Are Cramér‐Rao lower bounds an accurate estimate for standard deviations in in vivo magnetic resonance spectroscopy?. (19th April 2021)
- Record Type:
- Journal Article
- Title:
- Are Cramér‐Rao lower bounds an accurate estimate for standard deviations in in vivo magnetic resonance spectroscopy?. (19th April 2021)
- Main Title:
- Are Cramér‐Rao lower bounds an accurate estimate for standard deviations in in vivo magnetic resonance spectroscopy?
- Authors:
- Landheer, Karl
Juchem, Christoph - Abstract:
- Abstract : Due to inherent time constraints for in vivo experiments, it is infeasible to repeat multiple MRS scans to estimate standard deviations on the desired measured parameters. As such, the Cramér‐Rao lower bounds (CRLBs) have become the routine method to approximate standard deviations for in vivo experiments. Cramér‐Rao lower bounds, however, as the name suggests, are theoretically a lower bound on the standard deviation and it is not clear if and under what circumstances this approximation is valid. Realistic synthetic 3 T spectra were used to investigate the relationship between estimated CRLBs, true CRLBs and standard deviations. Here we demonstrate that, although the CRLBs are theoretically truly a lower bound on the standard deviation (not an equality) for the problem typically encountered in quantification, they are still an adequate approximation to standard deviation as long as the model perfectly characterizes the data. In the case when the macromolecule basis deviates from the measured macromolecules it was shown that the CRLBs can deviate from standard deviations by approximately 50% for N ‐acetylaspartic acid, creatine and glutamate and of the order of 100% or more for myo‐inositol and γ‐aminobutyric acid. In the case when the model perfectly reflects the data the CRLBs are within approximately 10% of standard deviations for all metabolites. The result of the CRLB being within 10% of standard deviations means that, for an accurate model, novelAbstract : Due to inherent time constraints for in vivo experiments, it is infeasible to repeat multiple MRS scans to estimate standard deviations on the desired measured parameters. As such, the Cramér‐Rao lower bounds (CRLBs) have become the routine method to approximate standard deviations for in vivo experiments. Cramér‐Rao lower bounds, however, as the name suggests, are theoretically a lower bound on the standard deviation and it is not clear if and under what circumstances this approximation is valid. Realistic synthetic 3 T spectra were used to investigate the relationship between estimated CRLBs, true CRLBs and standard deviations. Here we demonstrate that, although the CRLBs are theoretically truly a lower bound on the standard deviation (not an equality) for the problem typically encountered in quantification, they are still an adequate approximation to standard deviation as long as the model perfectly characterizes the data. In the case when the macromolecule basis deviates from the measured macromolecules it was shown that the CRLBs can deviate from standard deviations by approximately 50% for N ‐acetylaspartic acid, creatine and glutamate and of the order of 100% or more for myo‐inositol and γ‐aminobutyric acid. In the case when the model perfectly reflects the data the CRLBs are within approximately 10% of standard deviations for all metabolites. The result of the CRLB being within 10% of standard deviations means that, for an accurate model, novel quantification methods such as machine learning or deep learning will not be able to obtain substantially more precise estimates for the desired parameters than traditional maximum‐likelihood estimation. Abstract : CRLBs are theoretically a lower bound on the standard deviation (not an equality) for the problem of scan time constraints typically encountered in in vivo MRS. We show that CRLB are an adequate approximation to standard deviation, indicating that the estimators are nearly efficient, if the model perfectly characterizes the data. Near efficiency means that novel quantification methods such as machine learning will not be able to obtain substantially more precise estimates than traditional maximum‐likelihood estimation. … (more)
- Is Part Of:
- NMR in biomedicine. Volume 34:Number 7(2021)
- Journal:
- NMR in biomedicine
- Issue:
- Volume 34:Number 7(2021)
- Issue Display:
- Volume 34, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 34
- Issue:
- 7
- Issue Sort Value:
- 2021-0034-0007-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-04-19
- Subjects:
- Cramér‐Rao lower bounds -- in vivo MRS -- Monte Carlo -- MRS -- standard deviations
Nuclear magnetic resonance -- Periodicals
Magnetic Resonance Spectroscopy -- Periodicals
574 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/nbm.4521 ↗
- Languages:
- English
- ISSNs:
- 0952-3480
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6113.931000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17211.xml