AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation

Abstract The hypothalamus is a small structure of the brain with an essential role in metabolic homeostasis, sleep regulation, and body temperature control. Some neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and dementia syndromes are reported to be related to hypothalamic v...

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Main Authors: Ina Vernikouskaya, Hans-Peter Müller, Francesco Roselli, Albert C. Ludolph, Jan Kassubek, Volker Rasche
Format: Article
Language:English
Published: Nature Portfolio 2023-12-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-48649-6
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author Ina Vernikouskaya
Hans-Peter Müller
Francesco Roselli
Albert C. Ludolph
Jan Kassubek
Volker Rasche
author_facet Ina Vernikouskaya
Hans-Peter Müller
Francesco Roselli
Albert C. Ludolph
Jan Kassubek
Volker Rasche
author_sort Ina Vernikouskaya
collection DOAJ
description Abstract The hypothalamus is a small structure of the brain with an essential role in metabolic homeostasis, sleep regulation, and body temperature control. Some neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and dementia syndromes are reported to be related to hypothalamic volume alterations. Despite its crucial role in human body regulation, neuroimaging studies of this structure are rather scarce due to work-intensive operator-dependent manual delineations from MRI and lack of automated segmentation tools. In this study we present a fully automatic approach based on deep convolutional neural networks (CNN) for hypothalamic segmentation and volume quantification. We applied CNN of U-Net architecture with EfficientNetB0 backbone to allow for accurate automatic hypothalamic segmentation in seconds on a GPU. We further applied our approach for the quantification of the normalized hypothalamic volumes to a large neuroimaging dataset of 432 ALS patients and 112 healthy controls (without the ground truth labels). Using the automated volumetric analysis, we could reproduce hypothalamic atrophy findings associated with ALS by detecting significant volume differences between ALS patients and controls at the group level. In conclusion, a fast and unbiased AI-assisted hypothalamic quantification method is introduced in this study (whose acceptance rate based on the outlier removal strategy was estimated to be above 95%) and made publicly available for researchers interested in the conduction of hypothalamus studies at a large scale.
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spelling doaj.art-79b43200dd8a4952b61665a0bb55e6bb2023-12-10T12:15:17ZengNature PortfolioScientific Reports2045-23222023-12-0113111110.1038/s41598-023-48649-6AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentationIna Vernikouskaya0Hans-Peter Müller1Francesco Roselli2Albert C. Ludolph3Jan Kassubek4Volker Rasche5Department of Internal Medicine II, Ulm University Medical CenterDepartment of Neurology, University of UlmDepartment of Neurology, University of UlmDepartment of Neurology, University of UlmDepartment of Neurology, University of UlmDepartment of Internal Medicine II, Ulm University Medical CenterAbstract The hypothalamus is a small structure of the brain with an essential role in metabolic homeostasis, sleep regulation, and body temperature control. Some neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and dementia syndromes are reported to be related to hypothalamic volume alterations. Despite its crucial role in human body regulation, neuroimaging studies of this structure are rather scarce due to work-intensive operator-dependent manual delineations from MRI and lack of automated segmentation tools. In this study we present a fully automatic approach based on deep convolutional neural networks (CNN) for hypothalamic segmentation and volume quantification. We applied CNN of U-Net architecture with EfficientNetB0 backbone to allow for accurate automatic hypothalamic segmentation in seconds on a GPU. We further applied our approach for the quantification of the normalized hypothalamic volumes to a large neuroimaging dataset of 432 ALS patients and 112 healthy controls (without the ground truth labels). Using the automated volumetric analysis, we could reproduce hypothalamic atrophy findings associated with ALS by detecting significant volume differences between ALS patients and controls at the group level. In conclusion, a fast and unbiased AI-assisted hypothalamic quantification method is introduced in this study (whose acceptance rate based on the outlier removal strategy was estimated to be above 95%) and made publicly available for researchers interested in the conduction of hypothalamus studies at a large scale.https://doi.org/10.1038/s41598-023-48649-6
spellingShingle Ina Vernikouskaya
Hans-Peter Müller
Francesco Roselli
Albert C. Ludolph
Jan Kassubek
Volker Rasche
AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
Scientific Reports
title AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
title_full AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
title_fullStr AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
title_full_unstemmed AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
title_short AI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
title_sort ai assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network based automatic segmentation
url https://doi.org/10.1038/s41598-023-48649-6
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