» Articles » PMID: 33671490

Metabolic Diseases and Down Syndrome: How Are They Linked Together?

Overview
Journal Biomedicines
Date 2021 Mar 6
PMID 33671490
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Down syndrome is a genetic disorder caused by the presence of a third copy of chromosome 21, associated with intellectual disabilities. Down syndrome is associated with anomalies of both the nervous and endocrine systems. Over the past decades, dramatic advances in Down syndrome research and treatment have helped to extend the life expectancy of these patients. Improved life expectancy is obviously a positive outcome, but it is accompanied with the need to address previously overlooked complications and comorbidities of Down syndrome, including obesity and diabetes, in order to improve the quality of life of Down syndrome patients. In this focused review, we describe the associations between Down syndrome and comorbidities, obesity and diabetes, and we discuss the understanding of proposed mechanisms for the association of Down syndrome with metabolic disorders. Drawing molecular mechanisms through which Type 1 diabetes and Type 2 diabetes could be linked to Down syndrome could allow identification of novel drug targets and provide therapeutic solutions to limit the development of metabolic and cognitive disorders.

Citing Articles

Down syndrome and DYRK1A overexpression: relationships and future therapeutic directions.

Murphy A, Wilton S, Aung-Htut M, McIntosh C Front Mol Neurosci. 2024; 17:1391564.

PMID: 39114642 PMC: 11303307. DOI: 10.3389/fnmol.2024.1391564.


Trisomy 21-driven metabolite alterations are linked to cellular injuries in Down syndrome.

Liu J, Chen S, Huang G, Wen P, Zhou X, Wu Y Cell Mol Life Sci. 2024; 81(1):112.

PMID: 38433139 PMC: 10909777. DOI: 10.1007/s00018-024-05127-0.


Autoimmune, Autoinflammatory Disease and Cutaneous Malignancy Associations with Hidradenitis Suppurativa: A Cross-Sectional Study.

Brydges H, Onuh O, Friedman R, Barrett J, Betensky R, Lu C Am J Clin Dermatol. 2024; 25(3):473-484.

PMID: 38337127 DOI: 10.1007/s40257-024-00844-5.


Motor Skills and Executive Functions in Pediatric Patients with Down Syndrome: A Challenge for Tailoring Physical Activity Interventions.

Vandoni M, Giuriato M, Pirazzi A, Zanelli S, Gaboardi F, Pellino V Pediatr Rep. 2023; 15(4):691-706.

PMID: 37987287 PMC: 10661287. DOI: 10.3390/pediatric15040062.


Metabolic syndrome: Nutri-epigenetic cause or consequence?.

Silva-Ochoa A, Velastegui E, Falconi I, Garcia-Solorzano V, Rendon-Riofrio A, Sanguna-Soliz G Heliyon. 2023; 9(11):e21106.

PMID: 37954272 PMC: 10637881. DOI: 10.1016/j.heliyon.2023.e21106.


References
1.
Osaili T, Attlee A, Naveed H, Maklai H, Mahmoud M, Hamadeh N . Physical Status and Parent-Child Feeding Behaviours in Children and Adolescents with Down Syndrome in The United Arab Emirates. Int J Environ Res Public Health. 2019; 16(13). PMC: 6650949. DOI: 10.3390/ijerph16132264. View

2.
Okamoto Y, Folco E, Minami M, Wara A, Feinberg M, Sukhova G . Adiponectin inhibits the production of CXC receptor 3 chemokine ligands in macrophages and reduces T-lymphocyte recruitment in atherogenesis. Circ Res. 2007; 102(2):218-25. DOI: 10.1161/CIRCRESAHA.107.164988. View

3.
Peiris H, Raghupathi R, Jessup C, Zanin M, Mohanasundaram D, Mackenzie K . Increased expression of the glucose-responsive gene, RCAN1, causes hypoinsulinemia, β-cell dysfunction, and diabetes. Endocrinology. 2012; 153(11):5212-21. DOI: 10.1210/en.2011-2149. View

4.
Bergholdt R, Eising S, Nerup J, Pociot F . Increased prevalence of Down's syndrome in individuals with type 1 diabetes in Denmark: A nationwide population-based study. Diabetologia. 2006; 49(6):1179-82. DOI: 10.1007/s00125-006-0231-6. View

5.
Nordstrom M, Paus B, Andersen L, Kolset S . Dietary aspects related to health and obesity in Williams syndrome, Down syndrome, and Prader-Willi syndrome. Food Nutr Res. 2015; 59:25487. PMC: 4317472. DOI: 10.3402/fnr.v59.25487. View