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Niacin

Common Name: Niacin
Synonyms: Vitamin B3, niacinamide, nicotinamide, inositol hexaniacinate

Overview:

Niacin, also known as vitamin B3, is a water-soluble vitamin that helps the body convert carbohydrates into glucose, the fuel that keeps the many functions of the body running smoothly. Along with the other B vitamins, niacin is responsible for the breakdown of fats and proteins as well. Niacin is actually essential for the functioning of over 50 enzymes and plays an important role in maintaining muscle tone, a healthy digestive tract, maintaining a healthy nervous system and the production of the sex and sex related hormones in the adrenal glands and elsewhere in the body.

Vitamin B3 comes in two forms, niacin (nicotinic acid) and niacinamide (nicotinamide). Inositol hexaniacinate is a combination of niacin and inositol (another B vitamin). Each of these forms of niacin work in their own way on different processes when taken in high doses.

Good sources of niacin are seeds, yeast, bran, peanuts brown rice, whole wheat, barley, almonds and peas. Niacin can also be synthesized from the amino acid tryptophan. A niacin deficiency can occur when inadequate amounts of niacin or tryptophan are consumed. Niacin deficiency also occurs in cases of Hartnup’s disease (a genetic disease that involves defective tryptophan absorption) and carcinoid syndrome. Prolonged treatment with Isoniazid (an anti-tuberculosis medication) can also result in a niacin deficiency.

The severe and late stage of niacin deficiency is called pellagra. Pellagra occurred throughout the Europe and the United States where corn was the primary stable of the poor and working class. Although corn contains niacin, but it is bound that is not nutritionally available to humans. In the parts of the world where corn originated, Mexico and South America, pellagra is very uncommon. This is despite the fact that these parts of the world are also poor and corn is a staple. In this region corn is prepared by soaking in lime which then releases the niacin in a form that can be used by humans.

The symptoms of pellagra are commonly known as the 4 D’s, dermatitis, diarrhea, dementia and death. In the skin, a thick, scaly and dark pigmented rash appears, especially in areas exposed to sunlight. Digestive system involvement includes a bright red tongue, vomiting and diarrhea. The neurological symptoms of pellagra are headache, apathy, fatigue, depression, disorientation and memory loss. If not treated pellagra is ultimately results in death.

Benefits

Extensive research has been done on niacin and what it can do.

  1. Preliminary studies in animals have shown that niacin not only helps to prevent DNA damage but actually assists in its repair. This DNA repair helps prevent the appearance of disorders that can result from cellular damage at the DNA level such as cancer. In vitro (in the laboratory) studies of human cancer lines have shown that the niacin metabolite NAD (niacin and tryptophan are its prcursors) suppresses the tumor suppressor protein p53.
  2. The use of niacin supplements to lower elevated LDL (bad cholesterol) levels and triglycerides. It is also more effective in increasing HDL (good cholesterol) levels than cholesterol lowering medications. Several well documented double-blind, placebo-controlled studies have found that niacin can reduce LDL levels by about 10%, triglyceride levels by 25% while raising HDL by 20-30%. Niacin has also been shown to lower the levels of lipoprotein (responsible for atherosclerosis) by as much as 30%. It has also been shown to be a safe and effective treatment for high cholesterol in people with diabetes without raising the blood sugar levels.
  3. There has been some evidence that niacin can prolong the “honeymoon” period in the development of juvenile diabetes. This is the period when the pancreas is slowly losing its ability to produce insulin. Preliminary evidence suggested that niacinamide might slightly prolong this period. In another study, niacinamide and vitamin E along with intensive insulin therapy was more effective than insulin plus niacinamide alone in prolonging the honeymoon period.
  4. Recent studies have also shown that niacinamide may help improve blood sugar control in type tow diabetes.
  5. There has been some eveidence that niacinamide by profide benefits to those with osteoarthritis. In a double-blind study 72 people with arthritis were given 3,000mg of niacinamide in 6 equal doses per day or a placebo for 12 weeks. Those who received the supplement showed a 29% improvement in their symptoms. The only draw back is that at this dose liver damage is a concern.
  6. In one small double blind study, the form of niacin known as inositol hexaniacinate proved helpful in Raynaud’s phenomen. The dosage used was 4000,mg daily an amount that could cause liver damage.
  7. Diatary B3 along with other nutrients are important for normal vision and the prevention of cataracts. A study of 2900 people in Australia found that those who consumed the most protein, vitamin A, B1 (thiamine), B2 and B3 (niacin) were significantly less likely to develop cataracts. A follow up study also showed that many supplemental B complex vitamins including B3 exerted a protective effect against cataracts.
  8. Preliminary research is showing the benefits of niacin in anti-aging skin products, for the treatment of acne, and even possibly the prevention of skin cancer.
  9. Some have even linked niacin to an increase in HGH (human growth hormone).

Recommended Dosage:

It should be understood that the amounts of niacin needed to be helpful in most medical conditions are extremely high. These doses are considered “pharmacological and must be prescribed by a qualified healthcare practitioner.

These amounts of niacin should also be taken with a meal to avoid stomach irritation.

Precautions

  1. Using niacin to lower blood lipid levels should only be done under a doctor’s direct supervision.
  2. Pregnant or nursing mothers should not take more that the RDA for niacian
  3. Anyone with liver disease, jaundice, peptic ulcers or gastritis should use high doses of nicotinic acid with caution.
  4. Those taking high doses should have their liver enzymes monitored on a regular basis.
  5. Do not substitute slow or extended release form of nicotinc acid for the immediate release forms.
  6. Niacin can cause an uncomfortable flushing of the skin. This flush is transient and should subside.
  7. There are many drug interactions connected with niacin supplementation. Your healthcare practioner should be consulted before a niacin regime is undertaken.

Women who are pregnant or breastfeeding should consult a health care provider before using any supplements. The affects of this supplement has not been tested on children and those suffering from liver or kidney disease. It is recommended that in children and people with liver or kidney disease this supplementation not be used.

Web References

  1. http://healthlibrary.epnet.com/GetContent.aspx?token=e0498803-7f62-4563-8d47-5fe33da65dd4&chunkiid=21769
  2. http://www.pdrhealth.com/drug_info/nmdrugprofiles/nutsupdrugs/nia_0184.shtml
  3. http://www.umm.edu/altmed/ConsSupplements/VitaminB3Niacincs.html
  4. http://lpi.oregonstate.edu/infocenter/vitamins/niacin/

Printed Reference Material

  1. Adding vitamins to the mix: skin care products that can benefit the skin [press release]. American Academy of Dermatology; March 11, 2000.
  2. Antoon AY, Donovan DK. Burn Injuries. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of Pediatrics. Philadelphia, Pa: W.B. Saunders Company; 2000:287-294.
  3. Bays HE, Dujovne CA. Drug interactions of lipid-altering drugs. Drug Safety. 1998;19(5):355-371.
  4. Brown BG, Zhao XQ, Chalt A, et al. Simvastatin and niacin, antioxidant vitamins, or the combination for the prevention of coronary disease. N Engl J Med. 2001;345(22):1583-1592.
  5. Canner PL, Berge KG, Wenger NK, et al. Fifteen year mortality in Coronary Drug Project patients: long-term benefit with niacin. J Am Coll Cardiol. 1986; 8:1245-1255.
  6. Capuzzi DM, Guyton JR, Morgan JM, et al. Efficacy and safety of an extended-release niacin (Niaspan): a long-term study. Am J Cardiol. Dec 17, 1998;82:74U–81U.
  7. Carlson LA, Rosenhamer G. Reduction of mortality in the Stockholm ischemic Heart Disease Secondary Prevention Study by combined treatment with clofibrate and nicotinic acid. Acta Med Scand. 1988; 223:405-418.
  8. Cervantes-Laurean D, McElvaney NG, Moss J. Niacin. In: Shils ME, Olson JA, Shike M, Ross AC, eds. Modern Nutrition in Health and Disease. 9th ed. Baltimore, MD: Williams and Wilkins; 1999:401-411.
  9. Chojnowska-Jezierska J, Adamska-Dyniewska H. [Prolonged treatment with slow release nicotinic acid in patients with type II hyperlipidemia]. [Article in Polish]. Pol Arch Med Wewn. 1997; 98:391-399.
  10. Colletti RB, Neufeld EJ, Roff NK, et al. Niacin treatment of hypercholesterolemia in children. Pediatrics. 1993; 92:78-82.
  11. Cumming RG, Mitchell P, Smith W. Diet and cataract: the Blue Mountains Eye Study. Ophthalmology. 2000;107(3):450-456.
  12. De-Souza DA, Greene LJ. Pharmacological nutrition after burn injury. J Nutr. 1998;128:797-803.
  13. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC: National Academy Press; 1998.
  14. Ding RW, Kolbe K, Merz B, de Vries J, Weber E, Benet Z. Pharmacokinetics of nicotinic acid-salicylic acid interaction. Clin Pharmacol Ther. 1989;46(6):642-647.
  15. Elam M, Hunninghake DB, Davis KB, et al. Effects of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: a randomized trial. Arterial Disease Multiple Intervention Trial. JAMA. 2000;284:1263-1270.
  16. Elam MB, Hunninghake DB, Davis KB, et al. Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: The ADMIT Study: A randomized trial. JAMA. 2000; 284:1263-1270.
  17. Gaby AR. Natural treatments for osteoarthritis. Altern Med Rev. 1999;4(5):330-341.
  18. Gardner SF, Marx MA, White LM, et al. Combination of low-dose niacin and pravastatin improves the lipid profile in diabetic patients without compromising glycemic control. Ann Pharmacother. 1997;31(6):677-682.
  19. Gardner SF, Schneider EF, Granberry MC, Carter IR. Combination therapy with low-dose lovastatin and niacin is as effective as higher-dose lovastatin. Pharmacother. 1996;16:419–423.
  20. Garg A. Lipid-lowering therapy and macrovascular disease in diabetes mellitus. Diabetes. 1992;41(Suppl 2):111-115.
  21. Goldberg A, Alagona P Jr, Capuzzi DM, et al. Multiple-dose efficacy and safety of an extended-release form of niacin in the management of hyperlipidemia. Am J Cardiol. 2000; 85:1100-1105.
  22. Goldberg A, Alagona P, Capuzzi DM, et al. Multiple-dose efficacy and safety of an extended-release form of niacin in management of hyperlipidemia. Am J Cardiol. 2000;85:1100-1105.
  23. Gray DR, Morgan T, Chretian SD, Kashyap ML. Efficacy and safety of controlled-release niacin in dyslipoproteinemic veterans. Ann Intern Med. 1994; 121:252-258.
  24. Guyton JR, Blazing MA, Hagar J, et al. Extended-release niacin vs gemfibrozil for the treatment of low levels of high-density lipoprotein cholesterol. Niaspan
  25. Gemfibrozil Study Group. Arch Int Med. 2000; 160:1177-1184.
  26. Guyton JR, Capuzzi DM. Treatment of hyperlipidemia with combined niacin-statin regimens. Am J Cardiol. Dec 17, 1998;82:82U–84U.
  27. Guyton JR. Effect of niacin on atherosclerotic cardiovascular disease. Am J Cardiol. Dec 17, 1998;82:18U–23U.
  28. Guyton JR. Effect of niacin on atherosclerotic cardiovascular disease. Am J Cardiol. 1998; 82:18U-23U.
  29. Henkin Y, Oberman A, Hurst DC. Niacin revisited: clinical observations on an important but underutilized drug. Am J Med. 1991; 91:239-246.
  30. Illingworth DR, Stein EA, Mitchel YB, et al. Comparative effects of lovastatin and niacin in primary hypercholesterolemia. Arch Intern Med. 1994; 154:1586-1595.
  31. Jacques PF, Chylack LT Jr, Hankinson SE, et al. Long-term nutrient intake and early age related nuclear lens opacities. Arch Ophthalmol. 2001;119(7):1009-1019.
  32. Johansson JO, Egberg N, Asplund-Carlson A, Carlson LA. Nicotinic acid treatment shifts the fibrinolytic balance favorably and decreases plasma fibrinogen in hypertriglyceridaemic men. J Cardiovasc Risk. 1997; 4:165-171.
  33. Jokubaitis LA. Fluvastatin in combination with other lipid-lowering agents. Br J ClinPract. 1996;77A(Suppl):28-32.
  34. Jonas WB, Rapoza CP, Blair WF. The effect of niacinamide on osteoarthritis: A pilot study. Inflamm Res. 1996;45:330-334.
  35. King JM, Crouse JR, Terry JG, et al. Evaluation of effects of unmodified niacin on fasting and postprandial plasma lipids in normolipidemic men with hypoalphalipoproteinemia. Am J Med. 1994; 97:323-331.
  36. Kirschmann GJ, Kirschmann JD. Nutrition Almanac. 4th ed. New York: McGraw-Hill;1996:88-99.
  37. Kuroki F, Iida M, Tominaga M, et al. Multiple vitamin status in Crohn's disease. Dig Dis Sci. 1993;38(9):1614-1618.
  38. Kuzniarz M, Mitchell P, Cumming RG, Flood VM. Use of vitamin supplements and cataract: the Blue Mountains Eye Study. Am J Ophthalmol. 2001;132(1):19-26.
  39. Lin S-J, Defossez P-A, Guarente L. Requirement of NAD and SIR2 for life-span extension by calorie restriction in Saccharomyces cerevisiae. Science. 2000; 289:2126-2128.
  40. Matsui MS, Rozovski SJ. Drug-nutrient interaction. Clin Ther. 1982;4(6):423-440.
  41. McCarty MF. Niacinamide therapy for osteoarthritis – does it inhibit nitric oxide synthase induction by interleukin-1 in chondrocytes? Med Hypotheses. 1999;53(4):350-360.
  42. McKenney JM, Proctor JD, Harris S, Chinchili VM. A comparison of the efficacy and toxic effects of sustained-vs immediate-release niacin in hypercholesterolemic patients. JAMA. 1994; 271:672-677.
  43. Meyer NA, Muller MJ, Herndon DN. Nutrient support of the healing wound. New Horizons. 1994;2(2):202-214.
  44. Nutrients and Nutritional Agents. In: Kastrup EK, Hines Burnham T, Short RM, et al, eds. Drug Facts and Comparisons. St. Louis, Mo: Facts and Comparisons; 2000:4-5.
  45. O'Hara J, Nicol CG. The therapeutic efficacy of inositol nicotinate (Hexopal) in intermittent claudication: a controlled trial. Br J Clin Prac. 1988;42(9):377-381.
  46. Omray A. Evaluation of pharmacokinetic parameters of tetracylcine hydrochloride upon oral administration with vitamin C and vitamin B complex. Hindustan Antibiot Bull. 1981;23(VI):33-37.
  47. Physicians' Desk Reference. 54th ed. Montvale, NJ: Medical Economics Co., Inc.: 2000:1519-1523.
  48. Rader JI, Calvert RJ, Hathcock JN. Hepatic toxicity of unmodified and time-release preparations of niacin. Am J Med. 1992; 92:77-81.
  49. Rockwell KA. Potential interaction between niacin and transdermal nicotine. Ann Pharmacother. 1993;27(10):1283-1288.
  50. Saareks V, Mucha I, Sievi E, Riutta A. Nicotinic acid and pyridoxine modulate arachidonic acid metabolism in vitro and ex vivo in man. Pharmacol Toxicol. 1999; 84:274-280.
  51. Tato F, Vega GL, Grundy SM. Effects of crystalline nicotinic acid-induced hepatic dysfunction on serum low-density lipoprotein cholesterol and lecithin cholesteryl acyl transferase. Am J Cardiology. 1998; 81:805-807.
  52. Torkos S. Drug-nutrient interactions: a focus on cholesterol-lowering agents. Int J Integrative Med. 2000;2(3):9-13.
  53. Trueblood NA, Ramasamy R, Wang LF, Schaefer S. Niacin protects the isolated heart from ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol. 2000; 279:H764-H771.
  54. Tsalamandris C, Panagiotopoulos S, Sinha A, et al. Complementary effects of pravastatin and nicotinic acid in the treatment of combined hyperlipidaemia in diabetic and non-diabetic patients. J Cardiovasc Risk. 1994; 1:231-239.
  55. Visalli N, Cavallo MG, Signore A, et al. A multi-centre randomized trial of two different doses of nicotinamide in patients with recent-onset type 1 diabetes (the IMDIAB VI). Diabetes Metab Res Rev. 1999;15(3):181-185.
  56. Whelan AM, Price SO, Fowler SF, et al. The effect of aspirin on niacin-induced cutaneous reactions. J Fam Pract. 1992;34(2):165-168.
  57. Yee HS, Fong NT, Atorvastatin in the treatment of primary hypercholesterolemia and mixed dyslipidemias. Ann Pharmacother. 1998 Oct;32(10):1030-1043.

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