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Latent profile analysis of cognitive decline and depressive symptoms after intracerebral hemorrhage. | LitMetric

AI Article Synopsis

  • - The study focused on understanding cognitive decline and depression in patients who experienced Intracerebral Hemorrhage (ICH) by using Latent Profile Analysis (LPA) to identify different symptom profiles.
  • - Data from 784 ICH survivors were analyzed over about 46 months, revealing four distinct profiles linked to different combinations of depression and dementia risk, as well as associations with clinical and genetic factors.
  • - The findings indicate that specific brain imaging and genetic characteristics correlate with certain profiles, proposing that distinct biological mechanisms separate the risks for depression and dementia in ICH patients, and suggesting that LPA could be useful in studying other stroke survivors.

Article Abstract

Background: Cognitive impairment and depressive symptoms are highly prevalent after Intracerebral Hemorrhage (ICH). We leveraged Latent Profile Analysis (LPA) to identify profiles for cognitive decline and depression onset after ICH. We also investigated differences in clinical, genetic and neuroimaging characteristics across patients' profiles.

Methods: We analyzed data from the ICH study conducted at Massachusetts General Hospital between January 1998 and December 2019. We collected information from electronical health records, follow-up interviews, CT and MRI imaging, and APOE genotype. We conducted LPA and multinomial logistic regression analyses to: 1) identify distinct profiles for cognitive decline and depression onset after ICH; 2) identify clinical, neuroimaging and genetic factors predicting individuals' likelihood to express a specific profile.

Results: We followed 784 ICH survivors for a median of 45.8 months. We identified four distinct profiles in cognitive and depressive symptoms after ICH: low depression and dementia risk, early-onset depression and dementia, late-onset depression and dementia, high depression with low dementia risk. Cerebral small vessel disease severity and APOE genotype were specifically associated with the late-onset profile (both p < 0.05). Acute hematoma characteristics (size, intraventricular extension) and functional disability were specifically associated with the early-onset profile (all p < 0.05).

Conclusion: We identified four distinct profiles for cognitive and depressive symptoms after ICH, each displaying specific associations with individual patients' clinical, genetic and neuroimaging data. These associations reflect separate biological mechanisms influencing dementia and depression risk after ICH. Our findings support employing LPA in future ICH studies, and is likely applicable to stroke survivors at large.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662844PMC
http://dx.doi.org/10.1186/s12883-021-02508-xDOI Listing

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