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==Overview==
==Overview==
[[Lipoproteins]] other than [[HDL]] (termed non-HDL cholesterol), especially low density lipoprotein (LDL), can always attribute to the increased risk of [[atherosclerosis]] and [[coronary heart disease]].  High LDL may primarily be a consequence of [[inherited]] ([[genetic]]) diseases that affects the [[lipid metabolism]], or due to secondary causes other than the primary inherited disorders of lipid metabolism.      
High LDL may be caused by [[inherited]] diseases that affect the [[lipid metabolism]] or can be secondary to causes other than the primary genetic disorders of lipid metabolism.


==Causes==
==Causes==

Revision as of 16:51, 20 November 2013

Low Density Lipoprotein Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Rim Halaby, M.D. [3]; Vendhan Ramanujam M.B.B.S [4]

Overview

High LDL may be caused by inherited diseases that affect the lipid metabolism or can be secondary to causes other than the primary genetic disorders of lipid metabolism.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Causes by Organ System

Cardiovascular No underlying causes
Chemical/Poisoning Diterpenoids
Dental No underlying causes
Dermatologic No underlying causes
Drug Side Effect Atazanavir, azathioprine, bexarotene, calcineurin inhibitors, chlortalidone, corticosteroids, cyclosporine, desvenlafaxine, fish oil supplements, immunosuppressive agents, levonorgestrel, lopinavir, mycophenolate, nicotine, norgestrel, prednisone, progestin, rapamycin, rosiglitazone, sirolimus, thiazide, tocilizumab
Ear Nose Throat No underlying causes
Endocrine Androgens, dehydroepiandrosterone, growth hormone deficiency, hypercortisolism, hypothyroidism, polycystic ovarian syndrome, progestagens, subclinical hypothyroidism, testosterone
Environmental No underlying causes
Gastroenterologic No underlying causes
Genetic Acid sphingomyelinase deficiency, autosomal recessive hypercholesterolemia, familial combined hyperlipidemia, familial defective apolipoprotein B-100, familial hypercholesterolemia, IL 28B polymorphisms, Niemann-Pick disease, polygenic hypercholesterolemia
Hematologic No underlying causes
Iatrogenic No underlying causes
Infectious Disease Gram negative bacteremia, H. pylori, small bowel bacterial overgrowth syndrome
Musculoskeletal/Orthopedic No underlying causes
Neurologic No underlying causes
Nutritional/Metabolic Chenodeoxycholic acid, high carbohydrate diet, high saturated fat diet, omega-3 polyunsaturated fatty acids, polygenic hypercholesterolemia, primary hyperlipoproteinemia, primary hypolipoproteinemia, selenium deficiency
Obstetric/Gynecologic Polycystic ovarian syndrome
Oncologic No underlying causes
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal/Electrolyte Chronic kidney disease, nephrotic syndrome
Rheumatology/Immunology/Allergy Dysproteinemia, lipopolysaccharides, monoclonal gammopathy, paraproteinemia
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous No underlying causes

Causes in Alphabetical Order

References

  1. 1.0 1.1 Durrington, P. (2003). "Dyslipidaemia". Lancet. 362 (9385): 717–31. doi:10.1016/S0140-6736(03)14234-1. PMID 12957096. Unknown parameter |month= ignored (help)
  2. 2.0 2.1 Covington, MB. (2004). "Omega-3 fatty acids". Am Fam Physician. 70 (1): 133–40. PMID 15259529. Unknown parameter |month= ignored (help)
  3. Pejic, RN.; Lee, DT. "Hypertriglyceridemia". J Am Board Fam Med. 19 (3): 310–6. PMID 16672684.
  4. Kronenberg, F. (2005). "Dyslipidemia and nephrotic syndrome: recent advances". J Ren Nutr. 15 (2): 195–203. PMID 15827892. Unknown parameter |month= ignored (help)


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