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年龄和虚弱对老年抗中性粒细胞胞质抗体相关性血管炎患者发生终末期肾病、死亡和严重感染风险的影响:一项回顾性队列研究。

The effects of age and frailty on the risks of end-stage renal disease, death, and severe infection in older adults with antineutrophil cytoplasmic antibody-associated vasculitis: a retrospective cohort study.

机构信息

Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute, Massachusetts General Hospital, Boston, MA, USA; Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Lancet Rheumatol. 2024 Nov;6(11):e771-e779. doi: 10.1016/S2665-9913(24)00193-0. Epub 2024 Sep 18.

Abstract

BACKGROUND

Frailty, a measure of biological age, might predict poor outcomes in older adults better than chronological age. We aimed to compare the effect of age and frailty on end-stage renal disease, death, and severe infection within 2 years of diagnosis in older adults with incident antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis.

METHODS

This retrospective cohort study included individuals aged 65 years or older from the Mass General Brigham ANCA-associated vasculitis cohort in the USA who were treated between Jan 1, 2002, and Dec 31, 2019. Individuals with a diagnosis of eosinophilic granulomatosis with polyangiitis were excluded from the analysis. Baseline frailty was measured with a claims-based frailty index using data collected in the year before the date of treatment initiation in individuals with at least one health-care encounter before baseline; individuals who did not have an encounter within the 12 months before baseline were classified as pre-frail. Incidence rates of end-stage renal disease or death and severe infections (ie, infections leading to hospital admission or death) at 2 years were estimated, and multivariable analyses were performed to compare the association of age and frailty with these outcomes. Cumulative incidence rates and an additive interaction analysis were used to assess the interaction of age and frailty groupings.

FINDINGS

Of the 234 individuals included, 136 (58%) were women, 98 (42%) were men, 198 (85%) were White, and 198 (85%) were positive for myeloperoxidase-specific ANCA. Frailty was present in 25 (22%) of 116 individuals aged 65-74 years and 44 (37%) of 118 aged 75 years or older. In the multivariable analysis, an age of 75 years or older was associated with an increased risk of end-stage renal disease or death (hazard ratio [HR] 4·50 [95% CI 1·83-11·09]), however, frailty was not (1·08 [0·50-2·36]). Both an age of 75 years or older (HR 2·52 [95% CI 1·26-5·04]) and frailty (8·46 [3·95-18·14]) were independent risk factors for severe infections. The effect of frailty on the incidence of end-stage renal disease or death was greater in individuals aged 65-74 years (frail vs non-frail or pre-frail incidence rate 7·5 cases vs 2·0 cases per 100 person-years) than in those aged 75 years or older (13·5 cases vs 16·0 cases per 100 person-years). The effect of frailty on the incidence of serious infections varied by age, with large differences observed among both individuals aged 65-74 years (frail vs non-frail or pre-frail incidence rate 38·9 cases vs 0·8 cases per 100 person-years) and individuals aged 75 years or older (61·9 cases vs 12·3 cases per 100 person-years). Despite the observed differences between the age groups, the additive interaction terms were not statistically significant for either frailty and end-stage renal disease or death (p for interaction=0·276) or frailty and serious infections (p for interaction=0·650).

INTERPRETATION

Adults with ANCA-associated vasculitis aged 75 years or older had a higher incidence of end-stage renal disease, death, and severe infections within 2 years of diagnosis than adults aged 65-74 years. Frailty, an approximation of biological age, was a risk factor for severe infection. Assessment beyond chronological age could better inform management decisions in older adults with ANCA-associated vasculitis.

FUNDING

National Institutes of Health and National Institute of Arthritis and Musculoskeletal and Skin Diseases.

摘要

背景

衰弱是衡量生物年龄的指标,可能比实际年龄更能预测老年人的不良预后。本研究旨在比较年龄和衰弱对老年新发抗中性粒细胞胞浆抗体(antineutrophil cytoplasmic antibody,ANCA)相关性血管炎患者诊断后 2 年内终末期肾病、死亡和严重感染的影响。

方法

本回顾性队列研究纳入了美国麻省总医院 Brigham 抗中性粒细胞胞浆抗体相关性血管炎队列中年龄≥65 岁的患者,他们在 2002 年 1 月 1 日至 2019 年 12 月 31 日期间接受了治疗。本研究排除了嗜酸粒细胞性肉芽肿伴多血管炎患者。在基线时,使用基于索赔的衰弱指数来测量基线时的衰弱情况,该指数使用了在患者接受治疗前至少有一次医疗就诊的一年中的数据;在基线前 12 个月内没有就诊的患者被归类为衰弱前期。估计了诊断后 2 年内终末期肾病或死亡和严重感染(即导致住院或死亡的感染)的发生率,并进行了多变量分析,以比较年龄和衰弱与这些结局的相关性。使用累积发生率和加性交互分析评估了年龄和衰弱分组之间的交互作用。

结果

在纳入的 234 名患者中,136 名(58%)为女性,98 名(42%)为男性,198 名(85%)为白人,198 名(85%)为髓过氧化物酶特异性抗中性粒细胞胞浆抗体阳性。116 名年龄在 65-74 岁的患者中有 25 名(22%)存在衰弱,118 名年龄在 75 岁或以上的患者中有 44 名(37%)存在衰弱。在多变量分析中,年龄在 75 岁或以上与终末期肾病或死亡的风险增加相关(风险比[hazard ratio,HR]4.50,95%置信区间[confidence interval,CI]1.83-11.09),然而,衰弱并不相关(1.08,0.50-2.36)。年龄在 75 岁或以上(HR 2.52,95%CI 1.26-5.04)和衰弱(HR 8.46,95%CI 3.95-18.14)都是严重感染的独立危险因素。与年龄在 75 岁或以上的患者相比,年龄在 65-74 岁的患者中衰弱对终末期肾病或死亡的发生率的影响更大(衰弱组与非衰弱组或衰弱前期组的发病率分别为 7.5 例和 2.0 例/100 人年)。年龄在 75 岁或以上的患者中,衰弱对严重感染的发生率的影响差异较大(衰弱组与非衰弱组或衰弱前期组的发病率分别为 13.5 例和 16.0 例/100 人年)。严重感染的发生率在年龄组之间存在显著差异,65-74 岁的患者中(衰弱组与非衰弱组或衰弱前期组的发病率分别为 38.9 例和 0.8 例/100 人年)和 75 岁或以上的患者中(衰弱组与非衰弱组或衰弱前期组的发病率分别为 61.9 例和 12.3 例/100 人年)观察到的差异很大。尽管在年龄组之间存在差异,但衰弱与终末期肾病或死亡(交互作用的 p 值为 0.276)或衰弱与严重感染(交互作用的 p 值为 0.650)之间的加性交互作用项没有统计学意义。

结论

与年龄在 65-74 岁的患者相比,75 岁或以上的 ANCA 相关性血管炎患者在诊断后 2 年内终末期肾病、死亡和严重感染的发生率更高。衰弱,一种生物年龄的近似值,是严重感染的危险因素。对年龄以外的因素进行评估可以更好地为老年 ANCA 相关性血管炎患者的管理决策提供信息。

资金来源

美国国立卫生研究院和美国国立关节炎、肌肉骨骼和皮肤病研究所。

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