Journal Article DZNE-2025-01454

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Uncovering hypothalamic network disruption in ALS.

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2026
Steinkopff [Darmstadt]

Journal of neurology 273(1), 37 () [10.1007/s00415-025-13574-3]

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Abstract: Structural MRI studies have shown hypothalamic atrophy and altered white matter (WM) connectivity in amyotrophic lateral sclerosis (ALS), as a possible substrate of hypermetabolism in this condition. However, hypothalamic functional connectivity and its association with clinical features in ALS remain unclear. This study explored hypothalamic resting-state functional connectivity (RS-FC) in ALS patients compared to controls and its relationship with disease severity defined by the ALS Functional Rating Scale (ALSFRS-r), body mass index (BMI), disease duration, progression rate, survival, hypothalamic volume, and WM integrity.Seventy-one ALS patients and 39 healthy controls underwent structural and RS functional MRI. The bilateral hypothalamus was segmented, and a seed-based RS-FC analysis was performed. Group differences in hypothalamic RS-FC and their correlations with ALSFRS-r scores, BMI, disease duration, progression rate, survival, hypothalamic volume, and WM integrity were assessed. Tract-based spatial statistics was performed to estimate the correlation between WM damage in ALS and hypothalamic RS-FC.ALS patients showed increased hypothalamic RS-FC with caudate nuclei compared to controls. Additionally, greater disease severity correlated with increased hypothalamic RS-FC with the caudate nuclei and orbitofrontal cortex. Hypothalamic RS-FC mean values also associated with FA in the genu of corpus callosum and forceps minor and disease progression rate. No significant correlations were observed with other clinical features.These findings support hypothalamic alterations in ALS. Early detection of hypothalamic changes could be useful in prognostic stratification and evaluating intervention effects.

Keyword(s): Humans (MeSH) ; Amyotrophic Lateral Sclerosis: diagnostic imaging (MeSH) ; Amyotrophic Lateral Sclerosis: physiopathology (MeSH) ; Amyotrophic Lateral Sclerosis: pathology (MeSH) ; Female (MeSH) ; Male (MeSH) ; Middle Aged (MeSH) ; Hypothalamus: diagnostic imaging (MeSH) ; Hypothalamus: physiopathology (MeSH) ; Hypothalamus: pathology (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Aged (MeSH) ; Adult (MeSH) ; White Matter: diagnostic imaging (MeSH) ; White Matter: pathology (MeSH) ; Nerve Net: diagnostic imaging (MeSH) ; Nerve Net: physiopathology (MeSH) ; Disease Progression (MeSH) ; Connectome (MeSH) ; Amyotrophic lateral sclerosis ; Functional connectivity ; Hypermetabolism ; Hypothalamus ; MRI

Classification:

Contributing Institute(s):
  1. Clinical Study Center (Ulm) (Clinical Study Center (Ulm))
  2. Metabolic Changes in Neurodegeneration (AG Roselli)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)
  2. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Database coverage:
Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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Institute Collections > UL DZNE > UL DZNE-Clinical Study Center (Ulm)
Document types > Articles > Journal Article
Institute Collections > UL DZNE > UL DZNE-AG Roselli
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 Record created 2025-12-29, last modified 2026-01-12


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