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[11C]metomidate PET-CT versus adrenal vein sampling for diagnosing surgically curable primary aldosteronism: a prospective, within-patient trial.
Wu, Xilin; Senanayake, Russell; Goodchild, Emily; Bashari, Waiel A; Salsbury, Jackie; Cabrera, Claudia P; Argentesi, Giulia; O'Toole, Samuel M; Matson, Matthew; Koo, Brendan; Parvanta, Laila; Hilliard, Nick; Kosmoliaptsis, Vasilis; Marker, Alison; Berney, Daniel M; Tan, Wilson; Foo, Roger; Mein, Charles A; Wozniak, Eva; Savage, Emmanuel; Sahdev, Anju; Bird, Nicholas; Laycock, Kate; Boros, Istvan; Hader, Stefan; Warnes, Victoria; Gillett, Daniel; Dawnay, Anne; Adeyeye, Elizabeth; Prete, Alessandro; Taylor, Angela E; Arlt, Wiebke; Bhuva, Anish N; Aigbirhio, Franklin; Manisty, Charlotte; McIntosh, Alasdair; McConnachie, Alexander; Cruickshank, J Kennedy; Cheow, Heok; Gurnell, Mark; Drake, William M; Brown, Morris J.
Affiliation
  • Wu X; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Senanayake R; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Goodchild E; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Bashari WA; Metabolic Research Laboratories, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.
  • Salsbury J; NIHR Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Cabrera CP; Department of Diabetes and Endocrinology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Argentesi G; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • O'Toole SM; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Matson M; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Koo B; Metabolic Research Laboratories, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.
  • Parvanta L; NIHR Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Hilliard N; Department of Diabetes and Endocrinology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Kosmoliaptsis V; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Marker A; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Berney DM; Centre for Translational Bioinformatics, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Tan W; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Foo R; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Mein CA; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Wozniak E; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Savage E; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Sahdev A; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Bird N; Department of Endocrinology, Royal Hallamshire Hospital, Sheffield, United Kingdom.
  • Laycock K; Department of Radiology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Boros I; Department of Radiology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Hader S; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Warnes V; Department of Radiology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Gillett D; Department of Surgery, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Dawnay A; Department of Histopathology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Adeyeye E; Department of Histopathology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Prete A; Cardiovascular Research Institute, National University of Singapore, Singapore, Singapore.
  • Taylor AE; Cardiovascular Research Institute, National University of Singapore, Singapore, Singapore.
  • Arlt W; Barts and the London Genome Centre, School of Medicine and Dentistry, Blizard Institute, London, United Kingdom.
  • Bhuva AN; Barts and the London Genome Centre, School of Medicine and Dentistry, Blizard Institute, London, United Kingdom.
  • Aigbirhio F; Barts and the London Genome Centre, School of Medicine and Dentistry, Blizard Institute, London, United Kingdom.
  • Manisty C; Department of Radiology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • McIntosh A; Department of Radiology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • McConnachie A; Endocrine Hypertension, Department of Clinical Pharmacology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
  • Cruickshank JK; NIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Cheow H; Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
  • Gurnell M; Wolfson Brain Imaging Centre, University of Cambridge, Cambridge, United Kingdom.
  • Drake WM; Wolfson Brain Imaging Centre, University of Cambridge, Cambridge, United Kingdom.
  • Brown MJ; Department of Nuclear Medicine, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
Nat Med ; 29(1): 190-202, 2023 01.
Article in En | MEDLINE | ID: mdl-36646800
ABSTRACT
Primary aldosteronism (PA) due to a unilateral aldosterone-producing adenoma is a common cause of hypertension. This can be cured, or greatly improved, by adrenal surgery. However, the invasive nature of the standard pre-surgical investigation contributes to fewer than 1% of patients with PA being offered the chance of a cure. The primary objective of our prospective study of 143 patients with PA ( NCT02945904 ) was to compare the accuracy of a non-invasive test, [11C]metomidate positron emission tomography computed tomography (MTO) scanning, with adrenal vein sampling (AVS) in predicting the biochemical remission of PA and the resolution of hypertension after surgery. A total of 128 patients reached 6- to 9-month follow-up, with 78 (61%) treated surgically and 50 (39%) managed medically. Of the 78 patients receiving surgery, 77 achieved one or more PA surgical outcome criterion for success. The accuracies of MTO at predicting biochemical and clinical success following adrenalectomy were, respectively, 72.7 and 65.4%. For AVS, the accuracies were 63.6 and 61.5%. MTO was not significantly superior, but the differences of 9.1% (95% confidence interval = -6.5 to 24.1%) and 3.8% (95% confidence interval = -11.9 to 9.4) lay within the pre-specified -17% margin for non-inferiority (P = 0.00055 and P = 0.0077, respectively). Of 24 serious adverse events, none was considered related to either investigation and 22 were fully resolved. MTO enables non-invasive diagnosis of unilateral PA.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Positron Emission Tomography Computed Tomography / Hyperaldosteronism Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nat Med Journal subject: BIOLOGIA MOLECULAR / MEDICINA Year: 2023 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Positron Emission Tomography Computed Tomography / Hyperaldosteronism Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nat Med Journal subject: BIOLOGIA MOLECULAR / MEDICINA Year: 2023 Type: Article Affiliation country: United kingdom