A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany
- Author:
Pickardt THOMAS
1
;
Niggemeyer EVA
;
Bauer MM ULRIKE
;
Abdul-Khaliq HASHIM
Author Information
1. National Register for Congenital Heart Defects
- Keywords:
Congenital heart defects;
Multi-center research;
Biorepository;
Genetic research;
DNA
- From:
Genomics, Proteomics & Bioinformatics
2016;14(4):181-190
- CountryChina
- Language:Chinese
-
Abstract:
Congenital heart disease (CHD) is the most frequent birth defect (0.8%–1% of all live births). Due to the advance in prenatal and postnatal early diagnosis and treatment, more than 90%of these patients survive into adulthood today. However, several mid-and long-term morbidi-ties are dominating the follow-up of these patients. Due to the rarity and heterogeneity of the phe-notypes of CHD, multicenter registry-based studies are required. The CHD-Biobank was established in 2009 with the aim to collect DNA from patients and their parents (trios) or from affected families, as well as cardiovascular tissues from patients undergoing corrective heart surgery for cardiovascular malformations. Clinical/phenotype data are matched to the International Paediatric and Congenital Cardiac Code (IPCCC) and the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10). The DNA collection currently comprises samples from approximately 4200 participants with a wide range of CHD phenotypes. The collection covers about 430 trios and 120 families with more than one affected member. The cardiac tissue collection comprises 1143 tissue samples from 556 patients after open heart surgery.
