# Patient-reported disease burden and health care utilization of HAE-nl-C1INH: insights from a real-world survey

**Authors:** Douglas Jones, Nihal Narsipur, Sally W. Wade, Joseph R. Harper, Nami Park, Philippe Adams, Anurag Relan, Amanda Harrington, John Anderson

PMC · DOI: 10.1007/s10238-025-02010-5 · Clinical and Experimental Medicine · 2026-01-14

## TL;DR

People with HAE-nl-C1INH experience a heavier disease burden and more frequent symptoms compared to those with HAE Type 1/2, according to a real-world survey.

## Contribution

This study provides new insights into the distinct disease burden and healthcare utilization patterns in HAE-nl-C1INH compared to other HAE types.

## Key findings

- Participants with HAE-nl-C1INH had higher odds of frequent HAE attacks and orofacial-laryngeal swelling.
- HAE-nl-C1INH patients had worse health-related quality of life scores and more frequent doctor visits.
- They also had higher odds of having multiple concomitant conditions.

## Abstract

Hereditary angioedema (HAE), a rare genetic disorder, is classified into 3 types: Type 1 (low C1 esterase inhibitor [C1-INH]), Type 2 (dysfunctional C1-INH), and HAE-nl-C1INH (normal C1-INH levels). This study aimed to compare characteristics among individuals with HAE Type 1/2 and HAE-nl-C1INH. A cross-sectional online survey was conducted (June 2020–September 2021) among adults with HAE to capture various patient-specific data and health care utilization. Statistical analyses included Fisher exact test, t test, and odds ratios (OR) with 95% confidence intervals (CI). Eighty-nine participants were included (HAE Type 1/2, n = 44; HAE-nl-C1INH, n = 45). No significant differences in demographics, treatment characteristics, and HAE triggers were observed between groups. Participants with HAE-nl-C1INH were less likely to be diagnosed before 18 years of age (4% vs. 32%; OR, 0.10; 95% CI, 0.02–0.50) and had higher odds of experiencing frequent HAE attacks (47% vs. 14%; OR, 5.5; 95% CI, 2.0–15.7) than those with HAE Type 1/2. Participants with HAE-nl-C1INH also had increased odds of orofacial-laryngeal swelling (31% vs. 16%; OR, 2.3; 95% CI, 1.1–4.7), more frequent doctor visits (> 1 visit/month: 31% vs. 11%; OR, 3.5; 95% CI, 1.1–10.8), and more concomitant conditions (93% vs. 77%; OR, 3.8; 95% CI, 1.6–9.2). The total health-related quality of life score was significantly worse in participants with HAE-nl-C1INH (53.6 vs. 38.2; p = 0.0001). Participants with HAE-nl-C1INH experience a significantly greater disease burden than those with HAE Type 1/2, emphasizing the need for improved diagnosis, targeted treatment strategies, and a deeper understanding of the prevalence and pathophysiology of HAE-nl-C1INH.

## Linked entities

- **Proteins:** SERPING1 (serpin family G member 1)
- **Diseases:** Hereditary angioedema (MONDO:0019623), HAE (MONDO:0019623)

## Full-text entities

- **Genes:** SERPING1 (serpin family G member 1) [NCBI Gene 710] {aka C1IN, C1INH, C1NH, HAE1, HAE2}
- **Diseases:** genetic disorder (MESH:D030342), HAE Type 1/2 (MESH:D056829), HAE (MESH:D054179), orofacial-laryngeal swelling (MESH:D007819)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12819523/full.md

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Source: https://tomesphere.com/paper/PMC12819523