4.7 Article

Resting-state functional connectivity of the human hippocampus in periadolescent children: Associations with age and memory performance

期刊

HUMAN BRAIN MAPPING
卷 42, 期 11, 页码 3620-3642

出版社

WILEY
DOI: 10.1002/hbm.25458

关键词

adolescence; development; hippocampus; memory; resting‐ state functional connectivity

资金

  1. National Institute of Mental Health [R01-MH103220, R01-MH116782, R01-MH118013]
  2. National Institute on Aging [R01AG064247]
  3. Office of Integrative Activities [1539067]
  4. Office Of The Director
  5. Office of Integrative Activities [1539067] Funding Source: National Science Foundation

向作者/读者索取更多资源

The study examined the hippocampal rs-FC in healthy children before adolescence, finding associations between hippocampal rs-FC, brain networks, age, and hippocampal-dependent memory, but not with working memory. These findings contribute to our understanding of neural development and cognitive development theories.
The hippocampus is necessary for declarative (relational) memory, and the ability to form hippocampal-dependent memories develops through late adolescence. This developmental trajectory of hippocampal-dependent memory could reflect maturation of intrinsic functional brain networks, but resting-state functional connectivity (rs-FC) of the human hippocampus is not well-characterized for periadolescent children. Measuring hippocampal rs-FC in periadolescence would thus fill a gap, and testing covariance of hippocampal rs-FC with age and memory could inform theories of cognitive development. Here, we studied hippocampal rs-FC in a cross-sectional sample of healthy children (N = 96; 59 F; age 9-15 years) using a seed-based approach, and linked these data with NIH Toolbox measures, the Picture-Sequence Memory Test (PSMT) and the List Sorting Working Memory Test (LSWMT). The PSMT was expected to rely more on hippocampal-dependent memory than the LSWMT. We observed hippocampal rs-FC with an extensive brain network including temporal, parietal, and frontal regions. This pattern was consistent with prior work measuring hippocampal rs-FC in younger and older samples. We also observed novel, regionally specific variation in hippocampal rs-FC with age and hippocampal-dependent memory but not working memory. Evidence consistent with these findings was observed in a second, validation dataset of similar-age healthy children drawn from the Philadelphia Neurodevelopment Cohort. Further, a cross-dataset analysis suggested generalizable properties of hippocampal rs-FC and covariance with age and memory. Our findings connect prior work by describing hippocampal rs-FC and covariance with age and memory in typically developing periadolescent children, and our observations suggest a developmental trajectory for brain networks that support hippocampal-dependent memory.

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