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    Frontiers in neurology. 2020 Sep 16. doi: 10.3389/fneur.2020.00972. pmc: PMC7526256
    Renal Manifestations of Tuberous Sclerosis Complex: Key Findings From the Final Analysis of the TOSCA Study Focussing Mainly on Renal Angiomyolipomas.
    Kingswood JC1,  Belousova E2,  Benedik MP3,  Carter T4,  Cottin V5,  Curatolo P6,  Dahlin M7,  D'Amato L8,  Beaure d'Augères G9,  de Vries PJ10,  Ferreira JC11,  Feucht M12,  Fladrowski C13,  Hertzberg C14,  Jozwiak S15,  Lawson JA16,  Macaya A17,  Marques R18,  Nabbout R19,  O'Callaghan F20,  Qin J21,  Sander V22,  Shah S23,  Takahashi Y24,  Touraine R25,  Youroukos S26,  Zonnenberg B27,  Jansen AC28,  Sauter M29
    Author information
    1Cardiology Clinical Academic Group, Molecular and Clinical Sciences Research Centre, St Georges University of London, London, United Kingdom.
    2Research and Clinical Institute of Pediatrics, Pirogov Russian National Research Medical University, Moscow, Russia.
    3Child Neurology Department, SPS Pediatrična Klinika, Ljubljana, Slovenia.
    4TSA Tuberous Sclerosis Association, Nottingham, United Kingdom.
    5Hôpital Louis Pradel, Claude Bernard University Lyon 1, Lyon, France.
    6Child Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University Hospital, Rome, Italy.
    7Neuropediatric Department, Astrid Lindgren Children's Hospital, Stockholm, Sweden.
    8Novartis Farma S.p.A., Origgio, Italy.
    9Association Sclérose Tubéreuse de Bourneville, Gradignan, France.
    10Division of Child and Adolescent Psychiatry, University of Cape Town, Cape Town, South Africa.
    11Neurology Department, Centro Hospitalar Lisboa Ocidental, Lisbon, Portugal.
    12Medical University of Vienna, Universitätsklinik für Kinder-und Jugendheilkunde, Affiliated Partner of the ERN EpiCARE, Vienna, Austria.
    13Associazione Sclerosi Tuberosa ONLUS, Milan, Italy.
    14Zentrum für Neuropädiatrie und Sozialpädiatrie, Vivantes-Klinikum Neukölln, Berlin, Germany.
    15Department of Child Neurology, Medical University of Warsaw, Warsaw, Poland.
    16The Tuberous Sclerosis Multidisciplinary Management Clinic, Sydney Children's Hospital, Randwick, NSW, Australia.
    17Pediatric Neurology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
    18Novartis Farma S.p.A., Origgio, Italy.
    19Department of Pediatric Neurology, Necker Enfants Malades Hospital, Paris Descartes University, Paris, France.
    20Institute of Child Health, University College London, London, United Kingdom.
    21Department of Pediatrics, Peking University People's Hospital (PKUPH), Beijing, China.
    22Department of Neurology and Rehabilitation, Tallinn Children Hospital, Tallinn, Estonia.
    23Novartis Healthcare Pvt. Ltd., Hyderabad, India.
    24National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan.
    25Department of Genetics, CHU-Hôpital Nord, Saint-Étienne, France.
    26First Department of Paediatrics, Athens University, St. Sophia Children's Hospital, Athens, Greece.
    27Department of Internal Medicine, University Medical Center, Utrecht, Netherlands.
    28Pediatric Neurology Unit, Department of Pediatrics, UZ Brussel VUB, Brussels, Belgium.
    29Klinikverbund Allgäu gGmbH, Kempten, Germany.
    Abstract

    Renal angiomyolipomas are one of the most common renal manifestations in patients with tuberous sclerosis complex (TSC), with potentially life-threatening complications and a poor prognosis. Despite the considerable progress in understanding TSC-associated renal angiomyolipomas, there are no large scale real-world data. The aim of our present study was to describe in detail the prevalence and outcome of renal angiomyolipomas in patients with TSC, enrolled into the TuberOus SClerosis registry to increase disease Awareness (TOSCA) from 170 sites across 31 countries worldwide. We also sought to evaluate the relationship of TSC-associated renal angiomyolipomas with age, gender and genotype. The potential risk factors for renal angiomyolipoma-related bleeding and chronic kidney disease (CKD) were studied in patients who participated in the TOSCA renal angiomyolipoma substudy. Of the 2,211 eligible patients, 1,062 (48%) reported a history of renal angiomyolipomas. The median age of TSC diagnosis for the all subjects ( = 2,211) was 1 year. The median age of diagnosis of renal angiomyolipoma in the 1,062 patients was 13 years. Renal angiomyolipomas were significantly more prevalent in female patients ( < 0.0001). Rates of angiomyolipomas >3 cm ( = 0.0119), growing lesions ( = 0.0439), and interventions for angiomyolipomas ( = 0.0058) were also higher in females than males. Pre-emptive intervention for renal angiomyolipomas with embolisation, surgery, or mammalian target of rapamycin (mTOR) inhibitor may have abolished the gender difference in impaired renal function, hypertension, and other complications. The rate of interventions for angiomyolipomas was less common in children than in adults, but interventions were reported in all age groups. In the substudy of 76 patients the complication rate was too low to be useful in predicting risk for more severe CKD. In addition, in this substudy no patient had a renal hemorrhage after commencing on an mTOR inhibitor. Our findings confirmed that renal angiomyolipomas in subjects with mutations develop on average at the later age, are relatively smaller in size and less likely to be growing; however, by age 40 years, no difference was observed in the percentage of patients with and mutations needing intervention. The peak of appearance of new renal angiomyolipomas was observed in patients aged between 18 and 40 years, but, given that angiomyolipomas can occur later, lifelong surveillance is necessary. We found that pre-emptive intervention was dramatically successful in altering the outcome compared to historical controls; with high pre-emptive intervention rates but low rates of bleeding and other complications. This validates the policy of surveillance and pre-emptive intervention recommended by clinical guidelines.


    Copyright © 2020 Kingswood, Belousova, Benedik, Carter, Cottin, Curatolo, Dahlin, D'Amato, Beaure d'Augères, de Vries, Ferreira, Feucht, Fladrowski, Hertzberg, Jozwiak, Lawson, Macaya, Marques, Nabbout, O'Callaghan, Qin, Sander, Shah, Takahashi, Touraine, Youroukos, Zonnenberg, Jansen and Sauter.

    KEYWORDS: TOSCA, mTOR, registry, renal angiomyolipoma, tuberous sclerosis complex

    Publikations ID: 33041968
    Quelle: öffnen
     
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