Genetic Enteropathies Linked to Epithelial Structural Abnormalities and Enteroendocrine Deficiency: A Systematic Review.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
01 06 2021
Historique:
entrez: 12 5 2021
pubmed: 13 5 2021
medline: 10 7 2021
Statut: ppublish

Résumé

Congenital diarrhea and enteropathies linked to epithelial structural abnormalities constitute 3 different rare diseases: the tufting enteropathies (TE; EPCAM and SPINT2 mutations), microvillous inclusion disease (MVID; MYO5B and STX3 mutations), and tricho-hepato-enteric syndrome (THE; TTC37 and SKIV2L mutations). Moreover, enteroendocrine deficiencies (ED; PCSK1 and NEUROG3 mutations) share common clinical characteristics with TE, THE, and MVID in that the treatment requires, in most cases, long-term parenteral nutrition. Although numerous cases have been reported in the literature, aggregated data on morbidity and mortality are missing owing to the rarity of the diseases. We performed a systematic review of all published cases and retrieved 86 articles describing 323 patients (164 boys and 135 girls). The mortality rate was 20.28%, with a median age at death of 13.5 months (range 0-228 months); the mortality risk was 30.8/1000 person-year; in half of the cases, death was caused by infections. Parenteral nutrition was required in 95.4% of patients and weaning off from parenteral nutrition was achieved in 29.35% at a median age of 23 months (range 3.3-276 months). The patients with ED linked to PCSK1 were nearly all weaned at a median age of 14 months, but most of the patients became overweight. MVID patients with MYO5B mutations were most often born preterm. ED linked to NEUROG3 mutation and THE patients usually presented with intrauterine growth retardation. This review presents data from 323 patients with congenital diarrhea linked to EPCAM TE, SPINT2 TE, TTC37 THE, SKIV2L THE, MYO5B MVID, STX3 MVID, NEUROG3 ED, and PCSK1 ED mutations.

Identifiants

pubmed: 33976085
doi: 10.1097/MPG.0000000000003049
pii: 00005176-202106000-00010
doi:

Substances chimiques

Membrane Glycoproteins 0
SPINT2 protein, human 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

826-832

Informations de copyright

Copyright © 2021 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

Références

Thiagarajah JR, Kamin DS, Acra S, et al. PediCODE Consortium. Advances in evaluation of chronic diarrhea in infants. Gastroenterology 2018; 154:2045–2059.
Canani RB, Castaldo G, Bacchetta R, et al. Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies. Nat Rev Gastroenterol Hepatol 2015; 12:293–302.
Wang J, Cortina G, Wu SV, et al. Mutant neurogenin-3 in congenital malabsorptive diarrhea. N Engl J Med 2006; 355:270–280.
Sivagnanam M, Mueller JL, Lee H, et al. Identification of EpCAM as the gene for congenital tufting enteropathy. Gastroenterology 2008; 135:429–537.
Müller T, Hess MW, Schiefermeier N, et al. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. Nat Genet 2008; 40:1163–1165.
Heinz-Erian P, Müller T, Krabichler B, et al. Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea. Am J Hum Genet 2009; 84:188–196.
Hartley JL, Zachos NC, Dawood B, et al. Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy). Gastroenterology 2010; 138:2388–2398.
Fabre A, Charroux B, Martinez-Vinson C, et al. SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome. Am J Hum Genet 2012; 90:689–692.
Jackson RS, Creemers JW, Farooqi IS, et al. Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency. J Clin Invest 2003; 112:1550–1560.
Wiegerinck CL, Janecke AR, Schneeberger K, et al. Loss of syntaxin 3 causes variant microvillus inclusion disease. Gastroenterology 2014; 147:65–68.
Pépin L, Colin E, Tessarech M, et al. A new case of PCSK1 pathogenic variant with congenital proprotein convertase 1/3 deficiency and literature review. J Clin Endocrinol Metab 2019; 104:985–993.
Girard M, Lacaille F, Verkarre V, et al. MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease. Hepatology 2014; 60:301–310.
Overeem AW, Li Q, Qiu YL, et al. A molecular mechanism underlying genotype-specific intrahepatic cholestasis resulting from MYO5B mutations. Hepatology 2019; 72:213–229.
Fabre A, Petit LM, Hansen LF, et al. A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two families. Am J Med Genet A 2018; 176:727–732.

Auteurs

Morgane Caralli (M)

APHM, Hôpital Timone Enfants, Service de Pédiatrie Multidisciplinaire, Marseille, France.

Celine Roman (C)

APHM, Hôpital Timone Enfants, Service de Pédiatrie Multidisciplinaire, Marseille, France.

Marie-Edith Coste (ME)

APHM, Hôpital Timone Enfants, Service de Pédiatrie Multidisciplinaire, Marseille, France.

Bertrand Roquelaure (B)

APHM, Hôpital Timone Enfants, Service de Pédiatrie Multidisciplinaire, Marseille, France.

Christophe Buffat (C)

APHM, Hôpital de la Conception, Laboratoire de Biochimie et de Biologie Moléculaire, Marseille, France.
APHM Service de Génétique Médicale, Marseille, France.

Patrice Bourgeois (P)

Aix Marseille Univ, INSERM, MMG.
APHM Service de Génétique Médicale, Marseille, France.

Catherine Badens (C)

Aix Marseille Univ, INSERM, MMG.
APHM Service de Génétique Médicale, Marseille, France.

Alexandre Fabre (A)

APHM, Hôpital Timone Enfants, Service de Pédiatrie Multidisciplinaire, Marseille, France.
Aix Marseille Univ, INSERM, MMG.

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