Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall
BACKGROUND: Oxysterols (cholestane-3β,5α,6β-triol and 7-ketocholesterol) and N-palmitoyl-O-phosphocholineserine (PPCS) are sensitive biomarkers for Niemann-Pick disease type C (NPC) screening. However, false-positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or other inborn errors of metabolism. OBJECTIVE: To identify causes of false-positive biomarker profiles mimicking NPC. METHODS: We conducted a multicenter retrospective study of 15 patients with false-positive oxysterols and PPCS profiles referred between 2017 and 2022 to two French NPC reference laboratories. Clinical data were collected via standardized chart review. The impact of Sertraline on NPC-like biological features was evaluated using the filipin test in fibroblasts and biomarker analysis in sertraline-treated patients. RESULTS: Thirteen of 15 patients with false-positive biomarkers were treated with sertraline. Two patients who discontinued sertraline showed normalization of biomarkers. The filipin test revealed that Sertraline disrupts intracellular cholesterol trafficking, a hallmark of NPC cellular features. Finally, among 47 sertraline-treated patients without NPC-suspicion, 26 (55%) had biomarker profile mimicking NPC. INTERPRETATION: Sertraline use is frequently associated with elevated biomarkers that mimic NPC, representing a primary cause of false-positive results in NPC screening. Genetic analysis of NPC1 and NPC2 remains essential to confirm NPC diagnosis. Most sertraline-treated patients with false-positive biomarkers presented predominantly atypical psychiatric symptoms, though one exhibited a clinical picture highly suggestive of NPC following prolonged sertraline exposure. The long-term clinical effects of sertraline use need further evaluation.
Authors
- Daniele Mandia (ORCID: https://orcid.org/0000-0003-4069-0483)
- Magali Pettazzoni (ORCID: https://orcid.org/0000-0002-9569-912X)
- N. Schleinitz (ORCID: https://orcid.org/0000-0001-9449-3392)
- Olivier Flabeau
- Yann Nadjar (ORCID: https://orcid.org/0000-0003-1466-6957)
- Claudine Laurent‐Levinson (ORCID: https://orcid.org/0000-0001-6550-3635)
- Carole Lacout (ORCID: https://orcid.org/0000-0003-2875-6048)
- Isabelle Rouvet (ORCID: https://orcid.org/0000-0002-8881-4396)
- Giulia Dingeo (ORCID: https://orcid.org/0000-0001-8787-8526)
- C. Gourguechon (ORCID: https://orcid.org/0000-0003-0740-2419)
- Jérôme Guitton (ORCID: https://orcid.org/0000-0001-6180-5708)
- Cécile Pagan
- Maria Makrygianni (ORCID: https://orcid.org/0000-0002-1204-2529)
- Antony Citterio-Quentin
- Foudil Lamari
- Bénédicte Héron
- Samia Pichard
- Florient Potier
- Cyril Hanin
- Elsa Besse‐Pinot
Institutions
- Hôpital Necker-Enfants Malades (FR)
- Sorbonne Université (FR)
- Hôpital Armand-Trousseau (FR)
- Assistance Publique Hôpitaux de Marseille (FR)
- Centre de Référence Déficits Immunitaires Héréditaires (FR)
- Centre de Recherche en Neurosciences de Lyon (FR)
- Centre Hospitalier Universitaire Amiens-Picardie (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Hospices Civils de Lyon (FR)
- University of Clermont Auvergne (FR)
- Institut de Myologie (FR)
- Pitié-Salpêtrière Hospital (FR)
- Hygeia Hospital (GR)
- Centre Hospitalier de la Côte Basque (FR)
- Centre Hospitalier Universitaire de Clermont-Ferrand (FR)
- Hôpital de la Timone (FR)
- Université d'Angers (FR)
Publication Details
- Journal
- Annals of Clinical and Translational Neurology
- Published
- 2026-04-27
- DOI
- https://doi.org/10.1002/acn3.70411
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00