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| Image Credit: Dmitriy Kievskiy |
Errors in a gene known to cause a serious neurodevelopmental condition in infants are also linked to the development of Parkinson’s disease in adolescence and adulthood, according to new research
The study, published in the Annals of Neurology, looked at a gene called EPG5. Errors in this gene are already known to cause Vici syndrome – a rare and severe inherited neurodevelopmental condition that presents early in life and affects multiple organ systems. Now researchers at King’s College London, University College London (UCL), the University of Cologne and the Max Planck Institute for Biology of Ageing have found that errors in the same gene are linked to changes in nerve cells that lead to more common age-related conditions like Parkinson’s disease and dementia.
Professor Heinz Jungbluth, Professor of Pediatric Neurology at King’s College London and lead and co-senior author of the study, said:
"This research, supported by patient organizations, was prompted by our earlier observation of an apparent increased Parkinson’s disease risk in relatives of children with Vici syndrome, after our team at King’s had found EPG5 to be a driver of this condition."
Our work shows that, whilst rarely considered a priority, research into (ultra)rare conditions such as Vici syndrome (where fewer than 10 children are currently known to have the condition in the UK) may provide vital insights into much more common disorders and have substantial public health benefits."
“Understanding the causes of these devastating and often life-limiting diseases is essential for therapy development and thus offers hope for patients and their families."
In the largest study of its kind to date, the team of scientists analysed clinical and genetic data from 211 individuals from across the world with rare errors in EPG5. They found that the effects of these genetic errors are broader and more variable than previously known – while some individuals had life-limiting forms of Vici syndrome identified before or shortly after birth, others showed much milder symptoms, including delay in movement, speech, and learning.
The researchers also discovered that some of the patients included in the study went on to develop a breakdown of nerve cells in adolescence or early adulthood that led to Parkinson's disease and dementia. Brain scans analyzed in some cases showed additional iron build-up in the brain, a feature of other, closely linked neurodevelopmental disorders.
Dr Reza Maroofian, co-first author of the study from the UCL Queen Square Institute of Neurology, said:
"Our findings link EPG5 dysfunction to Parkinson’s disease, highlighting how neurodevelopmental and neurodegenerative disorders can be mechanistically interconnected and add to a growing list of such conditions. This study underscores how insights from rare pediatric brain disorders can inform our understanding of more common adult-onset neurodegenerative diseases, such as Parkinson’s and dementia."
The EPG5 gene is involved in an important cellular process called autophagy, where the cell breaks down unwanted or damaged components and either recycles them into new parts or disposes of them. The protein made by EPG5 is involved in the last stage of this process – attaching the parts for disposal to the cell’s waste disposal unit for removal from the cell.
To explore the biology underpinning their findings, the researchers used patient-derived cells and model organisms, including mice and the tiny roundworm C. elegans, and introduced errors into EPG5. These experiments showed that genetic errors in the gene disrupt the cell’s ability to clear damaged components from the cell, leading to the build-up of proteins closely associated with Parkinson’s disease.
Professor Jungbluth, who is also a Consultant Paediatric Neurologist at Evelina London Children’s Hospital, Guy’s and St Thomas’ NHS Foundation Trust, said: "Using the example of EPG5, our findings suggest a life-time continuum of early-onset neurodevelopmental and late-onset neurodegenerative disorders, and more specifically an intriguing link between aberrant nerve development and degeneration linked in the same fundamental cellular mechanism preserved throughout different species."
Dr Manolis Fanto, Reader in Functional Genomics at King’s College London and co-senior author of the study, added:
"This project highlights the importance of collaboration between basic and clinical neuroscientists to unravel the complex mechanistic consequences of inherited genetic conditions throughout all life stages."
The study provides new understanding of how errors in autophagy can underpin a range of lifelong neurological conditions and may help pave the way for future treatments that target these shared drivers of disease.
Authors: Hormos Salimi Dafsari MD, Celine Deneubourg PhD, Kritarth Singh PhD, Reza Maroofian PhD, Zita Suprenant MD, MPH, Ay Lin Kho PhD, Neil J Ingham PhD, Karen P Steel PhD, Preethi Sheshadri PhD, Franciska Baur MD, Lea Hentrich, Birgit Gerisch PhD, Mina Zamani PhD, Cesar Alves MD, PhD, Ata Siddiqui MD, Haidar S Dafsari MD, Mehri Salari MD, Anthony E. Lang MD, Michael Harris MA, Alice Abdelaleem MD, Saeid Sadeghian MD, Reza Azizimalamiri MD, Hamid Galehdari PhD, Gholamreza Shariati PhD, Alireza Sedaghat MD, Jawaher Zeighami MD, Daniel Calame MD, PhD, Dana Marafi MD, MSc, Ruizhi Duan PhD, Adrian Boehnke BS, Gary D. Clark MD, Jill A. Rosenfeld MS, Carrie A. Mohila MD, PhD, Dora Steel MD, Saurabh Chopra MD, Suvasini Sharma MD, Nicolai Kohlschmidt MD, Steffi Patzer MD, Afshin Saffari MD, Darius Ebrahimi-Fakhari MD, PhD, Büşra Eser Çavdartepe MD, Irene J Chang MD, Erika Beckman MS, CGC, Renate Peters MD, Andrew Paul Fennell MD, Bernice Lo PhD, Luisa Averdunk MD, Felix Distelmaier MD, Martina Baethmann MD, Frances Elmslie MD(res), Kairit Joost MD, PhD, Sheela Nampoothiri MNAMS, MSc, Dhanya Yesodharan MD, Hanna Mandel MD, Amy Kimball MS, Antonie D. Kline MD, Cyril Mignot MD, PhD, Boris Keren MD, Vincent Laugel MD, PhD, Katrin Õunap MD, PhD, Kalpana Devadathan MD, Frederique M.C. van Berkestijn MD, Arpana Silwal MD, MSc, Saskia Koene MD, PhD, Sumit Verma MD, Mohammed Yousuf Karim MBBChir, Chahynez Boubidi MD, PhD, Majid Aziz MD, Gehad ElGhazali MD, PhD, Lauren Mattas MS, CGC, Mohammad Miryounesi MD, PhD, Farzad Hashemi-Gorji MSc, Shahryar Alavi MSc, Nayereh Nouri MSc, Mehrdad Noruzinia MD, Saeideh Kavousi PhD, Arveen Kamath MD, Sandeep Jayawant MD, Russell Saneto PhD, Nourelhoda A. Haridy MD, Pinar Ozkan Kart MD, Ali Cansu MD, Madeleine Joubert MD, Claire Beneteau MD, Kyra E. Stuurman MD, Martina Wilke PhD, Tahsin Stefan Barakat MD, PhD, Homa Tajsharghi PhD, Annarita Scardamaglia BSc, Sadeq Vallian MSc, PhD, Semra Hız MD, Ali Shoeibi MD, Reza Boostani MD, Narges Hashemi MD, Meisam Babaei MD, Norah Saleh Alsaleh MD, Julie Porter MD, PhD, Tania Attié-Bitach MD, PhD, Pauline Marzin MD, Dorota Wicher MD, PhD, Jessica I. Gold MD, PhD, Elisabeth Schuler MD, Amna Kashgari MD, Rakan F. Alanazi MD, Wafaa Eyaid MD, Marc Engelen MD, PhD, Mirjam Langeveld MD, Burkhard Stüve MD, Yun Li, Gökhan Yigit PhD, Bernd Wollnik MD, Mariana H.G Monje MD, PhD, Dimitri Krainc MD, PhD, Niccolò E. Mencacci MD, PhD, Somayeh Bakhtiari PhD, Michael Kruer MD, Emanuela Argilli PhD, Elliott Sherr MD, PhD, Yalda Jamshidi PhD, Ehsan Ghayoor Karimiani MD, MRes, PhD, Yiu Wing Sunny Cheung PhD, Ivan Karin MD, Giovanni Zifarelli PhD, Peter Bauer MD, Wendy K Chung MD, PhD, James R. Lupski MD, PhD, Manju A. Kurian PhD, Jörg Dötsch MD, Jürgen-Christoph von Kleist-Retzow MD, Thomas Klopstock MD, Matias Wagner MD, Calvin Yip PhD, Andreas Roos PhD, Rita Carsetti MD, Carlo Dionisi-Vici MD, Mathias Gautel MD, PhD, Michael R Duchen PhD, Adam Antebi PhD, Henry Houlden MD, PhD, Manolis Fanto PhD, Heinz Jungbluth MD, PhD
Source/Credit: King’s College London
Reference Number: ns101125_01
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