Veterans Affairs (VA) Nebraska-Western Iowa Health Care System and University of Nebraska Medical Center, Omaha.
VA Boston Cooperative Studies Program Coordinating Center, Boston, Massachusetts.
Arthritis Rheumatol. 2024 Apr;76(4):638-646. doi: 10.1002/art.42731. Epub 2023 Dec 26.
Using trial data comparing treat-to-target allopurinol and febuxostat in gout, we examined participant characteristics associated with serum urate (SU) goal achievement.
Participants with gout and SU ≥6.8 mg/dL were randomized to allopurinol or febuxostat, titrated during weeks 0 to 24, and maintained weeks 25 to 48. Participants were considered to achieve SU goal if the mean SU from weeks 36, 42, and 48 was <6.0 mg/dL or <5 mg/dL if tophi were present. Possible determinants of treatment response were preselected and included sociodemographics, comorbidities, diuretic use, health-related quality of life (HRQoL), body mass index, and gout measures. Determinants of SU response were assessed using multivariable logistic regression with additional analyses to account for treatment adherence.
Of 764 study participants completing week 48, 618 (81%) achieved SU goal. After multivariable adjustment, factors associated with a greater likelihood of SU goal achievement included older age (adjusted odds ratio [aOR] 1.40 per 10 years), higher education (aOR 2.02), and better HRQoL (aOR 1.17 per 0.1 unit). Factors associated with a lower odds of SU goal achievement included non-White race (aORs 0.32-0.47), higher baseline SU (aOR 0.83 per 1 mg/dL), presence of tophi (aOR 0.29), and the use of diuretics (aOR 0.52). Comorbidities including chronic kidney disease, hypertension, diabetes, and cardiovascular disease were not associated with SU goal achievement. Results were not meaningfully changed in analyses accounting for adherence.
Several patient-level factors were predictive of SU goal achievement among patients with gout who received treat-to-target urate-lowering therapy (ULT). Approaches that accurately predict individual responses to treat-to-target ULT hold promise in facilitating personalized management and improving outcomes in patients with gout.
利用比较靶向治疗别嘌醇和非布司他治疗痛风的试验数据,我们研究了与血清尿酸(SU)达标相关的参与者特征。
SU≥6.8mg/dL 的痛风患者被随机分为别嘌醇或非布司他组,在第 0 至 24 周进行滴定治疗,并在第 25 至 48 周维持治疗。如果第 36、42 和 48 周的平均 SU<6.0mg/dL 或存在痛风石时<5mg/dL,则认为患者达到 SU 目标。预先选择了可能的治疗反应决定因素,包括社会人口统计学特征、合并症、利尿剂使用、健康相关生活质量(HRQoL)、体重指数和痛风指标。使用多变量逻辑回归评估 SU 反应的决定因素,并进行了额外的分析以考虑治疗依从性。
在完成第 48 周的 764 名研究参与者中,有 618 名(81%)达到 SU 目标。经过多变量调整,与 SU 目标达成更有可能相关的因素包括年龄较大(每增加 10 岁,调整后的优势比[aOR]为 1.40)、受教育程度较高(aOR 为 2.02)和更好的 HRQoL(aOR 为每 0.1 单位增加 1.17)。与 SU 目标达成可能性降低相关的因素包括非白种人(aOR 为 0.32-0.47)、较高的基线 SU(aOR 为每增加 1mg/dL 为 0.83)、存在痛风石(aOR 为 0.29)和使用利尿剂(aOR 为 0.52)。合并症包括慢性肾脏病、高血压、糖尿病和心血管疾病与 SU 目标达成无关。在考虑到依从性的分析中,结果没有明显变化。
在接受降尿酸治疗(ULT)的痛风患者中,有几个患者水平的因素可预测 SU 目标的达成。准确预测个体化对 ULT 治疗的反应的方法有望在促进痛风患者的个体化管理和改善结局方面发挥作用。