This study delineates a systemic molecular landscape of adolescent MDD defined by the coexistence of hypoxic compensation and neurotrophic/remodeling failure. The identified three-gene biosignature (SLC4A1, IGF1, MMP9) offers a promising, objective tool for the early diagnosis of adolescent depression, highlighting the immune-metabolic interface as a critical avenue for future precision medicine.
Yang et al. (Fri,) studied this question.