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The habenular volume and allelic polymorphism in major depressive disorder: preliminary findings. | LitMetric

AI Article Synopsis

  • The study investigates the role of the habenula, a brain structure linked to depression, specifically focusing on the impact of phosphodiesterase 7A (PDE7A) and genetic variations associated with it.
  • Researchers analyzed habenula volume using MRI in patients with major depressive disorder and healthy controls, while also examining specific genetic mutations.
  • Results indicated that, although overall habenula volume did not change in MDD patients, those carrying certain genetic mutations had a smaller left habenula, suggesting a potential link between genetic factors and habenula structure in depression.

Article Abstract

Objectives: The habenula is a brain structure implicated in depression, yet with unknown molecular mechanisms. Several phosphodiesterases (PDEs) have been associated with a risk of depression. Although the role of PDE7A in the brain is unknown, it has enriched expression in the medial habenula, suggesting that it may play a role in depression.

Methods: We analysed: (1) habenula volume assessed by 3-T magnetic resonance imaging (MRI) in 84 patients with major depressive disorder (MDD) and 41 healthy controls; (2) frequencies of 10 single nucleotide polymorphisms (SNPs) in gene in 235 patients and 41 controls; and (3) both indices in 80 patients and 27 controls. The analyses considered gender, age, body mass index and season of the MRI examination.

Results: The analysis did not reveal habenula volumetric changes in MDD patients regardless of SNPs. However, in the combined group, the carriers of one or more mutations among 10 SNPs in the gene had a lower volume of the left habenula (driven mainly by rs972362 and rs138599850 mutations) and consequently had the reduced habenular laterality index in comparison with individuals without mutations.

Conclusions: Our findings suggest the implication of the gene into mechanisms determining the habenula structure.

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Source
http://dx.doi.org/10.1080/15622975.2022.2086297DOI Listing

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