Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study
Long-term studies show that some metabolic syndrome (MS) components deteriorate renal function in autosomal dominant polycystic kidney disease (ADPKD) patients. The aim of this 6-year follow-up was to analyze early changes of all MS components and their associations with kidney function in the nondi...
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doaj-1966a861ac134cbbb863f6963385f58d2020-11-25T02:55:06ZengIndex Copernicus International S.A.Postępy Higieny i Medycyny Doświadczalnej0032-54491732-26932019-11-017359860710.5604/01.3001.0013.560501.3001.0013.5605Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up studyMaria Pietrzak-Nowacka0Krzysztof Safranow1Małgorzata Marchelek-Myśliwiec2Mariusz Bodnar3Sylwia Przysiecka4Monika Nowosiad-Magda5Kazimierz Ciechanowski6Department of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandDepartment of Biochemistry and Medical Chemistry, Pomeranian Medical University, Szczecin, PolandDepartment of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandDepartment of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandDepartment of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandDepartment of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandDepartment of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, Szczecin, PolandLong-term studies show that some metabolic syndrome (MS) components deteriorate renal function in autosomal dominant polycystic kidney disease (ADPKD) patients. The aim of this 6-year follow-up was to analyze early changes of all MS components and their associations with kidney function in the nondiabetic ADPKD patients with normal renal function, compared to controls. The follow-up physical and laboratory examinations were performed for 39 ADPKD patients (age 43.7 ± 11.4 years) and 44 controls (43.5 ± 9.1 years). We noticed a significant increase in weight, body mass index (BMI), waist, total and LDL cholesterol, C-peptide, uric acid, creatinine and significant decline of HbA1c and e-GFR in the ADPKD group. Increases in waist, uric acid and creatinine concentrations were significantly higher in the ADPKD patients than controls. Both groups showed similar rates of prediabetes, while diabetes developed in 5 controls (with 4 cases of type 2 diabetes and one case of type 1), but not in the ADPKD group (11% vs 0%, P = 0.06 for diabetes, 9% vs 0%, P = 0.12 for type 2 diabetes). The ADPKD group showed a significantly higher percentage of obesity, waist circumferences, systolic/diastolic blood pressure, concentrations of creatinine, urea and uric acid and lower e-GFR. The MS prevalence was comparable; however, the number of MS components was significantly higher in the ADPKD patients (median 2 vs. 1, p = 0.001). The presence of MS does not influence the rate of renal failure progression in nondiabetic ADPKD patients with normal renal function at a 6-year follow-up. http://phmd.pl/gicid/01.3001.0013.5605autosomal dominant polycystic kidney diseasekidney functiondiabetesmetabolic syndrome |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maria Pietrzak-Nowacka Krzysztof Safranow Małgorzata Marchelek-Myśliwiec Mariusz Bodnar Sylwia Przysiecka Monika Nowosiad-Magda Kazimierz Ciechanowski |
spellingShingle |
Maria Pietrzak-Nowacka Krzysztof Safranow Małgorzata Marchelek-Myśliwiec Mariusz Bodnar Sylwia Przysiecka Monika Nowosiad-Magda Kazimierz Ciechanowski Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study Postępy Higieny i Medycyny Doświadczalnej autosomal dominant polycystic kidney disease kidney function diabetes metabolic syndrome |
author_facet |
Maria Pietrzak-Nowacka Krzysztof Safranow Małgorzata Marchelek-Myśliwiec Mariusz Bodnar Sylwia Przysiecka Monika Nowosiad-Magda Kazimierz Ciechanowski |
author_sort |
Maria Pietrzak-Nowacka |
title |
Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
title_short |
Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
title_full |
Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
title_fullStr |
Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
title_full_unstemmed |
Evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
title_sort |
evolution of metabolic syndrome components in patients with autosomal-dominant polycystic kidney disease: a six-year follow-up study |
publisher |
Index Copernicus International S.A. |
series |
Postępy Higieny i Medycyny Doświadczalnej |
issn |
0032-5449 1732-2693 |
publishDate |
2019-11-01 |
description |
Long-term studies show that some metabolic syndrome (MS) components deteriorate renal function in autosomal dominant polycystic kidney disease (ADPKD) patients. The aim of this 6-year follow-up was to analyze early changes of all MS components and their associations with kidney function in the nondiabetic ADPKD patients with normal renal function, compared to controls.
The follow-up physical and laboratory examinations were performed for 39 ADPKD patients (age 43.7 ± 11.4 years) and 44 controls (43.5 ± 9.1 years).
We noticed a significant increase in weight, body mass index (BMI), waist, total and LDL cholesterol, C-peptide, uric acid, creatinine and significant decline of HbA1c and e-GFR in the ADPKD group. Increases in waist, uric acid and creatinine concentrations were significantly higher in the ADPKD patients than controls. Both groups showed similar rates of prediabetes, while diabetes developed in 5 controls (with 4 cases of type 2 diabetes and one case of type 1), but not in the ADPKD group (11% vs 0%, P = 0.06 for diabetes, 9% vs 0%, P = 0.12 for type 2 diabetes). The ADPKD group showed a significantly higher percentage of obesity, waist circumferences, systolic/diastolic blood pressure, concentrations of creatinine, urea and uric acid and lower e-GFR. The MS prevalence was comparable; however, the number of MS components was significantly higher in the ADPKD patients (median 2 vs. 1, p = 0.001).
The presence of MS does not influence the rate of renal failure progression in nondiabetic ADPKD patients with normal renal function at a 6-year follow-up.
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topic |
autosomal dominant polycystic kidney disease kidney function diabetes metabolic syndrome |
url |
http://phmd.pl/gicid/01.3001.0013.5605 |
work_keys_str_mv |
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