PSA nadir greate
128 1c) (HR = 1.20; P = 0.0082) and in the fully adjusted model for other CVD risk factors (HR = 1.17; P
132 MDD was associated with HF in separate fully adjusted models for HIV- and HIV+ participants (adjusted
133 ubstantially attenuated in the multivariable adjusted models for major cardiovascular disease (hazard
135 ression to estimate relative risks (RRs) and adjusted models for sex of the child, gestational age at
136 lar %-dilation and skin %-hyperemia in fully adjusted models (for glycohemoglobin A1c, standardized B
138 bjective cognitive function in either raw or adjusted models (fully adjusted: global cognitive functi
143 ase risk of death or retransplantation in an adjusted model (hazard ratio 1.12 [95% confidence interv
144 ase risk of death or retransplantation in an adjusted model (hazard ratio 1.12 [95% confidence interv
145 isk of posttransplant mortality in the fully adjusted model (hazard ratio [HR], 1.22; 95% confidence
146 but still statistically significant in fully adjusted models (hazard ratio, 1.38; 95% CI, 1.11-1.71).
147 with a 41% lower risk of HF in multivariable-adjusted models (hazard ratio: 0.59; 95% confidence inte
148 ssociated with incident CVD in multivariable-adjusted models (hazard ratio=1.61; 95% CI, 1.04-2.51).
160 or nonaffective psychoses among offspring in adjusted models (HR, 1.32; 95% CI, 1.13-1.54) and in mat
165 ing multivariable logistic regression and PS-adjusted models in the combined group, higher adherence
168 clusters and any musculoskeletal outcome in adjusted models.In a protein-replete cohort of adults, d
169 repair compared with nulliparous, in an age-adjusted model (incidence rate ratio 7.04, 95% CI 5.87-8
180 ons with cognitive function across crude and adjusted models (linear trend P values were 0.05 and <0.
190 iations were explored in three progressively adjusted models: Model 1, adjusted for age and baseline
192 s 9.3% lower in South Africa than Malawi, in adjusted models mortality was similar in both countries
193 s 9.3% lower in South Africa than Malawi, in adjusted models mortality was similar in both countries
197 had a greater incidence of CKD in the fully adjusted model (odds ratio for fourth versus first quart
198 yle was associated with less diary use in an adjusted model (odds ratio, 0.66; 95% confidence interva
200 Consistent findings emerged in covariate-adjusted models of antidepressant treatment, such that p
203 ated with spontaneous preterm birth based on adjusted models of temporal exposures, whereas the spati
210 ciated with spontaneous preterm birth in the adjusted model (OR = 0.90; 95% CI: 0.83, 0.97 per 20 ppb
211 cordance was also associated with Y25 CAC in adjusted models (OR: 1.55 and OR: 1.45, respectively).
215 ndently associated with higher WBC counts in adjusted models (P < .01); the highest quartile of WBC c
231 ase the risk of hospitalization in a similar adjusted model (relative risk, 1.39; 95% CI, 0.90-2.15).
235 re maintained in all covariate models (fully adjusted model: risk ratio, 0.89; 95% CI, 0.83-0.95), bu
236 essive symptoms, and health behaviors (fully adjusted model: risk ratio, 0.91; 95% CI, 0.80-1.04).
242 the first subsample, the full multivariable-adjusted model showed that participants with 28 to 32, 2
253 and surgical outcome and then developed two adjusted models that accounted for variations in (1) bas
255 association remained significant in mutually adjusted models that included the 25 x 25 factors (HR 1.
261 ension at baseline, in the time- and cluster-adjusted model, the use of the salt substitute was assoc
262 ; P = 0.005) than those in the IFA group; in adjusted models, the differences in length (47.6 +/- 0.0
271 cores than the control group in the baseline-adjusted models; the between-group mean difference was -
275 mortality risk in both unadjusted and fully adjusted models: TNF-alpha: hazard ratios (HRs)(1 pg/ml
280 0.10-0.81; P=0.02), although the propensity-adjusted model was significant when AF lasted at least 6
289 Unadjusted and multilevel, multivariable adjusted models were used to measure the association of
290 s reinforce the need for comprehensive, risk-adjusted modeling when assessing performance based on pr
292 dds ratio, 2.35; 95% CI, 1.12-4.94) in fully adjusted models, whereas the association of coronary art