Association between circadian rhythms and neurodegenerative diseases

Dysfunction in 24-h circadian rhythms is a common occurrence in ageing adults; however, circadian rhythm disruptions are more severe in people with age-related neurodegenerative diseases, including Alzheimer's disease and related dementias, and Parkinson's disease. Manifestations of circad...

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Published inLancet neurology Vol. 18; no. 3; pp. 307 - 318
Main Authors Leng, Yue, Musiek, Erik S, Hu, Kun, Cappuccio, Francesco P, Yaffe, Kristine
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.03.2019
Elsevier Limited
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ISSN1474-4422
1474-4465
1474-4465
DOI10.1016/S1474-4422(18)30461-7

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Summary:Dysfunction in 24-h circadian rhythms is a common occurrence in ageing adults; however, circadian rhythm disruptions are more severe in people with age-related neurodegenerative diseases, including Alzheimer's disease and related dementias, and Parkinson's disease. Manifestations of circadian rhythm disruptions differ according to the type and severity of neurodegenerative disease and, for some patients, occur before the onset of typical clinical symptoms of neurodegeneration. Evidence from preliminary studies suggest that circadian rhythm disruptions, in addition to being a symptom of neurodegeneration, might also be a potential risk factor for developing Alzheimer's disease and related dementias, and Parkinson's disease, although large, longitudinal studies are needed to confirm this relationship. The mechanistic link between circadian rhythms and neurodegeneration is still not fully understood, although proposed underlying pathways include alterations of protein homoeostasis and immune and inflammatory function. While preliminary clinical studies are promising, more studies of circadian rhythm disruptions and its mechanisms are required. Furthermore, clinical trials are needed to determine whether circadian interventions could prevent or delay the onset of neurodegenerative diseases.
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Y.L. and K.Y. conceived the review and developed the outline of this review. All authors contributed to the writing and revision of the manuscript.
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ISSN:1474-4422
1474-4465
1474-4465
DOI:10.1016/S1474-4422(18)30461-7