Frontiers in Endocrinology (Jul 2023)
Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review
- Denise H. van Abswoude,
- Denise H. van Abswoude,
- Denise H. van Abswoude,
- Denise H. van Abswoude,
- Karlijn Pellikaan,
- Karlijn Pellikaan,
- Karlijn Pellikaan,
- Karlijn Pellikaan,
- Naomi Nguyen,
- Anna G. W. Rosenberg,
- Anna G. W. Rosenberg,
- Anna G. W. Rosenberg,
- Anna G. W. Rosenberg,
- Kirsten Davidse,
- Kirsten Davidse,
- Kirsten Davidse,
- Kirsten Davidse,
- Franciska M. E. Hoekstra,
- Franciska M. E. Hoekstra,
- Ilse M. Rood,
- Christine Poitou,
- Christine Poitou,
- Christine Poitou,
- Graziano Grugni,
- Graziano Grugni,
- Graziano Grugni,
- Charlotte Høybye,
- Charlotte Høybye,
- Charlotte Høybye,
- Charlotte Høybye,
- Tania P. Markovic,
- Tania P. Markovic,
- Tania P. Markovic,
- Assumpta Caixàs,
- Assumpta Caixàs,
- Assumpta Caixàs,
- Antonino Crinò,
- Antonino Crinò,
- Antonino Crinò,
- Sjoerd A. A. van den Berg,
- Sjoerd A. A. van den Berg,
- Aart J. van der Lely,
- Aart J. van der Lely,
- Aart J. van der Lely,
- Laura C. G. de Graaff,
- Laura C. G. de Graaff,
- Laura C. G. de Graaff,
- Laura C. G. de Graaff,
- Laura C. G. de Graaff
Affiliations
- Denise H. van Abswoude
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Denise H. van Abswoude
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Denise H. van Abswoude
- Dutch Center of Reference for Prader–Willi Syndrome, Rotterdam, Netherlands
- Denise H. van Abswoude
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Karlijn Pellikaan
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Karlijn Pellikaan
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Karlijn Pellikaan
- Dutch Center of Reference for Prader–Willi Syndrome, Rotterdam, Netherlands
- Karlijn Pellikaan
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Naomi Nguyen
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Anna G. W. Rosenberg
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Anna G. W. Rosenberg
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Anna G. W. Rosenberg
- Dutch Center of Reference for Prader–Willi Syndrome, Rotterdam, Netherlands
- Anna G. W. Rosenberg
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Kirsten Davidse
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Kirsten Davidse
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Kirsten Davidse
- Dutch Center of Reference for Prader–Willi Syndrome, Rotterdam, Netherlands
- Kirsten Davidse
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Franciska M. E. Hoekstra
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Franciska M. E. Hoekstra
- Internal Medicine, Division of Nephrology, Reinier de Graaf Gasthuis, Delft, Netherlands
- Ilse M. Rood
- Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands
- Christine Poitou
- Assistance Publique-Hôpitaux de Paris, Rare Diseases Center of Reference ‘Prader-Willi Syndrome and Obesity with Eating Disorders’ (PRADORT), Nutrition Department, Institute of Cardiometabolism and Nutrition (ICAN), Pitié-Salpêtrière Hospital, Sorbonne Université, National Institute of Health and Medical Research (INSERM), Nutriomics, Paris, France
- Christine Poitou
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Christine Poitou
- European Reference Network on Rare Endocrine Conditions (ENDO-ERN)
- Graziano Grugni
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Graziano Grugni
- European Reference Network on Rare Endocrine Conditions (ENDO-ERN)
- Graziano Grugni
- 0Division of Auxology, Istituto Auxologico Italiano, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Piancavallo, Italy
- Charlotte Høybye
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Charlotte Høybye
- European Reference Network on Rare Endocrine Conditions (ENDO-ERN)
- Charlotte Høybye
- 1Department of Molecular Medicine and Surgery, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden
- Charlotte Høybye
- 2Department of Endocrinology, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden
- Tania P. Markovic
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Tania P. Markovic
- 3Metabolism & Obesity Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia
- Tania P. Markovic
- 4Charles Perkins Center and Sydney Medical School, University of Sydney, Sydney, NSW, Australia
- Assumpta Caixàs
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Assumpta Caixàs
- 5Department of Endocrinology and Nutrition, Parc Tauli Hospital Universitari, Institut d’Investigació i Innovació Parc Taulí (I3PT) Instituto de Salud Carlos III (CERCA-ISCIII), Sabadell, Spain
- Assumpta Caixàs
- 6Department of Medicine, Universitat Autònoma de Barcelona, Sabadell, Spain
- Antonino Crinò
- International Network for Research, Management & Education on adults with Prader-Willi Syndrome (INfoRMEd-PWS)
- Antonino Crinò
- 7Reference Center for Prader-Willi syndrome, Bambino Gesù Hospital, Research Institute, Palidoro, Italy
- Antonino Crinò
- 8Center for Rare Diseases and Congenital Defects, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy
- Sjoerd A. A. van den Berg
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Sjoerd A. A. van den Berg
- 9Department of Clinical Chemistry, Erasmus Medical Center (MC), University Medical Center Rotterdam, Rotterdam, Netherlands
- Aart J. van der Lely
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Aart J. van der Lely
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Aart J. van der Lely
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Laura C. G. de Graaff
- Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Laura C. G. de Graaff
- Center for Adults with Rare Genetic Syndromes, Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Laura C. G. de Graaff
- Dutch Center of Reference for Prader–Willi Syndrome, Rotterdam, Netherlands
- Laura C. G. de Graaff
- Academic Center for Growth Disorders, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands
- Laura C. G. de Graaff
- European Reference Network on Rare Endocrine Conditions (ENDO-ERN)
- DOI
- https://doi.org/10.3389/fendo.2023.1168648
- Journal volume & issue
-
Vol. 14
Abstract
BackgroundPrader-Willi syndrome (PWS) is a rare, complex, genetic disorder characterized by hyperphagia, hypotonia, delayed psychomotor development, low muscle mass and hypothalamic dysfunction. Adults with PWS often have obesity, hypertension and type 2 diabetes mellitus (DM2), known risk factors for cardiovascular disease (CVD) and chronic kidney disease (CKD). Early symptoms of CVD and CKD may be masked by intellectual disability and inability to express physical complaints. Furthermore, kidney diseases are often asymptomatic. Therefore, renal and cardiovascular disease might be missed in patients with PWS. Microalbuminuria is an early sign of microvascular damage in the kidneys and other vascular beds. Therefore, we screened our adult PWS cohort for the presence of elevated urinary albumin and (micro)albuminuria.MethodsWe retrospectively collected anthropometric measurements, blood pressure, medical history, medication use, urine dipstick and biochemical measurements form electronic patient files. In addition, we performed a systematic literature review on kidney disease in PWS.ResultsWe included 162 adults with genetically confirmed PWS (56% male, median age 28 years), of whom 44 (27%) had DM2. None had known CVD. All subjects had normal estimated glomerular filtration rate (eGFR) according to non-PWS reference intervals. Elevated urinary albumin or (micro)albuminuria was present in 28 (18%); 19 out of 75 (25%) had an increased urinary albumin-to-creatinine ratio (UACR) and 10 out of 57 (18%) had an increased urinary protein-to-creatinine ratio. Elevated urinary albumin was present at a young age (median age 26 (IQR 24-32) years) and was associated with an significantly higher BMI and LDL-cholesterol levels and higher prevalence of DM2, hypertension and dyslipidemia than those with normal UACR (p=0.027, p=0.019, p<0.001, p<0.001, p=0.011 and respectively).ConclusionUpon screening, one in every five adults with PWS had increased urinary albumin or (micro)albuminuria, early signs of microvascular disease. All had normal eGFR, according to non-PWS reference intervals, and none had a formal diagnosis of CVD. As muscle mass is low in PWS, creatinine levels and eGFR may be spuriously normal. Urinalysis in this patient group can be used as a screening tool for microvascular (kidney) disease. We propose an algorithm for the detection and management of microvascular disease in adults with PWS.
Keywords
- Prader-Willi Syndrome
- kidney function tests
- proteinuria
- urine tract infections
- cardiovascular disease
- kidney disease