Burnim Michael, Putcha Nirupama, LaFon David, Woo Han, Azar Antoine, Groenke Lars, Stampfli Martin, Schaub Alexander, Fawzy Ashraf, Balasubramanian Aparna, Fedarko Neal, Cooper Christopher B, Bowler Russell P, Comellas Alejandro, Krishnan Jerry A, Han MeiLan K, Couper David, Peters Stephen P, Drummond M Bradley, O'Neal Wanda, Paine Robert, Criner Gerard, Martinez Fernando J, Curtis Jeffrey L, Barr Graham, Huang Yvonne J, Woodruff Prescott, Dransfield Mark, Hansel Nadia N
Department of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Am J Respir Crit Care Med. 2025 Feb;211(2):215-221. doi: 10.1164/rccm.202311-2184OC.
Serum IgG deficiency is associated with morbidity in chronic obstructive pulmonary disease (COPD), but it is unclear whether concentrations in the lower end of the normal range still confer risk. To determine if levels above traditional cutoffs for serum IgG deficiency are associated with exacerbations among current and former smokers with or at risk for COPD. Former and current smokers in SPIROMICS (the Subpopulations and Intermediate Outcome Measures of COPD study) ( = 1,497) were studied: 1,026 with COPD and 471 at risk for COPD. In a subset ( = 1,031), IgG subclasses were measured. Associations between total IgG or subclasses and prospective exacerbations were evaluated with multivariable models adjusting for demographic characteristics, current smoking, smoking history, FEV percent predicted, inhaled corticosteroids, and serum IgA. The 35th percentile (1,225 mg/dl in this cohort) of IgG was the best cutoff by Akaike information criterion. Below this, there was increased exacerbation risk (incidence rate ratio [IRR], 1.28; 95% confidence interval [CI], 1.08-1.51). Among subclasses, IgG1 and IgG2 below the 35th percentile (354 and 105 mg/dl, respectively) were associated with increased risks of severe exacerbation (IgG1, IRR, 1.39; 95% CI, 1.06-1.84; IgG2, IRR, 1.50; 95% CI, 1.14-1.1.97). These associations remained significant when additionally adjusting for a history of exacerbations. Lower serum IgG is prospectively associated with exacerbations in individuals with or at risk for COPD. Among subclasses, lower IgG1 and IgG2 are prospectively associated with severe exacerbations. The optimal IgG cutoff was substantially higher than traditional cutoffs for deficiency, suggesting that subtle impairment of humoral immunity may be associated with exacerbations.
血清IgG缺乏与慢性阻塞性肺疾病(COPD)的发病相关,但尚不清楚正常范围下限的浓度是否仍会带来风险。为了确定高于血清IgG缺乏传统临界值的水平是否与现吸烟者和曾吸烟者中患有COPD或有COPD风险者的病情加重有关。对SPIROMICS(COPD研究的亚群和中间结局指标)中的既往吸烟者和现吸烟者(n = 1497)进行了研究:1026例患有COPD,471例有COPD风险。在一个亚组(n = 1031)中,测量了IgG亚类。使用多变量模型评估总IgG或亚类与预期病情加重之间的关联,并对人口统计学特征、当前吸烟情况、吸烟史、预测的FEV百分比、吸入性糖皮质激素和血清IgA进行了调整。根据赤池信息准则,IgG的第35百分位数(该队列中为1225mg/dl)是最佳临界值。低于此值,病情加重风险增加(发病率比[IRR],1.28;95%置信区间[CI],1.08 - 1.51)。在亚类中,低于第35百分位数(分别为354mg/dl和105mg/dl)的IgG1和IgG2与严重病情加重风险增加相关(IgG1,IRR,1.39;95%CI,1.06 - 1.84;IgG²,IRR,1.50;95%CI,1.14 - 1.97)。在额外调整病情加重史后,这些关联仍然显著。较低的血清IgG与患有COPD或有COPD风险者的病情加重存在前瞻性关联。在亚类中,较低的IgG1和IgG2与严重病情加重存在前瞻性关联。最佳IgG临界值远高于传统的缺乏临界值,这表明体液免疫的细微损害可能与病情加重有关。