Synopsis
This lecture briefly introduces the
Rhineland Study and summarizes the concepts of its MR protocol. The Rhineland Study investigates aging, in
particular of the human brain and related neurological disorders, across the adult
lifespan. The Rhineland Study will include up
to 30,000 subjects, aged 30 years or over at first visit, and reexamination
every three years. The emphasis is on quantitative measures, including one-hour
MRI examination of brain structure and function.Learning Objectives
1. Necessity and challenges of big
data in MRI
2. Different ways to collect big data
in MRI
3. By example: MRI in the Rhineland
Study
Overview: What is Big Data?
Over the past years there has been
an increasing interest in large-scale imaging studies of the general population
or specific patient groups. A common goal of these efforts is the development
of reliable imaging-based biomarkers that indicate an increased risk of certain diseases, which may result in specific preventive or therapeutic measures or the longitudinal assessment
of therapeutic relevance. Due to the large variability of neurological diseases
and age-related effects, as well as the typically associated small biophysical
changes in brain tissue at early (pre-symptomatic) stages, large sample sizes
are required in order to draw neuroscientifically relevant conclusions. A
pioneering example of large-scale MRI in a prospective cohort study is given by
the Rotterdam Study, which successfully collects neuroimaging data in the
general population for more than 20 years [1]. Large-scale MRI studies are challenging
with respect to logistics and technology of data acquisition, archiving and
processing. Thus, the term Big
Data has become increasingly popular in the MRI community. The five V’s of Big Data – Volume, Velocity, Variety, Veracity, and
Value – perfectly describe the
challenges of MRI in large-scale MRI studies: High-throughput exams produce
large amount of images at high data rates (Volume
and Velocity), which are inherently multimodal and the subsequent analysis results
in a plethora of different data types (Variety).
However, the quality of MR images varies strongly even if acquired with (presumed)
identical setup, e.g. due to subject-motion or scanner drifts (Veracity). Finally, hypothesis-driven
analysis of the data and mining of the data by means of multivariate
classification and feature extraction may provide novel insights and imaging-based
biomarkers, which may have an impact on future healthcare (Value).
Concepts: How to acquire Big Data?
Different approaches exist to gather
large-scale MRI data. Retrospective imaging studies perform meta-analysis on
massive amounts of data across many different studies and sites; a prominent
example is the ENIGMA study [2]. Instead,
a prospective study allows to collect data, acquired with identical set-up and methods
tailored to the study questions. A leading example was given by the Human
Connectome Project (HCP), which applies state-of-the-art MRI technology in 1000
subjects [3]. Another approach is given by multi-centric prospective studies,
where dedicated imaging protocols are harmonized across many different sites
and scanner types, aiming at increased sample size at cost of decreased acquisition
efficiency and quality. A successful example of this approach is the Alzheimer’s
Disease Neuroimaging Initiative (ADNI) [4]. Recently there have been increasing
efforts to utilize advanced MRI technology in very large-scale population
studies by means of dedicated centers. For example the recently started UK-Biobank
study aims at brain MRI of 100,000 subjects [5]. A similar concept, with the
additional goal of longitudinal examination, is implemented by the Rhineland
Study, which is carried out by the DZNE
(Bonn, Germany) [6]. The Rhineland
Study investigates aging, in particular of the human brain and related neurological
disorders, across the adult lifespan. The main study starts in March 2016 and
is carried out in three dedicated study centers of which two are currently operational.
All centers are identically equipped, each with a Siemens Prisma MRI scanner.
The Rhineland Study will include up to 30,000 subjects, aged 30 years or over
at first visit, and reexamination every three years. The emphasis is on
quantitative measures, including one-hour MRI examination of brain structure
and function.
Methods: MRI in the Rhineland Study
This lecture briefly introduces the
Rhineland Study and summarizes the concepts of its MR protocol. Forward-looking and robust sequences were implemented,
tailored for the advanced scanner hardware. The 40min core protocol consists of
sequences to acquire T1-weighted, T2-weigthed, SWI (QSM), resting state fMRI,
and multidimensional diffusion-weighted contrast in the whole brain with high
isotropic resolution, respectively. Also, carotid artery MRI and body fat
quantification with the Dixon technique is performed in every subject.
Additionally, a 10min “free protocol” with varying sequences addresses
additional research questions such as perfusion or metabolism in subgroups of
the cohort. A dedicated workflow for image analysis was implemented, consisting
of a centralized archiving and compute system as well as automated (minimal) processing
pipelines for each modality. A tailored daily quality assurance routine was
developed, including dedicated MR phantoms to quantify scanner performance across
study centers. The MRI protocol was implemented, tested, retested, and refined during
a thorough pilot phase in 2015. Results
will be presented in the lecture.
Outlook
Finally, the presentation will address
current practical and conceptual problems of big data in large-scale MRI studies,
e.g. the difficulty to store raw data, centralized vs. mesh computing, and the
overarching problem of freezing software, hardware, and protocols in long-term
studies. Some suggestions for future research directions are made to overcome
current limitations.
Acknowledgements
No acknowledgement found.References
[1] Ikram, M. A. et al.
(2015). The Rotterdam Scan Study: design update 2016 and main findings.
European Journal of Epidemiology, 30(12), 1299–1315.
[2] Thompson, P. M. et
al. (2014). The ENIGMA Consortium: Large-scale collaborative analyses of
neuroimaging and genetic data. Brain Imaging and Behavior, 8(2), 153–182.
[3] Van Essen, D. C. et al. (2012). The Human Connectome Project:
a data acquisition perspective. NeuroImage, 62(4), 2222–31.
[4] Jack, C. R., et al.
(2008). The Alzheimer’s Disease Neuroimaging Initiative (ADNI): MRI methods.
JMRI, 27(4), 685–91.
[5] Paul M. Matthews,
Cathie Sudlow
(2015): The UK Biobank. In: Brain,
138 issue 12 , 2015.
[6]
www.rhineland-study.de