精神分裂症患者的唾液皮质醇:过去十年对照研究的选择性回顾和荟萃分析

Walter Paganin , Sabrina Signorini
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引用次数: 0

摘要

背景压力和创伤是包括精神分裂症在内的各种精神疾病的重要诱因。下丘脑-垂体-肾上腺(HPA)轴的失调,尤其是皮质醇分泌异常,与精神分裂症的病理生理学有关。唾液皮质醇是一种方便的测量指标,可帮助人们了解 HPA 轴的活动。本系统综述和荟萃分析评估了精神分裂症患者与健康对照组的唾液皮质醇水平,评估了唾液皮质醇作为精神分裂症生物标志物的潜力。目的 评估精神分裂症患者与健康对照组的唾液皮质醇水平在基线和应激反应中的差异,确定唾液皮质醇作为精神分裂症生物标志物的可靠性。我们在 MEDLINE/PubMed、Cochrane Central 和 EMBASE 中检索了 2013 年 1 月 1 日至 2023 年 7 月 1 日期间发表的、报告基线或应激后唾液皮质醇水平的精神分裂症和对照组人类研究。非人类研究、非特异性精神分裂症诊断或皮质醇数据缺失不在排除之列。两位审稿人分别独立提取数据并评估质量,在达成共识的基础上解决差异问题。由于存在明显的异质性(基线的 I² = 94 %,应激反应的 I² = 75 %),因此采用了随机效应模型。结果最初选择了 19 项研究,其中 12 项研究因诊断为非特异性精神分裂症或皮质醇数据缺失而被排除。最终的荟萃分析包括七项研究,涉及 507 名精神分裂症患者和 175 名健康对照者。主要发现包括:基线皮质醇水平精神分裂症患者和健康对照组的基线唾液皮质醇水平无明显差异(汇总估计值:-0.02,95 % CI:-0.47-0.42)。皮质醇对压力的反应两组患者在压力后的皮质醇水平无明显差异(汇总估计值:0.03,95 % CI:-1.84-1.79)。研究变异性由于设计、患者特征和皮质醇测量技术的不同,各研究之间存在很大差异。尽管有一些证据表明精神分裂症患者的皮质醇动态发生了改变,但研究方法的高变异性以及药物使用和社会心理压力等混杂因素使最终结论变得复杂。个体差异和方法差异限制了唾液皮质醇诊断的准确性。要阐明唾液皮质醇在精神分裂症中的作用及其潜在的临床应用,今后的研究必须要有更大的样本量、统一的方法和对混杂变量的全面控制。
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Salivary cortisol in Schizophrenia: a selective review and meta-analysis of controlled studies of the past decade

Background

Stress and trauma significantly contribute to various psychiatric disorders, including schizophrenia. Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis, particularly abnormal cortisol secretion, is implicated in schizophrenia's pathophysiology. Salivary cortisol, a convenient measure, provides insights into HPA axis activity. This systematic review and meta-analysis assess salivary cortisol levels in individuals with schizophrenia compared to healthy controls, evaluating its potential as a biomarker for schizophrenia.

Aim

To assess the differences in salivary cortisol levels at baseline and in response to stress between patients with schizophrenia and healthy controls, determining the reliability of salivary cortisol as a biomarker for schizophrenia.

Methods

A systematic review and meta-analysis were conducted following PRISMA guidelines. We searched MEDLINE/PubMed, Cochrane Central, and EMBASE for human studies on schizophrenia and controls published from January 1, 2013, to July 1, 2023, reporting baseline or post-stress salivary cortisol levels. Exclusions were non-human studies, non-specific schizophrenia diagnoses, or missing cortisol data. Two reviewers independently extracted data and appraised quality, resolving discrepancies by consensus. Due to significant heterogeneity (I² = 94 % for baseline, 75 % for stress response), a random effects model was used.

Results

Nineteen studies were initially selected, with twelve excluded due to non-specific schizophrenia diagnoses and missing cortisol data. The final meta-analysis included seven studies with 507 schizophrenia patients and 175 healthy controls. Key findings include:

Baseline cortisol levels

No significant difference in baseline salivary cortisol levels between schizophrenia patients and healthy controls (pooled estimate: −0.02, 95 % CI: −0.47–0.42).

Cortisol response to stress

No significant difference in post-stress cortisol levels between the two groups (pooled estimate: 0.03, 95 % CI: −1.84–1.79).

Study variability

High variability across studies due to differences in design, patient characteristics, and cortisol measurement techniques. Despite some evidence of altered cortisol dynamics in schizophrenia, high variability in methodologies and confounding factors like medication use and psychosocial stressors complicate definitive conclusions.

Conclusion

The review underscores the potential of cortisol as a biomarker for stress response; however, its use in diagnosing schizophrenia remains inconclusive. Individual variability and methodological differences limit the diagnostic accuracy of salivary cortisol. Future research with larger sample sizes, uniform methodologies, and comprehensive control for confounding variables is essential to elucidate the role of salivary cortisol in schizophrenia and its potential clinical applications.

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来源期刊
Biomarkers in Neuropsychiatry
Biomarkers in Neuropsychiatry Medicine-Psychiatry and Mental Health
CiteScore
4.00
自引率
0.00%
发文量
12
审稿时长
7 weeks
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