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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
4 KA, pH and creatinine levels during DKA, and urine albumin and creatinine measurements were analyzed.
5 spectively, >= 0.4 absolute correlation with urine albumin and serum creatinine, known prognosticator
8 EXE intervention significantly reduced the urine albumin concentration (UAC) at week 12 and 24 endp
11 blacks (NHB) and Mexican Americans, whereas urine albumin concentrations were significantly higher i
13 icant reductions in cellular infiltrates and urine albumin, consistent with protection from kidney da
14 ed hypertension (P < 0.001), the increase of urine albumin creatinine ratio (P < 0.01), the fall in g
15 orrelation between serum level of PAI-1 with urine albumin creatinine ratio (UACR) (r = 0.501, p = 0.
16 re considered to have an abnormally elevated urine albumin creatinine ratio if the value was >/=17 mg
17 ell as the threshold reference value for the urine albumin creatinine ratio in the adult intensive ca
19 igh CV risk (history of vascular disease and urine-albumin creatinine ratio [UACR] >200 mg/g), and hi
21 ng both an eGFR under 60 ml/min/1.73m(2) and urine/albumin creatinine ratio over 300 mg/g (5.56, 1.57
22 was 37%, and prevalence of macroalbuminuria (urine/albumin creatinine ratio over 300 mg/g) was 3%.
24 6 (62%) had eGFR <60 ml/min per 1.73 m(2) or urine albumin-creatinine ratio >30 mg/g at discharge.
25 The use of ACE-I or ARB in participants with urine albumin-creatinine ratio >300 mg/g or diabetes was
26 ned as eGFR <60 mL.min(-1).1.73 m(-2) and/or urine albumin-creatinine ratio >300 mg/g) at baseline.
28 <20 vs. >=20 mL/min/1.73 m(2)), albuminuria (urine albumin-creatinine ratio <300 vs. >=300 mg/g), and
29 0, >/=90 mL.min(-1).1.73 m(-2)) and baseline urine albumin-creatinine ratio (>300, 30-</=300, <30 mg/
31 % CI 0.94 to 4.86; P = 0.004), a decrease in urine albumin-creatinine ratio (ETD 24 weeks, -25.0%, 95
32 covariates, including for baseline eGFR and urine albumin-creatinine ratio (UACR) in longitudinal an
33 serum creatinine, estimated GFR (eGFR), and urine albumin-creatinine ratio (UACR) in search of genet
35 ns that adjusted for known risk factors, the urine albumin-creatinine ratio (UACR) was a significant
37 ere consistent across categories of eGFR and urine albumin-creatinine ratio at baseline and across th
38 urine metabolite associations with eGFR and urine albumin-creatinine ratio in an older community-bas
39 ration rate less than 60 mL/min/1.73 m2 or a urine albumin-creatinine ratio of 30 mg/g or higher for
41 in the simvastatin-treated group, as was the urine albumin-creatinine ratio on day 7 postsurgery.
42 KIM-1), urine biomarkers (EGF/creatinine and urine albumin-creatinine ratio), and eGFR identified fou
43 seline brachial artery diameter (PAI-1, CRP, urine albumin-creatinine ratio), baseline mean flow (N-A
46 line estimated glomerular filtration rate or urine albumin-creatinine ratio, or prerandomization left
47 igher serum potassium, lower eGFR, increased urine albumin-creatinine ratio, younger age, female sex,
48 igher serum potassium, lower eGFR, increased urine albumin-creatinine ratio, younger age, female sex,
51 oth estimated glomerular filtration rate and urine-albumin-creatinine ratio to stratify risk more com
52 L/min/1.73 m, P=0.21) and albumin excretion (urine albumin/ creatinine 9.76+/-23.6 mg/g vs. 5.91+/-11
53 filtration rate <60 mL/min per 1.73 m(2) or urine albumin/creatinine >30 mg/g) and available echocar
55 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
57 ) at a 1992-1996 research clinic visit, when urine albumin/creatinine ratio (ACR) was measured in spo
58 dex (BMI), glomerular filtration rate (GFR), urine albumin/creatinine ratio (ACR), hypertension, majo
59 idence of CKD events and changes in eGFR and urine albumin/creatinine ratio (UACR) in participants ra
60 raacetic acid clearance) was associated with urine albumin/creatinine ratio (UACR) post-HTx in a subg
62 rotein cholesterol, creatinine, glucose, and urine albumin/creatinine ratio as standard risk factors,
63 mplete blood count, serum creatinine level), urine albumin/creatinine ratio measure, and a measure of
67 methods, we identified a biomarker panel of urine albumin/creatinine, urine EGF/creatinine, plasma K
68 effect was more pronounced in patients with urine albumin:creatinine ratio >=1000 mg/g, for whom the
69 participants of the JHS, aged 21-84 y, with urine albumin:creatinine ratio < 30 mg/g, and eGFR >= 60
71 imated glomerular filtration rate (eGFR) and urine albumin:creatinine ratio (UACR) in pooled patient-
72 ly grade 1-2 toxicities, including increased urine albumin:creatinine ratio (UACR), proteinuria, peri
73 ATP6AP2 knockout significantly increased urine albumin:creatinine ratio in both ND and HFD fed mi
74 incident CKD, albuminuria (defined as a spot urine albumin:creatinine ratio of >30 mg/g or albumin ex
75 FR, 31.7 ml per minute per 1.73 m(2); median urine albumin:creatinine ratio, 716.9; mean serum urate
77 eduction with once-daily diltiazem decreased urine albumin excretion (2967 +/- 784 mg/d at baseline c
78 =192) and albumin-creatinine ratio and 24-hr urine albumin excretion (n=189) in stable renal transpla
79 tion, specifically serum uric acid (SUA) and urine albumin excretion (UAE), and that high sodium inta
81 s admixture to identify associations between urine albumin excretion (urine albumin-to-creatinine rat
82 us studies have found an association between urine albumin excretion and Amerindian ancestry in Hispa
83 assessment of GFR in addition to monitoring urine albumin excretion and funduscopic changes to ensur
84 eated diabetic mice (P < 0.04) and had lower urine albumin excretion at 10 weeks than VEH-treated dia
90 ted from podocytes exhibited an elevation in urine albumin excretion that was accompanied by increase
93 nth-old mice revealed a 1.7-fold increase in urine albumin excretion, accelerated glomerulosclerosis,
94 ng to estimated glomerular filtration rates, urine albumin excretion, and diagnoses from medical reco
95 ment of glomerular filtration rate (GFR) and urine albumin excretion, and kidney injury was evaluated
96 t of diabetic nephropathy with elevations in urine albumin excretion, glomerular and renal hypertroph
98 sociation of urinary albumin excretion (spot urine albumin indexed to creatinine [UACR]) and the inci
99 ld G6PD-deficient mice (17-20 mo) had higher urine albumin levels and also had evidence for increased
100 children with type 1 diabetes with 1 or more urine albumin levels measured during routine diabetes ca
104 y, and microalbuminuria, measured using spot urine albumin (SUA) and urine albumin-creatinine ratio (
105 m creatinine to estimate kidney function and urine albumin to assess for kidney and endothelial damag
106 type 2 diabetes and chronic kidney disease (urine albumin to creatine ratio, 30-5000 mg/g, estimated
107 fined as diabetes with albuminuria (ratio of urine albumin to creatinine >/=30 mg/g), impaired glomer
108 cts underwent uric acid, iothalamte GFR, and urine albumin to creatinine (ACR) measurements annually
109 lf-reported hypertension), microalbuminuria (urine albumin to creatinine ratio >30 mg/g), and chronic
110 mated from calibrated serum creatinine, spot urine albumin to creatinine ratio (ACR), age, gender, an
112 ere 2.38 (95% CI, 1.03-4.29) in those with a urine albumin to creatinine ratio (UACR) less than 300 m
113 R) of 30 to less than 90 mL/min/1.73 m(2), a urine albumin to creatinine ratio (UACR) of 200 to less
114 ne if either eGFR under 60mL/min/1.73m(2) or urine albumin to creatinine ratio 3 mg/mmol or more.
115 lar filtration rate < 60 mL/min/1.73 m(2) or urine albumin to creatinine ratio 3 mg/mmol) were exclud
116 [eGFR] < 60 mL/min/1.73 m2) and albuminuria (urine albumin to creatinine ratio [uACR]) > 30 mg/g).
117 In diabetic mice, PRR knockdown decreased urine albumin to creatinine ratio and the renal expressi
118 ate of less than 45 mL/min/1.73 m2, and/or a urine albumin to creatinine ratio of greater than 30 mg/
119 and December 31, 2019, and had an available urine albumin to creatinine ratio within 90 days of a se
120 Spot urine protein to creatinine ratio, spot urine albumin to creatinine ratio, creatinine clearance,
121 etabolite associations within strata of age, urine albumin to creatinine ratio, diabetes and Hispanic
122 imated glomerular filtration rate and higher urine albumin to creatinine ratios were associated with
123 ith diabetes, hypertension, and albuminuria (urine albumin-to-creatinine ratio > or =300 mg/g) who al
124 ) <60 ml/min per 1.73 m(2); we defined MA as urine albumin-to-creatinine ratio >/=25 (women) or 17 (m
126 atinine ratio >/=30 mg/g), macroalbuminuria (urine albumin-to-creatinine ratio >/=300 mg/g), reduced
127 CKD (eGFR<60 ml/min per 1.73 m(2) [n=832] or urine albumin-to-creatinine ratio >30 mg/g [n=577]).
129 etes and albuminuric chronic kidney disease (urine albumin-to-creatinine ratio >=30 to <300 mg/g and
130 te >=25 to <=90 mL per min per 1.73 m(2), or urine albumin-to-creatinine ratio >=300 to <=5000 mg/g a
131 ar filtration rate < or >=60 mL/min/1.73 m2, urine albumin-to-creatinine ratio < or >=300 mg/g, or Ki
133 In type 1 diabetes, changes in the GFR and urine albumin-to-creatinine ratio (ACR) are related to c
134 imated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio (ACR) at baseline.
136 (730,577 person-years) from 14 studies with urine albumin-to-creatinine ratio (ACR) measurements and
137 change in albuminuria, measured as change in urine albumin-to-creatinine ratio (ACR) or urine protein
138 ntify associations of creatinine-based eGFR, urine albumin-to-creatinine ratio (ACR), and dipstick pr
139 ion (KFRE) uses the 4 variables of age, sex, urine albumin-to-creatinine ratio (ACR), and estimated g
142 15 to <30, or <15 ml/min per 1.73 m(2)) and urine albumin-to-creatinine ratio (ACR; >300, 30-300, or
144 r of added kidney measures was cysC-eGFR and urine albumin-to-creatinine ratio (DeltaC=0.019 [95% CI,
145 inor allele frequency=0.01, P=1.6x10(-8)) or urine albumin-to-creatinine ratio (rs527493184 at ZBTB16
146 d GFR (eGFR) <60 ml/min per 1.73 m(2) and/or urine albumin-to-creatinine ratio (UACR) >/= 3.5 mg/mmol
147 ension, we examined the relationship between urine albumin-to-creatinine ratio (UACR) and cardiac mec
150 e complementary prognostic value of baseline urine albumin-to-creatinine ratio (uACR) and plasma solu
151 ate (eGFR) of 25-<60 mL/min per 1.73 m(2), a urine albumin-to-creatinine ratio (UACR) of >100-<=5000
152 in per 1.73 m(2) of body surface area, and a urine albumin-to-creatinine ratio (UACR) of 300-5000 mg/
153 to less than 60 mL/min/1.73 m2, doubling of urine albumin-to-creatinine ratio (UACR) to 30 mg/g or g
154 Albuminuria, routinely assessed as spot urine albumin-to-creatinine ratio (UACR), indicates stru
156 rate clearance; albuminuria was estimated by urine albumin-to-creatinine ratio (UACR); and M/I was es
157 etes and albuminuric chronic kidney disease (urine albumin-to-creatinine ratio 30 to <300 mg/g and es
159 l included patients with type 2 diabetes and urine albumin-to-creatinine ratio 30 to 5000 mg/g and an
160 l included patients with type 2 diabetes and urine albumin-to-creatinine ratio 30 to 5000 mg/g and an
161 n rate 25 to 90 mL per min per 1.73 m(2), or urine albumin-to-creatinine ratio 300 to 5000 mg/g and e
162 tion 11 years, and GFR 153 mL/min and median urine albumin-to-creatinine ratio 36 mg/g), 69 progresse
163 ria; 60 had historic or current albuminuria (urine albumin-to-creatinine ratio [UACR] >=30 mg/g]), an
164 iltration rate [eGFR] >60 ml/min/1.73 m2 and urine albumin-to-creatinine ratio [uACR] <3 mg/mmol) at
165 y of type 2 diabetes, increased albuminuria (urine albumin-to-creatinine ratio [UACR] 30-3500 mg/g),
166 ssociations between urine albumin excretion (urine albumin-to-creatinine ratio [UACR]) and genomic re
167 ) study for the association between baseline urine albumin-to-creatinine ratio and estimated GFR (eGF
168 o had been assessed in 2006 to 2010 with the urine albumin-to-creatinine ratio and estimated glomerul
169 s when clinically indicated for measurement (urine albumin-to-creatinine ratio and hemoglobin A1c) or
170 rt failure) and include optional predictors (urine albumin-to-creatinine ratio and hemoglobin A1c), a
171 used parameters (glomerular filtration rate, urine albumin-to-creatinine ratio and urine protein-to-c
172 sistent for a prespecified baseline eGFR and urine albumin-to-creatinine ratio categories (P(interact
176 .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/
177 for estimated glomerular filtration rate and urine albumin-to-creatinine ratio in up to 12 207 Hispan
178 ml/min per 100 g body wt, P = 0.02), and the urine albumin-to-creatinine ratio increased markedly (co
179 imated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio into low-, moderate-,
180 mated glomerular filtration rate categories, urine albumin-to-creatinine ratio levels, and KDIGO risk
182 outcomes in patients with type 2 diabetes, a urine albumin-to-creatinine ratio of 30-5000 mg/g, an es
183 R 43 (SD 11) ml/min per 1.73 m(2) and median urine albumin-to-creatinine ratio of 362 mg/g (interquar
184 nt signs of kidney damage, such as increased urine albumin-to-creatinine ratio or a GFR below the thr
185 344, P=9.3x10(-11)) and validated 8 loci for urine albumin-to-creatinine ratio previously identified
186 eatment effect for death due to any cause by urine albumin-to-creatinine ratio was .01 [<300 mg/g HR
188 Calibration improved significantly when the urine albumin-to-creatinine ratio was added to the base
189 kidney measures (creat-eGFR, cysC-eGFR, and urine albumin-to-creatinine ratio) led to significant im
192 sted models for demographics, baseline eGFR, urine albumin-to-creatinine ratio, comorbidity, and meas
193 acute eGFR decline included higher baseline urine albumin-to-creatinine ratio, eGFR, systolic blood
194 was small but statistically significant when urine albumin-to-creatinine ratio, hemoglobin A1c, and s
195 , human immunodeficiency virus (HIV) status, urine albumin-to-creatinine ratio, hemoglobin, and lipid
196 tion group had higher hemoglobin A1c, higher urine albumin-to-creatinine ratio, increased glomerular
207 Tirzepatide treatment was associated with urine albumin-to-creatinine reduction after 24 weeks, wh