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1.
Br J Dermatol ; 165(5): 1011-21, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21787368

ABSTRACT

BACKGROUND: Skin ageing is said to be caused by multiple factors. The relationship with sun exposure is of particular interest because the detrimental cutaneous effects of the sun may be a strong motivator to sun protection. We report a study of skin ageing in participants of an epidemiological study of melanoma. OBJECTIVES: To determine the predictors of periorbital cutaneous ageing and whether it could be used as an objective marker of sun exposure. METHODS: Photographs of the periorbital skin in 1341 participants were graded for wrinkles, degree of vascularity and blotchy pigmentation and the resultant data assessed in relation to reported sun exposure, sunscreen use, body mass index (BMI), smoking and the melanocortin 1 receptor (MC1R) gene status. Data were analysed using proportional odds regression. RESULTS: Wrinkling was associated with age and heavy smoking. Use of higher sun-protection factor sunscreen was protective (P = 0·01). Age, male sex, MC1R variants ('r', P=0·01; 'R', P=0·02), higher reported daily sun exposure (P=0·02), increased BMI (P=0·01) and smoking (P=0·02) were risk factors for hypervascularity. Blotchy pigmentation was associated with age, male sex, higher education and higher weekday sun exposure (P=0·03). More frequent sunscreen use (P=0·02) and MC1R variants ('r', P=0·03; 'R', P=0·001) were protective. CONCLUSIONS: Periorbital wrinkling is a poor biomarker of reported sun exposure. Vascularity is a better biomarker as is blotchy pigmentation, the latter in darker-skinned individuals. In summary, male sex, sun exposure, smoking, obesity and MC1R variants were associated with measures of cutaneous ageing. Sunscreen use showed some evidence of being protective.


Subject(s)
Melanoma/pathology , Skin Aging/radiation effects , Skin Neoplasms/pathology , Sunlight/adverse effects , Adult , Aged , Case-Control Studies , Female , Genotype , Humans , Male , Middle Aged , Obesity/complications , Obesity/pathology , Observer Variation , Orbit , Receptor, Melanocortin, Type 1/genetics , Skin/blood supply , Skin Aging/genetics , Skin Pigmentation , Smoking/adverse effects , Sunburn/pathology
2.
Br J Cancer ; 97(9): 1211-7, 2007 Nov 05.
Article in English | MEDLINE | ID: mdl-17968426

ABSTRACT

Many factors involved in wound healing can stimulate tumour growth in the experimental setting. This study examined the relationship between wound complications and the development of systemic recurrence after treatment of primary breast cancer. One thousand and sixty-five patients diagnosed with operable primary invasive breast cancer between 1994 and 2001 were assessed for development of systemic recurrence according to whether or not a wound complication occurred after surgery, with a median follow-up of 54 months (range 15-119). There were 93 wound complications (9%). There was a statistically significant greater risk of developing systemic recurrence in patients with wound problems than those without (hazard ratio (HR) 2.87; 95% CI: 1.97, 4.18; P<0.0001). This remained in a multivariate analysis after adjustment for case mix variables, including Nottingham Prognostic Index (NPI) and oestrogen-progesterone receptor status (HR: 2.52; 95% CI: 1.69, 3.77; P<0.0001). In the good prognostic NPI group, 4 out of 27 patients (15%) with wound problems vs 11 out of 334 (3%) without wound problems developed systemic recurrence. The corresponding figures were 10 out of 35 (29%) vs 48 out of 412 (12 %) in the moderate prognostic group and 18 out of 29 (62%) vs 75 out of 199 (38%) in the poor prognostic group. In 29 patients NPI could not be calculated. Smokers at the time of diagnosis were more likely to develop metastatic disease than the non-smokers (HR: 1.50; 95% CI: 1.04, 2.15; P=0.03) after adjustment for other factors. The results suggest that patients with wound complications at primary surgery have increased rates of systemic recurrence of breast cancer.


Subject(s)
Breast Neoplasms/surgery , Carcinoma, Ductal, Breast/surgery , Neoplasm Recurrence, Local/etiology , Postoperative Complications , Adult , Aged , Aged, 80 and over , Breast Neoplasms/complications , Carcinoma, Ductal, Breast/complications , Female , Follow-Up Studies , Humans , Middle Aged , Survival Rate , Treatment Outcome , Wound Healing
3.
Br J Cancer ; 96(5): 836-40, 2007 Mar 12.
Article in English | MEDLINE | ID: mdl-17311024

ABSTRACT

In a large population-based series of invasive breast cancer patients, we investigated socioeconomic background (SEB) in relation to (a) stage at diagnosis; (b) treatment pattern; and (c) 5-year survival. Women diagnosed during 1998-2000 and resident in the Northern and Yorkshire regions of England were identified from the cancer registry database (N=12,768). Logistic regression and Cox proportional hazards analyses were used to estimate associations between SEB (defined using the Townsend Index for area of residence) and tumour stage, treatment pattern, and survival. Living in a more deprived area was associated with increased likelihood of being diagnosed with stage III or IV disease (age-adjusted odds ratio (OR) 1.13; 95% confidence interval (CI) 1.08-1.18 per quartile increase in Townsend score), and, after adjustment for age and stage, reduced odds of having surgery (OR 0.85; 95% CI 0.80-0.91), and receiving radiotherapy (OR 0.91; 95% CI 0.88-0.94). Amongst patients receiving surgery, those living in more deprived areas had decreased odds of having breast conserving surgery (age plus stage-adjusted OR 0.92; 95% CI 0.89-0.95). Living in a more deprived area was also associated with increased mortality (age- plus stage-adjusted hazard ratio 1.08; 95% CI 1.05-1.11). These effects may operate through several pathways, such as later presentation leading to advanced disease.


Subject(s)
Breast Neoplasms/mortality , Breast Neoplasms/pathology , Breast Neoplasms/therapy , Aged , Female , Health Services Accessibility , Humans , Medically Underserved Area , Middle Aged , Neoplasm Staging , Socioeconomic Factors , Survival Analysis , United Kingdom
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