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Letters to the EditorFull Access

The Temporal Relationship Between Alzheimer’s Disease and Depressive Symptoms: Variable Matters

To the Editor: In their recent comprehensive analysis, published in the June 2018 issue of the Journal, Donovan et al. (1) present convincing support of the hypothesis that emerging neuropsychiatric symptoms represent an early manifestation of preclinical Alzheimer’s disease. Donovan et al. appropriately viewed their analysis as a first step toward understanding the temporal relationship between Alzheimer’s disease and depressive symptoms in cognitively normal older adults, with the initial aim to examine association rather than causation.

Physiological aging is accompanied by a chronic low-grade proinflammatory state, which has been named “inflammaging” (2). Inflammaging likely acts as a prodromal cofactor in the subclinical course of Alzheimer’s disease (3). Neuroinflammation can also be associated with amyloid beta burden independently of inflammaging (4). In addition, several lines of evidence also associate inflammation with depressive symptoms (5). This makes the relationship between Alzheimer’s disease and depressive symptoms more complex. If Alzheimer’s disease causes inflammation that leads to depression, inflammation can be considered a mediating variable in the relationship between Alzheimer’s disease and depressive symptoms. Alternatively, if the strength of the relationship between Alzheimer’s disease and depressive symptoms is changing across levels of inflammation, then inflammation is a moderating variable. Eventually, inflammation could also be a confounding variable if it causes both Alzheimer’s disease and depressive symptoms independently.

From INSERM UMR1205, Brain Tech Lab, Université Grenoble Alpes, La Tronche, France.
Address correspondence to Dr. Wion ().

The author reports no financial relationships with commercial interests.

References

1 Donovan NJ, Locascio JJ, Marshall GA, et al.: Longitudinal association of amyloid beta and anxious-depressive symptoms in cognitively normal older adults. Am J Psychiatry 2018; 175:530–537LinkGoogle Scholar

2 Franceschi C, Bonafè M, Valensin S, et al.: Inflamm-aging: an evolutionary perspective on immunosenescence. Ann N Y Acad Sci 2000; 908:244–254Crossref, MedlineGoogle Scholar

3 Giunta B, Fernandez F, Nikolic WV, et al.: Inflammaging as a prodrome to Alzheimer’s disease. J Neuroinflammation 2008; 5:51Crossref, MedlineGoogle Scholar

4 Barger SW, Harmon AD: Microglial activation by Alzheimer amyloid precursor protein and modulation by apolipoprotein E. Nature 1997; 388:878–881Crossref, MedlineGoogle Scholar

5 Smith KJ, Au B, Ollis L, et al.: The association between C-reactive protein, Interleukin-6 and depression among older adults in the community: a systematic review and meta-analysis. Exp Gerontol 2018; 102:109–132Crossref, MedlineGoogle Scholar