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1 ARIC participants were enrolled from four communities ac
2 ARIC participants with elevated hs-CRP and low LDL-C had
3 ARIC-based limits for diastolic function improved risk d
4 ARIC-based reference limits for TDI e' (4.6 and 5.2 cm/s
6 KD using whole-blood DNA methylation of 2264 ARIC Study and 2595 Framingham Heart Study participants
10 a median follow-up of 7.3 and 13.1 years, 44 ARIC study participants and 275 CHS participants had SCD
12 d by genotyping an independent sample of 718 ARIC African Americans (minor allele frequency=1%; P=1.2
13 ing serum creatinine were measured among 807 ARIC participants with CKD (estimated GFR between 15 and
15 cantly associated with CKD progression among ARIC participants overall and among those without baseli
16 3, 8.5, and 14.4 per 1000 person-years among ARIC participants with an estimated GFR of >/=90, 60 to
19 ted Framingham, recalibrated Health ABC, and ARIC risk scores by 18%, 12%, and 13%, respectively.
20 correlates of circulating LCMUFAs in CHS and ARIC and US dietary sources of LCMUFAs in the 2003-2010
21 re related to circulating LCMUFAs in CHS and ARIC, consistent with food sources of LCMUFAs in NHANES,
22 ent congestive heart failure in both CHS and ARIC; hazard ratios were 1.34 (95% confidence interval,
24 r allele frequency 4.45 and 3.96% in FHS and ARIC, respectively) was associated with higher CKD preva
25 After adjustment for age, race, gender, and ARIC field center, among those with CKD, the relative ri
26 activity, lipid levels, blood pressure, and ARIC Study center, compared with adults who never smoked
27 dney function, the age-, gender-, race-, and ARIC field center-adjusted RR for PAD was 1.04 (95% conf
28 ecalibrated, Health ABC HF recalibrated, and ARIC risk scores were 0.610, 0.762, 0.783, and 0.797, re
29 tudied 9240 individuals without HF or CVD at ARIC visit 4 and followed them for a mean of 10.5 years.
30 ses were ascertained by electrocardiogram at ARIC follow-up visits, hospital discharge diagnosis, or
33 nical stroke who underwent a cerebral MRI at ARIC visit 3 (n = 1622) and a second cerebral MRI approx
34 cestry individuals from the population-based ARIC (Atherosclerosis Risk In Communities) Study cohort
35 had DBP between 80 to 89 mm Hg at baseline (ARIC visit 2), the adjusted odds ratio of having hs-cTnT
36 al CHD incidence was assessed from baseline (ARIC=1987-1989, CHS=1989-1990, REGARDS=2003-2007) throug
41 rticipants of four population-based cohorts (ARIC, CHS, FHS, RS; n = 19,877; 2,388 CKD cases), and te
42 3), the Atherosclerosis Risk in Communities (ARIC) (n = 12341) study, and the Health, Aging, and Body
43 in the Atherosclerosis Risk in Communities (ARIC) and Multi-Ethnic Study of Atherosclerosis cohorts.
44 in the Atherosclerosis Risk in Communities (ARIC) cohort (3679 African-Americans and 10 427 Whites)
46 rom the Atherosclerosis Risk in Communities (ARIC) cohort study who underwent 3-dimensional intracran
48 The Atherosclerosis Risk in Communities (ARIC) cohort was followed for a median of 13 years for C
49 rom the Atherosclerosis Risk in Communities (ARIC) cohort, we tested the hypotheses that the incidenc
50 rom the Atherosclerosis Risk in Communities (ARIC) cohort, which sampled middle-aged adults and their
53 examine Atherosclerosis Risk in Communities (ARIC) participants in midlife and to explore association
57 of the Atherosclerosis Risk in Communities (ARIC) study (76+/-5 years and 60% women) who underwent t
58 in the Atherosclerosis Risk in Communities (ARIC) Study (mean age-62 years, moderate CP-43% and seve
62 89, the Atherosclerosis Risk in Communities (ARIC) Study analyzed plasma fatty acids in cholesteryl e
63 of the Atherosclerosis Risk in Communities (ARIC) study and 4559 participants of the Cardiovascular
64 in the Atherosclerosis Risk in Communities (ARIC) Study and compared it with these other schemes.
65 in the Atherosclerosis Risk in Communities (ARIC) study and focusing on loss-of-function (LoF) varia
66 rom the Atherosclerosis Risk in Communities (ARIC) study and included 7,260 nondiabetic Caucasian ind
67 of the Atherosclerosis Risk in Communities (ARIC) Study and interrogated the regions of the nine pub
68 rom the Atherosclerosis Risk in Communities (ARIC) Study and quantified the independent association b
72 blished Atherosclerosis Risk in Communities (ARIC) Study criteria with the presence or absence of an
73 in the Atherosclerosis Risk in Communities (ARIC) study for the association between baseline urine a
78 The Atherosclerosis Risk in Communities (ARIC) study investigators, for example, typically report
79 The Atherosclerosis Risk in Communities (ARIC) study is a large, predominantly biracial, National
81 rom the Atherosclerosis Risk in Communities (ARIC) study matched for age, gender, and, for the majori
84 14 569 Atherosclerosis Risk in Communities (ARIC) study participants aged 45 to 64 years with mean f
85 in the Atherosclerosis Risk in Communities (ARIC) study participants at 5 examination visits between
86 ed 6516 Atherosclerosis Risk in Communities (ARIC) Study participants who were free of prevalent hype
87 14,590 Atherosclerosis Risk In Communities (ARIC) study participants with lipid measurements in 1987
88 iologic Atherosclerosis Risk in Communities (ARIC) study reported that plasma protein C may be protec
89 ased on Atherosclerosis Risk in Communities (ARIC) Study surveillance adjudicating 12,450 eligible ho
90 hin the Atherosclerosis Risk in Communities (ARIC) Study to determine the association between plasma
92 of the Atherosclerosis Risk in Communities (ARIC) Study was conducted from 1987-1989 through 2011-20
93 rom the Atherosclerosis Risk in Communities (ARIC) study were enrolled in the ARIC Carotid MRI Study.
95 in the Atherosclerosis Risk in Communities (ARIC) Study who attended visit 4 (1996-1998) were analyz
96 rom the Atherosclerosis Risk in Communities (ARIC) Study who were aged 45-64 years at baseline (1987-
97 in the Atherosclerosis Risk in Communities (ARIC) Study who were aged 47-68 years, had normal kidney
98 rom the Atherosclerosis Risk in Communities (ARIC) study who were free of cardiovascular disease at b
99 rom the Atherosclerosis Risk in Communities (ARIC) study who were free of coronary heart disease at b
100 of the Atherosclerosis Risk in Communities (ARIC) study who were free of prevalent HF at baseline we
101 in the Atherosclerosis Risk in Communities (ARIC) study who were in sinus rhythm, free of valvular d
102 in the Atherosclerosis Risk in Communities (ARIC) Study with acute incident MI, there was a decline
103 in the Atherosclerosis Risk in Communities (ARIC) study without cardiovascular disease at baseline (
104 of the Atherosclerosis Risk in Communities (ARIC) Study without heart failure or diabetes at baselin
105 rom the Atherosclerosis Risk in Communities (ARIC) Study, 14,280 middle-aged adults were categorized
106 in the Atherosclerosis Risk in Communities (ARIC) study, 21,222 in the Women's Genome Health Study (
107 in the Atherosclerosis Risk in Communities (ARIC) Study, a community-based prospective cohort of whi
108 rom the Atherosclerosis Risk in Communities (ARIC) Study, a large multicenter cohort study that enrol
109 of the Atherosclerosis Risk in Communities (ARIC) Study, a population-based cohort of adults in 4 US
110 in the Atherosclerosis Risk in Communities (ARIC) study, a prospective cohort study of subjects aged
111 S), the Atherosclerosis Risk in Communities (ARIC) Study, and the Cardiovascular Health Study (CHS).
112 rom the Atherosclerosis Risk in Communities (ARIC) study, and the GWAS for PT was conducted in 2,583
114 rom the Atherosclerosis Risk in Communities (ARIC) study, Cardiovascular Health Study (CHS), and Fram
115 in the Atherosclerosis Risk in Communities (ARIC) Study, comprising 6,429 men in four US communities
116 n-based Atherosclerosis Risk in Communities (ARIC) study, including associations with eGFR decline, v
117 ongoing Atherosclerosis Risk in Communities (ARIC) Study, the authors assessed the relation of tradit
118 of the Atherosclerosis Risk in Communities (ARIC) study, the Illumina Infinium HumanMethylation450 (
119 in the Atherosclerosis Risk in Communities (ARIC) Study, was used to assess LV dimensions in 1572 bl
120 dy, the Atherosclerosis Risk in Communities (ARIC) Study, we measured change in performance on 3 cogn
121 in the Atherosclerosis Risk in Communities (ARIC) Study, who received a complete periodontal examina
153 at the Atherosclerosis Risk in Communities (ARIC) visit 4 using both tooth loss and clinical signs o
154 The Atherosclerosis Risk in Communities (ARIC)-PET Amyloid Imaging Study, a prospective cohort st
156 tates (Atherosclerosis Risks in Communities [ARIC] and Cardiovascular Health Study [CHS]) to assess t
159 d the Atherosclerosis Risk In the Community (ARIC) visit 5 examination (2011-2013) and underwent tran
160 plored as a secondary analysis of the Dental ARIC (Atherosclerosis Risk in Communities) study using s
162 centile values for the hs-cTnT assay in DHS, ARIC, and CHS were 18, 22, and 36 ng/l (subcohort 1) and
165 core variables had a C statistic of 0.61 for ARIC study and 0.67 for CHS; the full multivariable mode
169 events involving hospitalization in the four ARIC communities had ICD-9-CM codes screened for AMI.
171 ere 0.78, 0.84, and 0.83 for the Framingham, ARIC, and San Antonio risk prediction models, respective
177 1.89 (95% confidence interval, 1.42-2.51) in ARIC, 1.25 (95% confidence interval, 0.81-1.92) in REGAR
181 ck versus white men 45 to 64 years of age in ARIC and REGARDS were 2.09 (95% confidence interval, 1.4
186 s is the first study to characterize CNPs in ARIC and the first genome-wide analysis of CNPs and uric
190 CP, no other loci were associated with CP in ARIC or aggressive periodontitis in the German sample.
191 de significant interactions were detected in ARIC for systolic blood pressure between PLEKHA7 (a know
194 hazards ratio estimates for incident IHD in ARIC (Pearson correlation [r]=0.62), indicating that the
196 the test of gene-environment interaction in ARIC EA participants, the index variant at MUC1 had 2.5
197 enome-wide significant local interactions in ARIC in the 4p16.1 region located mostly in an intergeni
199 festyle to 5.1% for a favorable lifestyle in ARIC, from 4.6% to 2.0% in WGHS, and from 8.2% to 5.3% i
200 nal effects and three epistatic SNP pairs in ARIC-three marginal SNPs were located within SLC2A9 and
202 r multivariable adjustment, hazard ratios in ARIC and REGARDS were 0.67 (95% confidence interval, 0.3
203 ardiovascular risk factors, hazard ratios in ARIC and REGARDS were 1.19 (95% confidence interval, 0.7
204 bes passed the threshold for significance in ARIC (P < 1 x 10(-7); Bonferroni), including probes in t
205 nteraction P = 2.9 x 10(-9)) with smoking in ARIC was not replicated in Health ABC, although estimate
207 ents occurred during 39 238 person-years; in ARIC, 330 events congestive heart failure events occurre
208 Association Detection Project in Industry), ARIC (Atherosclerosis Risk in Communities), and CHS (Car
209 validate these findings for CP in the larger ARIC cohort (n = 821 participants with severe CP, 2031-m
212 95% confidence interval, 1.20-2.73) but not ARIC (hazard ratio, 1.21; 95% confidence interval, 0.96-
218 , Atherosclerosis Risk in Communities Study (ARIC), and Multiethnic Study of Atherosclerosis (MESA).
219 e Atherosclerosis Risk in Communities Study (ARIC), the Cardiovascular Health Study (CHS), and the Re
220 e Atherosclerosis Risk in Communities study (ARIC), the Cardiovascular Health Study (CHS), and the Re
221 e Atherosclerosis Risk in Communities study (ARIC, n = 15,792; enrollment age, 45-64 years; enrollmen
222 e Atherosclerosis Risk in Communities Study (ARIC; n = 11,061 self-identified white and n = 4014 blac
223 2013, through the ARIC Neurocognitive Study (ARIC-NCS), participants underwent a detailed neurocognit
225 a large population-based prospective study, ARIC (Atherosclerosis Risk in Communities), and in the p
230 nterview, for participants not attending the ARIC-NCS visit, or by an International Classification of
232 he genetic correlation estimates between the ARIC risk factors and the EHR IHD were modestly linearly
234 coronary disease age 45 to 74 years from the ARIC (Atherosclerosis Risk In Communities) and CHS (Card
235 The authors studied 11,565 adults from the ARIC (Atherosclerosis Risk In Communities) cohort, analy
238 African Americans (27%) and whites from the ARIC cohort [aged 45-64 y at baseline (1987-1989)] were
241 ed on 2383 participants (1993-1995) from the ARIC study (Atherosclerosis Risk in Communities; 100% bl
242 ETHODS AND We used ECG measurements from the ARIC study (Atherosclerosis Risk in Communities; n=6731
243 an independent subsample (N = 1088) from the ARIC study, suggests that the ABO blood group may influe
244 80 African Americans) were selected from the ARIC Study--a prospective investigation of atheroscleros
246 otal of 16,169 European individuals from the ARIC, GHS, MARTHA and PROCARDIS studies, were meta-analy
247 dy included 11,715 middle-aged adults in the ARIC (Atherosclerosis Risk In Communities) cohort with h
248 mean baseline age 59 years, 43% male) in the ARIC (Atherosclerosis Risk In Communities) study and the
249 up.Among 14,082 participants enrolled in the ARIC (Atherosclerosis Risk in Communities) Study initial
250 d with acute or chronic heart failure in the ARIC (Atherosclerosis Risk In Communities) study surveil
251 f European descent (aged 45-64 years) in the ARIC (Atherosclerosis Risk in Communities) study were fo
256 models discriminated reasonably well in the ARIC and Multi-Ethnic Study of Atherosclerosis data (C s
262 ardiographic measures in participants in the ARIC study (Atherosclerosis Risk in Communities) (n=13 6
263 cular disease events or heart failure in the ARIC Study (Atherosclerosis Risk in Communities) underwe
267 , and the 12 independent risk factors in the ARIC study included age, male sex, black race, current s
269 spective cohort study of participants in the ARIC study who did not have diagnosed diabetes and who a
270 (P = 0.16 in North Carolina; P = 0.97 in the ARIC study) and did not segregate with type 2 diabetes i
271 y investigated in the female subgroup in the ARIC study, and the CARE and WOSCOPS trials included onl
272 his lack of association was confirmed in the ARIC study, even after the analysis was restricted to le
274 s and 1635 participants with diabetes in the ARIC study, who did not have cardiovascular disease, wer
278 s) (n = 2029, p value = 6.7 x 10(-3)) of the ARIC and was confirmed by replication in both EAs and AA
281 e optimism-corrected area under curve of the ARIC HF risk score increased from 0.773 (95% CI, 0.753-0
282 ighest category (>/=0.014 mug/L; 7.4% of the ARIC population) had significantly increased risk for CH
283 valvular disease from the fifth visit of the ARIC study (Atherosclerosis Risk in Communities) who und
286 The community surveillance component of the ARIC Study consisted of tracking residents 35 to 74 year
289 Most recently, in 2011-2013, through the ARIC Neurocognitive Study (ARIC-NCS), participants under
293 estimated from 4,089 women is comparable to ARIC in direction and magnitude (1.414.707.88, p=5.46x10
298 specificity of the automated algorithm with ARIC reviewer panel as the referent standard were 0.68 (
299 phenotype was most strongly correlated with ARIC metabolic phenotypes, including total:high-density
300 0 participants, the mean age was 62.4 years (ARIC, 57.9 years; MESA, 62.4 years; and CHS, 72.5 years)
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