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Abstract Number: 071

The Association Between Age at Diagnosis and Health-Related Quality of Life in Takayasu Arteritis

Jessica Bloom1, Kaci Pickett-Nairne2, Lori Silveira2, Cristina Burroughs3, Katrina Bargender4, Amy Bolton5, Christine Yeung6, Jennifer Gordon5, Peter A. Merkel7 and Karen James8, 1University of Colorado Aurora, CO, 2University of Colorado, 3University of South Florida, 4Vasculitis Patient-Powered Research Network, Caledonia, WI, 5Vasculitis Patient-Powered Research Network, 6University of Pennsylvania, 7University of Pennsylvania, Philadelphia, United Kingdom, 8University of Utah, Salt Lake City, UT

Meeting: 2026 Pediatric Rheumatology Symposium

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Session Information

Date: Thursday, March 19, 2026

Title: Posters: Special Category: Patient Engagement

Session Time: 6:00PM-7:00PM

Background/Purpose: Takayasu arteritis (TAK) can occur throughout the lifespan and impacts health-related quality of life (HRQoL). This study examined the relationship between age at diagnosis of TAK and HRQoL.

Methods: The source of data was a longitudinal, prospective cohort of patients with TAK followed in the physician- and patient-led Vasculitis Patient-Powered Research Network (VPPRN, online patient-reported data). The cohort was stratified by age at diagnosis: < 40 years (younger) and ≥ 40 years (older). Descriptive statistics were summarized. Univariable and multivariable linear regressions assessed associations between age at diagnosis and Patient-Reported Outcomes Measurement Information System (PROMIS) scores. The multivariable model adjusted for glucocorticoid use and age at HRQoL assessment.

Results: Analysis included 202 patients with TAK, 139 (68.8%) diagnosed at a younger age and 63 (31.2%) at an older age (Table 1). Both cohorts had a similar proportion of females (95%) and length of follow up at quality of life assessment (11.3 and 11.7 years respectively). Glucocorticoid use impacted HRQoL. In univariable analyses, only HRQoL scores related to sleep disturbance and physical functioning differed by age at diagnosis (Table 1). When adjusted, the HRQoL score related to sleep disturbance for those diagnosed younger was estimated to be 3.84 points lower (i.e. better) than those diagnosed older (95%CI: [-7.35, -0.34], p < 0.03), with no difference in HRQoL scores related to fatigue, depression, pain interference, satisfaction with participation in social roles, physical functioning, or anxiety between age at diagnosis groups (Table 2).

Conclusion: Compared to patients diagnosed with TAK at older ages, those diagnosed at younger ages have better HRQoL related to sleep disturbance and similar HRQoL related to fatigue, depression, pain interference, satisfaction with participation in social roles, physical functioning, and anxiety. Glucocorticoid use impacts the HRQoL of patients with TAK. Future studies of larger cohorts are needed during childhood and young adulthood to further assess the impact of age at diagnosis on HRQoL and guide interventional tools for people with TAK.

Table 1. Characteristics of patients with Takayasu Arteritis based on age at diagnosis.Supporting image 1Unknown or missing responses for each score were not included. *Statistical significance was set at 0.05.

Table 2. Multivariable analysis of differences in Patient-Reported Outcomes Measurement Information System scores based on age at diagnosis.Supporting image 2PROMIS, Patient-Reported Outcomes Measurement Information System. HRQoL, health-related quality of life.
Unknown or missing responses for each score were not included. *Statistical significance was set at 0.05.
‡Differences in scores between age at diagnosis groups were assessed via multivariable linear regression adjusting for age at time of quality-of-life assessment and glucocorticoid use if significant in the univariable analysis at p < 0.05 level. Sex was left out of univariable model due to the majority of patients being female. If the confidence interval includes zero, the difference is not significant. A positive estimated difference in scores represents a higher score for younger age at diagnosis than older age at diagnosis, while a negative difference represents a lower score in younger age at diagnosis than older age at diagnosis.


Disclosures: J. Bloom: None; K. Pickett-Nairne: None; L. Silveira: None; C. Burroughs: None; K. Bargender: None; A. Bolton: None; C. Yeung: None; J. Gordon: None; P. Merkel: AbbVie/Abbott, 2, 5, Alpine Pharmaceuticals, 2, Amgen, 2, 5, argenx, 2, AstraZeneca, 2, 5, Boehringer-Ingelheim, 2, 5, Bristol-Myers Squibb(BMS), 2, 5, CSL Behring, 2, Eicos, 5, Electra, 5, GlaxoSmithKlein(GSK), 2, 5, iCell, 2, Interius BioTherapeutics, 2, Kinevant Sciences, 2, Kyverna, 2, 11, Lifordi, 11, Metagenomi, 2, Neutrolis, 2, 5, Novartis, 2, NS Pharma, 2, Q32 Bio, 2, 11, Quell Therapeutics, 2, Regeneron Pharmaceuticals, 2, Sanofi, 2, Sparrow Pharmaceuticals, 2, 11, Takeda Pharmaceuticals, 2, 5, Visterra, 2; K. James: Sobi, 1.

To cite this abstract in AMA style:

Bloom J, Pickett-Nairne K, Silveira L, Burroughs C, Bargender K, Bolton A, Yeung C, Gordon J, Merkel P, James K. The Association Between Age at Diagnosis and Health-Related Quality of Life in Takayasu Arteritis [abstract]. Arthritis Rheumatol. 2026; 78 (suppl 3). https://acrabstracts.org/abstract/the-association-between-age-at-diagnosis-and-health-related-quality-of-life-in-takayasu-arteritis/. Accessed .
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All abstracts accepted to PRYSM are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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