A Comparative Study of Clinical and Dermoscopic Patterns of Psoriasis in Smokers and Non-Smokers Attending a Tertiary Care Hospital

Authors:
  • Saurabh D Raut , Assistant Professor, Department of Dermatology, Shri Balaji Institute of Medical Science, Raipur, India.
  • Ajit Kumar , Assistant Professor, Department of Dermatology, Shri Balaji Institute of Medical Science, Raipur, India.
  • Sandeep Agrawal , Assistant Professor, Department Of Community Medicine, Pt. JNM Medical College Raipur, India.

Article Information:

Published:November 9, 2024
Article Type:Original Research
Pages:83 - 85
Received:September 11, 2024
Accepted:October 28, 2024

Abstract:

Introduction Psoriasis is a chronic immune-mediated inflammatory skin disorder with multifactorial etiology involving genetic, environmental, and lifestyle factors. Smoking has been recognized as an important risk factor influencing disease severity and progression. Dermoscopy has emerged as a useful non-invasive diagnostic tool in psoriasis Aim To compare the clinical and dermoscopic patterns of psoriasis among smokers and non-smokers attending a tertiary care hospital. Materials and Methods: A hospital-based comparative cross-sectional study was conducted among 120 clinically diagnosed psoriasis patients attending the Dermatology outpatient department over one year. Patients were divided into smokers (n=60) and non-smokers (n=60). Detailed clinical examination and dermoscopic evaluation were performed. Disease severity was assessed using Psoriasis Area Severity Index (PASI). Data were analyzed using SPSS version 25. Results: The mean age of participants was 41.8 ± 12.4 years. Male predominance was observed among smokers. Chronic plaque psoriasis was the most common clinical type in both groups. Smokers demonstrated significantly higher PASI scores compared to non-smokers (p<0.05). Dermoscopic findings including regularly distributed dotted vessels, diffuse white scales, red globules, and hemorrhagic spots were more prominent among smokers. Nail involvement and scalp psoriasis were also significantly higher in smokers. Conclusion: Smoking is associated with increased severity and distinct dermoscopic patterns in psoriasis patients. Dermoscopy serves as a valuable non-invasive tool for assessment of disease activity and vascular changes in psoriasis.

Keywords:

Psoriasis Dermoscopy Smoking PASI Chronic plaque psoriasis Non-smokers.

Article :

Introduction:

Psoriasis is a chronic, relapsing, immune-mediated inflammatory skin disorder affecting approximately 2–3% of the global population.[1] It is characterized by erythematous scaly plaques resulting from hyperproliferation and abnormal differentiation of keratinocytes along with inflammatory infiltration.[2]

 

The etiopathogenesis of psoriasis is multifactorial and involves genetic predisposition, environmental triggers, infections, psychological stress, obesity, alcohol intake, and smoking.[3] Smoking has emerged as an important modifiable risk factor associated with the onset, severity, and persistence of psoriasis.[4] Nicotine and other tobacco components are believed to influence immune pathways, cytokine release, and oxidative stress leading to exacerbation of psoriatic lesions.[5]

 

Several epidemiological studies have demonstrated increased prevalence and severity of psoriasis among smokers compared to non-smokers.[6] Smoking is also associated with poor therapeutic response, increased nail involvement, palmoplantar psoriasis, and psoriatic arthritis.[7]

 

Dermoscopy is a non-invasive diagnostic tool increasingly used in dermatology for evaluation of inflammatory dermatoses.[8] In psoriasis, characteristic dermoscopic features include regularly distributed dotted vessels on a light red background with diffuse white scaling.[9] Dermoscopy helps differentiate psoriasis from other papulosquamous disorders and assists in monitoring treatment response.[10]

 

Studies evaluating dermoscopic differences between smokers and non-smokers with psoriasis are limited, especially in the Indian population. Therefore, the present study was conducted to compare clinical and dermoscopic patterns of psoriasis among smokers and non-smokers attending a tertiary care hospital.

Materials and Methods:

Study Design and Setting

This hospital-based comparative cross-sectional study was conducted in the Department of Dermatology at a tertiary care teaching hospital over a period of one year.

 

Study Population

A total of 120 clinically diagnosed psoriasis patients were included and divided into:

               Smokers: 60 patients

               Non-smokers: 60 patients

 

Inclusion Criteria

               Patients aged ≥18 years

               Clinically diagnosed psoriasis cases

               Patients willing to participate

 

Exclusion Criteria

               Patients on systemic immunosuppressive therapy

               Pregnant and lactating females

               Patients with severe systemic illness

               Patients unwilling to participate

 

Data Collection

Detailed demographic history, smoking history, duration of disease, family history, comorbidities, and treatment history were recorded.

 

Clinical Assessment

Clinical type of psoriasis, body surface area involvement, nail changes, scalp involvement, and joint symptoms were documented. Disease severity was assessed using Psoriasis Area Severity Index (PASI).

 

Dermoscopic Evaluation

Dermoscopic examination was performed using a handheld dermoscope under polarized mode. Features assessed included:

               Dotted vessels

               White scales

               Red globules

               Hemorrhagic spots

               Vascular arrangement

               Background erythema

 

Statistical Analysis

Data were analyzed using SPSS version 25. Chi-square test and Student’s t-test were used where appropriate. A p-value <0.05 was considered statistically significant.

Results:

Demographic Profile

Among smokers, 48 (80%) were males and 12 (20%) were females, whereas non-smokers included 32 (53.3%) males and 28 (46.7%) females.

Variable

Smokers

Non-Smokers

Mean age (years)

43.2 ± 11.8

40.4 ± 12.9

Male (%)

80%

53.3%

Female (%)

20%

46.7%

 

Clinical Characteristics

Chronic plaque psoriasis was the predominant clinical type in both groups.

Clinical Type

Smokers (%)

Non-Smokers (%)

Chronic plaque psoriasis

76.7

71.7

Guttate psoriasis

8.3

13.3

Palmoplantar psoriasis

10

6.7

Erythrodermic psoriasis

5

8.3

 

Mean PASI score was significantly higher among smokers (14.6 ± 5.2) compared to non-smokers (10.8 ± 4.6).

Nail involvement was observed in 46.7% smokers and 25% non-smokers.

Scalp involvement was present in 58.3% smokers and 38.3% non-smokers.

 

Dermoscopic Findings

Dermoscopic Feature

Smokers (%)

Non-Smokers (%)

Regular dotted vessels

91.7

83.3

Diffuse white scales

95

88.3

Red globules

48.3

26.7

Hemorrhagic spots

36.7

15

Background erythema

86.7

73.3

Dermoscopic vascular prominence and hemorrhagic spots were significantly more common among smokers (p<0.05).

 

Discussion:

The present study demonstrated that smoking is associated with increased clinical severity and distinctive dermoscopic findings in psoriasis patients. Male predominance among smokers was consistent with previous studies conducted by Naldi et al. and Armstrong et al.[11,12]

 

Smoking has been implicated in psoriasis pathogenesis through activation of inflammatory cytokines including TNF-α, IL-17, and IL-23 pathways.[13] Nicotine-induced oxidative stress and endothelial dysfunction may contribute to increased vascular proliferation observed dermoscopically in smokers.[14]

 

Higher PASI scores among smokers observed in the present study are comparable to findings reported by Fortes et al., who demonstrated dose-dependent association between smoking and psoriasis severity.[15]

 

Regular dotted vessels and diffuse white scales were common dermoscopic findings in both groups, consistent with observations by Lallas et al.[16] However, hemorrhagic spots and prominent vascular changes were more frequent among smokers, possibly due to smoking-induced microvascular alterations.[17]

 

Nail and scalp involvement were significantly more common among smokers. Similar findings were reported by Rai et al. and Gupta et al. in Indian studies.[18,19]

 

Dermoscopy proved to be a valuable non-invasive tool in assessing vascular and scaling patterns in psoriasis and may aid in evaluating disease severity and treatment response.[20].

Conclusion:

Smoking is significantly associated with greater disease severity, nail involvement, scalp lesions, and distinct dermoscopic vascular patterns in psoriasis patients. Dermoscopy provides important additional information regarding disease activity and vascular changes. Smoking cessation counseling should be integrated into psoriasis management for better clinical outcomes.

References:

1.        Griffiths CE, Barker JN. Pathogenesis and clinical features of psoriasis. Lancet. 2007;370(9583):263-71.

2.        Lowes MA, Bowcock AM, Krueger JG. Pathogenesis and therapy of psoriasis. Nature. 2007;445(7130):866-73.

3.        Nestle FO, Kaplan DH, Barker J. Psoriasis. N Engl J Med. 2009;361(5):496-509.

4.        Armstrong AW, Harskamp CT, Dhillon JS, Armstrong EJ. Psoriasis and smoking: A systematic review and meta-analysis. Br J Dermatol. 2014;170(2):304-14.

5.        Naldi L. Epidemiology of psoriasis. Curr Drug Targets Inflamm Allergy. 2004;3(2):121-8.

6.        Setty AR, Curhan G, Choi HK. Smoking and risk of psoriasis in women. Am J Med. 2007;120(11):953-9.

7.        Mallbris L, Granath F, Hamsten A, Ståhle M. Psoriasis is associated with lipid abnormalities at onset of skin disease. J Am Acad Dermatol. 2006;54(4):614-21.

8.        Errichetti E, Stinco G. Dermoscopy in general dermatology: A practical overview. Dermatol Ther (Heidelb). 2016;6(4):471-507.

9.        Lallas A, Kyrgidis A, Tzellos TG, Apalla Z, Karatolias A, Lefaki I, et al. Accuracy of dermoscopic criteria for diagnosis of psoriasis. Br J Dermatol. 2012;166(6):1198-205.

10.     Waskiel-Burnat A, Rakowska A, Sikora M, Ciechanowicz P, Olszewska M, Rudnicka L. Dermoscopy of psoriasis and psoriasiform dermatitis. Clin Dermatol. 2018;36(4):545-53.

11.     Naldi L, Chatenoud L, Linder D, Belloni A, Peserico A, Virgili AR, et al. Cigarette smoking, body mass index, and stressful life events as risk factors for psoriasis. J Invest Dermatol. 2005;125(1):61-7.

12.     Armstrong AW, Armstrong EJ, Fuller EN, Sockolov ME, Voyles SV. Smoking and pathogenesis of psoriasis. Arch Dermatol. 2011;147(8):949-56.

13.     Boehncke WH, Schön MP. Psoriasis. Lancet. 2015;386(9997):983-94.

14.     Wolk K, Mallbris L, Larsson P, Rosenblad A, Vingård E, Ståhle M. Excessive body weight and smoking associates with a high risk of onset of plaque psoriasis. Acta Derm Venereol. 2009;89(5):492-7.

15.     Fortes C, Mastroeni S, Leffondré K, Sampogna F, Melchi F, Mazzotti E, et al. Relationship between smoking and psoriasis. Arch Dermatol. 2005;141(12):1580-4.

16.     Lallas A, Argenziano G, Apalla Z, Gourhant JY, Zaballos P, Di Lernia V, et al. Dermoscopic patterns of common inflammatory skin disorders. Dermatol Clin. 2013;31(4):621-32.

17.     Kim GW, Jung HJ, Ko HC, Kim MB, Lee WJ, Lee SJ, et al. Dermoscopy can be useful in differentiating scalp psoriasis from seborrheic dermatitis. Ann Dermatol. 2011;23(4):437-41.

18.     Rai R, Srinivas CR, Shenoi SD, Balachandran C. Clinical profile of psoriasis in South India. Indian J Dermatol Venereol Leprol. 2011;77(5):541-4.

19.     Gupta S, Kumar B. Psoriasis and smoking: A prospective observational study. Indian Dermatol Online J. 2014;5(3):287-91.

20.     Errichetti E, Lacarrubba F, Micali G, Stinco G. Dermoscopy of inflammatory dermatoses (inflammoscopy): An up-to-date overview. Dermatol Pract Concept. 2019;9(3):169-80.

21.     Christophers E. Psoriasis—epidemiology and clinical spectrum. Clin Exp Dermatol. 2001;26(4):314-20.

22.     Dogra S, Yadav S. Psoriasis in India: Prevalence and pattern. Indian J Dermatol Venereol Leprol. 2010;76(6):595-601.

23.     Kurd SK, Troxel AB, Crits-Christoph P, Gelfand JM. The risk of depression and anxiety in patients with psoriasis. Arch Dermatol. 2010;146(8):891-5.

24.     Parisi R, Symmons DP, Griffiths CE, Ashcroft DM. Global epidemiology of psoriasis. J Invest Dermatol. 2013;133(2):377-85.

25.     Menter A, Gottlieb A, Feldman SR, Van Voorhees AS, Leonardi CL, Gordon KB, et al. Guidelines of care for management of psoriasis and psoriatic arthritis. J Am Acad Dermatol. 2008;58(5):826-50.