SCL-90量表评分与冠状动脉粥样硬化的相关性分析
Correlation Analysis between SCL-90 Scale Scores and Coronary Atherosclerosis
DOI: 10.12677/ACM.2023.1361470, PDF,    科研立项经费支持
作者: 何其辛*:南京医科大学第二临床医学院,江苏 南京;郭纪群*#, 俞 捷, 张国辉:镇江市第一人民医院心内科,江苏 镇江;戴庭豪:南京医科大学医学影像学院,江苏 南京
关键词: 心理因素冠心病碱性磷酸酶Gensini评分Psychological Factors Coronary Disease Alkaline Phosphatase Gensini’s Score
摘要: 目的:通过分析SCL-90量表评分与冠状动脉粥样硬化程度的相关性,探讨心理因素与冠心病的关系,并揭示其可能机制。方法:纳入50例2017年1月至2022年1月于镇江市第一人民医院心内科因疑诊冠心病而接受冠脉造影检查的住院患者,填写90项症状自评量表(SCL-90),最终30例患者满足入选条件,以量表得分评估10项心理因子分与冠状动脉粥样硬化程度之间的相关性。分组分析时选取22例术中诊断为冠脉粥样硬化或冠心病者为研究组,8例术中诊断为心肌桥或冠脉造影正常者为对照组。比较组间患者的一般临床资料和10项心理因子分结果。对Gensini评分与SCL-90量表因子分进行二变量Spearman相关分析,并将Gensini评分与SCL-90因子分在控制年龄性别的条件下进行偏相关分析。在控制性别的条件下将多项与冠心病存在关联的指标纳入偏相关分析矩阵,探索与SCL-90量表因子分存在相关性的指标。运用多元线性回归分析冠脉粥样硬化或冠心病的独立危险因素。结果:分组分析结果表明,冠脉明显病变组精神病因子分显著高于轻度病变组和对照组。抑郁因子分(r = 0.363, P = 0.048)、精神病因子分(r = 0.439, P = 0.015)与Gensini评分存在正相关性。且控制年龄和性别后抑郁因子分(r = 0.513, P = 0.005)、精神病因子分(r = 0.465, P = 0.013)与Gensini评分呈现出更强的相关性。多元回归分析表明,对于冠状动脉粥样硬化严重程度最具有预测价值的心理因素是抑郁(β = 0.512, T = 3.583, P = 0.001)。在控制了性别的情况下,精神病因子(r = 0.493, P = 0.007)和抑郁因子(r = 0.398, P = 0.033)与血清碱性磷酸酶水平也存在正相关性。结论:精神病因子、抑郁因子与冠状动脉粥样硬化程度正相关,其中抑郁为冠状动脉粥样硬化独立危险因素,具有一定预测价值。心理因素可能通过改变血清碱性磷酸酶水平间接促进冠脉粥样硬化进展。
Abstract: Objective: To explore the relationship between psychological factors and coronary heart disease by analyzing the correlation between SCL-90 scores and the severity of coronary atherosclerosis, and to reveal the possible mechanisms. Methods: Fifty inpatients who underwent coronary angiography due to suspected coronary heart disease at the First People’s Hospital of Zhenjiang from January 2017 to January 2022 were enrolled. They completed the 90-item Symptom Checklist-90 (SCL-90). Finally, 30 patients met the inclusion criteria, and the correlation between the scores of 10 psycho-logical factors and the severity of coronary atherosclerosis was evaluated. Twenty-two patients with a diagnosis of coronary atherosclerosis or coronary heart disease during the operation were select-ed as the study group, and eight patients with a diagnosis of myocardial bridge or normal coronary angiography were selected as the control group. The general clinical data and the results of the 10 psychological factors were compared between the two groups. The bivariate Spearman correlation analysis was used to analyze the correlation between Gensini’s score and SCL-90 factor score, and the partial correlation analysis was performed to control for age and gender. Under the condition of controlling for gender, multiple variables associated with coronary heart disease were included in the partial correlation analysis matrix to explore the indicators that are correlated with SCL-90 fac-tor score. Multiple linear regression analysis was used to analyze the independent risk factors for coronary atherosclerosis or coronary heart disease. Results: The results of the grouping analysis showed that the scores of the psychotic factor in the severe coronary artery disease group were sig-nificantly higher than those in the mild coronary artery disease group and the control group. The depression factor score (r = 0.363, P = 0.048) and psychotic factor score (r = 0.439, P = 0.015) were positively correlated with the Gensini’s score. After controlling for age and gender, the factor scores for depression (r = 0.513, P = 0.005) and psychosis (r = 0.465, P = 0.013) showed a stronger correla-tion with Gensini’s score. The multiple regression analysis showed that depression (β = 0.512, T = 3.583, P = 0.001) was the psychological factor with the highest predictive value for the severity of coronary atherosclerosis. Under the condition of controlling for gender, the psychotic factor (r = 0.493, P = 0.007) and the depression factor (r = 0.398, P = 0.033) were positively correlated with the level of serum alkaline phosphatase. Conclusion: The psychotic factor and depression factor are positively correlated with the severity of coronary atherosclerosis, and depression is an independ-ent risk factor for coronary atherosclerosis with certain predictive value. Psychological factors may indirectly promote the progression of coronary atherosclerosis by altering the level of serum alka-line phosphatase.
文章引用:何其辛, 郭纪群, 俞捷, 戴庭豪, 张国辉. SCL-90量表评分与冠状动脉粥样硬化的相关性分析[J]. 临床医学进展, 2023, 13(6): 10505-10514. https://doi.org/10.12677/ACM.2023.1361470

参考文献

[1] Davidson, K.W., Alcántara, C. and Miller, G.E. (2018) Selected Psychological Comorbidities in Coronary Heart Disease: Challenges and Grand Opportunities. American Psychologist, 73, 1019-1030. [Google Scholar] [CrossRef] [PubMed]
[2] Hemingway, H. and Marmot, M. (1999) Evidence Based Cardiology: Psychosocial Factors in the Aetiology and Prognosis of Coronary Heart Disease: Systematic Review of Prospective Co-hort Studies. BMJ, 318, 1460-1467. [Google Scholar] [CrossRef] [PubMed]
[3] 王征宇. 症状自评量(SCL-90) [J]. 上海精神医学, 1984(2): 68-70.
[4] Rampidis, G.P., Benetos, G., Benz, D.C., Giannopoulos, A.A. and Buechel, R.R. (2019) A Guide for Gensini Score Calculation. Atherosclerosis, 287, 181-183. [Google Scholar] [CrossRef] [PubMed]
[5] Gensini, G.G. (1983) A More Meaningful Scoring Sys-tem for Determining the Severity of Coronary Heart Disease. The American Journal of Cardiology, 51, 606. [Google Scholar] [CrossRef
[6] Malakar, A.K., Choudhury, D., Halder, B., Paul, P., Uddin, A. and Chakraborty, S. (2019) A Review on Coronary Artery Disease, Its Risk Factors, and Therapeutics. Journal of Cellular Physiology, 234, 16812-16823. [Google Scholar] [CrossRef] [PubMed]
[7] Ösby, U., Correia, N., Brandt, L., Ekbomb, A. and Sparén, P. (2000) Time Trends in Schizophrenia Mortality in Stockholm County, Sweden: Cohort Study. BMJ, 321, 483-484. [Google Scholar] [CrossRef] [PubMed]
[8] Kasteng, F., Eriksson, J., Sennfält, K. and Lindgren, P. (2011) Metabolic Effects and Cost-Effectiveness of Aripiprazole versus Olanzapine in Schizophrenia and Bipolar Disorder. Acta Psychiatrica Scandinavica, 124, 214-225. [Google Scholar] [CrossRef] [PubMed]
[9] 郭纪群, 葛均波. 血尿酸与冠状动脉粥样硬化程度的关系[J]. 中国心血管杂志, 2013, 18(5): 346-349.
[10] Lichtman, J.H., Froelicher, E.S., Blumenthal, J.A., et al. (2014) Depression as a Risk Factor for Poor Prognosis among Patients with Acute Coronary Syndrome: Systematic Review and Recommendations: A Scientific Statement from the American Heart Association. Circulation, 129, 1350-1369. [Google Scholar] [CrossRef
[11] Kleber, M.E., Delgado, G., Grammer, T.B., et al. (2015) Uric Acid and Cardiovascular Events: A Mendelian Randomization Study. Journal of the American Society of Nephrology, 26, 2831-2838. [Google Scholar] [CrossRef
[12] Lim, D.-H., Lee, Y., Park, G.-M., et al. (2019) Serum Uric Acid Level and Subclinical Coronary Atherosclerosis in Asymptomatic Individuals: An Observational Cohort Study. Athero-sclerosis, 288, 112-117. [Google Scholar] [CrossRef] [PubMed]
[13] Kunutsor, S.K., Apekey, T.A. and Khan, H. (2014) Liver Enzymes and Risk of Cardiovascular Disease in the General Population: A Meta-Analysis of Prospective Cohort Studies. Atherosclerosis, 236, 7-17. [Google Scholar] [CrossRef] [PubMed]
[14] Kaplan, M.M. (1972) Alkaline Phosphatase. New Eng-land Journal of Medicine, 286, 200-202. [Google Scholar] [CrossRef
[15] Matsubara, Y., Kiyohara, H., Teratani, T., Mikami, Y. and Kanai, T. (2022) Organ and Brain Crosstalk: The Liver-Brain Axis in Gastrointestinal, Liver, and Pancreatic Diseases. Neuropharmacology, 205, Article ID: 108915. [Google Scholar] [CrossRef] [PubMed]
[16] Ballaz, S.J. and Bourin, M. (2021) Cholecystokin-in-Mediated Neuromodulation of Anxiety and Schizophrenia: A “Dimmer-Switch” Hypothesis. Current Neuropharma-cology, 19, 925-938. [Google Scholar] [CrossRef
[17] 张萌萌, 徐又佳, 侯建明, 等. 骨质疏松实验室诊断及影响因素专家共识2022 [J]. 中国骨质疏松杂志, 2022, 28(9): 1249-1259.
[18] Huang, T.-L. and Lin, C.-C. (2015) Advances in Biomarkers of Major Depressive Disorder. In: Makowski, G.S., Ed., Advances in Clinical Chemis-try, Vol. 68, Academic Press, Cambridge, 177-204. [Google Scholar] [CrossRef] [PubMed]
[19] Ndrepepa, G., Xhepa, E., Braun, S., et al. (2017) Alkaline Phos-phatase and Prognosis in Patients with Coronary Artery Disease. European Journal of Clinical Investigation, 47, 378-387. [Google Scholar] [CrossRef] [PubMed]
[20] Sforzini, L., Pariante, C.M., Palacios, J.E., et al. (2019) Inflamma-tion Associated with Coronary Heart Disease Predicts Onset of Depression in a Three-Year Prospective Follow-up: A Preliminary Study. Brain, Behavior, and Immunity, 81, 659-664. [Google Scholar] [CrossRef] [PubMed]
[21] Kim, J.-M., Stewart, R., Kim, J.-W., et al. (2019) Modifying Effects of Depression on the Association between BDNF Methylation and Rognosis of Acute Coronary Syndrome. Brain, Be-havior, and Immunity, 81, 422-429. [Google Scholar] [CrossRef] [PubMed]
[22] Deter, H.C., Orth-Gomér, K., Rauch-Kröhnert, U., et al. (2021) De-pression, Anxiety, and Vital Exhaustion Are Associated with Pro-Coagulant Markers in Depressed Patients with Coro-nary Artery Disease—A Cross Sectional and Prospective Secondary Analysis of the SPIRR-CAD Trial. Journal of Psy-chosomatic Research, 151, Article ID: 110659. [Google Scholar] [CrossRef] [PubMed]
[23] Amare, A., Schubert, K., Klingler-Hoffmann, M., Co-hen-Woods, S. and Baune, B.T. (2017) The Genetic Overlap Between Mood Disorders and Cardiometabolic Diseases: A Systematic Review of Genome Wide and Candidate Gene Studies. Translational Psychiatry, 7, e1007. [Google Scholar] [CrossRef] [PubMed]
[24] Kang, H.-J., Stewart, R., Kim, J.-W., et al. (2020) Synergistic Effects of Depression and NR3C1 Methylation on Prognosis of Acute Coronary Syndrome. Scientific Reports, 10, Article No. 5519. [Google Scholar] [CrossRef] [PubMed]
[25] Kloner, R.A. (2019) The Brain-Heart Connection and the Northridge Earthquake. Cardiology in Review, 27, 171-172. [Google Scholar] [CrossRef