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Volume 56, Issue 4, Pages 709-710 (April 2007)


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Yes, let's abandon race—It does not accurately correlate with hair form

Nonhlanhla P. Khumalo, MBChB, FCDermCorresponding Author Informationemail address

Article Outline

References

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To the Editor: I read with interest the recent reports by Bigby et al in the Journal1, 2, 3 and thank them for raising this important issue. There is no doubt that there are variable human traits which probably resulted from environmental adaptation,4 and that some traits are likely to cluster in “race” groups that were under similar environmental factors as people who migrated “out of Africa.” The most obvious of these would be skin color and hair form.

Probably the most exhaustive study of hair form examined 8 parameters in hair from 7 populations.5 Participants of Asian ancestry were found to have the largest hair diameter and most consistent medulla. East African hair had the highest kink, curvature, crimp, and ratio of natural to straight hair.5 Computer-aided reconstruction of scalp biopsies demonstrated the spiral and straight nature of “African” and “Asian” follicles, respectively.6 These findings were recently confirmed by data demonstrating that asymmetric differentiation of layers of the bulb result in the curved follicle that is typical of “African hair.”7 Thus, the most significant findings to date, whether using hair form characteristics,5 computer-aided reconstruction,6 or immunohistochemistry7 have been that “African” and “Asian” hair represent extremes of the spectrum of hair morphology. The latter also possibly explains the pragmatic classification of hair into 3 major groups: African, Asian, and European, which is currently used in dermatology texts.

External features, although impressive, are not necessarily markers of other traits or even response to disease—they may be proxies of variable accuracy. For example, although people of African ancestry are reported to have higher mean blood pressures than white Americans, this race-linked association falls flat when one considers that the mean blood pressure in parts of Europe is significantly higher than that of African Americans.8

Even the recent testing—and subsequent targeted US Food and Drug Administration approval—of BiDil (NitroMed, Inc., Lexington, Mass) for hypertension in African Americans does not mean that this is the only group that can benefit from its use.9 In fact, components of BiDil (hydralazine and isosorbide dinitrate) have been known to be effective across populations for years. Current evidence suggests that for common diseases10, 11, 12 in populations, environmental factors are more important disease determinants than genetic traits. It is now also known that many previous associations of race with disease, like assessments of intellect, were in fact confounded by nurture (eg, socioeconomic status13).

Race is not a quantifiable biologic entity, and there is more variation within than between groups, yet its social effects are not insignificant.14 While race has been used to do untold harm—and as a South African, the experience is recent—its use in dermatology is a vexed question. For example, the definition of “African hair” is important because this hair form is associated with a higher prevalence of specific disorders (eg, acne keloidalis15). The latter may seem like a contradiction, especially in view of what I said above, until one realizes that race is in fact only a proxy for hair form. Within groups of “African” and “Asian” hair reside extremes of the spectrum of hair morphology, with the majority, typical of human variation, falling within these extremes. Even indigenous Africans in Africa display variations in hair form. I agree with Bigby et al that race should be abandoned, and whilst it is a useful, albeit nonspecific, surrogate for hair form, its use suggests a lack of rigor on our part.

There have been at least three previous attempts, as cited by Hrdy,5 to classify hair form. They have included: straight, wavy, frizzy, and woolly; straight, wavy, kinky, and woolly; and lastly straight, wavy, and helical. These classifications have all become historic records which may be a sign of our comfort with current terminology, the lack of representative participation in their development, or perhaps a case of teaching old dogs new tricks! There is need for a creative, inclusive, classification of hair form which should be user-friendly and could be an adaptation of one of the above. Fitzpatrick's16 “or other classifications” could also be adapted and evaluated for reliability as replacement for race, only if skin color is relevant in clinical reports. A credible development of such classifications could ensure their international acceptance. If it were not for disorders that are prevalent in specific hair forms and skin colors, attempts to clarify terminology would be unnecessary. Unlike other medical disciplines, where traits are often invisible polymorphisms, we have a unique opportunity in dermatology. Why should we settle for proxies and surrogates when we can be more specific?

References 

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1. 1Bigby M, Thaler D. Describing patients' “race” in clinical presentations should be abandoned. J Am Acad Dermatol. 2006;54:1074–1076. Full Text | Full-Text PDF (76 KB) | CrossRef

2. 2Bigby M, Bernhard JD. Proposed policy on identification of race, ethnicity, or skin color in case reports and studies submitted to the Journal of the American Academy of Dermatology. J Am Acad Dermatol. 2006;54:1077. Full Text | Full-Text PDF (56 KB) | CrossRef

3. 3Unaeze J, Bigby M. The frequency of reporting of race/ethnicity in case reports. J Am Acad Dermatol. 2006;54:1067–1070. Full Text | Full-Text PDF (93 KB) | CrossRef

4. 4Jablonski NG, Chaplin G. The evolution of human skin coloration. J Hum Evol. 2000;39:57–106. MEDLINE | CrossRef

5. 5Hrdy D. Quantitative hair form variation in seven populations. Am J Phys Anthropol. 1973;39:7–17. MEDLINE | CrossRef

6. 6Lindelof B, Forslind B, Hedblad MA, Kaveus U. Human hair form. Morphology revealed by light and scanning electron microscopy and computer aided three-dimensional reconstruction. Arch Dermatol. 1988;124:1359–1363.

7. 7Thibaut S, Gaillard O, Bouhanna P, Cannell DW, Bernard BA. Human hair shape is programmed from the bulb. Br J Dermatol. 2005;152:632–638. MEDLINE | CrossRef

8. 8Lawes CM, Vander Hoorn S, Law MR, Elliott P, MacMahon S, Rodgers A. Blood pressure and the global burden of disease 2000. Part 1: estimates of blood pressure levels. J Hypertens. 2006;24:413–422. MEDLINE

9. 9Gray area for new heart failure drug. Although the FDA approved BiDil for blacks with heart failure, it may work in anyone. Harv Heart Lett. 2005;16:1–2. MEDLINE

10. 10Yusuf S, Hawken S, Ounpuu S, Dans T, Avezum A, Lanas F, et al.for the INTERHEART Study Investigators Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004;364:937–952. Abstract | Full Text | Full-Text PDF (257 KB) | CrossRef

11. 11Puddu P, Cravero E, Puddu GM, Muscari A. Genes and atherosclerosis: at the origin of the predisposition. Int J Clin Pract. 2005;59:462–472. MEDLINE | CrossRef

12. 12Marks GB. Environmental factors and gene-environment interactions in the aetiology of asthma. Clin Exp Pharmacol Physiol. 2006;33:285–289. MEDLINE | CrossRef

13. 13Bronfenbrenner U. Nature with nurture: A reinterpretation of the evidence. In:  Montagu A editors. Race and IQ (1999 ed). New York: Oxford University Press; 1975;p. 153–183.

14. 14Smedley A, Smedley BD. Race as biology is fiction, racism as a social problem is real: anthropological and historical perspectives on the social construction of race. Am Psychol. 2005;60:16–26. CrossRef

15. 15Knable AL, Hanke CW, Gonin R. Prevalence of acne keloidalis nuchae in football players. J Am Acad Dermatol. 1997;37:570–574. Abstract | Full Text | Full-Text PDF (572 KB) | CrossRef

16. 16Fitzpatrick TB. The validity and practicability of sun-reactive skin types I through VI. Arch Dermatol. 1988;124:869–871.

Division of Dermatology, Groote Schuur Hospital, and The University of Cape Town, Cape Town, South Africa

Corresponding Author InformationCorrespondence to: N. P. Khumalo, MBChB, FCDerm, Division of Dermatology, Ward G23, Groote Schuur Hospital, Observatory 7925, South Africa

 Funding sources: None.

Conflicts of interest: None identified.

PII: S0190-9622(06)02846-5

doi:10.1016/j.jaad.2006.10.016


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