Carotenoids in familial hypobetalipoproteinemia disorders: Malabsorption in Caco2 cell models and severe deficiency in patients.

Abetalipoproteinemia Carotenoid absorption Chylomicron retention disease Familial hypocholesterolemia Lutein Zeaxanthin

Journal

Journal of clinical lipidology
ISSN: 1933-2874
Titre abrégé: J Clin Lipidol
Pays: United States
ID NLM: 101300157

Informations de publication

Date de publication:
04 Nov 2023
Historique:
received: 02 06 2023
revised: 17 10 2023
accepted: 21 10 2023
medline: 22 11 2023
pubmed: 22 11 2023
entrez: 21 11 2023
Statut: aheadofprint

Résumé

Familial hypobetalipoproteinemias (FHBL) are rare genetic diseases characterized by lipid malabsorption. We focused on abetalipoproteinemia (FHBL-SD1) and chylomicron retention disease (FHBL-SD3), caused by mutations in MTTP and SAR1B genes, respectively. Treatments include a low-fat diet and high-dose fat-soluble vitamin supplementations. However, patients are not supplemented in carotenoids, a group of lipid-soluble pigments essential for eye health. Our aim was to evaluate carotenoid absorption and status in the context of hypobetalipoproteinemia. We first used knock-out Caco-2/TC7 cell models of FHBL-SD1 and FHBL-SD3 to evaluate carotenoid absorption. We then characterized FHBL-SD1 and FHBL-SD3 patient status in the main dietary carotenoids and compared it to that of control subjects. In vitro results showed a significant decrease in basolateral secretion of α- and β-carotene, lutein, and zeaxanthin (-88.8 ± 2.2 % to -95.3 ± 5.8 %, -79.2 ± 4.4 % to -96.1 ± 2.6 %, -91.0 ± 4.5 % to -96.7 ± 0.3 % and -65.4 ± 3.6 % to -96.6 ± 1.9 %, respectively). Carotenoids plasma levels in patients confirmed significant deficiencies, with decreases ranging from -89 % for zeaxanthin to -98 % for α-carotene, compared to control subjects. Given the continuous loss in visual function despite fat-soluble vitamin treatment in some patients, carotenoid supplementation may be of clinical utility. Future studies should assess the correlation between carotenoid status and visual function in aging patients and investigate whether carotenoid supplementation could prevent their visual impairment.

Sections du résumé

BACKGROUND BACKGROUND
Familial hypobetalipoproteinemias (FHBL) are rare genetic diseases characterized by lipid malabsorption. We focused on abetalipoproteinemia (FHBL-SD1) and chylomicron retention disease (FHBL-SD3), caused by mutations in MTTP and SAR1B genes, respectively. Treatments include a low-fat diet and high-dose fat-soluble vitamin supplementations. However, patients are not supplemented in carotenoids, a group of lipid-soluble pigments essential for eye health.
OBJECTIVE OBJECTIVE
Our aim was to evaluate carotenoid absorption and status in the context of hypobetalipoproteinemia.
METHODS METHODS
We first used knock-out Caco-2/TC7 cell models of FHBL-SD1 and FHBL-SD3 to evaluate carotenoid absorption. We then characterized FHBL-SD1 and FHBL-SD3 patient status in the main dietary carotenoids and compared it to that of control subjects.
RESULTS RESULTS
In vitro results showed a significant decrease in basolateral secretion of α- and β-carotene, lutein, and zeaxanthin (-88.8 ± 2.2 % to -95.3 ± 5.8 %, -79.2 ± 4.4 % to -96.1 ± 2.6 %, -91.0 ± 4.5 % to -96.7 ± 0.3 % and -65.4 ± 3.6 % to -96.6 ± 1.9 %, respectively). Carotenoids plasma levels in patients confirmed significant deficiencies, with decreases ranging from -89 % for zeaxanthin to -98 % for α-carotene, compared to control subjects.
CONCLUSION CONCLUSIONS
Given the continuous loss in visual function despite fat-soluble vitamin treatment in some patients, carotenoid supplementation may be of clinical utility. Future studies should assess the correlation between carotenoid status and visual function in aging patients and investigate whether carotenoid supplementation could prevent their visual impairment.

Identifiants

pubmed: 37989694
pii: S1933-2874(23)00312-4
doi: 10.1016/j.jacl.2023.10.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 National Lipid Association. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Claire Bordat (C)

Aix-Marseille Université, INRAE, INSERM, C2VN, Marseille, France (Dr Bordat, Halimi, Drs Vairo, Reboul); Univ-Lyon, CarMeN laboratory, INSERM U1060, INRAE 1397, Université Claude Bernard Lyon-1, Pierre Benite 69495, France (Drs Bordat, Peretti).

Charlotte Cuerq (C)

Biochemistry Department, Hospices Civils de Lyon, Pierre-Benite 69495, France (Drs Cuerq, Blond).

Charlotte Halimi (C)

Aix-Marseille Université, INRAE, INSERM, C2VN, Marseille, France (Dr Bordat, Halimi, Drs Vairo, Reboul).

Donato Vairo (D)

Aix-Marseille Université, INRAE, INSERM, C2VN, Marseille, France (Dr Bordat, Halimi, Drs Vairo, Reboul).

Emilie Blond (E)

Biochemistry Department, Hospices Civils de Lyon, Pierre-Benite 69495, France (Drs Cuerq, Blond).

Liora Restier (L)

Pediatric Hepato-Gastroenterology and Nutrition Unit, Hôpital Femme Mère Enfant de Lyon HFME, Hospices Civils de Lyon HCL, Bron 69677, France (Drs Restier, Poinsot, Duclaux-Loras, Peretti).

Pierre Poinsot (P)

Pediatric Hepato-Gastroenterology and Nutrition Unit, Hôpital Femme Mère Enfant de Lyon HFME, Hospices Civils de Lyon HCL, Bron 69677, France (Drs Restier, Poinsot, Duclaux-Loras, Peretti).

Rémi Duclaux-Loras (R)

Pediatric Hepato-Gastroenterology and Nutrition Unit, Hôpital Femme Mère Enfant de Lyon HFME, Hospices Civils de Lyon HCL, Bron 69677, France (Drs Restier, Poinsot, Duclaux-Loras, Peretti).

Noël Peretti (N)

Univ-Lyon, CarMeN laboratory, INSERM U1060, INRAE 1397, Université Claude Bernard Lyon-1, Pierre Benite 69495, France (Drs Bordat, Peretti); Pediatric Hepato-Gastroenterology and Nutrition Unit, Hôpital Femme Mère Enfant de Lyon HFME, Hospices Civils de Lyon HCL, Bron 69677, France (Drs Restier, Poinsot, Duclaux-Loras, Peretti); CENS ELI-2D, 165 Chemin du Grand Revoyet, Pierre Bénite F - 69310, France (Dr Peretti).

Emmanuelle Reboul (E)

Aix-Marseille Université, INRAE, INSERM, C2VN, Marseille, France (Dr Bordat, Halimi, Drs Vairo, Reboul). Electronic address: Emmanuelle.Reboul@univ-amu.fr.

Classifications MeSH