期刊论文详细信息
BMC Public Health
Skin pigmentation, sun exposure and vitamin D levels in children of the Avon Longitudinal Study of Parents and Children
George Davey Smith2  Sarah J Lewis3  Debbie A Lawlor2  Andrew K Wills3  Andrew R Ness1  Carolina Bonilla3 
[1] School of Oral and Dental Sciences, University of Bristol, Bristol, UK;MRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK;School of Social and Community Medicine, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, UK
关键词: Genetic scores;    ALSPAC;    Vitamin D;    Sun exposure;    Pigmentation;   
Others  :  1129481
DOI  :  10.1186/1471-2458-14-597
 received in 2013-09-20, accepted in 2014-05-27,  发布年份 2014
PDF
【 摘 要 】

Background

It has been hypothesised that light skin pigmentation has arisen to ensure adequate levels of vitamin D as human populations moved out of Africa and into higher latitudes. Vitamin D, which is primarily obtained through exposure to sunlight (specifically ultraviolet radiation B (UVR-B)), has been inversely associated with several complex diseases. Greater sun exposure, on the other hand, is a well-known cause of skin cancer. The potential of UVR to be beneficial for some health outcomes but detrimental for others has prompted a public health debate on how to balance the positive and negative consequences of sun exposure. In this study we aimed to determine the validity of the evolutionary hypothesis linking lighter skin with higher vitamin D concentrations in a European population. Additionally, we aimed to examine the influence of pigmentation on personal behaviour towards sunlight exposure and the effects of this behaviour on vitamin D.

Methods

We combined genetic variants strongly associated with skin colour, tanning or freckling to create genetic scores for each of these phenotypes. We examined the association of the scores with pigmentary traits, sun exposure and serum 25-hydroxyvitamin D (25(OH)D) levels among children of the Avon Longitudinal Study of Parents and Children (ALSPAC, N = 661 to 5649).

Results

We found that fairer-skinned children, i.e. those with higher pigmentation score values, had higher levels of 25(OH)D (0.6 nmol/l; 95% CI 0.2, 1.0; per unit increase in skin colour score; N = 5649). These children also used more protection against the damaging effects of UVR.

Conclusions

In this population taking protective measures against sunburn and skin cancer does not seem to remove the positive effect that having a less pigmented skin has on vitamin D production. Our findings require further replication as skin pigmentation showed only a small effect on circulating 25(OH)D.

【 授权许可】

   
2014 Bonilla et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150226055516429.pdf 238KB PDF download
【 参考文献 】
  • [1]Jablonski NG, Chaplin G: In Light of Evolution IV: The Human Conditions Sackler Colloquium: Human skin pigmentation as an adaptation to UV radiation. Proc Natl Acad Sci U S 2010, 107 Suppl:8962-8968.
  • [2]Robins AH: Biological Perspectives on Human Pigmentation. Cambridge. UK: Cambridge University Press; 1991:253.
  • [3]Jablonski NG: The evolution of human skin and skin color. Annu Rev Anthropol 2004, 33:585-623.
  • [4]Wagner JK, Parra EJ, Norton LH, Jovel C, Shriver MD: Skin responses to ultraviolet radiation: effects of constitutive pigmentation, sex, and ancestry. Pigment Cell Res 2002, 15:385-90.
  • [5]Sturm RA: Skin colour and skin cancer - MC1R, the genetic link. Melanoma Res 2002, 12:405-16.
  • [6]Armas LAG, Dowell S, Akhter M, Duthuluru S, Huerter C, Hollis BW, Lund R, Heaney RP: Ultraviolet-B radiation increases serum 25-hydroxyvitamin D levels: the effect of UVB dose and skin color. J Am Acad Dermatol 2007, 57:588-93.
  • [7]Rockell JEP, Skeaff CM, Williams SM, Green TJ: Association between quantitative measures of skin color and plasma 25-hydroxyvitamin D. Osteoporos Int 2008, 19:1639-42.
  • [8]Hall LM, Kimlin MG, Aronov PA, Hammock BD, Slusser JR, Woodhouse LR, Stephensen CB: Vitamin D intake needed to maintain target serum 25-hydroxyvitamin D concentrations in participants with low sun exposure and dark skin pigmentation is substantially higher than current recommendations. J Nutr 2010, 140:542-50.
  • [9]Nessvi S, Johansson L, Jopson J, Stewart A, Reeder A, McKenzie R, Scragg RK: Association of 25-hydroxyvitamin D3 levels in adult New Zealanders with ethnicity, skin color and self-reported skin sensitivity to sun exposure. Photochem Photobiol 2011, 87:1173-8.
  • [10]Libon F, Cavalier E, Nikkels AF: Skin color is relevant to vitamin D synthesis. Dermatology 2013, 227:250-4.
  • [11]Norval M, Wulf HC: Does chronic sunscreen use reduce vitamin D production to insufficient levels? Br J Dermatol 2009, 161:732-6.
  • [12]Bogh MKB: Vitamin D production after UVB: aspects of UV-related and personal factors. Scand J Clin Lab Investig 2012, 243:24-31.
  • [13]Moan J, Porojnicu AC, Dahlback A, Setlow RB: Addressing the health benefits and risks, involving vitamin D or skin cancer, of increased sun exposure. Proc Natl Acad Sci U S A 2008, 105:668-73.
  • [14]Gerstenblith MR, Shi J, Landi MT: Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis. Pigment Cell Melanoma Res 2010, 23:587-606.
  • [15]Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Magnusson KP, Manolescu A, Karason A, Palsson A, Thorleifsson G, Jakobsdottir M, Steinberg S, Pálsson S, Jonasson F, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Kiemeney LA, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir U, Stefansson K: Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 2007, 39:1443-52.
  • [16]Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Jakobsdottir M, Steinberg S, Gudjonsson SA, Palsson A, Thorleifsson G, Pálsson S, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Vermeulen SH, Goldstein AM, Tucker MA, Kiemeney LA, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir U, Stefansson K: Two newly identified genetic determinants of pigmentation in Europeans. Nat Genet 2008, 40:835-837.
  • [17]Stokowski RP, Pant PVK, Dadd T, Fereday A, Hinds DA, Jarman C, Filsell W, Ginger RS, Green MR, van Der Ouderaa FJ, Cox DR: A genomewide association study of skin pigmentation in a South Asian population. Am J Hum Genet 2007, 81:1119-32.
  • [18]Candille SI, Absher DM, Beleza S, Bauchet M, McEvoy B, Garrison NA, Li JZ, Myers RM, Barsh GS, Tang H, Shriver MD: Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. PLoS One 2012, 7:e48294.
  • [19]Bonilla C, Gilbert R, Kemp JP, Timpson NJ, Evans DM, Donovan JL, Hamdy FC, Neal DE, Fraser WD, Davey SG, Lewis SJ, Lathrop M, Martin RM: Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin D and prostate cancer risk. Cancer Epidemiol Biomarkers Prev 2013, 22:597-606.
  • [20]Fraser A, Macdonald-Wallis C, Tilling K, Boyd A, Golding J, Davey Smith G, Henderson J, Macleod J, Molloy L, Ness A, Ring S, Nelson SM, Lawlor DA: Cohort Profile: the Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort. Int J Epidemiol 2013, 42:97-110.
  • [21]Boyd A, Golding J, Macleod J, Lawlor DA, Fraser A, Henderson J, Molloy L, Ness A, Ring S: Davey Smith G: Cohort Profile: the “children of the 90s”–the index offspring of the Avon Longitudinal Study of Parents and Children. Int J Epidemiol 2013, 42:111-27.
  • [22]Tolppanen A-M, Fraser A, Fraser WD, Lawlor DA: Risk factors for variation in 25-hydroxyvitamin D3 and D2 concentrations and vitamin D deficiency in children. J Clin Endocrinol Metab 2012, 97:1202-10.
  • [23]Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006, 38:904-9.
  • [24]Lawlor DA, Wills AK, Fraser A, Sayers A, Fraser WD, Tobias JH: Association of maternal vitamin D status during pregnancy with bone-mineral content in offspring: a prospective cohort study. Lancet 2013, 381:2176-83.
  • [25]Ladhani S, Srinivasan L, Buchanan C, Allgrove J: Presentation of vitamin D deficiency. Arch Dis Child 2004, 89:781-4.
  • [26]Glass D, Lens M, Swaminathan R, Spector TD, Bataille V: Pigmentation and vitamin D metabolism in Caucasians: low vitamin D serum levels in fair skin types in the UK. PLoS One 2009, 4:e6477.
  • [27]Frost P: Human skin-color sexual dimorphism: a test of the sexual selection hypothesis. Am J Phys Anthropol 2007, 781(December 2006):779-781.
  • [28]Jablonski NG, Chaplin G: The evolution of human skin coloration. J Hum Evol 2000, 39:57-106.
  • [29]Shriver MD, Parra EJ, Dios S, Bonilla C, Norton H, Jovel C, Pfaff C, Jones C, Massac A, Cameron N, Baron A, Jackson T, Argyropoulos G, Jin L, Hoggart CJ, McKeigue PM, Kittles RA: Skin pigmentation, biogeographical ancestry and admixture mapping. Hum Genet 2003, 112:387-99.
  • [30]Costin G-E, Hearing VJ: Human skin pigmentation: melanocytes modulate skin color in response to stress. FASEB J 2007, 21:976-94.
  • [31]Scott MC, Suzuki I, Abdel-Malek ZA: Regulation of the human melanocortin 1 receptor expression in epidermal melanocytes by paracrine and endocrine factors and by ultraviolet radiation. Pigment Cell Res 2002, 15:433-9.
  • [32]Aoki K: Sexual selection as a cause of human skin colour variation: Darwin ’s hypothesis revisited. Ann Hum Biol 2002, 29:589-608.
  • [33]Savage SA, Gerstenblith MR, Goldstein AM, Mirabello L, Fargnoli MC, Peris K, Landi MT: Nucleotide diversity and population differentiation of the melanocortin 1 receptor gene, MC1R. BMC Genet 2008, 9:31.
  • [34]Norton HL, Kittles RA, Parra E, McKeigue P, Mao X, Cheng K, Canfield VA, Bradley DG, McEvoy B, Shriver MD: Genetic evidence for the convergent evolution of light skin in Europeans and East Asians. Mol Biol Evol 2007, 24:710-22.
  • [35]Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu R-B, Zhukova OV, Kim J-J, Siniscalco M, New M, Li H, Kajuna SLB, Manolopoulos VG, Speed WC, Pakstis AJ, Kidd JR, Kidd KK: A global view of the OCA2-HERC2 region and pigmentation. Hum Genet 2012, 131:683-96.
  • [36]Verweij KJH, Burri AV, Zietsch BP: Evidence for genetic variation in human mate preferences for sexually dimorphic physical traits. PLoS One 2012, 7:e49294.
  • [37]Liu F, Bessonova L, Taylor TH, Ziogas A, Meyskens FL, Anton-Culver H: A unique gender difference in early onset melanoma implies that in addition to ultraviolet light exposure other causative factors are important. Pigment Cell Melanoma Res 2013, 26:128-35.
  • [38]Falk M, Anderson CD: Influence of age, gender, educational level and self-estimation of skin type on sun exposure habits and readiness to increase sun protection. Cancer Epidemiol 2013, 37:127-32.
  • [39]Melia J, Pendry L, Eiser JR, Harland C, Moss S: Evaluation of primary prevention initiatives for skin cancer: a review from a U.K. perspective. Br J Dermatol 2000, 143:701-708.
  • [40]Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang H-Y, Demirkan A, Den Hertog HM, Donnelly LA, Ehret GB, Esko T, Feitosa MF, Ferreira T, Fischer K, Fontanillas P, Fraser RM, Freitag DF, Gurdasani D, Heikkilä K, Hyppönen E, Isaacs A, et al.: Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet 2013, 45:1345-52.
  • [41]Holmes MV, Asselbergs FW, Palmer TM, Drenos F, Lanktree MB, Nelson CP, Dale CE, Padmanabhan S, Finan C, Swerdlow DI, Tragante V, van Iperen EP, Sivapalaratnam S, Shah S, Elbers CC, Shah T, Engmann J, Giambartolomei C, White J, Zabaneh D, Sofat R, McLachlan S, Doevendans PA, Balmforth AJ, Hall AS, North KE, Almoguera B, Hoogeveen RC, Cushman M, Fornage M, et al.: Mendelian randomization of blood lipids for coronary heart disease. Eur Heart J 2014. doi:10.1093/eurheartj/eht571
  文献评价指标  
  下载次数:31次 浏览次数:13次