PMID- 38327882 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240210 IS - 2220-3206 (Print) IS - 2220-3206 (Electronic) IS - 2220-3206 (Linking) VI - 14 IP - 1 DP - 2024 Jan 19 TI - Assessing myocardial indices and inflammatory factors to determine anxiety and depression severity in patients with chronic heart failure. PG - 53-62 LID - 10.5498/wjp.v14.i1.53 [doi] AB - BACKGROUND: Patients with chronic heart failure (CHF) have a progressive disease that is associated with poor quality of life and high mortality. Many patients experience anxiety and depression (A&D) symptoms, which can further accelerate disease progression. We hypothesized that indicators of myocardial function and inflammatory stress may reflect the severity of A&D symptoms in patients with CHF. Changes in these biomarkers could potentially predict whether A&D symptoms will deteriorate further in these individuals. AIM: To measure changes in cardiac and inflammatory markers in patients with CHF to determine A&D severity and predict outcomes. METHODS: We retrospectively analyzed 233 patients with CHF treated at the Jingzhou Hospital, Yangtze University between 2018-2022 and grouped them according to Self-Rating Anxiety Scale (SAS) and Self-Rating Depression Scale (SDS) scores. We compared clinical data in the no-A&D, mild-A&D, moderate-A&D, and severe-A&D groups, the SAS and SDS scores with the New York Heart Association (NYHA) functional classification, and cardiac markers and inflammatory factors between the no/mild-A&D and moderate/severe-A&D groups. Regression analysis was performed on the markers with P < 0.05 to determine their ability to predict A&D severity in patients and the area under the receiver operating characteristic curve (AUROC) was used to evaluate their accuracy. RESULTS: In the inter-group comparison, the following variables had an effect on A&D severity in patients with CHF: NYHA class, left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter, N-terminal pro-brain natriuretic peptide (NT-proBNP), interleukin-6 (IL-6), and tumor necrosis factor-alpha (P < 0.05). Other variables did not differ significantly between the A&D groups (P > 0.05). In addition, we found that higher NYHA classes were associated with higher the SAS and SDS scores (P < 0.05). Regression analysis showed that LVEF, NT-proBNP, and IL-6 were independent risk factors for A&D severity (P < 0.05). Among them, NT-proBNP had the best predictive ability as a single indicator (AUROC = 0.781). Furthermore, the combination of these three indicators exhibited a good predictive effect toward discriminating the extent of A&D severity among patients (AUROC = 0.875). CONCLUSION: Cardiac and inflammatory biomarkers, such as LVEF, NT-proBNP, and IL-6, are correlated with A&D severity in patients with CHF and have predictive value. CI - (c)The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved. FAU - Zhang, Li AU - Zhang L AD - Department of Cardiology, Jingzhou Hospital, Yangtze University, Jingzhou 434020, Hubei Province, China. FAU - Wang, Qiang AU - Wang Q AD - Department of Cardiology, Jingzhou Hospital, Yangtze University, Jingzhou 434020, Hubei Province, China. FAU - Cui, Hong-Sheng AU - Cui HS AD - Department of Cardiology, Jingzhou Hospital, Yangtze University, Jingzhou 434020, Hubei Province, China. FAU - Luo, Yuan-Yuan AU - Luo YY AD - Department of Intensive Care Unit, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510000, Guangdong Province, China. kellyyuan1983@163.com. LA - eng PT - Journal Article DEP - 20240119 PL - United States TA - World J Psychiatry JT - World journal of psychiatry JID - 101610480 PMC - PMC10845224 OTO - NOTNLM OT - Anxiety OT - Cardiac markers OT - Chronic heart failure OT - Depression OT - Inflammatory factors OT - Prediction COIS- Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article. EDAT- 2024/02/08 06:43 MHDA- 2024/02/08 06:44 PMCR- 2024/01/19 CRDT- 2024/02/08 04:12 PHST- 2023/11/06 00:00 [received] PHST- 2023/11/25 00:00 [revised] PHST- 2023/12/21 00:00 [accepted] PHST- 2024/02/08 06:44 [medline] PHST- 2024/02/08 06:43 [pubmed] PHST- 2024/02/08 04:12 [entrez] PHST- 2024/01/19 00:00 [pmc-release] AID - 10.5498/wjp.v14.i1.53 [doi] PST - epublish SO - World J Psychiatry. 2024 Jan 19;14(1):53-62. doi: 10.5498/wjp.v14.i1.53. eCollection 2024 Jan 19.