Volume 21, Issue 4 pp. 281-286
Original Article

In vivo quantification of epidermis pigmentation and dermis papilla density with reflectance confocal microscopy: variations with age and skin phototype

Sophie Garrido Lagarrigue

Sophie Garrido Lagarrigue

Toulouse University, Toulouse, France

CNRS UMR5165, Toulouse, France

INSERM U1056, Toulouse, France

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Jerome George

Jerome George

Pierre Fabre Dermo-Cosmétique, Toulouse, France

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Emmanuel Questel

Emmanuel Questel

Pierre Fabre Dermo-Cosmétique, Toulouse, France

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Christophe Lauze

Christophe Lauze

Pierre Fabre Biometrie, Toulouse, France

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Nicolas Meyer

Nicolas Meyer

Department of Dermatology, Toulouse University, Hôpital Larrey, Toulouse, France

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Jean-Michel Lagarde

Jean-Michel Lagarde

Pierre Fabre Dermo-Cosmétique, Toulouse, France

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Michel Simon

Michel Simon

Toulouse University, Toulouse, France

CNRS UMR5165, Toulouse, France

INSERM U1056, Toulouse, France

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Anne-Marie Schmitt

Anne-Marie Schmitt

Pierre Fabre Dermo-Cosmétique, Toulouse, France

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Guy Serre

Guy Serre

Toulouse University, Toulouse, France

CNRS UMR5165, Toulouse, France

INSERM U1056, Toulouse, France

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Carle Paul

Carle Paul

Toulouse University, Toulouse, France

CNRS UMR5165, Toulouse, France

INSERM U1056, Toulouse, France

Department of Dermatology, Toulouse University, Hôpital Larrey, Toulouse, France

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First published: 17 January 2012
Citations: 44
Carle Paul, Department of Dermatology, Paul Sabatier University, Larrey Hospital, 24 Chemin de Pouvourville, 31059 Toulouse, Cedex 9, France, Tel.: +33 5 67 778140, Fax: +33 5 67 778142, e-mail: [email protected]

Abstract

Abstract: Reflectance confocal microscopy (RCM) may help to quantify variations of skin pigmentation induced by different stimuli such as UV radiation or therapeutic intervention. The objective of our work was to identify RCM parameters able to quantify in vivo dermis papilla density and epidermis pigmentation potentially applicable in clinical studies. The study included 111 healthy female volunteers with phototypes I–VI. Photo-exposed and photo-protected anatomical sites were imaged. The effect of age was also assessed. Four epidermis components were specifically investigated: stratum corneum, stratum spinosum, basal epidermal layer and dermo-epidermal junction. Laser power, diameter of corneocytes and upper spinous keratinocytes, brightness of upper spinous and interpapillary spinous keratinocytes, number of dermal papillae and papillary contrast were systematically assessed. Papillary contrast measured at the dermo-epidermal junction appeared to be a reliable marker of epidermis pigmentation and showed a strong correlation with skin pigmentation assessed clinically using the Fitzpatrick’s classification. Brightness of upper spinous and interpapillary spinous keratinocytes was not influenced by the skin phototype. The number of dermal papillae was significantly lower in subjects with phototypes I–II as compared with darker skin subjects. A dramatic reduction in the number of dermal papillae was noticed with age, particularly in subjects with fair skin. The method presented here provides a new in vivo investigation tool for quantification of dermis papilla density and epidermal pigmentation. Papillary contrast measured at the dermo-epidermal junction may be selected as a marker of skin pigmentation for evaluation in clinical studies.

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