AI Article Synopsis

  • - This study explores the genetic factors related to major depressive disorder (MDD) and how they influence treatment responses, aiming to compile a comprehensive list of genetic variants linked to the disorder and its treatment effectiveness.
  • - Researchers reviewed numerous studies to identify genetic variants associated with MDD susceptibility and antidepressant response, finding 31 replicated variants for MDD and 18 for treatment response.
  • - The analysis showed that a significant portion of these variants could potentially harm gene function or regulate it, suggesting they could be useful in diagnosing MDD and predicting treatment outcomes, but more focused studies are needed to validate these findings.

Article Abstract

Background: The clinical heterogeneity in major depressive disorder (MDD), variable treatment response, and conflicting findings limit the ability of genomics toward the discovery of evidence-based diagnosis and treatment regimen. This study attempts to curate all genetic association findings to evaluate potential variants for clinical translation.

Methods: We systematically reviewed all candidates and genome-wide association studies for both MDD susceptibility and antidepressant response, independently, using MEDLINE, particularly to identify replicated findings. These variants were evaluated for functional consequences using different in silico tools and further estimated their diagnostic predictability by calculating positive predictive values.

Results: A total of 217 significantly associated studies comprising 1200 variants across 545 genes and 128 studies including 921 variants across 412 genes were included with MDD susceptibility and antidepressant response, respectively. Although the majority of associations were confirmed by a single study, we identified 31 and 18 replicated variants (in at least 2 studies) for MDD and antidepressant response. Functional annotation of these 31 variants predicted 20% coding variants as deleterious/damaging and 80.6% variants with regulatory effect. Similarly, the response-related 18 variants revealed 25% coding variant as damaging and 88.2% with substantial regulatory potential. Finally, we could calculate the diagnostic predictability of 19 and 5 variants whose positive predictive values ranges from 0.49 to 0.66 for MDD and 0.36 to 0.66 for response.

Conclusions: The replicated variants presented in our data are promising for disease diagnosis and improved response outcomes. Although these quantitative assessment measures are solely directive of available observational evidence, robust homogenous validation studies are required to strengthen these variants for molecular diagnostic application.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586057PMC
http://dx.doi.org/10.1093/ijnp/pyad001DOI Listing

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