Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-19T00:33:09.687Z Has data issue: false hasContentIssue false

Vitatmin C and bone markers: investigations in a Gambian population

Published online by Cambridge University Press:  05 March 2007

Karen Munday*
Affiliation:
Medical Research Council Human Nutrition Research, Elsie Widdowson Laboratory, Fulbourn Road, Cambridge, CB1 9NL, UK
*
Corresponding author: Karen Munday, fax +44 1223 437515, [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Vitamin C is an essential micronutrient. Absence from the diet will result in the deficiency disease scurvy, typically characterised by weakening of collagenous structures. High intakes of vitamin C have been associated with decreased incidence or severity of a number of diseases, including cancer and cardiovascular disease. These beneficial effects may be attributed to its antioxidant properties, although the exact mechanisms of action remain elusive. It is also unclear what intake levels are required for optimal health benefits. The task of defining optimal intakes is hindered by the lack of a reliable functional marker of tissue vitamin C status in man. Many different pathways have been investigated, but none of them have measurable outcome variables relating directly to scorbutic changes. The bone-collagen formation pathway has the potential to provide a functional index of tissue vitamin C adequacy. Vitamin C acts as a cofactor for the enzyme lysyl hydroxylase, which is required for the hydroxylation of lysine residues in procollagen chains. Pyridinoline is a mature collagen cross-link formed from three hydroxylysine residues, deoxypyridinoline is formed from two hydroxylysine and one lysine residue. Guinea-pig studies have shown an alteration in the pyridinium cross-link ratios in response to graded vitamin C intakes ‘Tsuchiya & Bates, 1998’. In order to investigate whether these changes can be seen in a human population group, a study was carried out in rural Gambia, where there is a marked seasonal variation in dietary vitamin C. The present review discusses the rationale behind the study and presents some preliminary results.

Type
Micronutrient Group Symposium on ‘Micronutrient supplementation: when and why?’
Copyright
Copyright © The Nutrition Society 2003

References

Acil, Y, Vetter, U, Brenner, R, Muller, PK & Brinckmann, J (1995) Ehlers-Danlos syndrome type VI: cross-link pattern in tissue and urine samples as a diagnostic marker. Journal of the American Academy of Dermatology 33, 522524CrossRefGoogle ScholarPubMed
Bates, CJ, Prentice, AM & Paul, AA (1994) Seasonal variation in vitamins A, C, riboflavin and folate intakes and status of pregnant and lactating women in rural Gambian community. European Journal of Clinical Nutrition 48, 660668Google Scholar
Benzie, IF (1999) Vitamin C: prospective functional markers for defining optimal nutritional status. Proceedings of the Nutrition Society 58, 469476CrossRefGoogle ScholarPubMed
Block, G (1991) Epidemiologic evidence regarding vitamin C and cancer. American Journal of Clinical Nutrition 54 1310S1314SCrossRefGoogle ScholarPubMed
Blumsohn, A & Eastell, R (1997) The performance and utility of biochemical markers of bone turnover: do we know enough to use them in clinical practice?. Annals of Clinical Biochemistry 34, 449459CrossRefGoogle ScholarPubMed
Blumsohn, A, Hannon, RA & Eastell, R (1995) Apparent instability of osteocalcin in serum as measured with different commercially available immunoassays. Clinical Chemistry 41, 318319CrossRefGoogle ScholarPubMed
Cole, TJ (1990) The LMS method for constructing normalized growth standards. European Journal of Clinical Nutrition 44, 4560Google ScholarPubMed
Dembure, PP, Janko, AR, Priest, JH & Elsas, LJ (1987) Ascorbate regulation of collagen biosynthesis in Ehlers-Danlos Syndrome, type VI. Metabolism 36, 687691CrossRefGoogle ScholarPubMed
Dibba, B, Prentice, A, Ceesay, M, Stirling, DM, Cole, TJ & Poskitt, EM (2000) Effect of calcium supplementation on bone mineral accretion in Gambian children accustomed to a low-calcium diet. American Journal of Clinical Nutrition 71, 544549CrossRefGoogle Scholar
Franceschi, RT & Iyer, BS (1992) Relationship between collagen synthesis and expression of the osteoblast phenotype in MC3T3-El cells. Journal of Bone and Mineral Research 1, 235246CrossRefGoogle Scholar
Frei, B (1997) Vitamin C as an Antiarthrogen: Mechanisms of Action New York Marcel Dekker IncGoogle Scholar
Ginty, F, Flynn, A & Cashman, K (1998) Inter and intra-individual variations in urinary excretion of pyridinium crosslinks of collagen in healthy young adults. European Journal of Clinical Nutrition 52, 7173CrossRefGoogle ScholarPubMed
Hall, SL & Greendale, GA (1998) The relation of dietary vitamin C intake to bone mineral density: results from the PEPI study. Calcified Tissue International 63, 183189CrossRefGoogle ScholarPubMed
Herbert, V, Shaw, S & Jayatilleke, E (1996) Vitamin C-driven free radical generation from iron. Journal of Nutrition 126 1213S – 1220SCrossRefGoogle ScholarPubMed
Hughes, RE, Hurley, RJ & Jones, E (1980) Dietary ascorbic acid and muscle carnitine (beta-OH-gamma-(trimethylamino) butyric acid) in guinea-pigs. British Journal of Nutrition 43, 385387CrossRefGoogle Scholar
Jackson, MJ, McArdle, A & McArdle, F (1998) Antioxidant micronutrients and gene expression. Proceedings of the Nutrition Society 57, 301305CrossRefGoogle ScholarPubMed
Jacques, PF, Chylack, LT Jr (1991) Epidemiologic evidence of a role for the antioxidant vitamins and carotenoids in cataract prevention. American Journal of Clinical Nutrition 53 352S – 355SCrossRefGoogle ScholarPubMed
Johnston, CS & Corte, C (1999) People with marginal vitamin C status are at high risk of developing vitamin C deficiency. Journal of the American Dietetic Association 99, 854856CrossRefGoogle ScholarPubMed
Johnston, CS, Solomon, RE & Corte, C (1996) Vitamin C depletion is associated with alterations in blood histamine and plasma free carnitine in adults. Journal of the American College of Nutrition 15, 586591CrossRefGoogle ScholarPubMed
Masi, L, Franchi, A, Santucci, M, Danielli, D, Arganini, L, Giannone, V et al. (1992) Adhesion, growth, and matrix production by osteoblasts on collagen substrata. Calcified Tissue International 51, 202212CrossRefGoogle ScholarPubMed
New, SA, Bolton-Smith, C, Grubb, DA & Reid, DM (1997) Nutritional influences on bone mineral density: a cross-sectional study in premenopausal women. American Journal of Clinical Nutrition 65, 18311839CrossRefGoogle Scholar
Panteghini, M & Pagani, F (1996) Biological variation in urinary excretion of pyridinium crosslinks: recommendations for the optimum specimen. Annals of Clinical Biochemistry 33, 3642CrossRefGoogle ScholarPubMed
Pasquali, M, Dembure, PP, Still, MJ & Elsas, LJ (1994) Urinary pyridinium cross-links: a non-invasive diagnostic test for Ehlers-Danlos Syndrome type VI (letter). New England Journal of Medicine 331, 132133CrossRefGoogle Scholar
Pinnell, SR, Krane, SM, Kenzora, JE & Glimcher, MJ (1972) A heritable disorder of connective tissue. Hydroxylysine-deficient collagen disease. New England Journal of Medicine 286, 10131020CrossRefGoogle ScholarPubMed
Podmore, ID, Griffiths, HR, Herbert, KE, Mistry, N, Mistry, P & Lunec, J (1998) Vitamin C exhibits pro-oxidant properties. Nature 392 559CrossRefGoogle ScholarPubMed
Poulsen, HE, Prieme, H & Loft, S (1998) Role of oxidative DNA damage in cancer initiation and promotion. European Journal of Cancer Prevention 7, 916Google ScholarPubMed
Prentice, A & Bates, CJ (1993) An appraisal of the adequacy of dietary mineral intakes in developing countries for bone growth and development in children. Nutrition Research Reviews 6, 5169CrossRefGoogle ScholarPubMed
Robins, SP (1988) Functional properties of collagen and elastin. Baillieres Clinical Rheumatology 2, 136CrossRefGoogle ScholarPubMed
Robins, SP, Duncan, A & Riggs, BL (1990) Direct measurement of free hydroxypyridinium crosslinks of collagen in urine as markers of bone resorption in osteoporosis Third International Symposium on Osteoporosis 464468 Christiansen C Overgaard K Copenhagen OsteopressGoogle Scholar
Sato, P & Udenfriend, S (1978) Scurvy-prone animals, including man, monkey, and guinea pig, do not express the gene for gulonolactone oxidase. Archives of Biochemistry and Biophysics 187, 158162CrossRefGoogle Scholar
Subar, AF & Block, G (1990) Use of vitamin and mineral supplements: demographics and amounts of nutrients consumed. The 1987 Health Interview Survey. American Journal of Epidemiology 132, 10911101CrossRefGoogle ScholarPubMed
Sugimoto, T, Nakada, M, Fukase, M, Imai, Y, Kinoshita, Y & Fujita, T (1986) Effects of ascorbic acid on alkaline phosphatase activity and hormone responsiveness in the osteoblastic osteo-sarcoma cell line UMR-106. Calcified Tissue International 39, 171174CrossRefGoogle Scholar
Tsuchiya, H & Bates, CJ (1997) Vitamin C and copper interactions in guinea-pigs and a study of collagen cross-links. British Journal of Nutrition 77, 315325CrossRefGoogle Scholar
Tsuchiya, H & Bates, C (1998) Changes in collagen cross-link ratios in bone and urine of guinea pigs fed graded dietary vitamin C: a functional index of vitamin C status. Journal of Nutritional Biochemistry 9, 402407CrossRefGoogle Scholar
Vuilleumier, JP & Keck, E (1989) Fluorometric assay of vitamin C in biological materials using a centrifugal analyser with fluorescence attachment. Journal of Micronutrient Analysis 5, 2534Google Scholar