Department of Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, MA, USA.
Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
BMC Pulm Med. 2021 Jul 14;21(1):235. doi: 10.1186/s12890-021-01585-5.
Secondary polycythemia is associated with cigarette smoking and chronic obstructive pulmonary disease (COPD). However, the prevalence of polycythemia in COPD and the contributing risk factors for polycythemia in COPD have not been extensively studied.
We analyzed the presence of secondary polycythemia in current and former smokers with moderate to very severe COPD at the five-year follow-up visit in the observational COPDGene study. We used logistic regression to evaluate the association of polycythemia with age, sex, race, altitude, current smoking status, spirometry, diffusing capacity for carbon monoxide (DLCO), quantitative chest CT measurements (including emphysema, airway wall thickness, and pulmonary artery to aorta diameter ratio), resting hypoxemia, exercise-induced hypoxemia, and long-term oxygen therapy.
In a total of 1928 COPDGene participants with moderate to very severe COPD, secondary polycythemia was found in 97 (9.2%) male and 31 (3.5%) female participants. In a multivariable logistic model, severe resting hypoxemia (OR 3.50, 95% CI 1.41-8.66), impaired DLCO (OR 1.28 for each 10-percent decrease in DLCO % predicted, CI 1.09-1.49), male sex (OR 3.60, CI 2.20-5.90), non-Hispanic white race (OR 3.33, CI 1.71-6.50), current smoking (OR 2.55, CI 1.49-4.38), and enrollment in the Denver clinical center (OR 4.42, CI 2.38-8.21) were associated with higher risk for polycythemia. In addition, continuous (OR 0.13, CI 0.05-0.35) and nocturnal (OR 0.46, CI 0.21-0.97) supplemental oxygen were associated with lower risk for polycythemia. Results were similar after excluding participants with anemia and participants enrolled at the Denver clinical center.
In a large cohort of individuals with moderate to very severe COPD, male sex, current smoking, enrollment at the Denver clinical center, impaired DLCO, and severe hypoxemia were associated with increased risk for secondary polycythemia. Continuous or nocturnal supplemental oxygen use were associated with decreased risk for polycythemia.
继发性红细胞增多与吸烟和慢性阻塞性肺疾病(COPD)有关。然而,COPD 患者中红细胞增多症的患病率以及 COPD 患者红细胞增多症的相关危险因素尚未得到广泛研究。
我们在观察性 COPDGene 研究中,对五年随访时处于中度至重度 COPD 的现吸烟者和曾经吸烟者中继发性红细胞增多症的发生情况进行了分析。我们使用逻辑回归来评估红细胞增多症与年龄、性别、种族、海拔、当前吸烟状况、肺量计检查、一氧化碳弥散量(DLCO)、定量胸部 CT 测量值(包括肺气肿、气道壁厚度和肺动脉与主动脉直径比)、静息性低氧血症、运动性低氧血症和长期氧疗之间的关系。
在总共 1928 名患有中度至重度 COPDGene 的参与者中,有 97 名男性(9.2%)和 31 名女性(3.5%)参与者出现继发性红细胞增多症。在多变量逻辑模型中,严重的静息性低氧血症(OR 3.50,95%CI 1.41-8.66)、DLCO 受损(OR 每下降 10%DLCO 预测值的 1.28,CI 1.09-1.49)、男性(OR 3.60,CI 2.20-5.90)、非西班牙裔白种人(OR 3.33,CI 1.71-6.50)、当前吸烟(OR 2.55,CI 1.49-4.38)和在丹佛临床中心入组(OR 4.42,CI 2.38-8.21)与红细胞增多症风险升高相关。此外,连续(OR 0.13,CI 0.05-0.35)和夜间(OR 0.46,CI 0.21-0.97)补充氧气与红细胞增多症风险降低相关。在排除贫血患者和在丹佛临床中心入组的患者后,结果相似。
在患有中重度 COPD 的大量患者中,男性、当前吸烟、在丹佛临床中心入组、DLCO 受损和严重低氧血症与继发性红细胞增多症的风险增加相关。连续或夜间补充氧气的使用与红细胞增多症风险降低相关。