卵圆孔未闭合并偏头痛患者NTRK3基因表达水平及其与临床指标相关性分析

Expression level of NTRK3 gene in patients with patent foramen ovale combined with migraine and its correlations with clinical indicators

  • 摘要:
    目的 评估卵圆孔未闭(PFO) 合并偏头痛(MA)患者的神经营养受体酪氨酸激酶3(NTRK3)基因表达水平及其与临床指标的相关性。
    方法 选取收治的86例PFO患者为研究对象, 根据临床症状不同分为合并MA组(n=46)、未合并MA组(n=40)。同期选取40例健康体检者作为对照组。采用逆转录-聚合酶链反应(RT-PCR)检测3组NTRK3基因表达水平。比较合并MA组、未合并MA组患者的PFO直径、静息下右向左分流(RLS)、Valsalva状态下RLS、头痛影响测验-6(HIT-6)评分、偏头痛残疾程度评价量表(MIDAS)评分。分析NTRK3基因表达水平与PFO合并MA患者临床指标的相关性; 分析PFO合并MA患者封堵术后MA缓解的影响因素。
    结果 合并MA组和未合并MA组的NTRK3基因表达水平低于对照组, 且合并MA组低于未合并MA组, 差异有统计学意义(P < 0.05)。合并MA组患者的静息下RLS、HIT-6评分、MIDAS评分高于未合并MA组, 差异有统计学意义(P < 0.05)。NTRK3基因表达水平与PFO合并MA患者静息下RLS、HIT-6评分、MIDAS评分存在负相关(P < 0.05)。NTRK3基因表达水平是PFO合并MA患者封堵术后MA缓解的保护性因素(OR=0.621, P=0.018)。
    结论 PFO合并MA患者的NTRK3基因表达水平显著较低, 其与临床指标以及预后存在显著相关性。

     

    Abstract:
    Objective To evaluate the expression level of neurotrophic receptor tyrosine kinase 3(NTRK3) gene in patients with patent foramen ovale (PFO) combined with migraine (MA) and its correlations with clinical indicators.
    Methods Eighty-six patients with PFO were selected as the study objects, and were divided into MA combined group (n=46) and non-MA combined group (n=40) according to different clinical symptoms. In the same period, 40 healting subjects were selected as the control group. Reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the expression of NTRK3 gene in the three groups. PFO diameter, right-to-left shingle (RLS) at rest, RLS in Valsalva state, Headache Impact Test-6 (HIT-6) score and Migraine Disability Assessment Scale (MIDAS) score were compared between patients in MA combined group and those in the non-MA combined group. The correlation of expression level of NTRK3 gene with the clinical indexes of PFO patients complicating with MA was analyzed; influencing factors of MA remission in patients with PFO combined with MA after plugging were analyzed.
    Results The expression level of NTRK3 gene in the combined MA group and the non-MA combined group was significantly lower than that in the control group, and the MA combined group was significantly lower than that in the non-MA combined group (P < 0.05). The resting RLS, HIT-6 scores and MIDAS scores of patients in the MA combined group were significantly higher than those in the non-MA combined group (P < 0.05). The expression level of NTRK3 gene was negatively correlated with RLS, HIT-6 and MIDAS scores at rest in PFO patients with MA (P < 0.05). The expression level of NTRK3 gene was a protective factor for MA remission in PFO patients with MA after plugging (OR=0.621, P=0.018).
    Conclusion The expression level of NTRK3 gene is significantly lower in PFO patients with MA, which is significantly correlated with clinical indicators and prognosis.

     

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