Glucagon-Like Peptide-1 Receptor Agonist Use and Renal Impairment: A Retrospective Analysis of an Electronic Health Records Database in the U.S. Population (original) (raw)

Abstract

Introduction

The study characterizes the use of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in patients with type 2 diabetes (T2D) with and without renal impairment and examines the effects of such use on the clinical outcomes of estimated glomerular filtration rate (eGFR) and glycated hemoglobin (A1c).

Methods

Data from the Practice Fusion electronic health records database from 1 January 2012 through 30 April 2015 were used. Adults with T2D who received serum creatinine laboratory tests and initiated therapy with a GLP-1 RA (N = 3225) or other glucose-lowering agent (GLA) (N = 37,074) were included in the analysis. The GLP-1 RA cohort was matched to cohorts initiating therapy any other GLA, and multivariable analyses examined the association between GLP-1 RA use and changes in eGFR or A1c at 1 year after therapy initiation.

Results

In this study, only 5.7% of patients with an eGFR of < 30 and ≥ 15 mL/min/1.73 m2 and 3.6% of patients with an eGFR of < 15 mL/min/1.73 m2 initiated therapy with a GLP-1 RA. Compared to other GLAs, at 1-year after initiation of therapy the use of a GLP-1 RA was associated with a significantly smaller decline in eGFR (− 0.80 vs. − 1.03 mL/min/1.73 m2; P = 0.0005), a significantly smaller likelihood of having a ≥ 30% reduction in eGFR (2.19 vs. 3.14%; P < 0.0001), and a significantly larger reduction in A1c (− 0.48 vs. − 0.43; P = 0.0064).

Conclusion

In clinical practice, the use of GLP-1 RAs in patients with a higher degree of renal impairment disease was limited. Compared to other GLAs, the use of GLP-1 RAs was associated with a significantly smaller decline in eGFR and a larger reduction in A1c over the 1 year following therapy initiation.

Funding

Eli Lilly and Company.

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Introduction

Chronic kidney disease (CKD) is a common type 2 diabetes (T2D) complication that is associated with an increased risk of adverse outcomes [1]. For example, the U.S. Renal Data System attributed diabetes as the primary cause of end-stage renal disease (ESRD) in 44.3% of incident dialysis patients in 2011 [[2](/article/10.1007/s13300-018-0377-5#ref-CR2 "U.S. Renal Data System. USRDS 2013 annual data report; atlas of chronic kidney disease and end-stage renal disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease [Internet], Bethesda, MD; 2014. Available from: https://www.usrds.org/atlas13.aspx

              .")\], and patients with comorbid T2D and CKD have been reported to experience increased rates of cardiovascular morbidity and mortality \[[3](/article/10.1007/s13300-018-0377-5#ref-CR3 "Pálsson R, Patel UD. Cardiovascular complications of diabetic kidney disease. Adv Chronic Kidney Dis. 2014;21:273–80.")\]. The presence of CKD also increases the complexity of T2D treatment, since the pharmacokinetic aspects of drugs cleared by the kidney can be influenced by renal impairment \[[4](/article/10.1007/s13300-018-0377-5#ref-CR4 "Davies MJ, Bain SC, Atkin SL, Rossing P, Scott D, Shamkhalova MS, et al. Efficacy and safety of liraglutide versus placebo as add-on to glucose-lowering therapy in patients with type 2 diabetes and moderate renal impairment (LIRA-RENAL): a randomized clinical trial. Diabetes Care. 2016;39:222–30.")\]. Treatment options are also limited for these patients, with biguanides, alpha-glucosidase inhibitors, and sodium–glucose cotransporter 2 (SGLT2) inhibitors not usable in patients with ESRD and T2D, and thiazelidinediones not usable in patients with ESRD and diabetes with cardiac disease \[[5](/article/10.1007/s13300-018-0377-5#ref-CR5 "Idorn T, Knop FK, Jørgensen MB, Jensen T, Resuli M, Hansen PM, et al. Safety and efficacy of liraglutide in patients with type 2 diabetes and end-stage renal disease: an investigator-initiated, placebo-controlled, double-blind, parallel-group, randomized trial. Diabetes Care. 2016;39:206–13.")\]. In addition, the incidence of hypoglycemia is increased in patients with both diabetes and CKD \[[6](/article/10.1007/s13300-018-0377-5#ref-CR6 "Alsahli M, Gerich JE. Hypoglycemia in patients with diabetes and renal disease. J Clin Med. 2015;4:948–64.")\].

Animal studies have indicated a renoprotective effect with the use of glucagon-like peptide-1 receptor agonist (GLP-1 RA) medications [7, 8]. Clinical studies have also shown GLP-1 RAs to be associated with decreased development and progression of nephropathy [9, 10], primarily driven by lower rates of new-onset persistent macroalbuminuria [11]. However, the U.S. Food Drug Administration (FDA) label for GLP-1 RA exenatide states that the drug “should not be used in patients with severe renal impairment or end-stage renal disease and should be used with caution in patients with renal transplantations” [[12](/article/10.1007/s13300-018-0377-5#ref-CR12 "AstraZeneca Pharmaceuticals. Byetta (exenatide) injection. Highlights of prescribing information. Revised February 2015. [Internet]. Available from: https://www.azpicentral.com/byetta/pi_byetta.pdf#page=1

              . Accessed 22 June 2017.")\], and the FDA’s label for lixisenatide recommends monitoring of renal function when initiating or escalating doses of the drug and states that the drug “is not recommended in patients with end stage renal disease” \[[13](/article/10.1007/s13300-018-0377-5#ref-CR13 "U.S. Drug and Food Administration (FDA). Adlyxin (lixisenatide) injection. Highlights of prescribing information. Revised July, 2016 [Internet]. Available from: 
                https://www.accessdata.fda.gov/drugsatfda_docs/nda/2016/208471Orig1s000lbl.pdf
                
              . Accessed 26 Sept 2017.")\].

To investigate how GLP-1 RAs are being prescribed in real-world settings, we have examined the frequency of initiation on drugs in this class across various estimated glomerular filtration rate (eGFR) categories in patients with T2D. In addition, given the burden of CKD among patients with T2D and the difficulties in treating such patients, in the current study we also explored the association between initiation of therapy with a GLP-1 RA and changes in glycated hemoglobin (A1c) and kidney function, as measured by the eGFR.

Methods

Data

The Practice Fusion electronic health record database furnished the study data, which covered the time period from 1 January 2012 through 30 April 2016. Practice Fusion’s web-based electronic health records (EHR) system contains data input by over 150,000 medical professionals primarily working in small, ambulatory practices and primary care practices and treating over 50 million patients in all 50 states [[14](/article/10.1007/s13300-018-0377-5#ref-CR14 "Marcus JR. A web-based electronic health record system for national surveillance. Online J Public Health Inform. [Internet]. 2013:5. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692859/

              . Accessed 19 Mar 2017.")\]. In particular, Practice Fusion provided recent records on patient characteristics, diagnoses, medications prescribed, laboratory test results, and observational data, such as weight and blood pressure. All records were de-identified and fully compliant with Health Insurance Portability and Accountability Act regulations. The research does not contain any studies with human participants or animals performed by any of the authors.

Inclusion and Exclusion Criteria

This study focused exclusively on patients identified as having T2D over the time period from 1 January 2013 through 1 May 2015 (i.e., the identification window), based upon a validated algorithm designed for EHR data [15]. Specifically, all patients who received at least one diagnosis of diabetes (International Classification of Diseases, Ninth Revision, Clinical Modification [ICD-9-CM], code 250.xx) were initially considered. Patients were excluded if they received any of the following: (1) more diagnoses of type 1 diabetes (T1D; ICD-9-CM codes 250.x1, 250.x3) than of T2D (ICD-9-CM codes of 250.x0, 250.x2) in addition to a prescription for glucagon; (2) more diagnoses of T1D than of T2D with no record of receipt of a GLA other than metformin; (3) a negative laboratory test result for c-peptide or a positive test result for diabetes autoantibody; or (4) a prescription for a urine acetone test strip.

Patients were included in the analysis if they initiated therapy with a glucose-lowering agent (GLA) during the identification window, with the first such date identified as the index date. Patients were excluded if they: (1) received a prescription for their index class of medication during the 1-year prior to the index date (i.e., during the pre-period); (2) received a diagnosis of pregnancy at any time from the start of the pre-period through the 1 year following the index date (i.e., the post-period); (3) were younger than 18 years as of the index date; or (4) appeared to have dropped out of the database at any time from the start of the pre-period through the end of the post-period. Patients were also required to have at least two recorded serum creatinine laboratory test results, with the first such test occurring some time after the start of the pre-period through to the index date and the second serum creatinine test recorded in the post-period. The eGFR was estimated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation [16]. Patients were classified based on their eGFR categories (eGFR ≥ 90 mL/min/1.73 m2; eGFR < 90 and ≥ 60 mL/min/1.73 m2; eGFR < 60 and ≥ 45 mL/min/1.73 m2; eGFR < 45 and ≥ 30 mL/min/1.73 m2; eGFR < 30 and ≥ 15 mL/min/1.73 m2; or eGFR < 15 mL/min/1.73 m2) [[17](/article/10.1007/s13300-018-0377-5#ref-CR17 "The Renal Association. CKD stages [Internet]. Available from: http://www.renal.org/information-resources/the-uk-eckd-guide/ckd-stages#sthash.s6SpVT7b.K0UCX4l0.dpbs

              . Accessed 17 Aug 2016.")\]. These criteria resulted in a sample of 40,299 patients—3225 of whom initiated therapy with a GLP-1 RA and 37,074 of whom initiated therapy with an alternative class of GLA. Figure [1](/article/10.1007/s13300-018-0377-5#Fig1) illustrates how each of the inclusion and exclusion criteria affected sample size.

Fig. 1

figure 1

Inclusion–exclusion criteria and sample size of study. GLA Glucose-lowering agent, GLP-1 RA glucagon-like peptide-1 receptor agonist, T2D type 2 diabetes

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Statistical Methods

The GLP-1 RA and other GLA cohorts were matched using Mahalanobis matching, with calipers defined by the propensity score [18]. Multivariable analyses were then used to examine differences between patients who were treated with a GLP-1 RA and those treated with an alternative GLA. The analyses examined changes in eGFR over the study period as well as the likelihood of having a ≥ 30% reduction in eGFR. A similar analysis was conducted for the subset of patients who also had a A1c laboratory test recorded during both the pre- and post-period, with the multivariable analysis examining the change in A1c. All multivariable analyses were controlled for patient demographics, observational patient characteristics, general health and comorbidities, prior medication use and resource utilization, as well as index A1c and eGFR values. Patient characteristics included age, sex, race, ethnicity, region of residence, and smoking status, while observational characteristics included body mass index and blood pressure. General health was proxied by the Charlson Comorbidity Index (CCI) [19, 20]. Diabetes-specific health was measured by the Diabetes Complications Severity Index (DCSI) [21]. Anxiety and depression were also studied, as these comorbidities have been shown to be both prevalent in patients with diabetes [22, 23] and associated with poorer patient outcomes, and as they are not included in either the CCI or the DCSI. Prior medication use focused on which classes of GLA drugs were prescribed in the pre-period, the number of classes of anti-hypertensive drugs prescribed, and whether any of the following medications were prescribed: angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, hypertension fixed-dose combination therapy, non-steroidal anti-inflammatory drugs (NSAIDs), aspirin, statins, and ezetimibe. Prior resource utilization captured the number of visits to a cardiologist or endocrinologist.

Given the results of the multivariable analyses, differences in continuous outcomes were examined using t statistics, with a P value of < 0.05 considered, a priori, to be statistically significant. When examining the probability of having a ≥ 30% reduction in eGFR, odds ratios (ORs) and 95% confidence intervals (CIs) were recorded. All analyses were conducted using SAS version 9.4 (SAS Institute, Cary, NC, USA).

Results

Table 1 presents unadjusted descriptive statistics both before and after matching and reveals significant differences between patients who initiated therapy with a GLP-1 RA compared to those who initiated therapy with an alternative class of GLA. Patients who initiated treatment with a GLP-1 RA were significantly younger (58.5 vs. 63.0 years; P < 0.001) and more likely to be identified as white (57.27 vs. 48.98%; P < 0.001) and non-Hispanic (73.21 vs. 69.43%; P < 0.001). These patients were also less likely to be identified as underweight/normal weight (3.97 vs. 10.96%) or overweight (14.36 vs. 25.48%) and more likely to be identified as class II obese (21.86 vs. 15.71%) or class III obese (26.70 vs. 14.43%). Examination of differences in pre-period general health, comorbidities, GLA use, other medication use, and visits to specialists generally suggested that patients who initiated therapy with a GLP-1 RA were in poorer health than patients who initiated therapy with other GLAs. For example, patients who started taking a GLP-1 RA were found to have a significantly higher CCI score (1.53 vs. 1.36; P < 0.001), and they were more likely to be diagnosed with comorbid depression (11.47 vs. 8.36%; P < 0.001). Furthermore, these patients were significantly more likely to have received a prescription for hypertensive drugs, NSAIDs, statins, aspirin, or ezetimibe. Patients who initiated therapy on a GLP-1 RA compared to alternative GLAs were prescribed more GLAs in the pre-period and had a significantly higher mean index A1c (8.47 vs 7.77%; P < 0.001).

Table 1 Patient characteristics pre- and post matching

Full size table

Matching resulted in a successful match rate of 91.97%, with 2966 patients who initiated therapy with a GLP-1 RA and 2966 controls who initiated therapy with another class of other GLA. As Table 1 illustrates, the matching resulted in removing most of the differences between the two cohorts. However, post-matching there still remained a statistically significant difference in the percentage of patients who were prescribed bolus insulin in the pre-period, with patients who initiated therapy with a GLP-1 RA more likely to have received such a prescription compared to controls (5.29 vs. 4.05%; P = 0.023). In the matched cohort, patients who initiated therapy with a GLP-1 RA were on average 58.8 years old, and 52.49% were female, while 56.61% were identified as white and 72.99% were identified as non-Hispanic.

While Table 1 presents the descriptive statistics pre- and post-matching, Table 2 presents the distribution of patients prior to matching based upon eGFR categories. As Table 2 illustrates, there were significant differences in the class of drug initiated across eGFR categories (P < 0.0001), with the proportions of patients starting therapy with a GLP-1 RA tending to decrease with lower eGFR category. For example, the proportions of patients who initiated therapy with a GLP-1 RA were 7.5% of patients with an eGFR of < 60 and ≥ 45 mL/min/1.73 m2, 6.9% of patients with an eGFR of < 45 and ≥ 30 mL/min/1.73 m2, 5.7% of patients with an eGFR of < 30 and ≥ 15 mL/min/1.73 m2, and 3.6% of patients with an eGFR of < 15 mL/min/1.73 m2. Patients who initiated therapy with other GLAs were generally less likely to be treated with metformin or a SGLT2 inhibitor and more likely to be treated with insulin for lower eGFR categories. Overall, 2.6% of patients had an eGFR of < 30 mL/min/1.73 m2 and 94.7% of these patients (2.4% of the overall population) initiated therapy on a medication other than GLP-1 RA. Consistent with these results, the mean baseline eGFR prior to matching was significantly higher for patients who initiated a GLP-1 Ra compared to those who initiated therapy with an alternative GLA (82.69 vs. 78.54 mL/min/1.73 m2; P < 0.001).

Table 2 The distribution of patients by estimated glomerular filtration status based upon initiation of therapy with a glucagon-like peptide-1 receptor agonist therapy or any other glucose-lowering agent

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Figure 2 illustrates the results of the multivariable analyses of the matched sample and reveals that patients who initiated therapy with a GLP-1 RA, compared to those who initiated therapy with an alternative GLA, had a statistically significantly smaller reduction in eGFR in the 1 year after therapy initiation (− 0.80 vs. − 1.03 mL/min/1.73 m2; P < 0.001). In addition, logistic regressions were estimated to examine the probability of patients having a ≥ 30% decrease in eGFR over the 1-year post-period. The results indicate that an estimated 2.19% of patients who initiated therapy on a GLP-1 RA had a reduction in eGFR of ≥ 30% compared to 3.14% of patients who initiated therapy with an alternative GLA (P < 0.001). The logistic regression results confirm this finding, with patients who initiated therapy with a GLP-1 RA found to be 30% less likely to have such a reduction over the 1-year post-period (OR 0.70, 95% CI 0.51–0.97).

Fig. 2

figure 2

Kidney function of GLP-1 RAs compared to GLAs over time. CI Confidence interval, eGFR estimated glomerular filtration rate, OR odds ratio

Full size image

In addition to examining eGFR, we also assessed A1c using a matched cohort of patients who had both an index and a post-period A1c score. There were 3158 patients who initiated therapy with a GLP-1 RA and 35,028 patients who initiated therapy with an alternative GLA who received at least one A1c test on or before the index date and another A1c test after the index date. Matching for this group resulted in a successful matched rate of 91.6%, with 2892 patients who initiated therapy with a GLP-1 RA and 2892 controls who initiated therapy with other GLAs. Given the similarity in sample sizes between this group of patients and the patients who received at least two serum creatinine tests, descriptive statistics pre- and post-matching are not presented. As with the eGFR cohort, after matching, the difference in the bolus insulin use prior to the index date remained statistically significant, with patients who initiated therapy with a GLP-1 RA significantly more likely to have received such a prescription (5.15 vs. 3.98%; P = 0.032). Results from the multivariable analyses conducted on the matched cohort (Fig. 3) revealed that patients who initiated therapy with a GLP-1 RA had a significantly larger reduction in A1c over the 1-year post-period compared to patients who initiated therapy with other GLAs (− 0.48 vs. − 0.43; P = 0.006). Multivariable analysis for the subset of individuals with an index eGFR of < 60 mL/min/1.73 m2 (N = 1067) revealed an even larger difference in A1c reduction for patients who initiated GLP-1 RA therapy compared to other GLA (− 0.41 vs − 0.22; P < 0.0001).

Fig. 3

figure 3

Reduction in glycated hemoglobin (A1c) with GLP-1 RA compared to other GLAs over time

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As a test of the sensitivity of the results, all analyses were conducted without matching of cohorts. There were no qualitative differences based upon these re-analyses. However, estimated differences in changes in eGFR and A1c were more pronounced in models without matching, where there was a mean difference of 0.36 mL/min/1.73 m2 in eGFR (− 0.83 vs − 1.19; P < 0.001) and a − 0.17% difference in A1c (− 0.50 vs. − 0.33; P < 0.001) associated with GLP-1 RA use compared to the use of other GLAS. The estimated likelihood of a ≥ 30% reduction in eGFR over the post-period was smaller (OR 0.77, 95% CI 0.59–0.99). Analyses were also performed with the inclusion of a variable that accounts for differences in timing between index and post-period measurements of eGFR and A1c. These analyses did not have any effect on the estimates of eGFR, although there was a slightly larger difference in A1c when patients who initiated therapy with a GLP-1 RA were compared to those who initiated therapy with other GLAs (− 0.46 vs − 0.40; P = 0.003).

Discussion

Therapy with GLP-1 RA is an established treatment option for patients with T2D and has been shown to both improve glycemic control and be associated with weight loss without increasing the risk of hypoglycemia [24]. However, due to the lack of controlled studies and label restrictions [[12](/article/10.1007/s13300-018-0377-5#ref-CR12 "AstraZeneca Pharmaceuticals. Byetta (exenatide) injection. Highlights of prescribing information. Revised February 2015. [Internet]. Available from: https://www.azpicentral.com/byetta/pi_byetta.pdf#page=1

              . Accessed 22 June 2017."), [25](/article/10.1007/s13300-018-0377-5#ref-CR25 "FDA. Victoza (liraglutide [rDNA origin] injection). Highlights of prescribing information [Internet]. Available from: 
                https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022341lbl.pdf
                
              . Accessed 19 Mar 2017.")\] there is limited use of this class in patients with moderate and severe renal impairment. This study found a decreasing use of GLP-1 RAs as renal impairment became more severe, with 5.7% of patients with an eGFR of < 30 and ≥ 15 mL/min/1.73 m2 and 3.6% of patients with an eGFR of < 15 mL/min/1.73 m2 initiating therapy with a GLP-1 RA. In the overall cohort, only 0.14% of patients had an eGFR of < 30 mL/min/1.73 m2 and initiated therapy with a GLP-1 RA, while 2.4% of patients had an eGFR of < 30 mL/min/1.73 m2 and initiated therapy with another GLA.

Multivariable analyses examined patient glycemic control over the 1-year post-period. The results of this study are consistent with those of clinical trials which illustrated that GLP-1 RAs are associated with reductions in A1c for patients with T2D [26,27,28], as well as for patients with T2D and moderate renal impairment [4]. The findings in this study are also consistent with those of retrospective, non-randomized studies that have illustrated the effectiveness of this class of drugs in real-world settings [29,30,31]. For example, a retrospective analysis of an electronic medical records database found that GLP-1 RA therapy, used with or without insulin, was associated with significant improvements in glycemic control [31]. Furthermore, the results are also in concert with analyses of claims databases which have shown that GLP-1 RAs are associated with greater improvement in glycemic outcomes relative to dipeptidyl peptidase-4 inhibitors [32, 33] and insulin glargine [34].

The smaller decline in eGFR and the lower likelihood of having a ≥ 30% reduction in eGFR associated with GLP-1 RA use compared to other GLAs found in this study generally complements the results of previous study types which have examined GLP-1 RA use and kidney function. For example, animal studies have shown that GLP-1 RA use is associated with natriuresis and diureses [35, 36] and that these agents also reduce risk factors of diabetic nephropathy, by reducing urine albumin levels [37] and inhibiting the development of hypertension [38]. Clinical trials have also illustrated the safety and potential benefits associated with use of GLP-1 RAs. For example, one clinical trial that compared GLP-1 RAs to placebo found no increased risk of acute renal failure associated with GLP-1 RA use [10], and another trial found similar rates of renal disorder adverse events among the two groups of patients [39]. In addition to their safety profile, the studies have also shown better patient outcomes associated with the use of GLP-1 RAs. For example, the SUSTAIN-6 study found semaglutide patients were significantly less likely to have new or worsening nephropathy [10] and the LEADER study showed a greater benefit of liraglutide with respect to cardiovascular outcomes in patients with an eGFR of < 60 ml/min/1.73 m2 [9]. The LEADER study also showed that use of liraglutide was associated with lower rates in the development and progression of diabetic kidney disease relative to placebo [40]. The AWARD-7 study, which compared dulaglutide and insulin glargine use, both combined with insulin lispro, in patients with T2D and stage 3 or 4 CKD found that the use of dulaglutide was associated with less eGFR decline at 26 weeks [41].

The findings reported herein must be interpreted within the context of the limitations of the study. First, a large percentage of T2D patients did not have recorded serum creatinine tests, suggesting that the results may not be generalizable to all patients. Second, the use of EHR data does not allow for confirmation that patients were filling and taking their prescribed medications. In addition, given the retrospective nature of the database, laboratory test results were not conducted at uniform time intervals for all patients. However, a sensitivity analysis revealed that the timing of these tests had no significant impact on the results. Third, the study focused exclusively on GLP-1 RAs as a class of medication and did not examine any potential differences among individual drugs. In addition, the study could not examine any potential impact of differences in GLP-1 RA doses on patient outcomes. Finally, it should be noted that the analysis focused on statistical significance, and practitioners should consider whether there are clinically important differences for the patients they treat. Specifically, the analysis focuses on whether there are statistical differences in outcomes and does not examine whether such differences represent meaningful changes to patients.

Conclusions

Consistent with FDA labeling, this study found that the use of GLP-1 RAs was very limited in patients with a higher degree of renal impairment. However, multivariable analyses which controlled for a wide range of factors, including index eGFR, found that the initiation of therapy on GLP-1 RA was associated with a smaller decline in eGFR and larger reductions in A1c relative to the initiation of therapy on alternative classes of GLAs. Although more research may be needed for this population and individual GLP-1 RA therapies may differ in their respective risk–benefit ratio in patients with renal impairment, the findings of this study suggests that this class of drugs may be underutilized.

References

  1. Neal B, Perkovic V, Matthews DR, Mahaffey KW, Fulcher G, Meininger G, et al. Rationale, design and baseline characteristics of the CANagliflozin cardioVascular Assessment Study-Renal (CANVAS-R): a randomized, placebo-controlled trial. Diabetes Obes Metab. 2017;19:387–93.
    Article CAS PubMed PubMed Central Google Scholar
  2. U.S. Renal Data System. USRDS 2013 annual data report; atlas of chronic kidney disease and end-stage renal disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease [Internet], Bethesda, MD; 2014. Available from: https://www.usrds.org/atlas13.aspx.
  3. Pálsson R, Patel UD. Cardiovascular complications of diabetic kidney disease. Adv Chronic Kidney Dis. 2014;21:273–80.
    Article PubMed PubMed Central Google Scholar
  4. Davies MJ, Bain SC, Atkin SL, Rossing P, Scott D, Shamkhalova MS, et al. Efficacy and safety of liraglutide versus placebo as add-on to glucose-lowering therapy in patients with type 2 diabetes and moderate renal impairment (LIRA-RENAL): a randomized clinical trial. Diabetes Care. 2016;39:222–30.
    Article CAS PubMed Google Scholar
  5. Idorn T, Knop FK, Jørgensen MB, Jensen T, Resuli M, Hansen PM, et al. Safety and efficacy of liraglutide in patients with type 2 diabetes and end-stage renal disease: an investigator-initiated, placebo-controlled, double-blind, parallel-group, randomized trial. Diabetes Care. 2016;39:206–13.
    Article CAS PubMed Google Scholar
  6. Alsahli M, Gerich JE. Hypoglycemia in patients with diabetes and renal disease. J Clin Med. 2015;4:948–64.
    Article CAS PubMed PubMed Central Google Scholar
  7. Park CW, Kim HW, Ko SH, Lim JH, Ryu GR, Chung HW, et al. Long-term treatment of glucagon-like peptide-1 analog exendin-4 ameliorates diabetic nephropathy through improving metabolic anomalies in db/db mice. J Am Soc Nephrol. 2007;18:1227–38.
    Article CAS PubMed Google Scholar
  8. Hendarto H, Inoguchi T, Maeda Y, Ikeda N, Zheng J, Takei R, et al. GLP-1 analog liraglutide protects against oxidative stress and albuminuria in streptozotocin-induced diabetic rats via protein kinase A-mediated inhibition of renal NAD(P)H oxidases. Metabolism. 2012;61:1422–34.
    Article CAS PubMed Google Scholar
  9. Marso SP, Daniels GH, Brown-Frandsen K, Kristensen P, Mann JFE, Nauck MA, et al. Liraglutide and cardiovascular outcomes in type 2 diabetes. N Engl J Med. 2016;375:311–22.
    Article CAS PubMed PubMed Central Google Scholar
  10. Marso SP, Bain SC, Consoli A, Eliaschewitz FG, Jódar E, Leiter LA, et al. Semaglutide and cardiovascular outcomes in patients with type 2 diabetes. N Engl J Med. 2016;375:1834–44.
    Article CAS PubMed Google Scholar
  11. Kalra S. Follow the LEADER—liraglutide effect and action in diabetes: evaluation of cardiovascular outcome results trial. Diabetes Ther. 2016;7:601–9.
    Article PubMed PubMed Central Google Scholar
  12. AstraZeneca Pharmaceuticals. Byetta (exenatide) injection. Highlights of prescribing information. Revised February 2015. [Internet]. Available from: https://www.azpicentral.com/byetta/pi_byetta.pdf#page=1. Accessed 22 June 2017.
  13. U.S. Drug and Food Administration (FDA). Adlyxin (lixisenatide) injection. Highlights of prescribing information. Revised July, 2016 [Internet]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2016/208471Orig1s000lbl.pdf. Accessed 26 Sept 2017.
  14. Marcus JR. A web-based electronic health record system for national surveillance. Online J Public Health Inform. [Internet]. 2013:5. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692859/. Accessed 19 Mar 2017.
  15. Klompas M, Eggleston E, McVetta J, Lazarus R, Li L, Platt R. Automated detection and classification of type 1 versus type 2 diabetes using electronic health record data. Diabetes Care. 2013;36:914–21.
    Article PubMed PubMed Central Google Scholar
  16. Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150:604–12.
    Article PubMed PubMed Central Google Scholar
  17. The Renal Association. CKD stages [Internet]. Available from: http://www.renal.org/information-resources/the-uk-eckd-guide/ckd-stages#sthash.s6SpVT7b.K0UCX4l0.dpbs. Accessed 17 Aug 2016.
  18. Rosenbaum PR, Rubin DB. Constructing a control group using multivariate matched sampling methods that incorporate the propensity score. Am Stat. 1985;39:33–8.
    Google Scholar
  19. Deyo RA, Cherkin DC, Ciol MA. Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases. J Clin Epidemiol. 1992;45:613–9.
    Article CAS PubMed Google Scholar
  20. Quan H, Sundararajan V, Halfon P, Fong A, Burnand B, Luthi J-C, et al. Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Med Care. 2005;43:1130–9.
    Article PubMed Google Scholar
  21. Chang H-Y, Weiner JP, Richards TM, Bleich SN, Segal JB. Validating the adapted diabetes complications severity index in claims data. Am J Manag Care. 2012;18:721–6.
    PubMed Google Scholar
  22. Grigsby AB, Anderson RJ, Freedland KE, Clouse RE, Lustman PJ. Prevalence of anxiety in adults with diabetes: a systematic review. J Psychosom Res. 2002;53:1053–60.
    Article PubMed Google Scholar
  23. Andreoulakis E, Hyphantis T, Kandylis D, Iacovides A. Depression in diabetes mellitus: a comprehensive review. Hippokratia. 2012;16:205–14.
    CAS PubMed PubMed Central Google Scholar
  24. Vergès B, Bonnard C, Renard E. Beyond glucose lowering: glucagon-like peptide-1 receptor agonists, body weight and the cardiovascular system. Diabetes Metab. 2011;37:477–88.
    Article PubMed Google Scholar
  25. FDA. Victoza (liraglutide [rDNA origin] injection). Highlights of prescribing information [Internet]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022341lbl.pdf. Accessed 19 Mar 2017.
  26. Buse JB, Henry RR, Han J, Kim DD, Fineman MS, Baron AD, et al. Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes. Diabetes Care. 2004;27:2628–35.
    Article CAS PubMed Google Scholar
  27. Buse JB, Nauck M, Forst T, Sheu WH-H, Shenouda SK, Heilmann CR, et al. Exenatide once weekly versus liraglutide once daily in patients with type 2 diabetes (DURATION-6): a randomised, open-label study. Lancet. 2013;381:117–24.
    Article CAS PubMed Google Scholar
  28. Nauck M, Frid A, Hermansen K, Shah NS, Tankova T, Mitha IH, et al. Efficacy and safety comparison of liraglutide, glimepiride, and placebo, all in combination with metformin, in type 2 diabetes: the LEAD (liraglutide effect and action in diabetes)-2 study. Diabetes Care. 2009;32:84–90.
    Article CAS PubMed PubMed Central Google Scholar
  29. Durden E, Lenhart G, Lopez-Gonzalez L, Hammer M, Langer J. Predictors of glycemic control and diabetes-related costs among type 2 diabetes patients initiating therapy with liraglutide in the United States. J Med Econ. 2016;19:403–13.
    Article PubMed Google Scholar
  30. Heymann A, Maor Y, Goldstein I, Todorova L, Schertz-Sternberg P, Karasik A. Efficacy of liraglutide in a real-life cohort. Diabetes Ther. 2014;5:193–206.
    Article CAS PubMed PubMed Central Google Scholar
  31. Singhal M, Unni S, Schauerhamer M, Nguyen H, Hurd J, McAdam-Marx C. Real-world glycemic control from glp-1ra therapy with and without concurrent insulin in patients with type 2 diabetes. J Manag Care Spec Pharm. 2017;23:267–75.
    Article PubMed Google Scholar
  32. Lee WC, Dekoven M, Bouchard J, Massoudi M, Langer J. Improved real-world glycaemic outcomes with liraglutide versus other incretin-based therapies in type 2 diabetes. Diabetes Obes Metab. 2014;16:819–26.
    Article CAS PubMed Google Scholar
  33. Li Q, Chitnis A, Hammer M, Langer J. Real-world clinical and economic outcomes of liraglutide versus sitagliptin in patients with type 2 diabetes mellitus in the United States. Diabetes Ther. 2014;5:579–90.
    Article CAS PubMed PubMed Central Google Scholar
  34. Thayer S, Wei W, Buysman E, Brekke L, Crown W, Grabner M, et al. The INITIATOR study: pilot data on real-world clinical and economic outcomes in US patients with type 2 diabetes initiating injectable therapy. Adv Ther. 2013;30(12):1128–1140.
  35. Kim M, Platt MJ, Shibasaki T, Quaggin SE, Backx PH, Seino S, et al. GLP-1 receptor activation and Epac2 link atrial natriuretic peptide secretion to control of blood pressure. Nat Med. 2013;19:567–75.
    Article CAS PubMed Google Scholar
  36. Rieg T, Gerasimova M, Murray F, Masuda T, Tang T, Rose M, et al. Natriuretic effect by exendin-4, but not the DPP-4 inhibitor alogliptin, is mediated via the GLP-1 receptor and preserved in obese type 2 diabetic mice. Am J Physiol Renal Physiol. 2012;303:F963–71.
    Article CAS PubMed PubMed Central Google Scholar
  37. Cummings BP, Stanhope KL, Graham JL, Baskin DG, Griffen SC, Nilsson C, et al. Chronic administration of the glucagon-like peptide-1 analog, liraglutide, delays the onset of diabetes and lowers triglycerides in UCD-T2DM rats. Diabetes. 2010;59:2653–61.
    Article CAS PubMed PubMed Central Google Scholar
  38. Liu Q, Adams L, Broyde A, Fernandez R, Baron AD, Parkes DG. The exenatide analogue AC3174 attenuates hypertension, insulin resistance, and renal dysfunction in Dahl salt-sensitive rats. Cardiovasc Diabetol. 2010;9:32.
    Article PubMed PubMed Central Google Scholar
  39. Tuttle KR, McKinney TD, Davidson JA, Anglin G, Harper KD, Botros FT. Effects of once-weekly dulaglutide on kidney function in patients with type 2 diabetes in phase II and III clinical trials. Diabetes Obes Metab. 2017;19:436–41.
    Article CAS PubMed Google Scholar
  40. Mann JFE, Ørsted DD, Brown-Frandsen K, Marso SP, Poulter NR, Rasmussen S, et al. Liraglutide and renal outcomes in type 2 diabetes. N Engl J Med. 2017;377:839–48.
    Article CAS PubMed Google Scholar
  41. Tuttle K, Lakshmanan M, Gross J, Rayner B, Busch R, Zimmermann A, et al. Dulaglutide versus glargine, both combined with lispro, mitigated eGFR decline in people with type 2 diabetes and moderate to severe chronic kidney disease (AWARD-7). Diabetes. 2017;66(Suppl 1A):LB37–8.
    Google Scholar

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Acknowledgements

Funding

Sponsorship for this study and article processing charges were funded by Eli Lilly and Company.

Editorial Assistance

Editorial assistance in the preparation of this article was provided by Patricia Platt and Michael Treglia of HealthMetrics Outcomes Research. Support for this assistance was funded by Eli Lilly and Company.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.

Disclosures

Kristina Boye is an employee and shareholder at Eli Lilly and Company. Fady Botros is an employee and shareholder at Eli Lilly and Company. Axel Haupt is an employee and shareholder at Eli Lilly and Company. Brad Woodward is an employee and shareholder at Eli Lilly and Company. Maureen Lage was compensated for her work on this project by Eli Lilly and Company.

Compliance with Ethics Guidelines

This article does not contain any studies with human participants or animals performed by any of the authors.

Data Availability

The datasets analyzed during the current study are not publicly available due to use restrictions agreed upon by Eli Lilly and Company and Practice Fusion.

Open Access

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Authors and Affiliations

  1. Global Patient Outcomes and Real World Evidence, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA
    Kristina S. Boye
  2. Diabetes, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA
    Fady T. Botros & Brad Woodward
  3. Early Phase Clinical Research—Diabetes and Complications, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA
    Axel Haupt
  4. HealthMetrics Outcomes Research, 27576 River Reach Drive, Bonita Springs, FL, 34134, USA
    Maureen J. Lage

Authors

  1. Kristina S. Boye
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  2. Fady T. Botros
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  3. Axel Haupt
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  4. Brad Woodward
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  5. Maureen J. Lage
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Corresponding author

Correspondence toMaureen J. Lage.

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Boye, K.S., Botros, F.T., Haupt, A. et al. Glucagon-Like Peptide-1 Receptor Agonist Use and Renal Impairment: A Retrospective Analysis of an Electronic Health Records Database in the U.S. Population.Diabetes Ther 9, 637–650 (2018). https://doi.org/10.1007/s13300-018-0377-5

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