Blood biomarkers for suicidality
a blood biomarker and suicidal risk technology, applied in the field of gene expression biomarkers, can solve the problems of no objective tools to assess and track changes in suicidal risk, suicide is a leading cause of death in psychiatric patients, etc., and achieve the effect of sufficient monitoring and treatmen
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example 1
Materials and Methods
[0050]In this Example, whole-genome gene expression profiling of blood samples was conducted to identify blood gene expression biomarkers for suicidality.
[0051]Human Subjects.
[0052]Male Caucasian subjects diagnosed with bipolar disorder (“Discovery Cohort”) were evaluated that had a diametrical change in suicidal ideation scores from no suicidal ideation to high suicidal ideation from visit to visit. The subjects were limited to minimize any potential gender-related and ethnicity-related state effects on gene expression. A demographic breakdown of the Discovery Cohort subjects is shown in Table 1A.
[0053]A “Validation Cohort”, in which the top biomarker findings from the Discovery Cohort testing were evaluated, consisted of an age-matched cohort of 9 male suicide completers obtained through the Marion County Coroner's Office (8 Caucasians, 1 African-American) (Table 1B). The subjects in the Validation Cohort were required to have a last observed alive post-mortem...
example 2
[0101]In this Example, SAT1 was validated by analyzing subsequent hospitalizations with and without suicidalilty and to previous hospitalizations with and without suicidality in two live follow-up cohorts, one bipolar (n=42) and one psychosis (schizophrenia / schizoaffective; n=46).
[0102]Particularly, the bipolar follow-up cohort (Table 9A) consisted of male Caucasian subjects in which whole-genome blood gene expression data, including levels of SAT 1, were obtained at the testing visits as described in Example 1. If the subjects had multiple testing visits, the visit with the highest SAT1 level was selected for this analysis. The subjects' subsequent number of hospitalizations with or without suicidality was tabulated from electronic medical records.
[0103]The psychosis (schizophrenia / schizoaffective) follow-up cohort (n=46) (Table 9B) similarly consisted of Caucasian subjects in which whole-genome blood gene expression data, including levels of SAT1, were obtained at testing visits a...
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