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In different types of GSD, hyperlipidemias are of a different origin. Hypertriglyceridemia is most prominent in GSD type Ia and associated with long\u2010term outcome morbidity, like pancreatitis and hepatic adenomas. In the ketotic subtypes of GSD, hypertriglyceridemia reflects the age\u2010dependent fasting intolerance, secondary lipolysis and increased mitochondrial fatty acid oxidation. The role of high protein diets is established for ketotic types of GSD, but non\u2010traditional dietary interventions (like medium\u2010chain triglycerides and the ketogenic diet) in hepatic GSD are still controversial and necessitate further studies. Patients with these rare inherited disorders of carbohydrate metabolism meet several criteria of the metabolic syndrome, therefore close monitoring for cardiovascular diseases in ageing GSD patients may be justified.<\/jats:p>","DOI":"10.1007\/s10545-015-9811-2","type":"journal-article","created":{"date-parts":[[2015,1,29]],"date-time":"2015-01-29T08:07:00Z","timestamp":1422518820000},"page":"537-543","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":54,"title":["Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directions"],"prefix":"10.1002","volume":"38","author":[{"given":"Terry G. 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