Abstract
Background
Chronic kidney disease (CKD) is highly prevalent but identification of patients at high risk for fast CKD progression before reaching end-stage renal disease in the short-term has been challenging. Whether factors associated with fast progression vary by diabetes status is also not well understood. We examined a large community-based cohort of adults with CKD to identify predictors of fast progression during the first 2 years of follow-up in the presence or absence of diabetes mellitus.
Methods
Within a large integrated healthcare delivery system in northern California, we identified adults with estimated glomerular filtration rate (eGFR) 30–59 ml/min/1.73 m2 by CKD-EPI equation between 2008 and 2010 who had no previous dialysis or renal transplant, who had outpatient serum creatinine values spaced 10–14 months apart and who did not initiate renal replacement therapy, die or disenroll during the first 2 years of follow-up. Through 2012, we calculated the annual rate of change in eGFR and classified patients as fast progressors if they lost > 4 ml/min/1.73 m2 per year. We used multivariable logistic regression to identify patient characteristics that were independently associated with fast CKD progression stratified by diabetes status.
Results
We identified 36,195 eligible adults with eGFR 30–59 ml/min/1.73 m2 and mean age 73 years, 55% women, 11% black, 12% Asian/Pacific Islander and 36% with diabetes mellitus. During 24-month follow-up, fast progression of CKD occurred in 23.0% of patients with diabetes vs. 15.3% of patients without diabetes. Multivariable predictors of fast CKD progression that were similar by diabetes status included proteinuria, age ≥ 80 years, heart failure, anemia and higher systolic blood pressure. Age 70–79 years, prior ischemic stroke, current or former smoking and lower HDL cholesterol level were also predictive in patients without diabetes, while age 18–49 years was additionally predictive in those with diabetes.
Conclusions
In a large, contemporary population of adults with eGFR 30–59 ml/min/1.73 m2, accelerated progression of kidney dysfunction within 2 years affected ~ 1 in 4 patients with diabetes and ~ 1 in 7 without diabetes. Regardless of diabetes status, the strongest independent predictors of fast CKD progression included proteinuria, elevated systolic blood pressure, heart failure and anemia.
Keywords: Diabetes, Chronic kidney disease, Progression, Risk factors, Proteinuria, Anemia, Blood pressure
Background
The population burden of chronic kidney disease (CKD) is high, with an estimated prevalence of 15% of U.S. adults in 2007–2012 [1] and 3.3–17.3% in 13 European populations [2]. CKD is independently associated with excess cardiovascular events, death, hospitalization and other adverse outcomes [3]. Stage 3 CKD, defined as an eGFR 30 to 59 ml/min/1.73 m2, makes up the largest fraction of CKD patients [1] and carries the highest potential to intervene early and affect the natural history of the disease.
Despite being relatively common, only a small fraction of patients with eGFR 30 to 59 ml/min/1.73 m2 progress to end-stage renal disease (ESRD) over their lifetime, with diabetes mellitus being one of the commonly attributed factors [4]. Previous research has focused primarily on the outcome of receipt of renal replacement therapy (chronic dialysis or receipt of renal transplant) that occurs often many years in the future [5–8] and is subject to important biases given that the definition of ESRD is currently based on receiving a procedure [9]. More rapid progression of CKD is associated with worse clinical outcomes (e.g., cardiovascular events and death) independent of current level of eGFR [10–14]. However, predicting which subset of patients are at high risk for progression of their CKD in the short-term is challenging but more clinically and policy relevant when prioritizing resources targeting the highest risk patients to potentially avoid or significantly delay the need for renal replacement therapy and potentially preventing cardiovascular and other adverse outcomes [15]. Prior research on fast progression of CKD has been limited by modest-sized samples, under-representation of racial/ethnic minorities, or being conducted during older eras not reflecting contemporary therapy and management [16–20]. Relatively little is known about whether predictors of the fast CKD progression of CKD varies by diabetes mellitus status, and this could have further clinical and population management implications.
Within a large, diverse cohort of adults with mild-to-moderate CKD, we evaluated contemporary two-year rates and predictors of fast progression of CKD. We hypothesized that there would be higher rates of fast progression in the presence of diabetes and that risk factors may differ based on the presence or absence of diabetes.
Methods
Source population
The study was based in KPNC, a large integrated healthcare delivery system currently providing comprehensive care to > 4.4 million members in the San Francisco and greater Bay Area. The KPNC membership is highly representative of the surrounding local and statewide population [21].
Cohort assembly
We identified all adult (≥ 18 years old) health plan members between January 1, 2008 and December 31, 2010 who had at least one ambulatory, non-emergency department serum creatinine measurement within a regional health plan laboratory and estimated glomerular filtration rate (eGFR) using the CKD-EPI equation [22]. Index date was defined using the first identified serum creatinine measurement during the inception period. We excluded patients whose index eGFR was not between the range of 30 and 59 ml/min/1.72 m2. In addition, we excluded patients who had less than 12 months of continuous health plan membership and pharmacy benefit before the index date (defined as the date of the first eGFR test during the inception period) to ensure adequate baseline information. We also excluded those who died, disenrolled or initiated renal replacement therapy (chronic dialysis or receipt of renal transplant) within 24 months after the index date. Deaths were identified from health plan administrative databases (including member proxy reporting), Social Security Administrative vital status files [23], and California state death certificate files [24]. Health plan disenrollment was defined as a continuous membership gap of > 30 days. We also excluded patients without outpatient, non-emergency department eGFR values spaced 10–14 months apart in order to approximate annual measurements during 2 years of follow-up.
Follow-up and definition of fast progression of CKD
Follow-up occurred through December 31, 2012 for occurrence of CKD progression in eligible patients. We searched only for outpatient, non-emergency department measurements of eGFR for each patient during the first 24 months of follow-up, during which the median number of eGFR measurements was 4 (interquartile range: 3 to 7). We then calculated the annual rate of change in eGFR by fitting a linear regression model where the dependent variable was eGFR consisting of only their baseline and the subsequent two outpatient, non-emergency eGFR values spaced 10–14 months apart during follow-up to ensure consistency across all patients. Fast progression of CKD was defined as experiencing a loss of eGFR > 4 ml/min/1.73 m2 per year [25].
Baseline covariates
Patient demographic characteristics (age, gender and self-reported race/ethnicity) were ascertained from health plan databases. Comorbid conditions were defined based on previously described validated algorithms using relevant information from hospitalization, outpatient and emergency department diagnosis and procedure codes; ambulatory pharmacy dispensing; and laboratory databases [3, 26, 27]. A list of specific definitions, codes and data sources are available on request. Conditions included myocardial infarction, heart failure, valvular heart disease, coronary revascularization (coronary artery bypass surgery, percutaneous coronary intervention), pacemaker placement, atrial fibrillation and/or flutter, ischemic stroke, transient ischemic attack, peripheral artery disease, cardiovascular risk factors (tobacco usage, diabetes mellitus, hypertension, dyslipidemia), other comorbid conditions (cancer, chronic liver disease, chronic lung disease, dementia, depression, extracranial hemorrhage, thyroid disease). We also ascertained data on ambulatory systolic and diastolic blood pressure, heart rate and body mass index, documented proteinuria based on measures of urine dipstick of 1+ or greater [3], as well as the most recent ambulatory level of hemoglobin, LDL cholesterol, HDL cholesterol and serum potassium.
Statistical approach
All analyses were conducted using SAS statistical software, version 9.3 (Cary, N.C.). Continuous variables were reported as means with standard deviations or medians with interquartile ranges; discrete variables were reported as frequencies and proportions. Given the large sample size, we calculated the difference between the means or proportions of the fast progressors versus non-fast progressors divided by the pooled estimate of the standard deviation, to indicate the standardized difference and considered a value of d ≥ 0.10 to represent a meaningful difference [28, 29].
We next calculated the crude risk of fast CKD progression over 24 months by dividing the number of fast progressors by the total number of patients and reported the associated 95% confidence intervals, stratified by baseline status of diabetes mellitus. To initially identify possible independent predictors of fast CKD progression with or without diabetes mellitus at baseline, we performed a two-step model selection process. First, we performed a multivariable logistic regression model stratified by presence or absence of diabetes including all baseline variables in Table 1 as of study entry date, except for specific laboratory measurements in which ≥15% of the patients had no data for that laboratory measurement, as well as any conditions with ≤1% prevalence at baseline. For self-reported race and eligible laboratory measurements, we included a category for unknown. Second, we included in the final multivariable stratified models patient age, gender, race, Hispanic ethnicity, hemoglobin levels and only the subset of other variables that were significantly associated with fast CKD progression using a cutoff of P < 0.05 from the initial logistic regression models. Finally, in sensitivity analyses, results were not significantly different if we included the 368 patients who initiated dialysis or received kidney transplantation within the first 2 years of follow-up as fast CKD progressors or if we included or excluded baseline eGFR level, so only results of the main analysis are presented (data not shown).
Table 1.
Baseline characteristics of adults with index eGFR 30 to 59 ml/min/1.73 m2 between January 1, 2008 and December 31, 2012 with annual measurements of kidney function, overall and stratified by those who did or did not experience fast progression of CKD
| Characteristic | Not Fast CKD Progression | Fast CKD Progression | D-Valuea |
|---|---|---|---|
| (N = 29,646) | (N = 6549) | ||
| Age, yr | |||
| Mean (SD) | 73.0 (10.0) | 73.3 (10.8) | 0.03 |
| Gender, n (%) | 0.00 | ||
| Women | 16,306 (55.0) | 3598 (54.9) | |
| Men | 13,340 (45.0) | 2951 (45.1) | |
| Race/Ethnicity, n (%) | |||
| White/European | 21,651 (73.0) | 4605 (70.3) | 0.05 |
| Black/African American | 3185 (10.7) | 790 (12.1) | 0.05 |
| Asian/Pacific Islander | 3442 (11.6) | 810 (12.4) | 0.05 |
| Native American | 90 (0.3) | 28 (0.4) | 0.05 |
| Other | 135 (0.5) | 45 (0.7) | 0.05 |
| Unknown | 1143 (3.9) | 271 (4.1) | 0.05 |
| Known Hispanic ethnicity, n (%) | 2816 (9.5) | 754 (11.5) | 0.07 |
| Smoking status, n (%) | 0.08 | ||
| Current or former smoker | 13,382 (45.1) | 3215 (49.1) | |
| Non-smoker | 16,264 (54.9) | 3334 (50.9) | |
| Cardiovascular history, n (%) | |||
| Acute myocardial infarction | 664 (2.2) | 222 (3.4) | 0.26 |
| Heart failure | 2675 (9.0) | 1001 (15.3) | 0.36 |
| Hospitalized ischemic stroke | 344 (1.2) | 105 (1.6) | 0.20 |
| Transient ischemic attack | 483 (1.6) | 128 (2.0) | 0.11 |
| Peripheral artery disease | 333 (1.1) | 103 (1.6) | 0.21 |
| Mitral and/or aortic valvular disease | 1973 (6.7) | 479 (7.3) | 0.06 |
| Atrial fibrillation and/or flutter | 3086 (10.4) | 830 (12.7) | 0.13 |
| Cardiac procedure history, n (%) | |||
| Coronary artery bypass graft surgery | 422 (1.4) | 112 (1.7) | 0.11 |
| Percutaneous coronary intervention | 820 (2.8) | 233 (3.6) | 0.16 |
| Pacemaker | 310 (1.0) | 106 (1.6) | 0.27 |
| Medical history, n (%) | |||
| Diabetes mellitus | 10,139 (34.2) | 3035 (46.3) | 0.31 |
| Proteinuria | 3032 (10.2) | 1458 (22.3) | 0.56 |
| Hypertension | 24,838 (83.8) | 5772 (88.1) | 0.22 |
| Diagnosed dementia | 685 (2.3) | 187 (2.9) | 0.13 |
| Diagnosed depression | 3899 (13.2) | 903 (13.8) | 0.03 |
| Dyslipidemia | 22,157 (74.7) | 5111 (78.0) | 0.11 |
| Chronic liver disease | 580 (2.0) | 156 (2.4) | 0.12 |
| Chronic lung disease | 6299 (21.2) | 1546 (23.6) | 0.08 |
| Hyperthyroidism | 865 (2.9) | 185 (2.8) | 0.02 |
| Hypothyroidism | 5555 (18.7) | 1216 (18.6) | 0.01 |
| Systemic cancer | 2042 (6.9) | 451 (6.9) | 0.00 |
| Extracranial hemorrhage | 553 (1.9) | 157 (2.4) | 0.16 |
| Body mass index, kg/m2, n (%) | 0.03 | ||
| < 18.5 | 247 (0.8) | 66 (1.0) | |
| 18.5–24.9 | 6664 (22.5) | 1418 (21.7) | |
| 25.0–29.9 | 10,290 (34.7) | 2180 (33.3) | |
| 30.0–39.9 | 9038 (30.5) | 2067 (31.6) | |
| ≥ 40.0 | 1497 (5.0) | 448 (6.8) | |
| Unknown | 1910 (6.4) | 370 (5.6) | |
| Systolic blood pressure, mmHg | |||
| Mean (SD) | 129.0 (16.5) | 132.9 (18.7) | 0.23 |
| Diastolic blood pressure, mmHg | |||
| Mean (SD) | 70.9 (10.4) | 71.1 (11.1) | 0.02 |
| Baseline medication use, n (%) | |||
| Angiotensin-converting enzyme inhibitor | 13,634 (46.0) | 3252 (49.7) | 0.09 |
| Angiotensin II receptor blocker | 4335 (14.6) | 1216 (18.6) | 0.17 |
| Diuretic | 17,136 (57.8) | 3997 (61.0) | 0.08 |
| Loop | 4470 (15.1) | 1502 (22.9) | 0.31 |
| Thiazide | 13,377 (45.1) | 2739 (41.8) | 0.08 |
| β-blocker | 15,256 (51.5) | 3759 (57.4) | 0.15 |
| Calcium channel blocker | 7607 (25.7) | 2110 (32.2) | 0.19 |
| Alpha-blocker | 3927 (13.2) | 1023 (15.6) | 0.12 |
| Aldosterone receptor antagonist | 691 (2.3) | 191 (2.9) | 0.14 |
| Isosorbide dinitrate + hydralazine | 66 (0.2) | 48 (0.7) | 0.73 |
| Hydralazine | 903 (3.0) | 374 (5.7) | 0.40 |
| Antiarrhythmic | 704 (2.4) | 189 (2.9) | 0.12 |
| Nitrate | 1478 (5.0) | 479 (7.3) | 0.25 |
| Digoxin | 1072 (3.6) | 303 (4.6) | 0.16 |
| Statin | 18,442 (62.2) | 4342 (66.3) | 0.11 |
| Other lipid-lowering agent | 1880 (6.3) | 505 (7.7) | 0.13 |
| Non-steroidal anti-inflammatory drug | 4028 (13.6) | 803 (12.3) | 0.07 |
| Antiplatelet agent | 1535 (5.2) | 422 (6.4) | 0.14 |
| Diabetic therapy | 7945 (26.8) | 2541 (38.8) | 0.33 |
| Erythropoietin | 160 (0.5) | 81 (1.2) | 0.51 |
| Baseline laboratory values | |||
| CKD-EPI eGFR, ml/min/1.73m2 | 0.07 | ||
| 45–59 | 20,263 (68.3) | 4675 (71.4) | |
| 30–44 | 9383 (31.7) | 1874 (28.6) | |
| Hemoglobin, g/dL, n (%) | 0.08 | ||
| ≥ 13.0 | 15,328 (51.7) | 2706 (41.3) | |
| 12.0–12.9 | 5160 (17.4) | 1326 (20.2) | |
| 11.0–11.9 | 2656 (9.0) | 937 (14.3) | |
| 10.0–10.9 | 994 (3.4) | 383 (5.8) | |
| 9.0–9.9 | 315 (1.1) | 117 (1.8) | |
| < 9.0 | 125 (0.4) | 42 (0.6) | |
| Unknown | 5068 (17.1) | 1038 (15.8) | |
| Low density lipoprotein cholesterol, mg/dL | |||
| Mean (SD) | 97.4 (33.1) | 94.0 (33.6) | 0.10 |
| Median (IQR) | 92.0 (75.0–116.0) | 88.0 (71.0–111.0) | |
| Range | 12.0–531.0 | 19.0–339.0 | |
| Missing, n (%) | 2997 (10.1) | 659 (10.1) | |
| High density lipoprotein cholesterol, mg/dL | |||
| Mean (SD) | 49.7 (14.2) | 48.3 (13.8) | 0.10 |
| Median (IQR) | 47.0 (40.0–57.0) | 46.0 (39.0–55.0) | |
| Range | 10.0–153.0 | 4.0–178.0 | |
| Missing, n (%) | 3560 (12.0) | 807 (12.3) | |
| Serum potassium, mmol/L | |||
| Mean (SD) | 4.5 (0.5) | 4.5 (0.5) | 0.03 |
| Median (IQR) | 4.5 (4.2–4.8) | 4.5 (4.2–4.8) | |
| Range | 2.1–6.7 | 2.6–7.3 | |
| Missing, n (%) | 2761 (9.3) | 376.7) | |
a Represents the Cohen’s D-value, calculated by dividing the difference of the group means by the standard deviation, with a D-value ≥ 0.10 considered a meaningful difference
Using the final models, we also examined model accuracy by evaluating calibration (i.e., how correctly the model predicts absolute risk) as well as discrimination (i.e., the ability of the model to identify higher vs. lower risk patients) to provide insights into the clinical utility of our findings [30].
Results
Cohort assembly and baseline characteristics
We identified 36,195 eligible adults with index eGFR 30 to 59 ml/min/1.73 m2 between January 1, 2008 and December 31, 2010, with 36% of patients having diabetes mellitus. In the overall cohort, mean age was 73.0 years with 55% being women, 11% black/African American, 12% Asian/Pacific Islander and 10% Hispanic (Table 1). Overall, 85% had hypertension and three quarters of patients had known dyslipidemia (Table 1).
During 2 years of follow-up, the median annual change in renal function in the overall cohort was 0.04 (interquartile range − 2.89 to 3.08) ml/min/1.73 m2. A total of 6549 patients (18.1%) experienced fast decline in kidney function over 24 months, with a higher crude risk in those with vs. without diabetes mellitus (Fig. 1). Fast progressors were more likely to have prior cardiovascular diseases (acute myocardial infarction, coronary artery bypass graft surgery, percutaneous coronary intervention, heart failure, atrial fibrillation/atrial flutter, pacemaker) as well as prior ischemic stroke, transient ischemic attack, peripheral artery disease, proteinuria, diabetes mellitus, hypertension, dementia, dyslipidemia, chronic liver disease, and thyroid disease (Table 1). Patients who experienced fast progression were also more likely to have higher mean systolic blood pressure than those who were not fast progressors. In addition, fast progressors were more likely to be receiving angiotensin II receptor blockers, loop diuretics, β-blockers, calcium channel blockers, alpha blockers, aldosterone receptor antagonists, isosorbide dinitrate/hydralazine, hydralazine, antiarrhythmic therapy, nitrates, digoxin, statin, other lipid lowering therapies, antiplatelet agents, diabetic therapy and erythropoietin (Table 1).
Fig. 1.
Risk of fast progression of CKD over 24 months among adults with eGFR 30 to 59 ml/min/1.73 m2, overall and stratified by baseline status of diabetes mellitus
Multivariable predictors of fast CKD progression by diabetes status
Given our hypothesis that predictors of being a fast progressor may vary in the presence or absence of diabetes, we performed models stratified by baseline diabetes status.
In patients without diabetes mellitus at entry, multivariable predictors of fast CKD progression included age ≥ 70 years, heart failure, prior ischemic stroke, prior pacemaker implantation, proteinuria, higher entry level of eGFR, lower hemoglobin levels and HDL cholesterol < 50 mg/dL (Table 2). There was a graded increased independent risk of fast progression with systolic blood pressure above 120 mmHg. Model calibration was outstanding across a range of absolute risk of fast CKD progression over 2 years (Fig. 2a and b), while model discrimination was moderate (c statistic 0.64).
Table 2.
Selected multivariable predictors of fast CKD progression over 24 months among adults with eGFR 30 to 59 ml/min/1.73 m2 stratified by baseline diabetes status
| Characteristic | Adjusteda Odds Ratio (95% Confidence Interval) for Fast Progression in Adults with Stage 3 CKD and no Diabetes N = 23,021 |
Adjustedb Odds Ratio (95% Confidence Interval) for Fast Progression in Adults with Stage 3 CKD and Diabetes N = 13,174 |
|---|---|---|
| Age group at study entry, yr | ||
| 18–49 | 1.16 (0.91–1.48) | 1.60 (1.22–2.10) |
| 50–59 | 0.72 (0.61–0.86) | 1.16 (1.00–1.34) |
| 60–69 | 0.81 (0.73–0.90) | 1.03 (0.92–1.14) |
| 70–79 | Reference | Reference |
| ≥ 80 | 1.25 (1.14–1.36) | 1.16 (1.03–1.30) |
| Male vs. female gender | 1.00 (0.92–1.08) | 0.99 (0.91–1.08) |
| Race | ||
| White/European | Reference | Reference |
| Black/African American | 1.02 (0.90–1.16) | 1.00 (0.88–1.14) |
| Asian/Pacific Islander | 1.00 (0.88–1.15) | 1.02 (0.91–1.15) |
| Native American | 1.57 (0.81–3.04) | 1.22 (0.67–2.20) |
| Other | 1.26 (0.68–2.34) | 1.24 (0.81–1.92) |
| Unknown | 0.88 (0.69–1.11) | 1.15 (0.94–1.42) |
| Hispanic ethnicity | 1.05 (0.90–1.21) | 1.03 (0.90–1.18) |
| Current/former smoking | 1.21 (1.12–1.30) | – |
| Medical history | ||
| Heart failure | 1.77 (1.57–1.99) | 1.58 (1.40–1.79) |
| Ischemic stroke | 1.50 (1.11–2.04) | – |
| Pacemaker | 1.43 (1.06–1.92) | – |
| Proteinuria | 1.86 (1.65–2.10) | 2.31 (2.10–2.55) |
| Valvular heart disease | – | 0.86 (0.71–1.03) |
| Systolic blood pressure, mmHg | ||
| ≤ 120 | Reference | Reference |
| 121–129 | 1.17 (1.04–1.30) | 1.14 (1.01–1.29) |
| 130–139 | 1.28 (1.15–1.41) | 1.23 (1.08–1.39) |
| 140–159 | 1.44 (1.28–1.62) | 1.47 (1.29–1.68) |
| 160–179 | 2.07 (1.75–2.46) | 1.99 (1.64–2.42) |
| ≥ 180 | 2.42 (1.80–3.24) | 2.21 (1.59–3.08) |
| Unknown | 1.12 (0.88–1.43) | 1.20 (0.94–1.53) |
| Laboratory values | ||
| Hemoglobin, g/dL | ||
| ≥ 13.0 | Reference | Reference |
| 12.0–12.9 | 1.38 (1.25–1.53) | 1.39 (1.23–1.56) |
| 11.0–11.9 | 2.02 (1.78–2.29) | 1.63 (1.43–1.87) |
| 10.0–10.9 | 2.09 (1.73–2.54) | 1.76 (1.47–2.11) |
| 9.0–9.9 | 1.46 (1.02–2.10) | 2.09 (1.55–2.81) |
| < 9.0 | 1.44 (0.85–2.43) | 2.15 (1.26–3.68) |
| Unknown | 1.13 (1.01–1.26) | 1.15 (1.02–1.30) |
| HDL cholesterol, mg/dL | ||
| ≥ 60 | Reference | – |
| 50–59 | 1.09 (0.97–1.23) | – |
| 40–49 | 1.16 (1.04–1.30) | – |
| 35–39 | 1.25 (1.08–1.45) | – |
| < 35 | 1.27 (1.07–1.50) | – |
| Unknown | 1.20 (1.07–1.36) | – |
| LDL cholesterol, mg/dL | ||
| ≥ 200 | – | Reference |
| 160–199 | – | 1.73 (1.06–2.84) |
| 130–159 | – | 1.07 (0.80–1.44) |
| 100–129 | – | 1.10 (0.89–1.35) |
| 70–99 | – | 1.03 (0.90–1.17) |
| < 70 | – | 0.93 (0.84–1.02) |
| Unknown | – | 1.07 (0.82–1.39) |
aAdjusted also for baseline level of eGFR and receipt of angiotensin II receptor blockers and calcium channel blockers at entry
bAdjusted also for baseline level of eGFR and receipt of diuretics, calcium channel blockers and hydralazine at entry
Fig. 2.
Accuracy of predictive model for fast CKD progression over 2 years in patients with eGFR 30 to 59 ml/min/1.73 m2 and no diabetes mellitus at entry, based on (a) comparison of observed vs. predicted risks within deciles of predicted risk and (b) model calibration across the spectrum of observed risk
In patients with diabetes mellitus at entry, results were largely similar to that found in non-diabetic patients with regards to heart failure, known proteinuria, higher entry level of eGFR, and the increased risk of fast progression with lower hemoglobin levels and higher systolic blood pressure, while there was a different association for age in which age 18–49 and ≥ 80 years were associated with higher adjusted odds of fast progression (Table 2). However, there was no significant multivariable association noted for current or former cigarette smoking, prior ischemic stroke, prior pacemaker implantation or lower HDL cholesterol level (Table 2). Similar to results in patients without diabetes, model calibration was outstanding across an even broader range of absolute risk of fast CKD progression over 2 years (Fig. 3a and b), while model discrimination was moderate (c statistic 0.66).
Fig. 3.
Accuracy of predictive model for fast CKD progression over 2 years in patients with eGFR 30 to 59 ml/min/1.73 m2 and diabetes mellitus at entry, based on (a) comparison of observed vs. predicted risks within deciles of predicted risk and (b) model calibration across the spectrum of observed risk
Discussion
There has been a growing appreciation that a significant proportion of patients with mild-to-moderate CKD do not progress in a predictable, slow linear pattern, with some patients either not progressing and others having a much faster decline in kidney function [31]. Identifying the subset of mild-to-moderate CKD patients who will subsequently experience fast CKD progression in the short-term has important clinical implications as they may benefit from more intensive monitoring and intervention. To address this, we examined a large, diverse community-based cohort with eGFR 30 to 59 ml/min/1.73 m2 and found that 23% of these patients with diabetes and 15% of those without experienced fast CKD progression, and that the significant multivariable factors regardless of diabetes status included age ≥ 80 years, proteinuria, higher systolic blood pressure, lower hemoglobin level, and known heart failure, even after accounting for initial level of eGFR and receipt of cardiovascular and renal-related medications.
While CKD “progression” has been investigated in various ways, the large majority of studies focused on the end point of ESRD defined as the receipt of chronic dialysis or renal transplantation [5–8]. Other studies have used varying definitions in the absolute or relative amount of drop in eGFR or reaching a particular level of eGFR [32]. While these are all potentially relevant outcomes, existing studies frequently use long time horizons and do not necessarily address the rate of change, which may be more important clinically to identify the subset of patients who are losing kidney function quickly in the short-term and may benefit from earlier, more frequent surveillance and intervention. Toward that end, our cohort of patients with Stage 3 CKD who had annual outpatient measurements of eGFR during 2 years of follow-up provides important insights into the rate of fast CKD progression and associated patient characteristics.
Our finding that documented proteinuria, a reflection of underlying structural kidney damage, is a strong predictor of short-term, fast CKD progression is consistent with other studies that have examined the development of ESRD or significant reductions in the absolute level of eGFR over a longer period of follow-up [5–8, 32].
In patients with diabetes, the youngest patients with CKD were also more likely to experience fast progression after accounting for other potential risk factors and use of cardioprotective and renoprotective therapies, which is consistent with other studies [32] and may reflect a difference in underlying cause(s) of CKD. In contrast, among patients without diabetes, those aged 50–69 years old were less likely than those aged 70–79 years old to have fast CKD progression. Patients ≥80 years were more likely to experience fast progression regardless of diabetes status. We found that current or former cigarette smoking was associated with fast CKD progression in the short-term among patients without diabetes, which is consistent with results from the Cardiovascular Health Study cohort that showed a 31% relative increase in the likelihood of a serum creatinine increase ≥0.3 mg/dL over 3 years [33]. Furthermore, among 1906 participants in the Italian Longitudinal Study on Aging (ISA) cohort, current smoking > 20 cigarettes/day was associated with a more than twofold higher odds (adjusted odds ratio 2.29, 95% CI:1.00–5.27) of an increase in serum creatinine > 0.3 mg/dL during mean 3.6-year follow-up [34]. However, conflicting results exist about the relationship between smoking history and longer-term endpoints such as the need for renal replacement therapy [35, 36].
Higher systolic blood pressure is a well-documented risk factor of development of ESRD [35, 37] or a 50% reduction in baseline eGFR in patients with CKD [38], but fewer studies have examined the influence of blood pressure on rate of change of eGFR. Among 220 participants with eGFR 30–59 ml/min/1.73 m2 enrolled in the Multi-Ethnic Study of Atherosclerosis (MESA), having a systolic blood pressure ≥ 130 mmHg was associated with a more than twofold higher adjusted odds (odds ratio 2.29, 95% CI:1.20–4.37) of CKD progression, defined as > 2.5 ml/min/1.73 m2 decline in eGFR over 5 years of follow-up when estimating GFR using combined serum creatinine and cystatin C data [39]. Our study supports and extends these findings in a much larger cohort showing a graded increased risk of fast CKD progression with systolic blood pressure > 120 mmHg even after additional adjustment for receipt of different antihypertensive agents.
Lower hemoglobin levels below 13.0 g/dL were also associated with a higher risk of fast progression. These results are consistent with an analysis of 6100 adults with systolic heart failure showing that a hematocrit < 36% (hemoglobin of approximately < 12.0 g/dL) was associated with a higher adjusted odds (odds ratio 1.30, 95% CI:1.18–1.45) of rapid decline in kidney function (defined as ≥6 ml/min/1.73 m2 decrease in eGFR per year) and was more prominent in those with CKD (adjusted odds ratio 1.71, 95% CI:1.43–2.05) [20]. In addition, hemoglobin levels were lower among 117 Stage 3 CKD patients who progressed (eGFR decline > 3 ml/min/1.73 m2 per year over 4 years) compared with 364 Stage 3 CKD patients considered non-progressors (< 1 ml/min/1.73 m2 per year over 4 years) [40].
There have been conflicting data about the association between different lipoproteins and the risks of ESRD or significant loss of kidney function in adults with CKD. For example, in the Chronic Renal Insufficiency Cohort (CRIC) Study, none of the lipoproteins studied (total, LDL, HDL, VLDL, Lp(a), apoA-I, apoB) were independently associated with development of ESRD or > 50% reduction in baseline eGFR [41]. In contrast, among a Japanese population with CKD [42], the highest two quartiles of triglyceride-to-HDL cholesterol ratio were associated with rapid decline (defined as > 5 ml/min/1.73 m2 reduction per year) compared with the lowest quartile, which supports our observation that a lower HDL level was associated with a graded, increased risk of fast CKD progression in the subset of patients without diabetes.
Despite evaluating a wide range of candidate predictors of fast progression of CKD, our model discrimination was moderate for models in patients with (c statistic 0.66) or without (c statistic 0.64) diabetes which is in contrast to models of initiation of renal replacement therapy which achieve much higher c statistics (0.84–0.90) [5, 8], depending on the severity of the CKD population studied and time horizon used. This highlights the challenge of accurately discriminating which subset of patients starting at an eGFR 30 to 59 ml/min/1.73 m2 will experience fast progression of CKD and the need for investigation of additional factors influencing this risk to potentially intervene earlier in the process to delay the progression to ESRD. Importantly, however, model calibration (i.e., the ability to correctly estimate absolute risk of fast CKD progression over 2 years) was outstanding in patients with and without diabetes at entry, which highlights the potential clinical value in providing prognostic information to patients with stage 3 CKD (Figs. 2 and 3).
The study was strengthened by inclusion of a large, racially/ethnically diverse sample of adults with mild-to-moderate CKD who had approximately annual outpatient, non-emergency department measurements of serum creatinine from baseline through the first 2 years of follow-up. This allowed us to examine annual rate of eGFR decline and to identify the subgroup of patients who experienced fast CKD progression. All relevant diagnoses, procedures, test results and treatments were comprehensively captured through a state-of-the-art electronic medical record system that facilitated assessment of relevant patient characteristics which may predict fast CKD progression. Our study also had some limitations. For each patient, we calculated an average annual rate of eGFR decline estimated using linear regression, but patients may experience non-linear patterns of change in kidney function not reflected using this approach. Since this was a retrospective study of patients receiving clinically obtained measures of eGFR (rather than a structured research protocol with annual assessment of kidney function), the findings may not apply to all patients with eGFR 30–59 ml/min/1.73 m2. We also used estimated GFR rather than measured GFR which may lead to some misclassification [43]. Similarly, results may not be completely generalizable to other clinical practice settings or to uninsured patients who may experience a different intensity of treatment or follow-up. Even though we examined a wide range of patient characteristics, we cannot rule out residual confounding affecting our model results. We were unable to comprehensively identify exposure to nephrotoxic insults or episodes of acute kidney injury from available data. Systematic information on other selected biomarkers that have been associated with different measures of CKD progression were also not available (e.g., urinary phosphorus excretion [44], serum calcium and phosphorus [40], serum bicarbonate [40, 45], NT-proBNP [19], or troponin T [19]).
Conclusions
In sum, within a large, contemporary population of adults with mild-to-moderate CKD, accelerated progression of kidney dysfunction within 2 years affected ~ 1 in 4 patients with diabetes and ~ 1 in 7 without diabetes. Regardless of diabetes status, the independent predictors of fast CKD progression included proteinuria, elevated systolic blood pressure, heart failure, anemia, and age ≥ 80 years. Age 18–49 years was also a predictor in those with diabetes, while additional predictors in patients without diabetes included smoking history, prior ischemic stroke, prior pacemaker implantation, and HDL cholesterol < 60 mg/dL. These findings may help in identifying the subset of patients who may benefit from more frequent monitoring of eGFR to identify fast CKD progression or proteinuria and subsequent intervention to potentially retard further loss of kidney function and other potentially associated adverse clinical outcomes such as cardiovascular events.
Acknowledgements
The authors would like to thank Susan S. Kim for her technical assistance.
Funding
This study was supported by a research grant through Dr. Go’s institution from AstraZeneca.
Availability of data and materials
The datasets generated and/or analyzed during the current study are not publicly available due to the data extracted from systems belonging to Kaiser Permanente Northern California.
Abbreviations
- CKD
Chronic kidney disease
- eGFR
Estimated glomerular filtration rate
- ESRD
End-stage renal disease
- KPNC
Kaiser Permanente Northern California
Authors’ contributions
ASG, JRY, TCT and JDO designed the study. ASG and JRY were responsible for assembling and analyzing the dataset and take responsibility for the accuracy of the findings. ASG, JRY and TCT drafted the manuscript. All authors read, provided critical revisions to and approved the final manuscript.
Ethics approval and consent to participate
This study was approved by the Kaiser Permanente Northern California institutional review board. A waiver of consent was obtained due to the nature of the study.
Consent for publication
Not applicable.
Competing interests
Drs. Cabrera, Stefansson and Greasley are employees of Astra-Zeneca. Ms. Yang, Ms. Tan and Dr. Ordonez declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets generated and/or analyzed during the current study are not publicly available due to the data extracted from systems belonging to Kaiser Permanente Northern California.