Serum insulin-like growth factor-1 and its association with epilepsy risk and cognitive function.

IF 2.6 Q4 CLINICAL NEUROLOGY
Jiahui Guo, Zhiruo Qiu, Bofei Chen, Haotian Li, Ping Su, Zhefeng Yuan, Dan Wu, Jiajia Fang
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Abstract

Background: Insulin-like growth factor 1 (IGF-1) has neurotrophic and neuroprotective properties, but its relationship with epilepsy risk and cognitive outcomes remains unclear. We investigated whether serum IGF-1 was associated with incident epilepsy and cognitive performance in a large population-based cohort.

Methods: We performed a prospective analysis of the UK Biobank including 466,857 participants with baseline serum IGF-1 measurements. Incident epilepsy was identified from hospital records and self-report. Associations with epilepsy risk were assessed using prespecified Cox proportional hazards models, restricted cubic splines, and sensitivity analyses. Cross-sectional and longitudinal analyses were used to examine cognitive outcomes.

Results: Over more than 15 years of follow-up, 4,532 participants developed incident epilepsy. Higher serum IGF-1 was consistently associated with a lower risk of incident epilepsy; in the primary model, each 1 nmol/L increase was associated with a lower hazard of incident epilepsy (HR = 0.978, 95% CI 0.973-0.984). The association was nonlinear and L-shaped, with a steeper increase in risk at lower IGF-1 concentrations and an apparent plateau above approximately 20 nmol/L. Per-standard-deviation, quartile-based, lagged, and alcohol-frequency sensitivity analyses showed similar results. In cross-sectional analyses of participants with epilepsy at baseline, higher IGF-1 was nominally associated with faster reaction time and better prospective memory, but neither association remained significant after false discovery rate correction. Exploratory longitudinal analyses in the epilepsy subgroup were limited by sample size and did not show significant cross-lagged associations. In the full cohort, higher baseline IGF-1 was associated with better subsequent performance in several cognitive domains, although these findings were not epilepsy-specific.

Conclusions: Lower serum IGF-1 was independently associated with a higher risk of incident epilepsy in this large population-based cohort. Evidence for cognitive associations was more limited, with only nominal cross-sectional findings in baseline epilepsy and exploratory, non-epilepsy-specific longitudinal signals. These results support further investigation of circulating IGF-1 as a candidate biomarker and biologically relevant pathway rather than as evidence of a causal or therapeutic target.

血清胰岛素样生长因子-1及其与癫痫风险和认知功能的关系。
背景:胰岛素样生长因子1 (IGF-1)具有神经营养和神经保护特性,但其与癫痫风险和认知结局的关系尚不清楚。我们研究了血清IGF-1是否与癫痫发作和认知能力有关。方法:我们对英国生物银行进行了前瞻性分析,包括466,857名基线血清IGF-1测量的参与者。从医院记录和自我报告中确定偶发性癫痫。使用预先设定的Cox比例风险模型、受限三次样条和敏感性分析评估与癫痫风险的关联。采用横断面和纵向分析来检查认知结果。结果:在超过15年的随访中,4532名参与者发生了癫痫发作。较高的血清IGF-1始终与较低的癫痫发作风险相关;在初级模型中,每增加1 nmol/L,癫痫发生率降低(HR = 0.978, 95% CI 0.973 ~ 0.984)。这种关联是非线性的,呈L形,IGF-1浓度较低时风险增加更陡,在大约20 nmol/L以上有一个明显的平台。按标准偏差、基于四分位数、滞后和酒精频率敏感性分析显示了类似的结果。在基线癫痫患者的横断面分析中,较高的IGF-1名义上与更快的反应时间和更好的前瞻性记忆相关,但在错误发现率校正后,这两种关联都不显着。癫痫亚组的探索性纵向分析受到样本量的限制,没有显示出显著的交叉滞后关联。在整个队列中,较高的基线IGF-1与随后在几个认知领域的更好表现相关,尽管这些发现并非癫痫特异性的。结论:在这个以人群为基础的大队列中,较低的血清IGF-1与较高的癫痫发作风险独立相关。认知关联的证据更为有限,在基线癫痫和探索性非癫痫特异性纵向信号中只有名义上的横断面发现。这些结果支持进一步研究循环IGF-1作为候选生物标志物和生物学相关途径,而不是作为因果或治疗靶点的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Epileptologica
Acta Epileptologica Medicine-Neurology (clinical)
CiteScore
2.00
自引率
0.00%
发文量
38
审稿时长
20 weeks
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