Анализа корелације нивоа Ц1QTNF9 и Хомо-Цис у серуму са тежином лезија коронарних артерија (КХБ)

Нивои серума C1QTNF9 и хомоцистеина код КХБ-а

  • Rui Wang Одељење кардиологије, болница Ксионган Суанву
  • Man Zhang Одељење кардиологије, болница Ксионган Суанву
  • Lafang Ran Одељење за кардиоваскуларну медицину, Болница Ренмин Универзитета у Вухану
  • Guozhang Tang Department of Cardiovascular Medicine, Renmin Hospital of Wuhan University
  • Lu Yu Одељење за кардиоваскуларне болести, Сарадничка болница Чужоу Медицинског универзитета Анхуј (Прва народна болница Чужоу)
Ključne reči: Коронарна болест срца, Д-димер, Хомоцистеин, Степен лезије угрожене плаке

Sažetak


[Objective] To investigate the connections between the vulnerability of coronary atherosclerotic plaques and the severity of coronary artery lesions in patients with coronary heart disease (CHD) and the serum levels of C1q/tumor necrosis factor-related protein 9 (C1QTNF9), homocysteine (Homo-Cys), and D-dimer (D-D).

[Methods] Research participants were 396 individuals with suspected coronary heart disease (CHD) who came to the hospital between June 2022 and October 2025 with symptoms like tightness and pain in their chest. Through coronary angiography (CAG) examination, The CHD group consisted of 248 patients with CHD, while the control group consisted of 148 people without CHD. The two patient groups' serum levels of C1QTNF9, Homo-Cys, and D-D were compared. Three types of CHD patients were identified based on the findings of the blood flow reserve fraction test: those with no plaque, those with stable plaque, and those with susceptible plaque. Using the Gensini scoring standards, the patients were divided into three groups according to the CAG examination results: low-risk (less than 20 points), medium-risk (20–40 points), and high-risk (more than 40 points). The patients were split into one lesion group, two lesion groups, and three or more lesion groups. Serum levels of C1QTNF9, Homo-Cys, and D-D were compared and associations were examined in CHD patients with varying coronary artery plaque stabilities, coronary artery lesion counts, and Gensini scores.

[Results] The CHD group's serum C1QTNF9 level was lower than the control group's, despite the Homo-Cys and D-D levels being significantly greater (P<0.05). Both the stable and vulnerable plaque groups had lower serum C1QTNF9 levels than the plaque-free group, while the plaque-free group had higher levels of Homo-Cys and D-D. Furthermore, the susceptible plaque group had a lower serum level of C1QTNF9 than the stable plaque group, and the blood levels of Homo-Cys and D-D were higher than those in the stable plaque group (P<0.05). While the levels of Homo-Cys and D-D progressively increased, the serum C1QTNF9 level steadily decreased as the number of coronary artery lesion branches grew. P<0.05 indicated that these changes were statistically significant. Both the intermediate-risk and high-risk groups had lower serum C1QTNF9 levels than the low-risk group, while the low-risk group had greater levels of Homo-Cys and D-D. Additionally, the high-risk group's serum C1QTNF9 level was lower than the intermediate-risk group's, while the intermediate-risk group's Homo-Cys and D-D levels were higher (P<0.05). The number of vulnerable plaques, the number of coronary artery lesions, and the Gensini score were all negatively correlated with the serum C1QTNF9 level (P<0.05), while the number of vulnerable plaques, the number of coronary artery lesions, and the serum Homo-Cys and D-D levels showed a positive correlation (P<0.05) with the Gensini score. Serum Homo-Cys was favorably connected with D-D (P<0.05), while serum C1QTNF9 was negatively correlated with Homo-Cys and D-D (P<0.05).

[Conclusion] In patients with CHD, the serum C1QTNF9 level is decreased, whereas the Homo-Cys and D-D levels are increased. The serum C1QTNF9, Homo-Cys, and D-D levels are closely related to the stability of coronary atherosclerotic plaques and the severity of coronary artery lesions. Moreover, these indicators interact with each other and jointly participate in the disease progression of CHD patients.

Reference

1.You X, Gao B. Association between Intestinal Flora Metabolites and Coronary Artery Vulnerable Plaque Characteristics in Coronary Heart Disease. Br J Hosp Med (Lond). 2025 Mar 26;86(3):1-13. doi: 10.12968/hmed.2024.0772. PMID: 40135300.
2.Wang H, Huang Z, Wang J, Yue S, Hou Y, Ren R, Zhang Y, Cheng Y, Zhang R, Mu Y. Predictive value of system immune-inflammation index for the severity of coronary stenosis in patients with coronary heart disease and diabetes mellitus. Sci Rep. 2024 Dec 28;14(1):31370. doi: 10.1038/s41598-024-82826-5. PMID: 39732905; PMCID: PMC11682039.
3.Yang B, Jia Z. Diagnostic value of nocturnal trend changes in a dynamic electrocardiogram for coronary heart disease. BMC Cardiovasc Disord. 2024 Oct 16;24(1):561. doi: 10.1186/s12872-024-04213-2. PMID: 39407107; PMCID: PMC11481414.
4.Li Y, Zhai Y, Hu S, Liu J, Zhang W, Yue J, Wang Z. Remnant cholesterol, lipid ratios, and the severity of coronary artery lesions: a retrospective cohort study in patients with coronary heart disease. Front Cardiovasc Med. 2025 Mar 10;12:1516326. doi: 10.3389/fcvm.2025.1516326. PMID: 40129766; PMCID: PMC11930836.
5.Methods In Medicine CAM. Retracted: Analysis of Coronary Artery Lesion Degree and Related Risk Factors in Patients with Coronary Heart Disease Based on Computer-Aided Diagnosis of Coronary Angiography. Comput Math Methods Med. 2023 Jul 26;2023:9814137. doi: 10.1155/2023/9814137. PMID: 37538457; PMCID: PMC10396684.
6.Zhang B, Yang D, Xu M, Wu JJ, Ling ZH. Carotid Ultrasound Combined with Plasma Atherosclerosis Index (AIP) in the Severe Analysis of Coronary Heart Disease Treated with Atorvastatin. Altern Ther Health Med. 2024 Dec;30(12):436-442. PMID: 38581319.
7.Li L, Zhang Y, Ma M, Liu F, Shang Y, Yuan Q, Li X, Ju B. Does erectile dysfunction predict cardiovascular risk? A cross-sectional study of clinical characteristics in patients with erectile dysfunction combined with coronary heart disease. Front Cardiovasc Med. 2024 Mar 18;11:1341819. doi: 10.3389/fcvm.2024.1341819. PMID: 38562188; PMCID: PMC10984325.
8.Miaomiao S, Jiaqi Z, Xiaomeng L, Shanshan L, Jie W, Kaicheng L, Mei J, Ming S. Myocardial intramural course may reduce left ventricular ejection fraction of patients suffering from coronary heart disease. Front Cardiovasc Med. 2025 Feb 27;12:1451173. doi: 10.3389/fcvm.2025.1451173. PMID: 40083823; PMCID: PMC11903404.
9.Yang Z, Xu L, Gao Y, Zhang C, Wang A. Tailored personas for self-management in home-based cardiac rehabilitation for patients with coronary heart disease: A qualitative study. Int J Nurs Stud. 2025 Mar;163:105000. doi: 10.1016/j.ijnurstu.2025.105000. Epub 2025 Jan 19. PMID: 39854909.
10.Carney RM, Freedland KE, Rich MW. Treating Depression to Improve Survival in Coronary Heart Disease: What Have We Learned? J Am Coll Cardiol. 2024 Jul 30;84(5):482-489. doi: 10.1016/j.jacc.2024.05.038. PMID: 39048281.
11.Lan Y, Luo FK, Yu Y, Wang XY, Wang PQ, Xiong XJ. [Coronary heart disease: innovative understanding from traditional Chinese medicine and treatment by classic formulas]. Zhongguo Zhong Yao Za Zhi. 2024 Jul;49(13):3684-3692. Chinese. doi: 10.19540/j.cnki.cjcmm.20240326.501. PMID: 39041141.
12.Zhao M, Feng L, Li W. Network Pharmacology and Experimental Verification: SanQi-DanShen Treats Coronary Heart Disease by Inhibiting the PI3K/AKT Signaling Pathway. Drug Des Devel Ther. 2024 Oct 9;18:4529-4550. doi: 10.2147/DDDT.S480248. PMID: 39399124; PMCID: PMC11471080.
13.Ma R, Zhou X, Zhang G, Wu H, Lu Y, Liu F, Chang Y, Ding Y. Association between composite dietary antioxidant index and coronary heart disease among US adults: a cross-sectional analysis. BMC Public Health. 2023 Dec 5;23(1):2426. doi: 10.1186/s12889-023-17373-1. PMID: 38053099; PMCID: PMC10699074.
14.Liu Y, Zhu B, Zhou W, Du Y, Qi D, Wang C, Cheng Q, Zhang Y, Wang S, Gao C. Triglyceride-glucose index as a marker of adverse cardiovascular prognosis in patients with coronary heart disease and hypertension. Cardiovasc Diabetol. 2023 Jun 9;22(1):133. doi: 10.1186/s12933-023-01866-9. PMID: 37296406; PMCID: PMC10257289.
15.Tao S, Yu L, Li J, Huang L, Huang X, Zhang W, Xie Z, Tan Y, Yang D. Association between the triglyceride-glucose index and 1-year major adverse cardiovascular events in patients with coronary heart disease and hypertension. Cardiovasc Diabetol. 2023 Nov 8;22(1):305. doi: 10.1186/s12933-023-02018-9. PMID: 37940943; PMCID: PMC10633928.
16.Kopparam RV, Grady D, Redberg RF. Coronary Heart Disease Testing Before Kidney Transplant-A Call for Revised Guidance. JAMA Intern Med. 2023 Apr 1;183(4):287-288. doi: 10.1001/jamainternmed.2022.6841. PMID: 36806879.
17.Hou XZ, Wu Q, Lv QY, Yang YT, Li LL, Ye XJ, Yang CY, Lv YF, Wang SH. Development and external validation of a risk prediction model for depression in patients with coronary heart disease. J Affect Disord. 2024 Dec 15;367:137-147. doi: 10.1016/j.jad.2024.08.218. Epub 2024 Sep 2. PMID: 39233236.
18.Li W, Liao X, Geng D, Yang J, Chen H, Hu S, Dai M. Mindfulness therapy for patients with coronary heart disease: A systematic review and meta-analysis. Int J Nurs Pract. 2024 Dec;30(6):e13276. doi: 10.1111/ijn.13276. Epub 2024 Aug 11. PMID: 39129297; PMCID: PMC11608930.
19.Du L, Wang Y, Ma H, Fan J, Wang S, Liu J, Wang X. Exploring novel markers for coronary heart disease associated with systemic lupus erythematosus: A review. Medicine (Baltimore). 2024 Dec 13;103(50):e40773. doi: 10.1097/MD.0000000000040773. PMID: 39686502; PMCID: PMC11651451.
20.Shen R, Zhang Y. Relationship between amino acid metabolism and inflammation in coronary heart disease (Review). Int J Mol Med. 2025 Aug;56(2):120. doi: 10.3892/ijmm.2025.5561. Epub 2025 Jun 6. PMID: 40476584; PMCID: PMC12176267.
21.Kong H, Cen J, Yang X, Xu Z, Liang J, Xiong Q, Zhu J. Research Progress in the Relationship Between Trimethylamine Oxide and Coronary Heart Disease. Altern Ther Health Med. 2024 Nov;30(11):220-227. PMID: 38430149.
22.Chen Y, Jia W, Guo J, Yang H, Sheng X, Wei L, Li J. Association between the C-reactive protein-triglyceride glucose index and new-onset coronary heart disease among metabolically heterogeneous individuals. Cardiovasc Diabetol. 2025 Aug 1;24(1):316. doi: 10.1186/s12933-025-02876-5. PMID: 40751146; PMCID: PMC12317589.
23.Zhang H, Jing L, Zhai C, Xiang Q, Tian H, Hu H. Intestinal Flora Metabolite Trimethylamine Oxide Is Inextricably Linked to Coronary Heart Disease. J Cardiovasc Pharmacol. 2023 Mar 1;81(3):175-182. doi: 10.1097/FJC.0000000000001387. PMID: 36607700; PMCID: PMC9988214.
Objavljeno
2026/03/06
Broj časopisa
Rubrika
Original paper