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Deep Phenotyping at Scale: Study Protocol for the Korean Mood Disorder Genetic Study-Depression (KOMOGEN-D).

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Recruiting women with recurrent major depressive disorder (MDD) through clinical interviews enhances genetic analysis. This deep phenotyping approach yields high-quality data for understanding MDD

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KOMOGEN‐Ddeep phenotypinggenome‐wide association studymajor depressive disorderpsychiatric geneticstargeted recruitment

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Area of Science:

  • Psychiatry and Genetics
  • Epidemiology
  • Clinical Research Methodology

Background:

  • Genetic analysis of major depressive disorder (MDD) is challenged by sample heterogeneity and diagnostic inaccuracies.
  • Current genome-wide association studies (GWAS) often use self-reports or electronic health records, introducing biases.
  • A need exists for large, well-characterized cohorts to explore genetic and environmental factors in MDD.

Purpose of the Study:

  • To describe a novel methodology for recruiting and phenotyping large cohorts for genetic studies of MDD.
  • To enhance sample homogeneity by focusing on specific patient subgroups.
  • To overcome logistical challenges in large-scale clinical research.

Main Methods:

  • Targeted ascertainment of cases through hospital-based recruitment.
  • In-depth phenotyping using structured clinical interviews conducted by trained personnel.
  • Recruitment of women with recurrent depressive episodes to increase sample homogeneity.
  • Collaboration with 47 hospitals across South Korea, training 347 interviewers.

Main Results:

  • Recruited 5704 cases and 4995 controls over 4 years, meeting significant recruitment targets.
  • Confirmed cases exhibit recurrent, severe MDD with detailed clinical features.
  • Successfully navigated challenges including COVID-19 restrictions and medical crises.
  • Developed a scalable deep phenotyping strategy for MDD genetic research.

Conclusions:

  • The described methodology yields deeply phenotyped, homogeneous cohorts suitable for genetic analysis of MDD.
  • This approach can identify genetic influences on specific MDD subtypes and clinical features.
  • The study design is adaptable for international collaboration to build larger MDD genetic research cohorts.