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Prognostic imaging biomarkers for diabetic kidney disease (iBEAt): study protocol.
Gooding, Kim M; Lienczewski, Chrysta; Papale, Massimo; Koivuviita, Niina; Maziarz, Marlena; Dutius Andersson, Anna-Maria; Sharma, Kanishka; Pontrelli, Paola; Garcia Hernandez, Alberto; Bailey, Julie; Tobin, Kay; Saunavaara, Virva; Zetterqvist, Anna; Shelley, David; Teh, Irvin; Ball, Claire; Puppala, Sapna; Ibberson, Mark; Karihaloo, Anil; Metsärinne, Kaj; Banks, Rosamonde E; Gilmour, Peter S; Mansfield, Michael; Gilchrist, Mark; de Zeeuw, Dick; Heerspink, Hiddo J L; Nuutila, Pirjo; Kretzler, Matthias; Welberry Smith, Matthew; Gesualdo, Loreto; Andress, Dennis; Grenier, Nicolas; Shore, Angela C; Gomez, Maria F; Sourbron, Steven.
Afiliação
  • Gooding KM; Diabetes and Vascular Medicine, University of Exeter Medical School, Barrack Road, Exeter, EX2 5AX, UK. K.M.Gooding@exeter.ac.uk.
  • Lienczewski C; NIHR Exeter Clinical Research Facility, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK. K.M.Gooding@exeter.ac.uk.
  • Papale M; Department of Nephrology, University of Michigan, Ann Arbor, USA.
  • Koivuviita N; Department of Emergency and Organ Transplantation, Nephrology Unit, University of Bari Aldo Moro, Bari, Italy.
  • Maziarz M; Department of Medicine, Division of Nephrology, Turku University Hospital, Turku, Finland.
  • Dutius Andersson AM; Turku PET Centre, University of Turku, Turku, Finland.
  • Sharma K; Department of Clinical Sciences in Malmö, Lund University Diabetes Centre, Lund University, Malmo, Sweden.
  • Pontrelli P; Department of Clinical Sciences in Malmö, Lund University Diabetes Centre, Lund University, Malmo, Sweden.
  • Garcia Hernandez A; Department of Imaging, Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
  • Bailey J; Department of Emergency and Organ Transplantation, Nephrology Unit, University of Bari Aldo Moro, Bari, Italy.
  • Tobin K; Astellas Pharma Europe B.V, Meppel, The Netherlands.
  • Saunavaara V; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Zetterqvist A; Department of Renal Medicine and Renal Transplantation, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Shelley D; Department of Medical Physics, Division of Medical Imaging, Turku University Hospital, Turku, Finland.
  • Teh I; Department of Clinical Sciences in Malmö, Lund University Diabetes Centre, Lund University, Malmo, Sweden.
  • Ball C; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Puppala S; Advanced Imaging Centre, University of Leeds, Leeds, UK.
  • Ibberson M; Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
  • Karihaloo A; NIHR Exeter Clinical Research Facility, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
  • Metsärinne K; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Banks RE; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • Gilmour PS; Novo Nordisk Research Center Seattle, Inc., Seattle, USA.
  • Mansfield M; Department of Medicine, Division of Nephrology, Turku University Hospital, Turku, Finland.
  • Gilchrist M; Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, UK.
  • de Zeeuw D; The Drug Development Team, Leiden, The Netherlands.
  • Heerspink HJL; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Nuutila P; Diabetes and Vascular Medicine, University of Exeter Medical School, Barrack Road, Exeter, EX2 5AX, UK.
  • Kretzler M; Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, Groningen, The Netherlands.
  • Welberry Smith M; University of Groningen, Groningen, The Netherlands.
  • Gesualdo L; Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, Groningen, The Netherlands.
  • Andress D; University of Groningen, Groningen, The Netherlands.
  • Grenier N; Department of Medicine, Division of Nephrology, Turku University Hospital, Turku, Finland.
  • Shore AC; Turku PET Centre, University of Turku, Turku, Finland.
  • Gomez MF; Department of Nephrology, University of Michigan, Ann Arbor, USA.
  • Sourbron S; Computational Medicine and Bioinformatics, University of Michigan, Ann Arbour, USA.
BMC Nephrol ; 21(1): 242, 2020 06 29.
Article em En | MEDLINE | ID: mdl-32600374
ABSTRACT

BACKGROUND:

Diabetic kidney disease (DKD) remains one of the leading causes of premature death in diabetes. DKD is classified on albuminuria and reduced kidney function (estimated glomerular filtration rate (eGFR)) but these have modest value for predicting future renal status. There is an unmet need for biomarkers that can be used in clinical settings which also improve prediction of renal decline on top of routinely available data, particularly in the early stages. The iBEAt study of the BEAt-DKD project aims to determine whether renal imaging biomarkers (magnetic resonance imaging (MRI) and ultrasound (US)) provide insight into the pathogenesis and heterogeneity of DKD (primary aim) and whether they have potential as prognostic biomarkers in DKD (secondary aim).

METHODS:

iBEAt is a prospective multi-centre observational cohort study recruiting 500 patients with type 2 diabetes (T2D) and eGFR ≥30 ml/min/1.73m2. At baseline, blood and urine will be collected, clinical examinations will be performed, and medical history will be obtained. These assessments will be repeated annually for 3 years. At baseline each participant will also undergo quantitative renal MRI and US with central processing of MRI images. Biological samples will be stored in a central laboratory for biomarker and validation studies, and data in a central data depository. Data analysis will explore the potential associations between imaging biomarkers and renal function, and whether the imaging biomarkers improve the prediction of DKD progression. Ancillary substudies will (1) validate imaging biomarkers against renal histopathology; (2) validate MRI based renal blood flow measurements against H2O15 positron-emission tomography (PET); (3) validate methods for (semi-)automated processing of renal MRI; (4) examine longitudinal changes in imaging biomarkers; (5) examine whether glycocalyx and microvascular measures are associated with imaging biomarkers and eGFR decline; (6) explore whether the findings in T2D can be extrapolated to type 1 diabetes.

DISCUSSION:

iBEAt is the largest DKD imaging study to date and will provide valuable insights into the progression and heterogeneity of DKD. The results may contribute to a more personalised approach to DKD management in patients with T2D. TRIAL REGISTRATION Clinicaltrials.gov ( NCT03716401 ).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Insuficiência Renal Crônica / Rim Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Insuficiência Renal Crônica / Rim Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article