In vivo data of epidermal thickness evaluated by optical coherence tomography: Effects of age, gender, skin type, and anatomic site

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Summary

Background

The knowledge of epidermal thickness (ET) is of great significance in many areas of medical and biological research.

Objectives

We aimed to assess optical coherence tomography (OCT) in terms of precision, and to investigate the influence of several constitutional factors, such as age, gender, skin type, and anatomic site, on the mean ET using OCT in vivo.

Methods

Eighty-three subjects were studied using OCT in vivo. Intra- and inter-day repeatability measurements were performed. The mean ET was assessed in six different body sites of young (20–40 years old) and old (60–80 years old) Caucasians, respectively. An ethnic group was included into the study.

Results

OCT proved to be a precise technique in terms of repeatability and reproducibility as expressed in low coefficients of variation. Comparison of young and old Caucasians demonstrated a significant decrease of ET with age in all anatomic sites investigated. ET assessed in males and females did not significantly differ, except for forehead skin which is significantly thinner in old females than in males. ET observed in Caucasians did not significantly differ from ET measured in ethnic individuals. Anatomic sites insignificantly influenced ET on an inter-individual level. However, differences of ET between body sites on an intra-individual level are significant.

Conclusions

This was the first systematic in vivo study on ET investigating several influencing parameters of the epidermal dimension in a reasonable study sample by means of OCT. The results presented here may serve as ET reference data in a variety of clinical and experimental matters.

Introduction

The knowledge of the skin thickness is of great significance in many areas of medical and biological research. For example, to understand cutaneous reactions to biochemical or biophysical stimuli, knowledge of epidermal thickness (ET) and its dependence on factors such as gender, age, skin type, and anatomic site are important. Many authors have reported on assessment of ET in relation to various factors without drawing firm conclusions [1], [2], [3], [4], [5], [6]. These investigations have had different purposes, for example, including collection of baseline data on normal skin [4], investigation of the effect of previous sun exposure comparing different sites of the body [3], the relation between ET and pigmentation [2], or the effect of different constitutive factors [7]. Most previous in vivo studies on ET used confocal laser scanning microscopy (CM). These explorative investigations included only a few subjects [3], [4], [5], [8], and studies presenting larger samples (n > 50) have generally been based on histologic investigations either from many different parts of the body or from one anatomic site only [1], [7], [9], [10].

Histology represents the gold standard for morphological investigation of the skin, though biopsy may alter the original morphology, is non-repeatable on the same site and always requires an iatrogenic trauma. In the past decade, advances in optics, fiber as well as laser technology, have enabled the development of novel non-invasive optical biomedical imaging techniques including CM and optical coherence tomography (OCT) [11], [12], [13], [14], [15], [16]. The latter is a promising non-invasive technique capable of generating cross-sectional images of tissue microstructure. The method works analogously to an ultrasound scanner—the major difference is [17], [18], however, that ultrasound pulses are replaced by a fiber-optic Michelson interferometer with a low-coherence-length broadband light source (infrared). The corresponding short coherence length permits a spatial resolution in depth direction of less than 10 μm. The lateral resolution, typically 10–15 μm in conventional OCT, is given by the numerical aperture of the employed objective as long as single scattering prevails. Depending on the scattering properties of tissue and some accepted loss in resolution, a penetration depth of about 1 mm can be achieved using conventional OCT scanners [19], [20], [21].

OCT is particularly capable to present morphological features of the epidermis and papillary dermis. In previous studies, skin appendages including hair follicles and eccrine ducts were identified by OCT [21], [22]. In a pilot study on ET, we observed a high correlation between OCT measurements and formalin-based histology, although the agreement of both methods was not satisfactory. However, agreement between OCT and cryostat-histology has recently been documented in a large-scale method comparison study [23]. Hence, OCT may be considered a very useful tool to study ET in vivo. In the present systematic investigation, we aimed, first, to study the performance the OCT method in terms of precision, second, to investigate the influence of several constitutional factors, such as age, gender, skin type, and anatomic site, on ET using OCT in vivo.

Section snippets

Study population

In total, 83 healthy subjects were included who gave their informed consent for the participation in the study. This study adhered to the Declaration of Helsinki. There were 71 Caucasians with skin types I–III (Fitzpatrick-classification) including subjects aged between 20 and 40 years, referred to as the younger group, and subjects aged between 60 and 80 years, referred to as the older group (Table 1). In addition, 12 subjects (20–40 years old) with skin types IV–VI were recruited, referred to

OCT precision

As shown in Table 1, there was no significant (P > 0.05) difference between the groups investigated with regard to the age of males and females. Intra- and inter-day repeatability of the OCT measurements in the stay-on modus showed a slightly better performance than the removal modus as indicated by a smaller CV on average (5.5% versus 8.5%). There were no significant differences between the intra- and inter-day measurements, respectively (ANOVA, P > 0.05). The CV value for intra-observer

Discussion

During recent years, the epidermis has been studied in vivo by means of non-invasive techniques such as high-frequency ultrasound, CM, and OCT [3], [4], [8], [17]. Nevertheless, these explorative studies included only small sample sizes and were not designed to establish definitive ET data in relation to various factors. Different OCT algorithms have been proposed for the assessment of ET in vivo [19], [22], [23], [24], [25]. Recently, we have demonstrated that the determination of mean ET

Acknowledgments

This study was performed in cooperation with the Ruhr Centre of Competence for Medical Engineering (KMR, Bochum, Germany) supported by the Federal Ministry of Education and Research (BMBF), grant no. 13N8079.

References (36)

  • J. Lock-Andersen et al.

    Epidermal thickness, skin pigmentation and constitutive photosensitivity

    Photodermatol Photoimmunol Photomed

    (1997)
  • K. Sauermann et al.

    Age-related changes of human skin investigated with histometric measurements by confocal laser scanning microscopy

    Skin Res Technol

    (2002)
  • S. Neerken et al.

    Characterization of age-related effects in human skin: a comparative study that applies confocal laser scanning microscopy and optical coherence tomography

    J Biomed Opt

    (2004)
  • S. Nouveau-Richard et al.

    In vivo epidermal thickness measurement: ultrasound vs. confocal imaging

    Skin Res Technol

    (2004)
  • J. Sandby-Moller et al.

    Epidermal thickness at different body sites: relationship to age, gender, pigmentation, blood content, skin type and smoking habits

    Acta Derm Venereol

    (2003)
  • P. Corcuff et al.

    Morphometry of human epidermis in vivo by real-time confocal microscopy

    Arch Dermatol Res

    (1993)
  • W.F.W. Southwood

    The thickness of the skin

    Plast Reconstr Surg

    (1955)
  • M.C. Branchet et al.

    Skin thickness changes in normal aging skin

    Gerontology

    (1990)
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