ライフサイエンスコーパス: adjusted for age, sex

1 h 20/40 or better (HR, 1.56; 95% CI, 1.06-2.30; P = 0.024), adjusted for age, sex, and statistically significant covariat

2 h HF was 2.16 (95% confidence interval [CI]: 1.39 to 3.35); adjusted for age, sex, and Charlson comorbidity index; HR: 1.

3 ntia (adjusted hazard ratio [aHR], 1.28; 95% CI, 1.13-1.46) adjusted for age, sex, and race.

4 anoma (odds ratio 2.90, 95% confidence interval 1.07-7.90), adjusted for age, sex, body mass index, and statin use.

5 By Cox analyses adjusted for age, sex, injury severity score, Glascow Coma Sc

6 rences were assessed with multivariable regression analyses adjusted for age, sex, body mass index, smoking, physical act

7 In a multivariable analysis adjusted for age, sex, revised International Prognostic Scori

8 In survival analysis adjusted for age, sex, and comorbidity, cystatin C was near-l

9 year cohort (born before 1940 or born in 1940 or later) and adjusted for age, sex, and race, were used to estimate hazard

10 incident parkinsonism per SD decrease in global cognition, adjusted for age, sex, and study subcohort.

11 hisms (SNPs) with natural log-transformed PTH concentration adjusted for age, sex, season, study site, and principal comp

12 Risk differences adjusted for age, sex, and race/ethnicity (ARDs) assessed tre

13 The HR for falls-adjusted for age, sex, ethnic origin, history of recent fall,

14 the product and marginal effects of the GRS and SSB intake adjusted for age-, sex-, and cohort-specific covariates, with

15 son-years were calculated, and incidence rate ratios (IRRs) adjusted for age, sex, socioeconomic status, smoking, alcohol

16 In a multivariable model adjusted for age, sex, education, dietary and lifestyle facto

17 However, a Cox proportional hazards model, adjusted for age, sex, and genotype for the Duffy antigen/rec

18 A Cox regression model, adjusted for age, sex, race/ethnicity, initial TT indication,

19 on to OH and SBP variability, using a Cox regression model, adjusted for age; sex; smoking status; alcohol intake; SBP; D

20 mortality was assessed with Cox proportional hazards models adjusted for age, sex, AMD severity, VA, history of cataract

21 In Cox proportional hazards models adjusted for age, sex, race, clinical site, education level,

22 Calculations were based on proportional hazards models adjusted for age, sex, race, HIV risk group, calendar year, c

23 In models adjusted for age, sex, chronic disease, socioeconomic status

24 Spatial mixed models adjusted for age, sex, and race were fit to calculate county-

25 cation and IOP were assessed using linear regression models adjusted for age, sex, body mass index, ethnicity, and the me

26 a with those testing negative in logistic regression models adjusted for age, sex, hospital, calendar time, time from ill

27 Multiple Poisson regression models adjusted for age, sex, smoking, socioeconomic status, and bod

28 c melanomas were evaluated using logistic regression models adjusted for age, sex, study center, and primary status (sing

29 cardiovascular mortality, and total mortality in the models adjusted for age, sex, and centre (random effect).

30 95, 2.32), and 2.57 (1.66, 4.04) (P < 0.001 for trend) once adjusted for age, sex, smoking, LDL-cholesterol, BMI, waist c

31 000 person-years were calculated, and incidence rate ratios adjusted for age, sex, and socioeconomic status were estimate

32 s of all outcomes, we used multivariable linear regression, adjusted for age, sex, HIV status, and socioeconomic status.

33 We used logistic regression, adjusted for age, sex, race, state (Iowa or North Carolina),

34 idual plaque bacterial counts in unadjusted models or those adjusted for age, sex, and race (P >0.1 for all).

35 ndependently associated with death or lung transplantation, adjusted for age, sex, and type of PAH.

36 k of progression to dementia and the independent variables, adjusted for age, sex, education, comorbidities, and cognitio

37 Relative risk of death was adjusted for age, sex, race/ethnicity, and season using Poiss

38 We adjusted for age, sex, and commuting between restriction and

39 In the multivariable model, we adjusted for age, sex, smoking, alcohol consumption, educatio

40 Analyses accounted for the complex sampling design and were adjusted for age, sex, and race.

41 Models accounted for familial relatedness and were adjusted for age, sex, total arsenic levels, and population s

42 survival (MSS) estimates up to 5 years after diagnosis were adjusted for age, sex, and 8th edition American Joint Committ

43 Survival models were adjusted for age, sex, alcohol intake, smoking history, and e

44 Models were adjusted for age, sex, and BMO area.

45 All models were adjusted for age, sex, ethnicity, and waist circumference at

46 Models were adjusted for age, sex, race/ethnicity, education, employment

47 d with the use of Cox proportional hazards models that were adjusted for age, sex, body mass index, smoking status, educa

48 In multivariable models that were adjusted for age, sex, urban or rural residence, and socioeco

49 P values were adjusted for age, sex, carotid artery site, and family relati

50 nal 7 were also significant in Cox regression analyses when adjusted for age, sex, and N-terminal probrain natriuretic pe