N-Acetylcysteine for Hereditary Cystatin C Amyloid Angiopathy

Key Information
Year
2025
summary/abstract

Key Points

Question

What is the safety, tolerability, and efficacy of N-acetylcysteine (NAC) for patients with hereditary cystatin C amyloid angiopathy (HCCAA)?

Findings

In this open-label, nonrandomized clinical trial of 17 participants carrying the L68Q-CST3 sequence variation with HCCAA, high-dose NAC therapy reduced levels of biomarkers of disease progression in skin and plasma. NAC was safe and well tolerated; a total of 5 cerebrovascular bleeds occurred during the study without permanent neurological sequela.

Meaning

Data from this open-label phase 2a nonrandomized clinical trial support the safety and potential efficacy of NAC as a therapeutic treatment of neurological consequences in patients with HCCAA.

Abstract

Importance

Hereditary cystatin C amyloid angiopathy (HCCAA) is a lethal, dominantly inherited disease primarily affecting Icelandic young adults that leads to severe cerebral amyloid angiopathy, with no effective therapy.

Objective

To investigate safety, tolerance, and therapeutic potential of N-acetylcysteine (NAC) in lowering disease-associated biomarkers in sequence variation carriers.

Design, Setting, and Participants

This phase 2a open-label clinical trial was conducted from March 2019 to December 2021 at a single study center at Landspitali University Hospital in Reykjavik, Iceland, and included 17 confirmed carriers of the L68Q-CST3 sequence variation.

Intervention

High-dose NAC treatment was administered at 2400 mg daily for 9 months. Participants underwent regular monitoring for hemorrhages and disease progression, including blood and skin biopsy samples obtained every 3 months for biomarker testing.

Main Outcomes and Measures

The primary outcomes were drug tolerability and safety, cognitive status, and reduction in disease-associated biomarkers in skin biopsies. Secondary outcomes included changes in blood and plasma biomarker levels.

Results

Of 17 carriers treated, 6 were male and 11 were female, and mean (SD) participant age was 40.0 (4.2) years. Analysis of the primary outcomes showed that NAC was safe and well tolerated. Five cerebral bleeds occurred during the treatment period without permanent neurological sequela; no death occurred. There was significant reduction in median (IQR) disease-specific biomarker levels in skin after treatment, including collagen IV (baseline: 3.69% [2.48%-5.16%]; after treatment: 2.60% [1.99%-2.97%]; P < .001), fibronectin (baseline: 3.17% [2.09%-5.05%]; after treatment: 2.37% [1.87%-3.42%]; P = .01), vimentin (baseline: 1.60% [1.24%-2.37%]; after treatment: 1.31% [0.97%-1.68%]; P < .001), and SMAD (baseline: 2.25% [0.55%-4.36%]; after treatment: 1.56% [0.20%-2.54%]; P < .001) via Wilcoxon matched-pairs signed rank test. Secondary outcomes included a significant increase in reduced glutathione levels and decreased high-molecular-weight cystatin C aggregate levels in plasma after NAC treatment.

Conclusions and Relevance

In this single-center nonrandomized clinical trial, NAC was safe and well tolerated and decreased disease-associated biomarker and amyloid deposition, suggesting NAC may offer a preventive strategy against HCCAA.

Trial Registration

ClinicalTrialsRegister.eu Identifier: 2017-004776-56external link, opens in a new tab

DOI
10.1001/jamaneurol.2025.0326
Authors
Asbjorg Osk Snorradottir 1,2, Alvaro Gutierrez-Uzquiza 3,4, Paloma Bragado 3, Michael E March 5, Charlly Kao 5, Enrico Bernardo Arkink 1,6, Solveig Jonsdottir 7, Arna Sigurdardottir 1, Helgi J Isaksson 2, Hekla Liv Mariasdóttir 7, Olga Yr Bjorgvinsdottir 7, Natalia M Kowal 7,8, Hugrun L Heimisdottir 7, Astros Sverrisdottir 9, Astridur Palsdottir 1, Hans Tomas Bjornsson 1,10,11, Hakon Hakonarson 1,5,12,13