Individual brain metabolic connectome indicator based on Kullback-Leibler Divergence Similarity Estimation predicts progression from mild cognitive impairment to Alzheimer's dementia.

Purpose: Positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG) reveals altered cerebral metabolism in individuals with mild cognitive impairment (MCI) and Alzheimer's dementia (AD). Previous metabolic connectome analyses derive from groups of patients but do not support the prediction...

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Publicado en:European Journal of Nuclear Medicine & Molecular Imaging Vol. 47; no. 12; pp. 2753 - 2765
Autores principales: Wang, Min, Jiang, Jiehui, Yan, Zhuangzhi, Alberts, Ian, Ge, Jingjie, Zhang, Huiwei, Zuo, Chuantao, Yu, Jintai, Rominger, Axel, Shi, Kuangyu
Formato: Journal Article
Publicado: Springer Nature Nov2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Nov2020
      vid: 47
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      pub: Springer Nature
      place: New York, New York
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        144190215
        10.1007/s00259-020-04814-x
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        atl: Individual brain metabolic connectome indicator based on Kullback-Leibler Divergence Similarity Estimation predicts progression from mild cognitive impairment to Alzheimer's dementia.
      aug:
        au:
          Wang, Min
          Jiang, Jiehui
          Yan, Zhuangzhi
          Alberts, Ian
          Ge, Jingjie
          Zhang, Huiwei
          Zuo, Chuantao
          Yu, Jintai
          Rominger, Axel
          Shi, Kuangyu
        affil: Shanghai Institute for Advanced Communication and Data Science, Shanghai University, 99 Shangda Road, 200444, Shanghai, China
      sug:
      ab: Purpose: Positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG) reveals altered cerebral metabolism in individuals with mild cognitive impairment (MCI) and Alzheimer's dementia (AD). Previous metabolic connectome analyses derive from groups of patients but do not support the prediction of an individual's risk of conversion from present MCI to AD. We now present an individual metabolic connectome method, namely the Kullback-Leibler Divergence Similarity Estimation (KLSE), to characterize brain-wide metabolic networks that predict an individual's risk of conversion from MCI to AD. Methods: FDG-PET data consisting of 50 healthy controls, 332 patients with stable MCI, 178 MCI patients progressing to AD, and 50 AD patients were recruited from ADNI database. Each individual's metabolic brain network was ascertained using the KLSE method. We compared intra- and intergroup similarity and difference between the KLSE matrix and group-level matrix, and then evaluated the network stability and inter-individual variation of KLSE. The multivariate Cox proportional hazards model and Harrell's concordance index (C-index) were employed to assess the prediction performance of KLSE and other clinical characteristics. Results: The KLSE method captures more pathological connectivity in the parietal and temporal lobes relative to the typical group-level method, and yields detailed individual information, while possessing greater stability of network organization (within-group similarity coefficient, 0.789 for sMCI and 0.731 for pMCI). Metabolic connectome expression was a superior predictor of conversion than were other clinical assessments (hazard ratio (HR) = 3.55; 95% CI, 2.77–4.55; P < 0.001). The predictive performance improved further upon combining clinical variables in the Cox model, i.e., C-indices 0.728 (clinical), 0.730 (group-level pattern model), 0.750 (imaging connectome), and 0.794 (the combined model). Conclusion: The KLSE indicator identifies abnormal brain networks predicting an individual's risk of conversion from MCI to AD, thus potentially constituting a clinically applicable imaging biomarker.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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