| Literature DB >> 27567817 |
Han Zhang1, Xiaobo Chen1, Feng Shi1, Gang Li1, Minjeong Kim1, Panteleimon Giannakopoulos2, Sven Haller3,4,5,6, Dinggang Shen1,7.
Abstract
Temporal synchronization-based functional connectivity (FC) has long been used by the neuroscience community. However, topographical FC information may provide additional information to characterize the advanced relationship between two brain regions. Accordingly, we proposed a novel method, namely high-order functional connectivity (HOFC), to capture this second-level relationship using inter-regional resemblance of the FC topographical profiles. Specifically, HOFC first calculates an FC profile for each brain region, notably between the given brain region and other brain regions. Based on these FC profiles, a second layer of correlations is computed between all pairs of brain regions (i.e., correlation's correlation). On this basis, we generated an HOFC network, where "high-order" network properties were computed. We found that HOFC was discordant with the traditional FC in several links, indicating additional information being revealed by the new metrics. We applied HOFC to identify biomarkers for early detection of Alzheimer's disease by comparing 77 mild cognitive impairment patients with 89 healthy individuals (control group). Sensitivity in detection of group difference was consistently improved by ∼25% using HOFC compared to using FC. An HOFC network analysis also provided complementary information to an FC network analysis. For example, HOFC between olfactory and orbitofrontal cortices was found significantly reduced in patients, besides extensive alterations in HOFC network properties. In conclusion, our results showed promise in using HOFC to comprehensively map the human brain connectome.Entities:
Keywords: Alzheimer’s disease; biomarker; early detection; functional connectivity; functional magnetic resonance imaging (fMRI); high-order connectivity; mild cognitive impairment; resting state fMRI
Mesh:
Year: 2016 PMID: 27567817 PMCID: PMC5437847 DOI: 10.3233/JAD-160092
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472