This study proposes to investigate comorbidities associated with suicidal behavior in old adults. This
systematic review follows the PRISMA methodology [6]. After review, a meta-analysis will proceed.
We used the PRISMA statement and defined the PECOS strategy, such as Population (P) = old adults; exposure (E) = mental disorders; comparison (C) = without mental disorders; outcome (O) = suicidal behavior; and study design(S) = all kinds of studies with an association any comorbidities in old adults and suicidal behavior published in the last ten years. To be eligible to be included in the review, studies had to meet the following criteria: They had to include a paper that reported suicidal ideation, suicide attempt, or suicide in old adults and comorbidities. We excluded every study that did not describe a possible association between comorbidities and suicidal behavior (suicidal ideation, suicide attempt, or suicide) in old adults. Previous reviews were included to verify the understanding and findings of other researchers. Being an old adult was over 60 years old. Two authors systematically searched, read, and shared the findings of the eligible papers.
Following the PRISMA, the defined papers’ titles and abstracts are eligible and non-restricted languages without time limits. Furthermore, it was systematically identified by searching electronic databases Embase [Emtree - Major Focus Exp.], Pubmed [Mesh Terms], and Lilacs - Complete collection of the Virtual Health Library [Title/abstracts], in November 2024.
It will use the Newcastle–Ottawa Quality Assessment Scale (NOQAS) to measure the methodological quality of studies, controlling for publication bias in case-control and cohort studies [7]. Two reviewers (LPR and JFRR) will independently assess the studies' quality. Disagreements will be resolved through discussion and consensus or with arbitration by a third reviewer (LLC). Based on the total NOQAS score, studies will be categorized into risk of bias levels: Minimal risk of bias: Score of 7 or more; Low risk of bias: Score of 5 to 6; Medium risk of bias: Score of 3 to 4; High risk of bias: Score of 0 to 2. Quality assessment will be used to contextualize the findings. It may inform sensitivity analyses, such as excluding studies with a high risk of bias to assess the robustness of the overall results.
The data will be extracted into two tables describing insomnia-related factors. Factors associated with insomnia in the two parallel reviews will be compared through exploratory factor analysis to identify and extract commonalities. Data extraction will be performed independently by two reviewers (JFRR and LPR) using a pre-piloted, standardized data extraction form. Discrepancies will be resolved through discussion and consensus or with arbitration by a third reviewer (GMAF). The data extraction form will capture the following information from each included study:
Study characteristics: Author(s), year of publication, country of study, study design, sample size, population characteristics (age, gender, clinical characteristics).
3.6.1. Data Synthesis and Meta-analysis:
Meta-analyses will be conducted using SPSS software version 29 [or equivalent]. We will use random-effects models to account for potential heterogeneity between studies. Heterogeneity will be assessed using the I2 statistic, with values of 25%, 50%, and 75% indicating low, moderate, and high heterogeneity, respectively. If substantial heterogeneity is detected (I2 > 50%), we will explore potential sources of heterogeneity through subgroup analyses (e.g., by study design, population characteristics, insomnia measurement method) and sensitivity analyses (e.g., excluding studies with high risk of bias). Publication bias will be assessed using funnel plots and Egger's test if a sufficient number of studies are included in meta-analyses (at least 10).
3.6.2. Optional analysis:
3.6.2.1. Umbrella Review:
If the systematic review demonstrates a large number of previous reviews, a joint analysis of the data can be performed.