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      Obesity is common in chronic kidney disease and associates with greater antihypertensive usage and proteinuria: evidence from a cross‐sectional study in a tertiary nephrology centre

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          Obesity is a treatable risk factor for chronic kidney disease progression. We audited the reporting of body‐mass index in nephrology outpatient clinics to establish the characteristics of individuals with obesity in nephrology practice. Body‐mass index, clinical information and biochemical measures were recorded for patients attending clinics between 3 rd August, 2018 and 18 th January, 2019. Inferential statistics and Pearson correlations were used to investigate relationships between body‐mass index, type 2 diabetes, hypertension and proteinuria. Mean ± SD BMI was 28.6 ± 5.8 kg/m 2 (n = 374). Overweight and obesity class 1 were more common in males ( P = .02). Amongst n = 123 individuals with obesity and chronic kidney disease, mean ± SD age, n (%) female and median[IQR] eGFR were 64.1 ± 14.2 years, 52 (42.3%) and 29.0[20.5] mL/min/BSA, respectively. A positive correlation between increasing body‐mass index and proteinuria was observed in such patients ( r = 0.21, P = .03), which was stronger in males and those with CKD stages 4 and 5. Mean body‐mass index was 2.3 kg/m 2 higher in those treated with 4‐5 versus 0‐1 antihypertensives ( P = .03). Amongst n = 59 patients with obesity, chronic kidney disease and type 2 diabetes, 2 (3.5%) and 0 (0%) were prescribed a GLP‐1 receptor analogue and SGLT2‐inhibitor, respectively. Our data provides a strong rationale not only for measuring body‐mass index but also for acting on the information in nephrology practice, although prospective studies are required to guide treatment decisions in people with obesity and chronic kidney disease.

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          A new equation to estimate glomerular filtration rate.

          Equations to estimate glomerular filtration rate (GFR) are routinely used to assess kidney function. Current equations have limited precision and systematically underestimate measured GFR at higher values. To develop a new estimating equation for GFR: the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Cross-sectional analysis with separate pooled data sets for equation development and validation and a representative sample of the U.S. population for prevalence estimates. Research studies and clinical populations ("studies") with measured GFR and NHANES (National Health and Nutrition Examination Survey), 1999 to 2006. 8254 participants in 10 studies (equation development data set) and 3896 participants in 16 studies (validation data set). Prevalence estimates were based on 16,032 participants in NHANES. GFR, measured as the clearance of exogenous filtration markers (iothalamate in the development data set; iothalamate and other markers in the validation data set), and linear regression to estimate the logarithm of measured GFR from standardized creatinine levels, sex, race, and age. In the validation data set, the CKD-EPI equation performed better than the Modification of Diet in Renal Disease Study equation, especially at higher GFR (P < 0.001 for all subsequent comparisons), with less bias (median difference between measured and estimated GFR, 2.5 vs. 5.5 mL/min per 1.73 m(2)), improved precision (interquartile range [IQR] of the differences, 16.6 vs. 18.3 mL/min per 1.73 m(2)), and greater accuracy (percentage of estimated GFR within 30% of measured GFR, 84.1% vs. 80.6%). In NHANES, the median estimated GFR was 94.5 mL/min per 1.73 m(2) (IQR, 79.7 to 108.1) vs. 85.0 (IQR, 72.9 to 98.5) mL/min per 1.73 m(2), and the prevalence of chronic kidney disease was 11.5% (95% CI, 10.6% to 12.4%) versus 13.1% (CI, 12.1% to 14.0%). The sample contained a limited number of elderly people and racial and ethnic minorities with measured GFR. The CKD-EPI creatinine equation is more accurate than the Modification of Diet in Renal Disease Study equation and could replace it for routine clinical use. National Institute of Diabetes and Digestive and Kidney Diseases.
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            Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy

            Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium-glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes.
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              Evaluation and management of chronic kidney disease: synopsis of the kidney disease: improving global outcomes 2012 clinical practice guideline.

              The Kidney Disease: Improving Global Outcomes (KDIGO) organization developed clinical practice guidelines in 2012 to provide guidance on the evaluation, management, and treatment of chronic kidney disease (CKD) in adults and children who are not receiving renal replacement therapy. The KDIGO CKD Guideline Development Work Group defined the scope of the guideline, gathered evidence, determined topics for systematic review, and graded the quality of evidence that had been summarized by an evidence review team. Searches of the English-language literature were conducted through November 2012. Final modification of the guidelines was informed by the KDIGO Board of Directors and a public review process involving registered stakeholders. The full guideline included 110 recommendations. This synopsis focuses on 10 key recommendations pertinent to definition, classification, monitoring, and management of CKD in adults.
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                Author and article information

                Contributors
                william.martin@ucd.ie
                Journal
                Clin Obes
                Clin Obes
                10.1111/(ISSN)1758-8111
                COB
                Clinical Obesity
                Blackwell Publishing Ltd (Chichester, UK )
                1758-8103
                1758-8111
                26 August 2020
                December 2020
                : 10
                : 6 ( doiID: 10.1111/cob.v10.6 )
                : e12402
                Affiliations
                [ 1 ] Diabetes Complications Research Centre Conway Institute of Biomolecular and Biomedical Research, School of Medicine, University College Dublin Dublin Ireland
                [ 2 ] Department of Nephrology St. Vincent's University Hospital Dublin Ireland
                [ 3 ] Department of Clinical Chemistry St. Vincent's University Hospital Dublin Ireland
                [ 4 ] Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg Gothenburg Sweden
                [ 5 ] Division of Investigative Science Imperial College London London UK
                Author notes
                [*] [* ] Correspondence

                Dr. William P. Martin, Diabetes Complications Research Centre, Conway Institute of Biomolecular and Biomedical Research, School of Medicine, University College Dublin, Dublin, Ireland.

                Email: william.martin@ 123456ucd.ie

                Author information
                https://orcid.org/0000-0001-7005-3966
                https://orcid.org/0000-0002-0961-2607
                Article
                COB12402
                10.1111/cob.12402
                7685118
                32845571
                f10af299-0c17-4bfe-bdc4-ad6d7b5777f8
                © 2020 The Authors. Clinical Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federation.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 May 2020
                : 09 July 2020
                : 03 August 2020
                Page count
                Figures: 3, Tables: 3, Pages: 12, Words: 8781
                Funding
                Funded by: European Foundation for the Study of Diabetes , open-funder-registry 10.13039/501100001648;
                Award ID: BI 2017_3
                Funded by: Health Research Board , open-funder-registry 10.13039/100010414;
                Award ID: 203930/B/16/Z
                Funded by: Medicinska Forskningsrådet , open-funder-registry 10.13039/501100006310;
                Award ID: 2015‐02733
                Funded by: Science Foundation Ireland , open-funder-registry 10.13039/501100001602;
                Award ID: 12/YI/B2480
                Funded by: Wellcome Trust , open-funder-registry 10.13039/100010269;
                Award ID: 203930/B/16/Z
                Categories
                Original Research Article
                Original Research Articles
                Custom metadata
                2.0
                December 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.4 mode:remove_FC converted:24.11.2020

                chronic kidney disease,diabetes mellitus,diabetic kidney disease,obesity,overweight

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