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MR Brain Screening in ADPKD Patients: To Screen or not to Screen?

BACKGROUND: Adult polycystic kidney disease (ADPKD) still represents a major cause of renal failure and intracranial aneurisms (IA) have a higher prevalence in ADPKD than in the general population. Current guidelines suggest performing brain MRI only in the subjects with a positive familiar history...

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Autores principales: Capelli, I., Zoli, M., Righini, M., Faccioli, L., Aiello, V., Spinardi, L., Gori, D., Friso, F., Rustici, A., Bortolotti, C., Graziano, C., Mantovani, V., Sciascia, N., Mazzatenta, D., Seri, M., Pastore Trossello, M., La Manna, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894296/
https://www.ncbi.nlm.nih.gov/pubmed/34586427
http://dx.doi.org/10.1007/s00062-021-01050-0
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author Capelli, I.
Zoli, M.
Righini, M.
Faccioli, L.
Aiello, V.
Spinardi, L.
Gori, D.
Friso, F.
Rustici, A.
Bortolotti, C.
Graziano, C.
Mantovani, V.
Sciascia, N.
Mazzatenta, D.
Seri, M.
Pastore Trossello, M.
La Manna, G.
author_facet Capelli, I.
Zoli, M.
Righini, M.
Faccioli, L.
Aiello, V.
Spinardi, L.
Gori, D.
Friso, F.
Rustici, A.
Bortolotti, C.
Graziano, C.
Mantovani, V.
Sciascia, N.
Mazzatenta, D.
Seri, M.
Pastore Trossello, M.
La Manna, G.
author_sort Capelli, I.
collection PubMed
description BACKGROUND: Adult polycystic kidney disease (ADPKD) still represents a major cause of renal failure and intracranial aneurisms (IA) have a higher prevalence in ADPKD than in the general population. Current guidelines suggest performing brain MRI only in the subjects with a positive familiar history of IAs or subarachnoid hemorrhage (SAH). This is a retrospective case-control analysis to evaluate the usefulness of a MR screening program in ADPKD patients. METHODS: We retrospectively analyzed all ADPKD patients followed in our outpatient clinic between 2016 and 2019 who underwent a brain MRI screening. We evaluated the presence of IAs and others brain abnormalities and compared our results with a non-ADPKD population (n = 300). We performed univariate and multivariate regression analysis to evaluate if general and demographic features, laboratory findings, clinical parameters and genetic test results correlated with IAs or other brain abnormalities presence. RESULTS: Among the patients evaluated 17 out of 156 (13.6%) ADPKD patients had IAs, compared to 16 out of 300 (5.3%) non-ADPKD controls (p < 0.005). Considering ADPKD patients presenting IAs, 12 (70.6%) had no family history for IAs or SAH. Genetic analysis was available for 97 patients: in the sub-population with IAs, 13 (76.5%) presented a PKD1 mutation and none a PKD2 mutation. We found that arachnoid cysts (AC) (p < 0.001) and arterial anatomical variants (p < 0.04) were significantly more frequent in ADPKD patients. CONCLUSION: In our population ADPKD patients showed a higher prevalence of IAs, AC and arterial variants compared to non-ADPKD. Most of the IAs were found in patients presenting a PKD1 mutation. We found a significant number of alterations even in those patients without a family history of IAs or SAH. The practice of submitting only patients with familial IAs or kidney transplantation candidates to MRI scan should be re-evaluated.
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spelling pubmed-88942962022-03-08 MR Brain Screening in ADPKD Patients: To Screen or not to Screen? Capelli, I. Zoli, M. Righini, M. Faccioli, L. Aiello, V. Spinardi, L. Gori, D. Friso, F. Rustici, A. Bortolotti, C. Graziano, C. Mantovani, V. Sciascia, N. Mazzatenta, D. Seri, M. Pastore Trossello, M. La Manna, G. Clin Neuroradiol Original Article BACKGROUND: Adult polycystic kidney disease (ADPKD) still represents a major cause of renal failure and intracranial aneurisms (IA) have a higher prevalence in ADPKD than in the general population. Current guidelines suggest performing brain MRI only in the subjects with a positive familiar history of IAs or subarachnoid hemorrhage (SAH). This is a retrospective case-control analysis to evaluate the usefulness of a MR screening program in ADPKD patients. METHODS: We retrospectively analyzed all ADPKD patients followed in our outpatient clinic between 2016 and 2019 who underwent a brain MRI screening. We evaluated the presence of IAs and others brain abnormalities and compared our results with a non-ADPKD population (n = 300). We performed univariate and multivariate regression analysis to evaluate if general and demographic features, laboratory findings, clinical parameters and genetic test results correlated with IAs or other brain abnormalities presence. RESULTS: Among the patients evaluated 17 out of 156 (13.6%) ADPKD patients had IAs, compared to 16 out of 300 (5.3%) non-ADPKD controls (p < 0.005). Considering ADPKD patients presenting IAs, 12 (70.6%) had no family history for IAs or SAH. Genetic analysis was available for 97 patients: in the sub-population with IAs, 13 (76.5%) presented a PKD1 mutation and none a PKD2 mutation. We found that arachnoid cysts (AC) (p < 0.001) and arterial anatomical variants (p < 0.04) were significantly more frequent in ADPKD patients. CONCLUSION: In our population ADPKD patients showed a higher prevalence of IAs, AC and arterial variants compared to non-ADPKD. Most of the IAs were found in patients presenting a PKD1 mutation. We found a significant number of alterations even in those patients without a family history of IAs or SAH. The practice of submitting only patients with familial IAs or kidney transplantation candidates to MRI scan should be re-evaluated. Springer Berlin Heidelberg 2021-09-29 2022 /pmc/articles/PMC8894296/ /pubmed/34586427 http://dx.doi.org/10.1007/s00062-021-01050-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Capelli, I.
Zoli, M.
Righini, M.
Faccioli, L.
Aiello, V.
Spinardi, L.
Gori, D.
Friso, F.
Rustici, A.
Bortolotti, C.
Graziano, C.
Mantovani, V.
Sciascia, N.
Mazzatenta, D.
Seri, M.
Pastore Trossello, M.
La Manna, G.
MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title_full MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title_fullStr MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title_full_unstemmed MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title_short MR Brain Screening in ADPKD Patients: To Screen or not to Screen?
title_sort mr brain screening in adpkd patients: to screen or not to screen?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894296/
https://www.ncbi.nlm.nih.gov/pubmed/34586427
http://dx.doi.org/10.1007/s00062-021-01050-0
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