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      Effects of Metreleptin on Proteinuria in Patients With Lipodystrophy

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          Abstract

          Context

          Patients with lipodystrophy have high prevalence of proteinuria.

          Objective

          To assess kidney disease in patients with generalized (GLD) vs partial lipodystrophy (PLD), and the effects of metreleptin on proteinuria in patients with lipodystrophy.

          Design, Setting, Patients, Intervention

          Prospective, open-label studies of metreleptin treatment in patients with GLD and PLD at the National Institutes of Health.

          Outcome Measures

          The 24-hour urinary albumin and protein excretion rates, estimated glomerular filtration rate (eGFR), and creatinine clearance (CrCl) were measured at baseline and during up to 24 months of metreleptin treatment. Patients with increases in medications affecting outcome measures were excluded.

          Results

          At baseline, patients with GLD had significantly greater albuminuria, proteinuria, eGFR, and CrCl compared with patients with PLD. CrCl was above the normal range in 69% of patients with GLD and 39% with PLD ( P = 0.02). With up to 24 months of metreleptin treatment, there were significant reductions in albuminuria and proteinuria in patients with GLD, but not in those with PLD. No changes in eGFR or CrCl were observed in patients with GLD or PLD during metreleptin treatment.

          Conclusions

          Patients with GLD had significantly greater proteinuria than those with PLD, which improved with metreleptin treatment. The mechanisms leading to proteinuria in lipodystrophy and improvements in proteinuria with metreleptin are not clear. Hyperfiltration was also more common in GLD vs PLD but did not change with metreleptin.

          Abstract

          Patients with generalized lipodystrophy (GLD) had greater proteinuria and more hyperfiltration vs those with partial lipodystrophy (PLD). Metreleptin improved proteinuria in GLD, but not PLD.

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          Author and article information

          Journal
          J Clin Endocrinol Metab
          J. Clin. Endocrinol. Metab
          jcem
          The Journal of Clinical Endocrinology and Metabolism
          Endocrine Society (Washington, DC )
          0021-972X
          1945-7197
          September 2019
          16 April 2019
          16 April 2020
          : 104
          : 9
          : 4169-4177
          Affiliations
          [1 ]Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland
          [2 ]Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland
          [3 ]Office of the Clinical Director, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland
          Author notes
          Correspondence and Reprint Requests:  Rebecca J. Brown, MD, Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Building 10-CRC, Room 6-5942, 10 Center Drive, Bethesda, Maryland 20892. E-mail: brownrebecca@ 123456mail.nih.gov .
          Author information
          http://orcid.org/0000-0002-2589-7382
          Article
          PMC6688455 PMC6688455 6688455 jcem_201900200
          10.1210/jc.2019-00200
          6688455
          30990519
          93f9a3e3-4725-4705-a857-b7293a59901f
          Published by Oxford University Press on behalf of the Endocrine Society 2019

          This article is a U.S. Government work-for-hire and is therefore in the public domain in the U.S.

          History
          : 25 January 2019
          : 10 April 2019
          Page count
          Pages: 9
          Funding
          Funded by: National Institute of Diabetes and Digestive and Kidney Diseases 10.13039/100000062
          Categories
          Clinical Research Articles
          Obesity and Adipocyte Biology

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