Genetic study clarifies the causes of the most severe heart muscle diseases of children

The researchers at the University of Helsinki and Helsinki University Hospital have collected a globally unique KidCMP cohort of children with severe cardiomyopathies from the past 21 years, and characterized them genetically. The researchers discovered that the genetic knowledge had direct implications for predicting the disease course and treatment decisions.

Cardiac muscle degeneration (cardiomyopathy) is the most common cause of severe cardiac dysfunction and life-threatening cardiac arrhythmias in children. These severe disorders often lead to consideration of heart transplant. However, their actual cause - the genetic basis - has been poorly characterized.

A collaborative effort of pediatric cardiologists of Helsinki University Hospital and University of Helsinki, led by Docent Tiina Ojala and Academy Professor Anu Suomalainen Wartiovaara, with Catalina Vasilescu, MSc, as the lead author, succeeded to collect a globally unique KidCMP cohort of children with severe cardiomyopathies from the past 21 years, and analyzed them genetically.

Genetic study clarifies the causes of the most severe heart muscle diseases of children.

 

The unique patient collection was enabled by the local cardiology clinic being the only center of cardiac transplantations in Finland. The median age of diagnosis of our patients with severe disease was just four months.

Using Next-Generation DNA sequencing methodology with rigorous subsequent validation of findings, the investigators uncovered the genetic causes in 40% of the patients.

"The results highlighted an extremely variable genetic background, each family presenting a different pathogenic variant that often arose during the patient’s own embryonal development", Professor Wartiovaara tells.

The authors discovered that the genetic knowledge had direct implications for predicting the disease course and treatment decisions.

"All children had life-threatening diseases early on, and some genetic defects predicted a primarily progressive disorder requiring cardiac transplant. However, if intensively treated, some gene defects predicted a recuperative course, without a transplant", Dr. Ojala says.

Personalized medicine is one of the goals of the current medical research, where the understanding of the genetic cause and disease mechanism in each individual will promote tailored forms of treatment. The study published by the University of Helsinki investigators makes an important step in this direction by deciphering genetic causes in children and their implications for treatment decisions.

The findings were reported in Journal of the American College of Cardiology.

For more information, please contact:

Tiina Ojala, MD PhD, pediatric cardiologist
Hospital of Children and Adolescents, Helsinki University Hospital             
Email: tiina.h.ojala@helsinki.fi                                                                                                                                      

Anu Suomalainen Wartiovaara, MD, PhD, Academy Professor
Research Program of Molecular Neurology, Faculty of Medicine, University of Helsinki
FinMIT Centre of Excellence of the Academy of Finland
Email: anu.wartiovaara@helsinki.fi

Reference: Catalina Vasilescu, Tiina H. Ojala, Virginia Brilhante, Simo Ojanen,  Helena M. Hinterding, Eino Palin, Tero-Pekka Alastalo, Juha Koskenvuo, Anita Hiippala, Eero Jokinen, Timo Jahnukainen, Jouko Lohi, Jaana Pihkala, Tiina A. Tyni, Christopher J. Carroll, Anu Suomalainen Wartiovaara. Genetic Basis of Severe Childhood-Onset Cardiomyopathies Journal of the American College of Cardiology Volume 72, Issue 19, November 2018; DOI: 10.1016/j.jacc.2018.08.2171

Audio-summary by journal editor Fuster:
https://s3.amazonaws.com/ADFJACC/JACC7219/JACC7219_fustersummary_04

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