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20: Niacin (Chapter 20c)

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    117148
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    Abstract

    The term "niacin" refers to three compounds: nico­tin­amide, nico­tinic acid, and nico­tin­amide ribose. They are precursors of nico­tin­amide adenine dinucleo­tide (NAD) and nico­tin­amide adenine dinucleo­tide phosphate (NADP), both of which function in a variety of oxidation and reduction reactions and are associated with both cata­bolic and anabolic processes. Pellagra, a disease of the "4Ds" (diarrhea, dermatitis, dementia, and death) is the syndrome of niacin deficiency. Although rare, outbreaks of pellagra still occur when diets are based on maize (without nixtamalization), a cereal low in bioavailable niacin. Secondary niacin deficiency may also develop in diseases that inter­fere with absorp­tion of niacin or tryp­to­phan (a precursor of niacin) (e.g., chronic colitis, liver cirrhosis) or reduce the con­ver­sion of tryp­to­phan to niacin (e.g., chronic alcoholism, prolonged isoniazid treat­ment for tuberculosis). Rich food sources of niacin include meat, poultry, and fish, followed by dairy products and enriched or fortified cereals. Coffee is also a good source of niacin. Absorption of niacin from food ranges from about 23% to 70% and is lowest from cereals and highest from animal products. Certain food preparation and pro­ces­sing practices may influence the content and bio­avail­ability of niacin in food. Intakes and requirements for niacin are expressed as niacin equivalents (NEs) to consider the contribution of tryp­to­phan to niacin (i.e., 60mg tryp­to­phan yields 1mg niacin). Dietary reference values for niacin are set as NE per day, or alternatively expressed as mg NE/MJ or mg NE/1000 kcal based on the relationship between the requirements for niacin and energy. Niacin toxicity may occur when large pharmacological doses of niacin are taken to prevent or treat metabolic diseases such as dyslipidemia. Tolerable Upper Intake Levels (ULs) are based on dermal vasodilative flushing.

    At present, the best biomarker of niacin status is the measure­ment of two urinary meta­bolites: N'‑methyl­nico­tin­amide and N'‑methyl-2-pyridine-5-carbox­amide (2‑pyridone) using HPLC. Sampling strategies employed include 24h urines with results expressed as concen­trations of individual meta­bolites (mg/d), or random spot urines when the ratio (2‑pyridone to N'‑methyl­nico­tin­amide), or concen­trations relative to creatinine (mg/g creatinine) are used. Interpretive criteria for adults are available for urinary excretion of these niacin meta­bolites expressed relative to creatinine and as the ratio (2‑pyridone / N'‑methyl­nico­tin­amide). WHO has developed provisional criteria for the severity of public health problem of niacin deficiency. Concentrations of the co-enzyme NAD in erythro­cytes (but not whole blood) or the ratio of erythro­cyte NAD to NADP (called niacin index) are said to be sensitive to short-term changes in niacin intake, even in the absence of clinical signs of deficiency. Hence, they may serve as a sensitive and reliable functional biomarker for risk of niacin deficiency. With the development of a rapid LC-MS/MS method for their analysis, further investigation of erythro­cyte NAD and NADP concen­trations as biomarkers of niacin status is warranted.

    • 20.1: Niacin - Introduction (20c.1)
      This page discusses the importance of niacin (vitamin B3) in converting tryptophan into NAD, vital for metabolic processes, gene expression, and DNA repair. Niacin prevents deficiency symptoms like pellagra, which is common in areas with low niacin bioavailability. It has potential therapeutic uses in cholesterol regulation and neuroprotection. Dietary sources include meat and fortified cereals, with recommended intakes set at 12-16mg/day for men and 11-14mg/day for women.
    • 20.2: Indices of niacin status (20c.2)
      This page discusses recent advancements in assessing niacin status, particularly through urinary metabolites. It highlights the efficacy of niacin fortification in reducing pellagra prevalence and scrutinizes current biomarker reliance. While the urine analysis of metabolites like N'-methyl-nicotinamide and 2-pyridone is emphasized, the effectiveness of these metrics is questioned in mild deficiency cases and impacted by protein intake.


    This page titled 20: Niacin (Chapter 20c) is shared under a CC BY 4.0 license and was authored, remixed, and/or curated by Rosalind S. Gibson via source content that was edited to the style and standards of the LibreTexts platform.