PMID- 30941882 OWN - NLM STAT- MEDLINE DCOM- 20200916 LR - 20210109 IS - 1463-1326 (Electronic) IS - 1462-8902 (Print) IS - 1462-8902 (Linking) VI - 21 IP - 8 DP - 2019 Aug TI - Temporal variation of renal function in people with type 2 diabetes mellitus: A retrospective UK clinical practice research datalink cohort study. PG - 1817-1823 LID - 10.1111/dom.13734 [doi] AB - AIM: To characterize the longitudinal variability of estimated glomerular filtration rate (eGFR) in people with type 2 diabetes mellitus (T2DM), including variation between categories and individuals. METHODS: People with T2DM and sufficient recorded serum creatinine measurements were identified from the Clinical Practice Research Datalink (T2DM diagnosis from 1 January 2009 to 1 January 2011 with 5 years follow-up); eGFR was calculated using the CKD-EPI equation. RESULTS: In total, 7766 individuals were included; 32.8%, 50.2%, 12.4%, 4.0% and 0.6% were in glomerular filtration rate (GFR) categories G1, G2, G3a, G3b and G4, respectively. Overall, eGFR decreased by 0.44 mL/min/1.73 m(2) per year; eGFR increased by 0.80 mL/min/1.73 m(2) between index and year 1, then decreased by 0.75 mL/min/1.73 m(2) annually up to year 5. Category G1 showed a steady decline in eGFR over time; G2, G3a and G3b showed an increase between index and year 1, followed by a decline. Category G4 showed a mean eGFR increase of 1.85 mL/min/1.73 m(2) annually. People in categories G3-G4 moved across a greater number of GFR categories than those in G1 and G2. Individual patients' eGFR showed a wide range of values (change from baseline at year 5 varied from -80 to +59 mL/min/1.73 m(2) ). CONCLUSION: Overall, eGFR declined over time, although there was considerable variation between GFR categories and individuals. This highlights the difficulty in prescribing many glucose-lowering therapies, which require dose adjustment for renal function. The study also emphasizes the importance of regular monitoring of renal impairment in people with T2DM. CI - (c) 2019 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. FAU - Spanopoulos, Dionysis AU - Spanopoulos D AD - Market Access, Boehringer Ingelheim Ltd, Bracknell, UK. FAU - Okhai, Hajra AU - Okhai H AD - Diabetes Research Centre, University of Leicester, Leicester, UK. FAU - Zaccardi, Francesco AU - Zaccardi F AD - Diabetes Research Centre, University of Leicester, Leicester, UK. FAU - Tebboth, Abigail AU - Tebboth A AUID- ORCID: 0000-0001-8201-3507 AD - Market Access, Boehringer Ingelheim Ltd, Bracknell, UK. FAU - Barrett, Brendan AU - Barrett B AD - Medical Affairs, Boehringer Ingelheim Ltd, Bracknell, UK. FAU - Busse, Michael AU - Busse M AD - Medical Affairs, Boehringer Ingelheim Ltd, Bracknell, UK. FAU - Webb, Joanne AU - Webb J AD - Medical Affairs, Eli Lilly and Company, Basingstoke, UK. FAU - Khunti, Kamlesh AU - Khunti K AUID- ORCID: 0000-0003-2343-7099 AD - Diabetes Research Centre, University of Leicester, Leicester, UK. LA - eng GR - Boehringer Ingelheim Ltd/International PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20190506 PL - England TA - Diabetes Obes Metab JT - Diabetes, obesity & metabolism JID - 100883645 RN - AYI8EX34EU (Creatinine) SB - IM MH - Adult MH - Aged MH - Creatinine/blood MH - Databases, Factual MH - Diabetes Mellitus, Type 2/*blood/complications/physiopathology MH - Diabetic Nephropathies/*etiology MH - Disease Progression MH - Female MH - Glomerular Filtration Rate MH - Humans MH - Kidney/physiopathology MH - Longitudinal Studies MH - Male MH - Middle Aged MH - Retrospective Studies MH - Risk Factors MH - *Time Factors MH - United Kingdom PMC - PMC6767485 OTO - NOTNLM OT - UK OT - primary care OT - renal impairment OT - type 2 diabetes COIS- A.T. and M.B. are employees of Boehringer Ingelheim, the study sponsor. D.S. and B.B. were also employees of Boehringer Ingelheim at the time the study was conducted. J.W. is an employee of Eli Lilly and Company. H.O. and F.Z. received funding from the study sponsors for the analysis and conduct of the study. K.K. has acted as a consultant and or speaker for Napp, Novartis, Novo Nordisk, Sanofi-Aventis, Lilly and Merck Sharp & Dohme, and has received grants in support of investigator and investigator-initiated trials from Novartis, Novo Nordisk, Sanofi-Aventis, Lilly, Pfizer, Boehringer Ingelheim and Merck Sharp & Dohme. EDAT- 2019/04/04 06:00 MHDA- 2020/09/17 06:00 PMCR- 2019/09/30 CRDT- 2019/04/04 06:00 PHST- 2019/01/11 00:00 [received] PHST- 2019/03/19 00:00 [revised] PHST- 2019/03/31 00:00 [accepted] PHST- 2019/04/04 06:00 [pubmed] PHST- 2020/09/17 06:00 [medline] PHST- 2019/04/04 06:00 [entrez] PHST- 2019/09/30 00:00 [pmc-release] AID - DOM13734 [pii] AID - 10.1111/dom.13734 [doi] PST - ppublish SO - Diabetes Obes Metab. 2019 Aug;21(8):1817-1823. doi: 10.1111/dom.13734. Epub 2019 May 6.