2023
DOI: 10.1016/j.heliyon.2023.e14653
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Shared peripheral blood biomarkers for Alzheimer’s disease, major depressive disorder, and type 2 diabetes and cognitive risk factor analysis

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Cited by 4 publications
(3 citation statements)
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References 92 publications
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“…Although there are broad genetic data available for AD, for genes such as Apolipoprotein E, MPKA and amyloid precursor protein/presenilin-I, the majority of patients typically undergo genetic testing already at the late stages of the disease, where no intervention can prevent the occurrence of the disease and the cognitive dysfunction has already become irreversible. Studies have identified co-expressed genes for AD, type 2 diabetes mellitus (T2DM) and MDD using bioinformatics analysis ( 27-29 ). A total of seven co-deregulated genes, namely structural maintenance of chromosomes 4, cell division cycle 27, hepatocyte nuclear factor 1 homeobox A, RhoD, Cut-like homeobox 1, PDZ and LIM Domain 5 and transthyretin, were considered to have a diagnostic value for AD, T2DM and MDD ( 27 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although there are broad genetic data available for AD, for genes such as Apolipoprotein E, MPKA and amyloid precursor protein/presenilin-I, the majority of patients typically undergo genetic testing already at the late stages of the disease, where no intervention can prevent the occurrence of the disease and the cognitive dysfunction has already become irreversible. Studies have identified co-expressed genes for AD, type 2 diabetes mellitus (T2DM) and MDD using bioinformatics analysis ( 27-29 ). A total of seven co-deregulated genes, namely structural maintenance of chromosomes 4, cell division cycle 27, hepatocyte nuclear factor 1 homeobox A, RhoD, Cut-like homeobox 1, PDZ and LIM Domain 5 and transthyretin, were considered to have a diagnostic value for AD, T2DM and MDD ( 27 ).…”
Section: Discussionmentioning
confidence: 99%
“…Studies have identified co-expressed genes for AD, type 2 diabetes mellitus (T2DM) and MDD using bioinformatics analysis ( 27-29 ). A total of seven co-deregulated genes, namely structural maintenance of chromosomes 4, cell division cycle 27, hepatocyte nuclear factor 1 homeobox A, RhoD, Cut-like homeobox 1, PDZ and LIM Domain 5 and transthyretin, were considered to have a diagnostic value for AD, T2DM and MDD ( 27 ). Another genomic study previously provided evidence for a significant causal genetic effect of depression on AD using the analysis of single nucleotide polymorphism profiles ( 30 , 31 ).…”
Section: Discussionmentioning
confidence: 99%
“… Shu et al (2022) identified Five hub proteins between AD and T2D. Zhang et al (2023b) identified seven hub genes of co-DEGs between T2DM, MDD, and dementia. Huang C. et al (2022) confirmed through multiple comparisons that CACNA2D3, NUMB, and IER3 simultaneously participate in AD and T2D, and analyzed interacting chemicals, transcription factors, and miRNAs.…”
Section: Identification Of Shared Candidate Biomarkers Between Ad And...mentioning
confidence: 99%