Automatic and manual segmentation of the piriform cortex: Method development and validation in patients with temporal lobe epilepsy and Alzheimer's disease

Author:

Steinbart David12ORCID,Yaakub Siti N.23ORCID,Steinbrenner Mirja1ORCID,Guldin Lynn S.2,Holtkamp Martin1,Keller Simon S.45,Weber Bernd67,Rüber Theodor7ORCID,Heckemann Rolf A.8,Ilyas‐Feldmann Maria1,Hammers Alexander2,

Affiliation:

1. Charité ‐ Universitätsmedizin Berlin Freie Universität and Humboldt‐Universität zu Berlin, Department of Neurology, Epilepsy‐Center Berlin‐Brandenburg Berlin Germany

2. King's College London & Guy's and St Thomas’ PET Centre School of Biomedical Engineering and Imaging Sciences, St Thomas’ Hospital London UK

3. School of Psychology, Faculty of Health University of Plymouth Plymouth UK

4. Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology University of Liverpool Liverpool UK

5. Department of Neuroradiology The Walton Centre NHS Foundation Trust Liverpool UK

6. Center for Economics and Neuroscience University of Bonn Bonn Germany

7. Institute of Experimental Epileptology and Cognition Research University Hospital Bonn Bonn Germany

8. Department of Medical Radiation Sciences University of Gothenburg Gothenburg Sweden

Abstract

AbstractThe piriform cortex (PC) is located at the junction of the temporal and frontal lobes. It is involved physiologically in olfaction as well as memory and plays an important role in epilepsy. Its study at scale is held back by the absence of automatic segmentation methods on MRI. We devised a manual segmentation protocol for PC volumes, integrated those manually derived images into the Hammers Atlas Database (n = 30) and used an extensively validated method (multi‐atlas propagation with enhanced registration, MAPER) for automatic PC segmentation. We applied automated PC volumetry to patients with unilateral temporal lobe epilepsy with hippocampal sclerosis (TLE; n = 174 including n = 58 controls) and to the Alzheimer's Disease Neuroimaging Initiative cohort (ADNI; n = 151, of whom with mild cognitive impairment (MCI), n = 71; Alzheimer's disease (AD), n = 33; controls, n = 47). In controls, mean PC volume was 485 mm3 on the right and 461 mm3 on the left. Automatic and manual segmentations overlapped with a Jaccard coefficient (intersection/union) of ~0.5 and a mean absolute volume difference of ~22 mm3 in healthy controls, ~0.40/ ~28 mm3 in patients with TLE, and ~ 0.34/~29 mm3 in patients with AD. In patients with TLE, PC atrophy lateralised to the side of hippocampal sclerosis (p < .001). In patients with MCI and AD, PC volumes were lower than those of controls bilaterally (p < .001). Overall, we have validated automatic PC volumetry in healthy controls and two types of pathology. The novel finding of early atrophy of PC at the stage of MCI possibly adds a novel biomarker. PC volumetry can now be applied at scale.

Funder

Wellcome Trust

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

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