The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management - PubMed (original) (raw)
Review
doi: 10.1016/S2213-8587(13)70191-8. Epub 2013 Dec 23.
Henry N Ginsberg 2, M John Chapman 3, Børge G Nordestgaard 4, Jan Albert Kuivenhoven 5, Maurizio Averna 6, Jan Borén 7, Eric Bruckert 8, Alberico L Catapano 9, Olivier S Descamps 10, G Kees Hovingh 11, Steve E Humphries 12, Petri T Kovanen 13, Luis Masana 14, Päivi Pajukanta 15, Klaus G Parhofer 16, Frederick J Raal 17, Kausik K Ray 18, Raul D Santos 19, Anton F H Stalenhoef 20, Erik Stroes 11, Marja-Riitta Taskinen 21, Anne Tybjærg-Hansen 22, Gerald F Watts 23, Olov Wiklund 24; European Atherosclerosis Society Consensus Panel
Affiliations
- PMID: 24731657
- PMCID: PMC4201123
- DOI: 10.1016/S2213-8587(13)70191-8
Review
The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management
Robert A Hegele et al. Lancet Diabetes Endocrinol. 2014 Aug.
Abstract
Plasma triglyceride concentration is a biomarker for circulating triglyceride-rich lipoproteins and their metabolic remnants. Common mild-to-moderate hypertriglyceridaemia is typically multigenic, and results from the cumulative burden of common and rare variants in more than 30 genes, as quantified by genetic risk scores. Rare autosomal recessive monogenic hypertriglyceridaemia can result from large-effect mutations in six different genes. Hypertriglyceridaemia is exacerbated by non-genetic factors. On the basis of recent genetic data, we redefine the disorder into two states: severe (triglyceride concentration >10 mmol/L), which is more likely to have a monogenic cause; and mild-to-moderate (triglyceride concentration 2-10 mmol/L). Because of clustering of susceptibility alleles and secondary factors in families, biochemical screening and counselling for family members is essential, but routine genetic testing is not warranted. Treatment includes management of lifestyle and secondary factors, and pharmacotherapy. In severe hypertriglyceridaemia, intervention is indicated because of pancreatitis risk; in mild-to-moderate hypertriglyceridaemia, intervention can be indicated to prevent cardiovascular disease, dependent on triglyceride concentration, concomitant lipoprotein disturbances, and overall cardiovascular risk.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Figures
Figure 1. Redefinition of hypertriglyceridaemic states on the basis of new genetic data
Triglyceride concentrations of more than 10 mmol/L, especially in young patients, are more likely to be due to monogenic causes combined with secondary factors, whereas patients with triglyceride concentrations of 2–10 mmol/L represent a single group, based on the interplay of several genes (both heterozygous mutations of large effect, and the cumulative burden of small-effect variants, causing a high genetic risk score; figure 2), together with secondary factors. Plasma triglyceride concentrations and approximate population percentages are based on data for more than 70 000 adults (>20 years of age) from the Copenhagen General Population Study.
Figure 2. Genetic risk scores for triglyceride-associated risk alleles
Unweighted risk scores composed of risk alleles at 32 triglyceride-associated loci were summed across individuals and compared between patients with hypertriglyceridaemia and controls. The minimum unweighted risk score is 0, whereas the maximum unweighted risk score is 64, but most scores in the population range between 22 and 46. Compared with healthy controls, the relative frequency distribution of triglyceride genetic risk scores was significantly increased in 504 patients with hypertriglyceridaemia (p=1·6×10−53). Figure reproduced from Johansen and colleagues by permission of Elsevier.
Comment in
- Treatment of severe hypertriglyceridaemia.
Preiss D, McMurray JJ, Sattar N. Preiss D, et al. Lancet Diabetes Endocrinol. 2014 Nov;2(11):860. doi: 10.1016/S2213-8587(14)70052-X. Epub 2014 Mar 20. Lancet Diabetes Endocrinol. 2014. PMID: 25439459 No abstract available. - Treatment of severe hypertriglyceridaemia--authors' reply.
Chapman MJ, Ginsberg HN, Hegele RA. Chapman MJ, et al. Lancet Diabetes Endocrinol. 2014 Nov;2(11):860-1. doi: 10.1016/S2213-8587(14)70054-3. Epub 2014 Mar 20. Lancet Diabetes Endocrinol. 2014. PMID: 25439460 No abstract available.
Similar articles
- Demystifying the management of hypertriglyceridaemia.
Watts GF, Ooi EM, Chan DC. Watts GF, et al. Nat Rev Cardiol. 2013 Nov;10(11):648-61. doi: 10.1038/nrcardio.2013.140. Epub 2013 Sep 24. Nat Rev Cardiol. 2013. PMID: 24060958 Review. - Investigation and management of hypertriglyceridaemia.
Ferns G, Keti V, Griffin B. Ferns G, et al. J Clin Pathol. 2008 Nov;61(11):1174-83. doi: 10.1136/jcp.2008.055756. J Clin Pathol. 2008. PMID: 18955574 Review. - Clinical review on triglycerides.
Laufs U, Parhofer KG, Ginsberg HN, Hegele RA. Laufs U, et al. Eur Heart J. 2020 Jan 1;41(1):99-109c. doi: 10.1093/eurheartj/ehz785. Eur Heart J. 2020. PMID: 31764986 Free PMC article. Review. - Hypertriglyceridaemia: an update.
Wierzbicki AS, Kim EJ, Esan O, Ramachandran R. Wierzbicki AS, et al. J Clin Pathol. 2022 Dec;75(12):798-806. doi: 10.1136/jclinpath-2021-207719. Epub 2022 Jun 16. J Clin Pathol. 2022. PMID: 35710321 Review. - Treatment of primary hypertriglyceridemia states--General approach and the role of extracorporeal methods.
Stefanutti C, Julius U. Stefanutti C, et al. Atheroscler Suppl. 2015 May;18:85-94. doi: 10.1016/j.atherosclerosissup.2015.02.017. Atheroscler Suppl. 2015. PMID: 25936310 Review.
Cited by
- Whole blood gene expression analysis of spontaneous hypertriglyceridemia in dogs suggests an underlying pro-thrombotic process.
Baker LA, Minor KM, Tate N, Furrow E. Baker LA, et al. PLoS One. 2024 Nov 12;19(11):e0313343. doi: 10.1371/journal.pone.0313343. eCollection 2024. PLoS One. 2024. PMID: 39531449 Free PMC article. - Beyond the Guidelines: Perspectives on Management of Pediatric Patients with Hypertriglyceridemia.
Gagnon CA, Ashraf AP. Gagnon CA, et al. Curr Atheroscler Rep. 2024 Nov;26(11):617-628. doi: 10.1007/s11883-024-01237-z. Epub 2024 Sep 30. Curr Atheroscler Rep. 2024. PMID: 39347913 Free PMC article. Review. - Clinico-Laboratory Profile of Hypertriglyceridemia Thalassemia Syndrome: A Case Series in a Paediatric Tertiary Care Centre.
Kapat A, Murmu R, Mandal S, Biswas K, Bhakta S, Mandal AK. Kapat A, et al. Cureus. 2024 Aug 27;16(8):e67936. doi: 10.7759/cureus.67936. eCollection 2024 Aug. Cureus. 2024. PMID: 39328659 Free PMC article. - Conditions Associated With Hypertriglyceridemia in Adult Patients in a Tertiary Care Center in Basrah, Iraq.
Altemeemy I, Alibrahim NT, Alzajaji QB, Mansour AA. Altemeemy I, et al. Cureus. 2024 Aug 23;16(8):e67609. doi: 10.7759/cureus.67609. eCollection 2024 Aug. Cureus. 2024. PMID: 39185300 Free PMC article. - A significant presence in atherosclerotic cardiovascular disease: Remnant cholesterol: A review.
Wang L, Zhang Q, Wu Z, Huang X. Wang L, et al. Medicine (Baltimore). 2024 Jul 5;103(27):e38754. doi: 10.1097/MD.0000000000038754. Medicine (Baltimore). 2024. PMID: 38968507 Free PMC article. Review.
References
- Boullart AC, de Graaf J, Stalenhoef AF. Serum triglycerides and risk of cardiovascular disease. Biochim Biophys Acta. 2012;1821:867–75. - PubMed
- Chapman MJ, Ginsberg HN, Amarenco P, et al. the European Atherosclerosis Society Consensus Panel Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management. Eur Heart J. 2011;32:1345–61. - PMC - PubMed
- Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive Summary of the Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA. 2001;285:2486–97. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- RG/08/008/25291/BHF_/British Heart Foundation/United Kingdom
- CTP-79853/CAPMC/ CIHR/Canada
- P01 HL028481/HL/NHLBI NIH HHS/United States
- MOP-13430/CAPMC/ CIHR/Canada
- MOP-79523/CAPMC/ CIHR/Canada
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical