Hypertriglyceridemia
Hypertriglyceridemia | |
---|---|
Other names | Elevated levels of triglycerides |
hypercalcemia |
Hypertriglyceridemia is the presence of high amounts of triglycerides in the blood. Triglycerides are the most abundant fatty molecule in most organisms. Hypertriglyceridemia occurs in various physiologic conditions and in various diseases, and high triglyceride levels are associated with atherosclerosis, even in the absence of hypercholesterolemia (high cholesterol levels) and predispose to cardiovascular disease.
Chronically elevated serum triglyceride levels are a component of metabolic syndrome and metabolic dysfunction-associated steatotic liver disease, both of which typically involve obesity and contribute significantly to cardiovascular mortality in industrialised countries as of 2021. Extreme triglyceride levels also increase the risk of acute pancreatitis.
Hypertriglyceridemia itself is usually symptomless, although high levels may be associated with skin lesions known as xanthomas.[1]
Signs and symptoms
Most people with elevated triglycerides experience no symptoms. Some forms of primary hypertriglyceridemia can lead to specific symptoms: both familial chylomicronemia and primary mixed hyperlipidemia include skin symptoms (eruptive xanthoma), eye abnormalities (lipaemia retinalis), hepatosplenomegaly (enlargement of the liver and spleen), and neurological symptoms. Some experience attacks of abdominal pain that may be mild episodes of pancreatitis. Eruptive xanthomas are 2–5 mm papules, often with a red ring around them, that occur in clusters on the skin of the trunk, buttocks and extremities.[2] Familial dysbetalipoproteinemia causes larger, tuberous xanthomas; these are red or orange and occur on the elbows and knees. Palmar crease xanthomas may also occur.[1][2]
The diagnosis is made on blood tests, often performed as part of screening. Once diagnosed, other blood tests are usually required to determine whether the raised triglyceride level is caused by other underlying disorders ("secondary hypertriglyceridemia") or whether no such underlying cause exists ("primary hypertriglyceridemia"). There is a hereditary predisposition to both primary and secondary hypertriglyceridemia.[1]

Acute pancreatitis may occur in people whose triglyceride levels are above 1000 mg/dL (11.3 mmol/L).[1][2][3] Hypertriglyceridemia is associated with 1–4% of all cases of pancreatitis. The symptoms are similar to pancreatitis secondary to other causes, although the presence of xanthomas or risk factors for hypertriglyceridemia may offer clues.[3]
Causes
- Overeating[4][5]
- Obesity
- central obesity, hypertension, and hyperglycemia)
- Excess alcohol consumption
- Kidney failure, nephrotic syndrome
- Genetic predisposition; some forms of familial hyperlipidemia such as familial combined hyperlipidemia i.e. Type II hyperlipidemia
- Lipoprotein lipase deficiency - Deficiency of this water-soluble enzyme, that hydrolyzes triglycerides in lipoproteins, leads to elevated levels of triglycerides in the blood.
- Cholesteryl ester storage disease
- Certain medications e.g. protease inhibitors
- Hypothyroidism (underactive thyroid)
- Lupus and associated autoimmune responses [6]
- Glycogen storage disease type 1.
- Propofol
- HIV medications
Diagnosis
The diagnosis is made on blood tests, often performed as part of screening. The normal triglyceride level is less than 150 mg/dL (1.7 mmol/L).[1][5] Once diagnosed, other blood tests are usually required to determine whether the raised triglyceride level is caused by other underlying disorders ("secondary hypertriglyceridemia") or whether no such underlying cause exists ("primary hypertriglyceridaemia"). There is a hereditary predisposition to both primary and secondary hypertriglyceridemia.[1]
Guidelines

The National Cholesterol Education Program has set guidelines for triglyceride levels:[7][8]
Level | Interpretation | |
---|---|---|
( dL )
|
(mmol/L) | |
< 150 | < 1.70 | Normal range – low risk |
150–199 | 1.70–2.25 | Slightly above normal |
200–499 | 2.26–5.65 | Some risk |
500 or higher | > 5.65 | Very high – high risk |
These levels are tested after fasting 8 to 12 hours. Triglyceride levels remain temporarily higher for a period after eating.
The AHA recommends an optimal triglyceride level of 100 mg/dL (1.1 mmol/L) or lower to improve heart health.[9]
Screening
In 2016, the United States Preventive Services Task Force concluded that testing the general population under the age of 40 without symptoms is of unclear benefit.[10][11]
Treatment
Lifestyle changes including weight loss, exercise and dietary modification may improve hypertriglyceridemia.
The decision to treat hypertriglyceridemia with medication depends on the levels and on the presence of other risk factors for cardiovascular disease. Very high levels that would increase the risk of pancreatitis is treated with a drug from the
Epidemiology
As of 2006, the prevalence of hypertriglyceridemia in the United States was 30%.[5]
Research
Analysis of the genes in depression and anxiety showed those linked solely to depression were also linked to hypertriglyceridemia.[21]
Etymology
The word hypertriglyceridemia uses
See also
References
- ^ PMID 22962670.
- ^ PMID 17420495.
- ^ S2CID 24193233.
- PMID 1397701.
- ^ PMID 16672684.
- PMID 28402248.
- ^ "Triglycerides". MedlinePlus. Archived from the original on 28 February 2014. Retrieved 2015-04-23.
- ^ Crawford, H., Micheal. Current Diagnosis & Treatment Cardiology. 3rd ed. McGraw-Hill Medical, 2009. p19
- ^ "What's considered normal?". Triglycerides: Why do they matter?. Mayo Clinic. 28 September 2012.
- S2CID 20592431.
- PMID 27532917.
- PMID 35243465.
- ^ S2CID 33149001.
- PMID 11834142.
- PMID 21712404.
- ISBN 978-1-58829-551-4.
- PMID 29290214.
- PMID 19698935.
- S2CID 15570639.
- S2CID 23706094.
- S2CID 233259875.
External links
- Lowering Triglycerides (EMedicineHealth.com; October 2020)