CMR-Analysis (including machine learning)
Teodora Chitiboi, PhD
Research Scientist
Siemens Healthcare GmbH, Hamburg, Germany
Hamburg, Germany
Andreea Bianca Popescu
Research Scientist
Siemens SRL, Brasov, Romania, Romania
Athira J. Jacob, MSc
Research Scientist
Siemens Medical Solutions USA, Inc., Princeton, NJ, United States
Plainsboro, New Jersey, United States
Jens Wetzl, PhD
Research Scientist
Magnetic Resonance, Siemens Healthcare GmbH, Erlangen, Germany
Erlangen, Germany
Bogdan Gheorghita
Research Scientist
Transilvania University of Brasov, Romania
Lucian Itu
Research Engineer
Siemens SRL, Brasov, Romania, Romania
Heiko Mahrholdt, MD
Leitender Arzt für Bildgebung in der Kardiologie
Robert-Bosch-Krankenhaus Stuttgart, Germany
Andreas Seitz
Senior Physician in Internal Medicine and Cardiology
Robert-Bosch Hospital Stuttgart, Germany
Puneet Sharma, PhD
Research & Technology Manager
Siemens Medical Solutions USA, Inc., Princeton, NJ, United States
Princeton, New Jersey, United States
Teodora Chitiboi, PhD
Research Scientist
Siemens Healthcare GmbH, Hamburg, Germany
Hamburg, Germany
Machine learning solutions for automatic segmentation are still limited by the amount of annotated data available for training. We propose to synthetically generate T1 maps from CINE MRI with deep learning style transfer for pre-training. We show that by pre-training on synthetic data we can improve segmentation results on unseen maps, with or without finetuning on annotated data from a new center.
9101 subjects were selected from the UK Biobank resource1 (access application 30769), where acquisition included a short axis CINE stack and one short axis ShMOLLI T1 map2. CINE data was automatically segmented using a previously trained model3 and images with wrong segmentations were manually removed leaving 8977 subjects (CINE data). For 90 subjects reserved for testing, the T1 maps were manually segmented (Mapping1 data), while for the rest no manual annotations were performed. Instead, a CycleGan network4 was trained on 1755 paired images (256 for validation) to learn a style transfer between CINE and mapping images (Figure 1). The model was used to generate 8807 synthetic maps (synthetic) with matching segmentations from CINE.
Dataset Mapping2 contains 144 separately acquired clinical subjects (52 normal, 49 myocarditis, 20 sarcoidosis, 23 systemic disease), where T1 MOLLI maps were acquired pre and post contrast and T2 mapping was performed. The maps were manually segmented. Data was randomly divided for training, validation, and testing (100/15/29). All data was acquired at 1.5T (MAGNETOM Aera, Siemens Healthcare, Erlangen, Germany).
A dense Unet5 (Figure 1) was trained for myocardium segmentation from T1 maps using 100%, 50%, 25%, and 10% of the data in Mapping2. The models were trained either from scratch or after pre-training with CINE or synthetic data, and were tested on Mapping1 and Mapping2.
When the goal is to segment T1 maps from a new center, i.e. Mapping1, without requiring manual annotations, the model pre-trained on synthetic and finetuned on the separately acquired Mapping2 significantly outperforms the model trained on Mapping2 only (Figure 2). Pre-training on CINE directly, without the synthetic image generation step, does not lead to an improvement, while training on CINE and synthetic only leads to poorer results.
When finetuning on data from the same distribution as the testing data, pre-training on synthetic before finetuning on Mapping2 also brings a significant improvement, when evaluation on the test subset of Mapping2. When reducing the amount of training/finetuning data from Mapping2, the impact of pre-training is significantly larger (Figure 3).
Using synthetically generated T1 maps with deep learning style transfer helps improve segmentation results, without the need for additional manual annotations for the data from a new center, but also when finetuning on scarce data.
The concepts presented are based on research results that are not commercially available.