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1 ein, lactate dehydrogenase, electrolytes, or urine albumin.
2 tive sample of subjects, the distribution of urine albumin and creatinine concentrations was examined
3 assessment of albuminuria includes measuring urine albumin and creatinine in an untimed spot urine co
8 blacks (NHB) and Mexican Americans, whereas urine albumin concentrations were significantly higher i
10 ed hypertension (P < 0.001), the increase of urine albumin creatinine ratio (P < 0.01), the fall in g
11 re considered to have an abnormally elevated urine albumin creatinine ratio if the value was >/=17 mg
12 ell as the threshold reference value for the urine albumin creatinine ratio in the adult intensive ca
13 ned as eGFR <60 mL.min(-1).1.73 m(-2) and/or urine albumin-creatinine ratio >300 mg/g) at baseline.
14 0, >/=90 mL.min(-1).1.73 m(-2)) and baseline urine albumin-creatinine ratio (>300, 30-</=300, <30 mg/
16 serum creatinine, estimated GFR (eGFR), and urine albumin-creatinine ratio (UACR) in search of genet
18 ns that adjusted for known risk factors, the urine albumin-creatinine ratio (UACR) was a significant
19 ere consistent across categories of eGFR and urine albumin-creatinine ratio at baseline and across th
21 in the simvastatin-treated group, as was the urine albumin-creatinine ratio on day 7 postsurgery.
22 seline brachial artery diameter (PAI-1, CRP, urine albumin-creatinine ratio), baseline mean flow (N-A
27 L/min/1.73 m, P=0.21) and albumin excretion (urine albumin/ creatinine 9.76+/-23.6 mg/g vs. 5.91+/-11
28 filtration rate <60 mL/min per 1.73 m(2) or urine albumin/creatinine >30 mg/g) and available echocar
30 1.3 vs. 1.0+/-1.0 mg/dl, p<0.001) and higher urine albumin/creatinine levels (3.6+/-2.3 vs. 3.3+/-2.0
31 ) at a 1992-1996 research clinic visit, when urine albumin/creatinine ratio (ACR) was measured in spo
32 dex (BMI), glomerular filtration rate (GFR), urine albumin/creatinine ratio (ACR), hypertension, majo
33 raacetic acid clearance) was associated with urine albumin/creatinine ratio (UACR) post-HTx in a subg
34 rotein cholesterol, creatinine, glucose, and urine albumin/creatinine ratio as standard risk factors,
35 mplete blood count, serum creatinine level), urine albumin/creatinine ratio measure, and a measure of
37 incident CKD, albuminuria (defined as a spot urine albumin:creatinine ratio of >30 mg/g or albumin ex
39 eduction with once-daily diltiazem decreased urine albumin excretion (2967 +/- 784 mg/d at baseline c
40 =192) and albumin-creatinine ratio and 24-hr urine albumin excretion (n=189) in stable renal transpla
41 tion, specifically serum uric acid (SUA) and urine albumin excretion (UAE), and that high sodium inta
43 s admixture to identify associations between urine albumin excretion (urine albumin-to-creatinine rat
44 us studies have found an association between urine albumin excretion and Amerindian ancestry in Hispa
45 assessment of GFR in addition to monitoring urine albumin excretion and funduscopic changes to ensur
46 eated diabetic mice (P < 0.04) and had lower urine albumin excretion at 10 weeks than VEH-treated dia
51 ted from podocytes exhibited an elevation in urine albumin excretion that was accompanied by increase
54 nth-old mice revealed a 1.7-fold increase in urine albumin excretion, accelerated glomerulosclerosis,
55 t of diabetic nephropathy with elevations in urine albumin excretion, glomerular and renal hypertroph
56 sociation of urinary albumin excretion (spot urine albumin indexed to creatinine [UACR]) and the inci
57 ld G6PD-deficient mice (17-20 mo) had higher urine albumin levels and also had evidence for increased
61 fined as diabetes with albuminuria (ratio of urine albumin to creatinine >/=30 mg/g), impaired glomer
62 cts underwent uric acid, iothalamte GFR, and urine albumin to creatinine (ACR) measurements annually
63 lf-reported hypertension), microalbuminuria (urine albumin to creatinine ratio >30 mg/g), and chronic
64 mated from calibrated serum creatinine, spot urine albumin to creatinine ratio (ACR), age, gender, an
66 Spot urine protein to creatinine ratio, spot urine albumin to creatinine ratio, creatinine clearance,
67 imated glomerular filtration rate and higher urine albumin to creatinine ratios were associated with
68 ith diabetes, hypertension, and albuminuria (urine albumin-to-creatinine ratio > or =300 mg/g) who al
69 ) <60 ml/min per 1.73 m(2); we defined MA as urine albumin-to-creatinine ratio >/=25 (women) or 17 (m
71 atinine ratio >/=30 mg/g), macroalbuminuria (urine albumin-to-creatinine ratio >/=300 mg/g), reduced
72 CKD (eGFR<60 ml/min per 1.73 m(2) [n=832] or urine albumin-to-creatinine ratio >30 mg/g [n=577]).
74 (730,577 person-years) from 14 studies with urine albumin-to-creatinine ratio (ACR) measurements and
75 ntify associations of creatinine-based eGFR, urine albumin-to-creatinine ratio (ACR), and dipstick pr
77 15 to <30, or <15 ml/min per 1.73 m(2)) and urine albumin-to-creatinine ratio (ACR; >300, 30-300, or
78 d GFR (eGFR) <60 ml/min per 1.73 m(2) and/or urine albumin-to-creatinine ratio (UACR) >/= 3.5 mg/mmol
79 ension, we examined the relationship between urine albumin-to-creatinine ratio (UACR) and cardiac mec
80 iltration rate [eGFR] >60 ml/min/1.73 m2 and urine albumin-to-creatinine ratio [uACR] <3 mg/mmol) at
81 ssociations between urine albumin excretion (urine albumin-to-creatinine ratio [UACR]) and genomic re
82 ) study for the association between baseline urine albumin-to-creatinine ratio and estimated GFR (eGF
83 used parameters (glomerular filtration rate, urine albumin-to-creatinine ratio and urine protein-to-c
86 .6 to 3.0), and 4.8 (95% CI, 3.2 to 7.2) for urine albumin-to-creatinine ratio groups of 11 to 29 mg/
87 ml/min per 100 g body wt, P = 0.02), and the urine albumin-to-creatinine ratio increased markedly (co
88 sted models for demographics, baseline eGFR, urine albumin-to-creatinine ratio, comorbidity, and meas
89 , human immunodeficiency virus (HIV) status, urine albumin-to-creatinine ratio, hemoglobin, and lipid
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