Cerebrospinal Fluid Homovanillic and 5-Hydroxyindoleacetic Acids in a Large Pediatric Population; Establishment of Reference Intervals and Impact of Disease and Medication.


Journal

Clinical chemistry
ISSN: 1530-8561
Titre abrégé: Clin Chem
Pays: England
ID NLM: 9421549

Informations de publication

Date de publication:
27 Sep 2024
Historique:
received: 19 01 2024
accepted: 31 07 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 27 9 2024
Statut: aheadofprint

Résumé

Cerebrospinal fluid (CSF) homovanillic (HVA), and 5-hydroxyindoleacetic acids (5-HIAA) are biomarkers of neurological diseases affecting the dopaminergic and serotoninergic pathways. Establishing reference intervals for these metabolites faces the challenges of a lack of healthy controls and a negative correlation with age, making stratified intervals unrealistic. We propose a pipeline to determine continuous reference intervals for HVA and 5-HIAA using an indirect method. We also studied the confounding effects of different variables and explored the impact of antiepileptic and neuroleptic treatments on HVA and 5-HIAA values. The study used least squares regression to fit age-concentration curves from a cohort of pediatric patients (n = 1533), where the residuals represent metabolite values excluding age effect. Presuming that HVA and 5-HIAA primary deficiencies characterize a distinct subpopulation, we fitted a two-component finite mixture model in age-normalized data and set reference intervals at the central 95% of the nondeficient population. Patients with primary genetic deficiencies of HVA and/or 5-HIAA consistently fall outside the proposed continuous reference intervals. Using the new continuous reference intervals reduces the number of secondary deficiencies detected compared with using stratified values. No correlations were observed between CSF HVA and 5-HIAA values across the studied drug categories (antiseizure and neuroleptic medications). In addition, biopterin values positively influenced both metabolite concentrations. The proposed continuous reference intervals caused a substantial reduction in the number of secondary deficiencies detected, most of which demonstrated no conclusive correlations between the diseases and altered HVA and 5-HIAA values.

Sections du résumé

BACKGROUND BACKGROUND
Cerebrospinal fluid (CSF) homovanillic (HVA), and 5-hydroxyindoleacetic acids (5-HIAA) are biomarkers of neurological diseases affecting the dopaminergic and serotoninergic pathways. Establishing reference intervals for these metabolites faces the challenges of a lack of healthy controls and a negative correlation with age, making stratified intervals unrealistic. We propose a pipeline to determine continuous reference intervals for HVA and 5-HIAA using an indirect method. We also studied the confounding effects of different variables and explored the impact of antiepileptic and neuroleptic treatments on HVA and 5-HIAA values.
METHODS METHODS
The study used least squares regression to fit age-concentration curves from a cohort of pediatric patients (n = 1533), where the residuals represent metabolite values excluding age effect. Presuming that HVA and 5-HIAA primary deficiencies characterize a distinct subpopulation, we fitted a two-component finite mixture model in age-normalized data and set reference intervals at the central 95% of the nondeficient population.
RESULTS RESULTS
Patients with primary genetic deficiencies of HVA and/or 5-HIAA consistently fall outside the proposed continuous reference intervals. Using the new continuous reference intervals reduces the number of secondary deficiencies detected compared with using stratified values. No correlations were observed between CSF HVA and 5-HIAA values across the studied drug categories (antiseizure and neuroleptic medications). In addition, biopterin values positively influenced both metabolite concentrations.
CONCLUSION CONCLUSIONS
The proposed continuous reference intervals caused a substantial reduction in the number of secondary deficiencies detected, most of which demonstrated no conclusive correlations between the diseases and altered HVA and 5-HIAA values.

Identifiants

pubmed: 39331696
pii: 7781974
doi: 10.1093/clinchem/hvae139
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Association for Diagnostics & Laboratory Medicine 2024. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Helena Rodriguez-Gonzalez (H)

Clinical Biochemistry Department, Hospital Sant Joan de Déu, Barcelona, Spain.
B2SLab, Departament d'Enginyeria de Sistemes, Automàtica i Informàtica Industrial, Universitat Politècnica de Catalunya, Barcelona, Spain.
Networking Biomedical Research Centre in the subject area of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.

Aida Ormazabal (A)

Clinical Biochemistry Department, Hospital Sant Joan de Déu, Barcelona, Spain.
Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.

Mercedes Casado (M)

Clinical Biochemistry Department, Hospital Sant Joan de Déu, Barcelona, Spain.
Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.

Angela Y Arias (AY)

Clinical Biochemistry Department, Hospital Sant Joan de Déu, Barcelona, Spain.

Clara Oliva (C)

Departament de Bioquímica Clinica, Institut de Bioquímica Clínica, Centre de Diagnostic Biomedic, Hospital Clinic, Barcelona, Spain.

Maria Barranco-Altirriba (M)

B2SLab, Departament d'Enginyeria de Sistemes, Automàtica i Informàtica Industrial, Universitat Politècnica de Catalunya, Barcelona, Spain.
Networking Biomedical Research Centre in the subject area of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.

Ricard Casadevall (R)

Dirección de Estrategia Digital y Datos, Hospital Sant Joan de Déu, Barcelona, Spain.

Francesc García-Cuyas (F)

Dirección de Estrategia Digital y Datos, Hospital Sant Joan de Déu, Barcelona, Spain.

Andrés Nascimento (A)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Carlos Ortez (C)

Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Daniel Natera-de Benito (D)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Thais Armangué (T)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Maria M O'Callaghan (MM)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Natalia Juliá-Palacios (N)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Alejandra Darling (A)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Juan Darío Ortigoza-Escobar (JD)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Carmen Fons (C)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Angels García-Cazorla (A)

Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.
Pediatric Neurology Department, Neuromuscular and Applied Research in Neuromuscular Diseases Units, Neurometabolic Unit, Movement Disorders Unit, Synaptic Metabolism Lab, MetabERN, EpiCARE and ERN-RND, Hospital Sant Joan de Déu, Barcelona, Spain.

Alexandre Perera-Lluna (A)

B2SLab, Departament d'Enginyeria de Sistemes, Automàtica i Informàtica Industrial, Universitat Politècnica de Catalunya, Barcelona, Spain.
Networking Biomedical Research Centre in the subject area of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.
Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.

Rafael Artuch (R)

Clinical Biochemistry Department, Hospital Sant Joan de Déu, Barcelona, Spain.
Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.
Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Barcelona, Spain.

Classifications MeSH