International Psoriasis Council

Advancing Knowledge. Improving Care.

Holistic Lifestyle Assessment and Psoriasis Susceptibility

Helen Young, MB, ChB, PhD, FRCP

The University of Manchester

Manchester, United Kingdom

IPC Councilor

Bio

PUBLICATIONS

Life’s Essential 8, Genetic Susceptibility and the Risk of Psoriatic Disease: A Prospective Cohort Study. Ouyang F, Yang H, Di Z, et al. Br J Dermatol. 2024 Nov 18;191(6):897-905. doi: 10.1093/bjd/ljae268. PMID: 38912785.

Why This Article Was Chosen

Psoriasis, which affects approximately 60 million people worldwide, has a strong genetic component, with heritability estimated at 66%.1,2 Genetic studies have, to date, observed the strongest association within the major histocompatibility complex (MHC) region on chromosome 6 and provided evidence for the IL23/IL17 pathway in disease pathogenesis.3-5 

Despite the association between psoriasis and other comorbid medical conditions, previous research, to date, has suggested that there is no interaction between the genetic risk of psoriasis and lifestyle factors.6 The authors of this paper conducted a prospective cohort study, utilizing data from the UK Biobank, to further explore any possible association between lifestyle and other modifiable risk factors of cardiovascular disease with the onset of new cases of psoriatic disease and to investigate whether genetic susceptibility could modify such associations.

Commentary

Psoriatic disease, including psoriasis and psoriatic arthritis, is associated with comorbidities such as cardiovascular disease (CVD), diabetes, hypertension, metabolic syndrome, anxiety, and depression.7,8 These psoriasis-associated comorbidities represent a substantial burden on both society and individuals. Consequently, exploring modifiable and easily monitored risk factors holds considerable importance for preventing and managing psoriasis.

Life’s Essential 8 (LE8) is an updated metric introduced by the American Heart Association (AHA) in 2022 to assess cardiovascular health holistically. It builds on Life’s Simple 7 (introduced in 2010) by incorporating sleep as a new component. Ultimately, LE8 encompasses diet, physical activity, nicotine exposure, sleep health, body mass index (BMI), blood lipids, blood glucose, and blood pressure.9  Each component is assigned a score on a scale of 0–100, and the overall composite score for cardiovascular health, ranging from 0–100, is calculated as the unweighted average of the 8 component scores. Following the guidelines of the AHA, composite scores are categorized into three groups: high level of cardiovascular health (80–100 points), moderate cardiovascular health (50–79 points), and low cardiovascular health (0–49 points).9 Genetic factors play a significant role in the onset of psoriatic disease, with the HLA-C*06:02 allele considered a major genetic risk factor for early-onset psoriasis. Inheriting this allele is associated with a 4–5-fold increased risk of developing psoriasis.10,11 To date, genome-wide association studies have accounted for approximately 30% of the disease.

The authors of this aimed to investigate the longitudinal association between LE8 score and the risk of psoriatic disease, to specifically explore the association of lifestyle factors (as measured with LE8 score) with the onset of new cases of psoriatic disease and to investigate further whether genetic susceptibility could modify such associations.

The data for the study were derived from the UK Biobank, which has > 500,000 participants aged between 37 and 73 years and was initially established to investigate genetic and nongenetic determinants of various diseases comprehensively.12  After excluding participants who lacked data related to the LE8 components, had missing genetic information, had self-reported or already had been diagnosed with psoriatic disease at baseline, and those with incomplete follow-up data, a total of 261,642 participants were included. During an average follow-up of 12.3 years, 1,501 participants developed psoriatic disease. Compared with participants with low LE8 scores, the hazard ratio (HR)s of developing psoriatic disease for those with moderate and high LE8 scores were 0.51 (95% CI 0.43–0.59) and 0.34 (95% CI 0.27–0.42) after adjustments, respectively. However, the key take-home message from this study was that dose-response analysis revealed a linear negative association between continuous LE8 score and the risk of developing psoriatic disease (P<0.001), with no evidence of nonlinear association detected. Genetic susceptibility to psoriatic disease did not modify this association (P interaction = 0.63), meaning that maintaining good cardiovascular health could help prevent psoriatic disease and its associated risks. Further subgroup analyses revealed that women had a more pronounced beneficial association between LE8 scores and psoriatic disease risk (P interaction = 0.02) than men. However, the authors cautioned that, given the study’s observational nature, the association between LE8 and psoriatic disease risk should not be interpreted as causal.

In summary, this study suggests that maintaining good cardiovascular health could prevent the development of psoriatic disease in the entire population, regardless of genetic background. It emphasizes the crucial role of holistic lifestyle assessment (such as LE8 score) in prevention strategies/messaging.

References

  1. Parisi R, et al. Iskandar I, Kontopantelis E, et al. National, Regional, and Worldwide Epidemiology of Psoriasis: Systematic Analysis and Modelling Study. BMJ. 2020;369:m1590.
  2. Grjibovski AM, Olsen AO, Magnus P, et al.  Psoriasis in Norwegian Twins: Contribution of Genetic and Environmental Effects. J Eur Acad Dermatol Venereol. 2007;21:1337-43.
  3. Tsoi LC, Stuart PE, Tian C, et al. Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis Associated Variants. Nat Commun. 2017;8:15382.
  4. Nair RP, Ding J, Callis Duffin K,  et al. Psoriasis Bench to Bedside: Genetics Meets Immunology. Arch Dermatol. 2009;145: 462-4.
  5. Mahil SK, Capon F, Barker JN. Genetics of Psoriasis. Dermatol Clin. 2015;33:1-11.
  6. Shen M, Xiao Y, Jing D, et al. Associations of Combined Lifestyle and Genetic Risks with Incident Psoriasis: A Prospective Cohort Study Among UK Biobank Participants of European Ancestry. J Am Acad Dermatol. 2022; 87:343–50.
  7. Armstrong AW, Read C. Pathophysiology, Clinical Presentation, and Treatment of Psoriasis: A Review. JAMA  2020; 323:1945–60.
  8. Mrowietz U, Sümbül M, Gerdes S. Depression, a Major Comorbidity of Psoriatic Disease, is Caused by Metabolic Inflammation. J Eur Acad Dermatol Venereol. 2023; 37:1731–8.
  9. Lloyd-Jones DM, Allen NB, Anderson CAM, et al. Life’s Essential 8: Updating and Enhancing the American Heart Association’s Construct of Cardiovascular Health: A Presidential Advisory from the American Heart Association. Circulation. 2022; 146:e18–43.
  10. Nair RP, Stuart PE, Nistor I, et al. Sequence and Haplotype Analysis Supports HLA-C as the Psoriasis Susceptibility 1 Gene. Am J Hum Genet. 2006; 78:827–51.
  11. Strange A, Capon F, Spencer CCA, et al.  A Genome-wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1. Nat Genet. 2010; 42:985–90.
  12. Sudlow C, Gallacher J, Allen N, et al. UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age. PLoS Med. 2015; 12:e1001779.

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