Serum multi-trace elements and post-stroke cognitive impairment: a prospective observational cohort study.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Ruolin Zhou, Weijie Zhai, Lingjie Meng, Chunxiao Wei, Li Sun
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引用次数: 0

Abstract

Post-stroke cognitive impairment (PSCI) significantly affects stroke survivors. Identifying modifiable risk factors for PSCI is essential. Serum multi-trace elements are crucial for neurological function but vary in concentration among older adults. It remains unclear whether increasing multi-trace elements can reduce the incidence of PSCI. We investigated the associations between baseline serum multi-trace elements and PSCI. The Montreal Cognitive Assessment defined PSCI. We used logistic regression analyses to evaluate the association between serum multi-trace elements and PSCI. Subsequently, we assessed the associations between serum multi-trace elements and three different cognitive domains using the Kruskal-Wallis test. We further evaluated improvements in the predictive ability of serum multi-trace elements. Finally, 626 patients (mean age: 62.85 ± 7.54 years) were followed up for a median of 1.2 years. Lower concentrations of serum iron (odds ratio [OR] = 2.498, 95% confidence interval [CI]: 1.505-4.145) and zinc (OR = 2.015, 95% CI: 1.233-3.293) were associated with a higher PSCI risk. Higher concentrations of serum iron (OR = 0.368, 95% CI: 0.227-0.595) and magnesium (OR = 0.273, 95% CI: 0.164-0.454), along with lower concentrations of serum copper (OR = 0.544, 95% CI: 0.34-0.872), were significantly correlated with a lower PSCI risk. Cognitive impairments varied across multi-trace elements. Serum iron affected wider cognition, while magnesium and copper levels were strongly associated with language and executive function. Adding serum multi-trace elements to the conventional model improved PSCI risk reclassification (area under curve: 0.676-0.718). Multi-trace elements may influence PSCI progression. This study was registered with the Chinese Clinical Trial Registry (URL: https://www.chictr.org.cn/ ; unique identifier: ChiCTR1900022675).

血清多微量元素与脑卒中后认知障碍:一项前瞻性观察队列研究。
脑卒中后认知障碍(PSCI)对脑卒中幸存者有显著影响。确定可改变的PSCI风险因素是必要的。血清多微量元素对神经功能至关重要,但在老年人中浓度不同。目前尚不清楚增加多微量元素是否可以减少PSCI的发病率。我们研究了基线血清多微量元素与PSCI之间的关系。蒙特利尔认知评估定义了PSCI。我们使用逻辑回归分析来评估血清多微量元素与PSCI之间的关系。随后,我们使用Kruskal-Wallis测试评估了血清多微量元素与三种不同认知领域之间的关系。我们进一步评估了血清多微量元素预测能力的改善。最终,626例患者(平均年龄:62.85±7.54岁)被随访,中位时间为1.2年。较低浓度的血清铁(比值比[OR] = 2.498, 95%可信区间[CI]: 1.505-4.145)和锌(OR = 2.015, 95% CI: 1.233-3.293)与较高的PSCI风险相关。较高浓度的血清铁(OR = 0.368, 95% CI: 0.227-0.595)和镁(OR = 0.273, 95% CI: 0.164-0.454)以及较低浓度的血清铜(OR = 0.544, 95% CI: 0.34-0.872)与较低的PSCI风险显著相关。认知障碍因多种微量元素而异。血清铁影响更广泛的认知,而镁和铜水平与语言和执行功能密切相关。在常规模型基础上加入血清多微量元素可改善PSCI风险再分类(曲线下面积:0.676-0.718)。多种微量元素可能影响PSCI的进展。本研究已在中国临床试验注册中心注册(URL: https://www.chictr.org.cn/;唯一标识符:ChiCTR1900022675)。
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
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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