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Facts about skin from the New Zealand Dermatological Society Incorporated. Topic index: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Ageing skin

Learning objectives
Introduction
Ultraviolet radiation
Biologic effects of light on normal skin
Skin Phototypes
Immune response
Chronic response to exposure to UVR
Activity

Learning objectives

Introduction

Skin changes with age. Some of this is intrinsic and some is extrinsic ageing due to environmental exposure, mainly photoageing. Smoking and other pollutants also age the skin, causing delayed healing after injury and enhancing facial lines.

Intrinsic ageing results in thinning of the epidermis and dermis, structural defects and immunological failure. These features are exaggerated in photo-aged skin, accompanied by lines, colour changes and neoplasia.

Photoageing is due to the effects of ultraviolet radiation (UVR) on the skin. The influence of visible light or infrared radiation is comparatively minor unless thermal burns arise.

Ultraviolet radiation

UVR is arbitrarily split into UVC (200-290 nm), UVB (290-320nm) and UVA (320-400nm). UVA is further divided into UVAI (340-400 nm) and UVAII (320-340 nm). Solar UVC does not pass through the ozone layer so is not present on the earth's surface.


The electromagnetic spectrum

UVR is at its greatest on the earth's surface when the sun is vertically overhead as it passes through thinner atmosphere than when the sun is at a greater angle. Thus:

There is also greater total UV:

Variation is greater for UVB than for UVA.

The global solar ultraviolet index (UVI) describes the level of solar UVR at the Earth's surface and ranges from 1 to 11+.

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UVR on clear day compared with cloudy day

UVR in different seasons
Measurements of UVR according to the time of day, Waikato Hospital 1989

The biological effects of light on normal skin

UVR causes biological effects on various tissues when it is absorbed. Injury to nucleic acids results in abnormal structures such as cyclobutane dimers and adducts. There are several repair mechanisms in normal individuals but their malfunction results in the development of aging changes and skin cancer.

The acute response of the skin to exposure to UVR has rapid onset (minutes to days) and short duration (hours to weeks).

Erythema mainly results from UVB i.e. wavelengths <320nm. It arises from dilation of the superficial blood vessels produced by cytokines. Solar-induced erythema is delayed by a few hours after exposure. Delayed tanning is noticeable two days after exposure and most intense a week afterwards. It is due to melanogenesis and distribution of melanin to keratinocytes throughout the epidermis. UVA and even visible radiation may cause melanogenesis, but UVB is the most effective in initiating it.

Further exposure to UVR causes less damage:

UVB converts precursors in the skin into vitamin-D. The liver, then the kidneys, change vitamin-D into calcitriol (1,25 dihydroxycholecalciferol), which is required for calcium homeostasis.

Skin cancers are due to progressive mutations in DNA. They are induced by:

Skin Phototypes

Fitzpatrick Skin Phototypes 1 to 6 are used to classify the effect of sun exposure on an individual's skin. Types 1 & 2 are at high risk of skin cancer, particularly when exposed to intense sunlight.

Type 1: Very fair. Burns easily, doesn't tan
Type 2: Fair. Burns easily, tans lightly
Type 3: Olive. Burns somewhat, tans readily
Type 4: Light brown. Burns rarely, tans well
Type 5: Dark brown. Doesn't burn, tans deeply
Type 6: Black

Type I: Solar keratoses

Type 2: Sunburn

Type 3: Suntan

Type 4: Melasma

Type 5: Acne

Type 6: Early vitiligo
Skin phototypes

Immune response

UVR results in profound alterations of both local and systemic immune responses:

Chronic response to exposure to UVR

Sun damage (photoageing) includes:


Thin transparent and wrinkled skin

Furrows due to muscle movement
and loss of subcutaneous fat

Freckles and lentigines

Senile purpura
Signs of photoageing

Glogau skin types

Glogau skin types refer to the degree of photoageing:

Activity

Determine Fitzpatrick Skin Phototype in 20 patients over 60 years of age. Compare this to their Glogau skin type.

 

Page 2 of 15. Next topic: Epidemiology of non-melanoma skin cancer. Back to: Skin lesions course contents.

Related information

References:

On DermNet NZ:

Information for patients

Other websites:

Books about skin diseases:

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Author: Clin Assoc Prof Amanda Oakley

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If you have any concerns with your skin or its treatment, see a dermatologist for advice.