Hailun Xie, Lishuang Wei, Qiwen Wang, Shuangyi Tang, Jialiang Gan
{"title":"载脂蛋白 A-I 水平与结直肠癌患者生存率的关系:一项回顾性研究","authors":"Hailun Xie, Lishuang Wei, Qiwen Wang, Shuangyi Tang, Jialiang Gan","doi":"10.3389/fendo.2024.1318416","DOIUrl":null,"url":null,"abstract":"Abnormal lipid levels have been associated with cancer incidence and progression. However, limited studies have investigated the relationship between apolipoprotein A-I (ApoA-I) and colorectal cancer (CRC). This study assessed the significance of ApoA-I levels in progression-free survival (PFS) and overall survival (OS) of patients with CRC.Survival curves were compared using Kaplan–Meier analysis, while the predictive values of various lipid indicators in CRC prognosis were evaluated based on receiver operating characteristic curves. The factors influencing PFS and OS in patients with CRC were analyzed using Cox proportional hazards regression models. Finally, the relationship between ApoA-I level and disease recurrence was investigated through logistic regression analysis. The optimal Apo-I level was determined through maximally selected rank statistics.Using the optimal ApoA-I cutoff value (0.9 g/L), the 1,270 patients with CRC were categorized into low (< 0.9 g/L, 275 cases) and high (≥0.9 g/L, 995 cases) ApoA-I groups. Compared with other lipid indicators, ApoA-I demonstrated superior predictive accuracy. The high ApoA-I group exhibited significantly higher survival rates than the low ApoA-I group (PFS, 64.8% vs. 45.2%, P < 0.001; OS, 66.1% vs. 48.6%, P < 0.001). Each one-standard-deviation increase in ApoA-I level was related to a 12.0% decrease in PFS risk (hazard ratio [HR] 0.880; 95% confidence interval [CI], 0.801–0.968; P = 0.009) and an 11.2% decrease in OS risk (HR 0.888; 95%CI, 0.806–0.978; P = 0.015). Logistic regression analysis revealed that patients with low ApoA-I had a 32.5% increased risk of disease recurrence (odds ratio [OR] 0.675; 95%CI, 0.481–0.946; P = 0.0225) compared with those with high ApoA-I. PFS/OS nomograms based on ApoA-I demonstrated excellent prognostic prediction accuracy.Serum ApoA-I level may be a valuable and non-invasive tool for predicting PFS and OS in patients with CRC.","PeriodicalId":505784,"journal":{"name":"Frontiers in Endocrinology","volume":"24 12","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Apolipoprotein A-I levels in the survival of patients with colorectal cancer: a retrospective study\",\"authors\":\"Hailun Xie, Lishuang Wei, Qiwen Wang, Shuangyi Tang, Jialiang Gan\",\"doi\":\"10.3389/fendo.2024.1318416\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abnormal lipid levels have been associated with cancer incidence and progression. However, limited studies have investigated the relationship between apolipoprotein A-I (ApoA-I) and colorectal cancer (CRC). This study assessed the significance of ApoA-I levels in progression-free survival (PFS) and overall survival (OS) of patients with CRC.Survival curves were compared using Kaplan–Meier analysis, while the predictive values of various lipid indicators in CRC prognosis were evaluated based on receiver operating characteristic curves. The factors influencing PFS and OS in patients with CRC were analyzed using Cox proportional hazards regression models. Finally, the relationship between ApoA-I level and disease recurrence was investigated through logistic regression analysis. The optimal Apo-I level was determined through maximally selected rank statistics.Using the optimal ApoA-I cutoff value (0.9 g/L), the 1,270 patients with CRC were categorized into low (< 0.9 g/L, 275 cases) and high (≥0.9 g/L, 995 cases) ApoA-I groups. Compared with other lipid indicators, ApoA-I demonstrated superior predictive accuracy. The high ApoA-I group exhibited significantly higher survival rates than the low ApoA-I group (PFS, 64.8% vs. 45.2%, P < 0.001; OS, 66.1% vs. 48.6%, P < 0.001). Each one-standard-deviation increase in ApoA-I level was related to a 12.0% decrease in PFS risk (hazard ratio [HR] 0.880; 95% confidence interval [CI], 0.801–0.968; P = 0.009) and an 11.2% decrease in OS risk (HR 0.888; 95%CI, 0.806–0.978; P = 0.015). Logistic regression analysis revealed that patients with low ApoA-I had a 32.5% increased risk of disease recurrence (odds ratio [OR] 0.675; 95%CI, 0.481–0.946; P = 0.0225) compared with those with high ApoA-I. 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引用次数: 0
摘要
血脂水平异常与癌症的发生和发展有关。然而,对载脂蛋白A-I(ApoA-I)与结直肠癌(CRC)之间关系的研究却很有限。本研究评估了载脂蛋白 A-I 水平在 CRC 患者无进展生存期(PFS)和总生存期(OS)中的意义。研究采用 Kaplan-Meier 分析法比较了生存曲线,并根据接收者操作特征曲线评估了各种血脂指标在 CRC 预后中的预测价值。采用Cox比例危险回归模型分析了影响CRC患者PFS和OS的因素。最后,通过逻辑回归分析研究了载脂蛋白A-I水平与疾病复发之间的关系。采用最佳载脂蛋白A-I临界值(0.9 g/L),将1270例CRC患者分为低载脂蛋白A-I组(< 0.9 g/L,275例)和高载脂蛋白A-I组(≥ 0.9 g/L,995例)。与其他血脂指标相比,载脂蛋白 A-I 的预测准确性更高。高载脂蛋白A-I组的生存率明显高于低载脂蛋白A-I组(PFS, 64.8% vs. 45.2%, P < 0.001; OS, 66.1% vs. 48.6%, P < 0.001)。载脂蛋白A-I水平每增加一个标准差,PFS风险降低12.0%(危险比[HR]0.880;95%置信区间[CI],0.801-0.968;P = 0.009),OS风险降低11.2%(HR 0.888;95%CI,0.806-0.978;P = 0.015)。逻辑回归分析显示,与高载脂蛋白A-I患者相比,低载脂蛋白A-I患者的疾病复发风险增加了32.5%(几率比 [OR] 0.675;95%CI,0.481-0.946;P = 0.0225)。基于载脂蛋白A-I的PFS/OS提名图显示了极佳的预后预测准确性。
Apolipoprotein A-I levels in the survival of patients with colorectal cancer: a retrospective study
Abnormal lipid levels have been associated with cancer incidence and progression. However, limited studies have investigated the relationship between apolipoprotein A-I (ApoA-I) and colorectal cancer (CRC). This study assessed the significance of ApoA-I levels in progression-free survival (PFS) and overall survival (OS) of patients with CRC.Survival curves were compared using Kaplan–Meier analysis, while the predictive values of various lipid indicators in CRC prognosis were evaluated based on receiver operating characteristic curves. The factors influencing PFS and OS in patients with CRC were analyzed using Cox proportional hazards regression models. Finally, the relationship between ApoA-I level and disease recurrence was investigated through logistic regression analysis. The optimal Apo-I level was determined through maximally selected rank statistics.Using the optimal ApoA-I cutoff value (0.9 g/L), the 1,270 patients with CRC were categorized into low (< 0.9 g/L, 275 cases) and high (≥0.9 g/L, 995 cases) ApoA-I groups. Compared with other lipid indicators, ApoA-I demonstrated superior predictive accuracy. The high ApoA-I group exhibited significantly higher survival rates than the low ApoA-I group (PFS, 64.8% vs. 45.2%, P < 0.001; OS, 66.1% vs. 48.6%, P < 0.001). Each one-standard-deviation increase in ApoA-I level was related to a 12.0% decrease in PFS risk (hazard ratio [HR] 0.880; 95% confidence interval [CI], 0.801–0.968; P = 0.009) and an 11.2% decrease in OS risk (HR 0.888; 95%CI, 0.806–0.978; P = 0.015). Logistic regression analysis revealed that patients with low ApoA-I had a 32.5% increased risk of disease recurrence (odds ratio [OR] 0.675; 95%CI, 0.481–0.946; P = 0.0225) compared with those with high ApoA-I. PFS/OS nomograms based on ApoA-I demonstrated excellent prognostic prediction accuracy.Serum ApoA-I level may be a valuable and non-invasive tool for predicting PFS and OS in patients with CRC.