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1 nterval: 1.11, 1.82, P = 8.0 x 10(-9), fully-adjusted model).
2 vascular death and total mortality (in fully adjusted models).
3 0.229] log-ISI per unit, P = 0.001 in fully adjusted models).
4 ompared with the lowest tertile in the fully adjusted model.
5 nd mortality remained significant in a fully adjusted model.
6 , 1.06) after adding balance measures to the adjusted model.
7 when clinical variables were included in the adjusted model.
8 ficant association with brain atrophy in the adjusted model.
9 er CIMT (95% CI: 0.4, 1.7%) based on a fully adjusted model.
10 onfidence interval [CI]: 1.09 to 1.33) in an adjusted model.
11 t significant predictors of diary use in the adjusted model.
12 al, 2.23-5.21) to be diagnosed with AS in an adjusted model.
13 comes were compared between the groups in an adjusted model.
14 Similar results were found in the adjusted model.
15 when surveillance was removed from otherwise adjusted models.
16 % confidence interval]: 1.52 [1.07-2.16]) in adjusted models.
17 g/mL; odds ratio 1.80; 95% CI, 1.21-2.68) in adjusted models.
18 ficantly associated with 30-day mortality in adjusted models.
19 were associated with a lower risk of CRC in adjusted models.
20 ociation between H2RA use and incident HF in adjusted models.
21 8) tertiles based on traditional risk factor-adjusted models.
22 ted with all-cause or CVD mortality in fully adjusted models.
23 ed with peak Vo2 levels at baseline in fully adjusted models.
24 found in risk of lung cancer death in fully adjusted models.
25 enza A(H1N1)pdm09 infection was estimated in adjusted models.
26 idney transplantation in both unadjusted and adjusted models.
27 g and higher prepregnancy body mass index in adjusted models.
28 ociated with CRC-specific mortality in fully adjusted models.
29 (p-values < 0.13), which did not persist in adjusted models.
30 nsitivity analyses included propensity score-adjusted models.
31 D, but results were not significant in fully adjusted models.
32 t significantly associated with CVD in fully adjusted models.
33 ion, and stroke (global p = 0.0035) in fully adjusted models.
34 nd all RRs remained significant in the fully adjusted models.
35 ine-adjusted arsenic, respectively) in fully adjusted models.
36 d statistically significant in multivariable adjusted models.
37 not positively associated with CRC in fully adjusted models.
38 egression analysis in age- and multivariable-adjusted models.
39 in unadjusted and multiple propensity score-adjusted models.
40 th risk of HF in both age- and multivariable-adjusted models.
41 ) and log DI (beta: 2.21, P = 0.02) in fully adjusted models.
42 al estate-owned foreclosures on SBP in fully adjusted models.
43 nd was not associated with outcomes in fully adjusted models.
44 cancers were in significant excess in fully adjusted models.
45 Results were similar in adjusted models.
46 onfidence interval: 1.00, 1.92) in minimally adjusted models.
47 AD and analytes correlations were studied in adjusted models.
48 % confidence interval: 10, 208; P = 0.01) in adjusted models.
49 rectal cancer incidence, using multivariable-adjusted models.
50 k was associated with stroke in age- and sex-adjusted models.
51 HR, 1.55; 95% CI, 1.04-2.32 in multivariable adjusted models.
52 with the lowest variation in body weight in adjusted models.
53 I<16.0, 2.53; 95% CI, 1.26-5.07) in mutually adjusted models.
54 ardiac troponin I (hs-cTnI) were included in adjusted models.
55 ow-up period were examined in unadjusted and adjusted models.
56 ts and the general population in demographic-adjusted models.
57 other types of cancer based on results from adjusted models.
58 d with the lowest quartiles in multivariable adjusted models.
59 cancer risk in unadjusted and multivariable-adjusted models.
60 h LTL in either basic or confounder/mediator-adjusted models.
61 es, and no difference was found in the fully adjusted model (-0.39; 95% CI, -1.24 to 0.45; P = .36).
63 ity or major disability in the multivariable-adjusted models (1.07 (0.89 to 1.29) and 0.85 (0.72 to 1
67 r tanning was associated with sunburn in the adjusted model: 82.3% (95% CI, 77.9%-86.0%) of indoor ta
80 1% (95% CI, 0.47% to 0.55%), and in mutually adjusted models, a less than primary education level was
82 n before or after eGFR reporting in crude or adjusted models accounting for case mix and facility cha
89 linical outcomes, and healthcare costs using adjusted models among the 1052 patients who underwent CA
93 ansplant were calculated using multivariable-adjusted models and examined across health insurance and
95 neurological outcome in a baseline variable-adjusted model, and target temperature did not significa
96 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).
103 m total and LDL cholesterol in multivariable-adjusted models (beta: 0.199, SE: 0.056, P < 0.001 and b
110 ificantly associated with incident HF in age-adjusted models, but not after multivariable adjustment.
111 associated with lower verbal IQ in minimally adjusted models; but after adjustment for socioeconomic
113 d incremental value for psoriasis in a fully adjusted model (chi2 = 4.48, P = .03) in predicting coro
115 re estimated at 2.1 (95% CI, 1.6-2.3) in the adjusted model, compared with 1.7 (95% CI, 1.1-2.0) if t
141 ne were associated with reduced fecundity in adjusted models (fecundability odds ratio (FOR) = 0.69 (
145 surrogacy for the surrogate covariate in the adjusted model for all-cause mortality: PSA nadir greate
149 MDD was associated with HF in separate fully adjusted models for HIV- and HIV+ participants (adjusted
150 ubstantially attenuated in the multivariable adjusted models for major cardiovascular disease (hazard
153 ide intake and adolescents' bone measures in adjusted models (for 183 females, all p values >/= .10 a
154 lar %-dilation and skin %-hyperemia in fully adjusted models (for glycohemoglobin A1c, standardized B
155 bjective cognitive function in either raw or adjusted models (fully adjusted: global cognitive functi
159 10 years, P < .001), which was confirmed in adjusted models (hazard ratio [HR], 0.55 [95% CI, 0.41-0
160 ssociated with the CVH score in age- and sex-adjusted models (hazard ratio, 0.77 per 1-unit increase
163 ge-, nativity-, and metropolitan demographic-adjusted models, high segregation was associated with a
171 ct except adjustment for age category (fully adjusted model HR, 1.26; 95% CI, 1.21-1.32; P < .001).
175 ears, P < .001), which was confirmed in risk-adjusted models (HR, 0.29 [95% CI, 0.19-0.43], P < .001)
176 or nonaffective psychoses among offspring in adjusted models (HR, 1.32; 95% CI, 1.13-1.54) and in mat
179 ssion glucose was assessed with multivariate adjusted models in 409 of the 421 randomized patients wh
180 ing multivariable logistic regression and PS-adjusted models in the combined group, higher adherence
181 education and cognitive change in unweighted adjusted models, in models incorporating inverse probabi
182 clusters and any musculoskeletal outcome in adjusted models.In a protein-replete cohort of adults, d
191 , 1.94; 95% CI, 1.26-2.97; P = 0.002) in the adjusted models independent of human leukocyte antigen m
194 confidence interval for IFG based on a fully adjusted model: isoleucine 2.29 (1.31-4.01), leucine 1.8
203 had a greater incidence of CKD in the fully adjusted model (odds ratio for fourth versus first quart
204 yle was associated with less diary use in an adjusted model (odds ratio, 0.66; 95% confidence interva
205 incident HF hospitalization in multivariable-adjusted models (odds ratio, 3.30 [1.66-6.52]; P=0.001 f
208 ated with spontaneous preterm birth based on adjusted models of temporal exposures, whereas the spati
212 ciated with spontaneous preterm birth in the adjusted model (OR = 0.90; 95% CI: 0.83, 0.97 per 20 ppb
214 reasing odds of incident depression in fully adjusted models (OR for the fifth compared with first qu
215 cordance was also associated with Y25 CAC in adjusted models (OR: 1.55 and OR: 1.45, respectively).
219 ndently associated with higher WBC counts in adjusted models (P < .01); the highest quartile of WBC c
229 ted with decreased mortality according to an adjusted model: posterior surgical approach (hazard rati
232 ts the overall model was validated, with the adjusted model predicting a 30% reduction in type-2 diab
234 onditions of participation are based on risk-adjusted models produced by the Scientific Registry for
235 Similar results were observed with the HD-PS adjusted model (prostate cancer-specific mortality: aHR,
239 re maintained in all covariate models (fully adjusted model: risk ratio, 0.89; 95% CI, 0.83-0.95), bu
240 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
247 djusted for sex) and a full SCA risk factors-adjusted model (significance, P<0.01=0.05/5, number of t
250 with longer disease duration (P = 0.002) in adjusted models, suggesting a milder disease course.
257 and surgical outcome and then developed two adjusted models that accounted for variations in (1) bas
259 association remained significant in mutually adjusted models that included the 25 x 25 factors (HR 1.
267 ; P = 0.005) than those in the IFA group; in adjusted models, the differences in length (47.6 +/- 0.0
275 cores than the control group in the baseline-adjusted models; the between-group mean difference was -
281 mortality risk in both unadjusted and fully adjusted models: TNF-alpha: hazard ratios (HRs)(1 pg/ml
294 s reinforce the need for comprehensive, risk-adjusted modeling when assessing performance based on pr
295 dds ratio, 2.35; 95% CI, 1.12-4.94) in fully adjusted models, whereas the association of coronary art
296 trate the interaction, a predicted covariate-adjusted model, which was used to derive estimates for t
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