高危监测人群中阻塞性睡眠呼吸暂停与胰腺癌的关联:CAPS和PCYST队列研究
Association of obstructive sleep apnea with pancreatic cancer in high-risk patients under surveillance in CAPS and PCYST cohorts.
文献信息
| PMID | 42859088 |
|---|---|
| 原文 | 在 PubMed 查看原文 ↗ |
| 发表日期 | 2026 |
| 作者 | Hassan Sinan |
| 作者单位 | Departments of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University, Baltimore, MD, United States of America. |
| 期刊 | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] |
| SCI 分区 | Q2 |
| IF | 3.8 |
| 研究类型 | 临床研究 · 临床 |
| 所属专科 | 咽喉科 |
中文摘要
背景: 阻塞性睡眠呼吸暂停(OSA)与癌症发病率和死亡率增加有关。我们假设OSA可能是接受胰腺癌监测的患者肿瘤进展的危险因素。
方法: 对两个约翰霍普金斯医院接受胰腺监测的队列进行回顾性病历审查;纳入胰腺癌筛查研究(CAPS)中具有家族性/遗传性风险的患者,以及PCYST研究中偶然发现胰腺囊肿的患者。按OSA状态比较进展为胰腺导管腺癌(PDAC)和肿瘤进展(PDAC、高级别不典型增生或胰腺神经内分泌肿瘤)的时间,并校正协变量。
结果: 在CAPS队列的893例患者中,174例(19.5%)在监测前或监测期间被诊断为OSA;在PCYST队列的1585例患者中,376例(23.7%)被诊断为OSA。在合并队列中,OSA与进展为PDAC的风险增加相关(未校正HR:3.12,95% CI:[1.82, 5.34],p < 0.001)。OSA还与男性、较高的BMI、脂肪肝、脂肪胰、糖尿病和吸烟史相关(所有p < 0.01)。在校正协变量后,OSA仍与PDAC风险相关(校正HR:2.56 [1.44, 4.55],p = 0.001)。与肿瘤进展相关的因素包括OSA(校正HR:1.93 [1.25, 2.97],p = 0.003)、年龄增长(每5岁校正HR:1.14 [1.05, 1.24],p = 0.003)、脂肪肝(校正HR:1.76 [1.19, 2.60],p = 0.005)和糖尿病(校正HR:1.77 [1.16, 2.71],p = 0.008)。
结论: 因家族性/遗传性风险和/或偶然发现的胰腺囊肿而接受胰腺监测的患者,如果被诊断为OSA,则发生胰腺癌的可能性更大。
英文摘要
BACKGROUND: Obstructive sleep apnea (OSA) has been linked with increased cancer incidence and mortality. We hypothesized that OSA may be a risk factor for neoplastic progression among patients undergoing pancreatic cancer surveillance.
METHODS: Retrospective medical record review of two Johns Hopkins Hospital cohorts undergoing pancreas surveillance; patients with familial/genetic risk enrolled in the Cancer of the Pancreas Screening (CAPS) study and patients with incidentally detected pancreatic cysts, enrolled in the PCYST study. Time-to-progression to pancreatic ductal adenocarcinoma (PDAC) and neoplastic progression (either PDAC, high-grade dysplasia or pancreatic neuroendocrine tumor) were compared by OSA status, adjusting for covariates.
RESULTS: OSA was diagnosed prior to or during surveillance in 174 (19.5%) of 893 patients in CAPS and 376 (23.7%) of 1585 patients in the PCYST cohort. In the combined cohorts, OSA was associated with increased risk of progression to PDAC (unadjusted HR: 3.12, 95% CI: [1.82, 5.34], p < 0.001). OSA was also associated with male sex, higher BMI, fatty liver, fatty pancreas, diabetes, and history of smoking (all p < 0.01). After covariate adjustment, OSA remained associated with PDAC risk (adjusted HR: 2.56 [1.44, 4.55], p = 0.001). Factors associated with neoplastic progression included OSA (adjusted HR: 1.93 [1.25, 2.97], p = 0.003), increasing age (age-per 5-years adjusted HR: 1.14 [1.05, 1.24], p = 0.003), fatty liver (adjusted HR: 1.76 [1.19, 2.60], p = 0.005), and diabetes (adjusted HR: 1.77 [1.16, 2.71], p = 0.008).
CONCLUSIONS: Patients undergoing pancreatic surveillance for their familial/genetic risk and/or incidentally detected pancreatic cysts have a greater likelihood of developing pancreatic cancer if they've been diagnosed with OSA.