miR-124-3p target genes identify globus pallidus role in suicide ideation recovery in borderline personality disorder

Macarena S. Aloi, Guillermo F. Poblete, John Oldham, Michelle A. Patriquin, David A. Nielsen, Thomas R. Kosten, Ramiro Salas
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Abstract

Borderline personality disorder (BPD) is characterized by patterns of unstable affect, unstable interpersonal relationships, and chronic suicidal tendencies. Research on the genetics, epigenetics, and brain function of BPD is lacking. MicroRNA-124-3p (miR-124-3p) was recently identified in a Genome-Wide Association Study as likely associated with BPD. Here, we identified the anatomical brain expression of genes likely modulated by miR-124-3p and compared morphometry in those brain regions in BPD inpatients vs. controls matched for psychiatric comorbidities. We isolated lists of targets likely modulated by miR-124-3p from TargetScan (v 8.0) by their preferentially conserved targeting (Aggregate PCT > 0.99, see Supplementary Table 1). We applied Process Genes List (PGL) to identify regions of interest associated with the co-expression of miR-124-3p target genes. We compared the gray matter volume of the top region of interest co-expressing those genes between BPD inpatients (n = 111, 46% female) and psychiatric controls (n = 111, 54% female) at The Menninger Clinic in Houston, Texas. We then correlated personality measures, suicidal ideation intensity, and recovery from suicidal ideation with volumetrics. Gene targets of miR-124-3p were significantly co-expressed in the left Globus Pallidus (GP), which was smaller in BPD than in psychiatric controls. Smaller GP volume was negatively correlated with agreeableness and with recovery from suicidal ideation post-treatment. In BPD, GP volume may be reduced through miR-124-3p regulation and suppression of its target genes. Importantly, we identified that a reduction of the GP in BPD could serve as a potential biomarker for recovery from suicidal ideation.

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miR-124-3p靶基因确定了丘脑在边缘型人格障碍患者自杀意念恢复中的作用
边缘型人格障碍(BPD)的特点是情绪不稳定、人际关系不稳定和长期自杀倾向。目前尚缺乏对 BPD 的遗传学、表观遗传学和大脑功能的研究。最近,一项全基因组关联研究发现,MicroRNA-124-3p(miR-124-3p)可能与 BPD 有关。在此,我们确定了可能受 miR-124-3p 调节的基因在大脑解剖学上的表达,并比较了 BPD 住院患者与精神疾病合并症匹配对照组在这些脑区的形态测量。我们从 TargetScan(v 8.0)中分离出了可能受 miR-124-3p 调节的靶标列表,这些靶标具有优先保守性(Aggregate PCT > 0.99,见补充表 1)。我们应用过程基因列表(PGL)来确定与 miR-124-3p 靶基因共表达相关的感兴趣区域。我们比较了德克萨斯州休斯敦梅宁格诊所的 BPD 住院患者(111 人,46% 为女性)和精神疾病对照组(111 人,54% 为女性)共同表达这些基因的顶级感兴趣区的灰质体积。然后,我们将人格测量、自杀意念强度和自杀意念恢复情况与容积相关联。miR-124-3p的基因靶标在左侧苍白球(Globus Pallidus,GP)中显著共表达,而BPD患者的GP体积小于精神病对照组。较小的GP体积与合群性和治疗后自杀意念的恢复呈负相关。在 BPD 中,GP 的体积可能通过 miR-124-3p 的调控及其靶基因的抑制而缩小。重要的是,我们发现在 BPD 中 GP 的缩小可作为自杀意念恢复的潜在生物标志物。
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