There is a significant amount of research examining the link between psoriasis and common mental health disorders; however, studies on less common psychiatric disorders, such as bipolar disorder (BD), remain limited. We conducted a systematic review of studies in the PubMed and Cochrane databases that explored the relationship between BD and psoriasis. Additionally, we evaluated the impact of lithium on psoriasis in patients with BD and included a quality assessment of all the studies. This review covers five studies that addressed the connection between psoriasis and psychiatric disorders, three studies on medical conditions in patients with BD, and four studies examining the effects of lithium intake on psoriasis in BD patients. We found substantial evidence supporting a link between psoriasis and BD, suggesting that psoriasis is an independent risk factor for BD. Patients with psoriasis are also more likely to use psychotropic medications. A limited number of studies indicate that lithium therapy may trigger or worsen psoriasis. We also explore the mechanisms of lithium-induced or -aggravated psoriasis, highlighting the intricate interplay between lithium treatment, inositol depletion, and psoriasis in patients with BD. In a placebo-controlled, randomized study, inositol supplementation could mitigate psoriasis in patients taking lithium. Additional research is needed to evaluate the efficacy of inositol supplementation for patients with psoriasis who need to continue lithium treatment for their BD. Psoriasis is a chronic inflammatory skin disease affecting 2-3% of the global population. It is characterized by an abnormal immune response involving dendritic cells, T helper (Th)1/Th17 lymphocytes, and keratinocytes, each engaging in a pathologic interplay that leads to systemic effects mediated by the cytokine milieu beyond skin changes. Psoriasis has a significant impact on the quality of life of affected individuals. Patients with psoriasis, especially those with severe forms, experience numerous comorbidities, including psychiatric disorders. People who suffer from psoriasis face an increased risk of developing various mental illnesses, including depression and anxiety, potentially linked to the increased inflammatory cytokine burden that affects neuropsychiatric pathways. The visible effects of psoriasis may also lead to significant stress, reduced self-esteem, and stigma, further contributing to adverse psychiatric outcomes. There is significant amount of research concerning the link between psoriasis and common mental disorders, such as major depressive disorder (MDD). Studies on less common psychiatric disorders, like bipolar disorder (BD), remain limited. BD affects approximately 1-3% of the global population and is characterized by alternating episodes of depression and mania (or hypomania). It leads to considerable changes in mood and energy levels, resulting in severe impairments in personal, social, and occupational functioning. Lithium is a well-established treatment for BD and is effective for managing acute mania and maintaining mood stability. Lithium possesses mood-stabilizing, antimanic, antidepressant, and anti-suicidal properties; however, its use can often complicate matters, because it may trigger or worsen psoriasis, which in turn significantly contributes to non-compliance with lithium therapy. The mechanisms by which lithium affects psoriasis remain poorly understood, with there being limited literature exploring psoriasis in patients with BD who are receiving lithium therapy.
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http://dx.doi.org/10.1016/j.clindermatol.2025.01.001 | DOI Listing |
The stress-induced keratin intermediate filament gene/protein (K16) is spatially restricted to the suprabasal compartment of the epidermis and extensively used as a biomarker for psoriasis, hidradenitis suppurativa, atopic dermatitis and other inflammatory disorders. However, its role in these conditions remains poorly defined. Here we show that K16 negatively regulates type-I interferon (IFN) signaling and innate immune responses.
View Article and Find Full Text PDFClin Exp Dermatol
January 2025
College of Medicine, The University of Arizona, Tucson, AZ, USA.
BMC Immunol
January 2025
Laboratoire Génomique, Bioinformatique, et Chimie Moléculaire, Conservatoire National des Arts et Métiers, 2 rue Conté 75003, Paris, EA7528, France.
Introduction: We have reanalyzed the genomic data from the International Collaboration for the Genomics of HIV (ICGH), focusing on HIV-1 Elite Controllers (EC).
Methods: A genome-wide association study (GWAS) was performed, comparing 543 HIV-1 EC individuals with 3,272 uninfected controls (CTR) of European ancestry. 8 million single nucleotide polymorphisms (SNPs) and HLA class I and class II gene alleles were imputed to compare EC and CTR.
Immunol Res
January 2025
Department of Rheumatology and Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
This study assessed trends in age-standardized incidence (ASIR), prevalence (ASPR), and mortality rates (ASMR) per 100,000 population for asthma, Type 1 Diabetes Mellitus (T1DM), Inflammatory Bowel Disease (IBD), Multiple Sclerosis (MS), Psoriasis, and Rheumatoid Arthritis (RA) in China from 1990 to 2021 and projected ASIR trends through 2046. Data were obtained from the Global Burden of Disease (GBD) 2021 study. Trends in ASIR, ASPR, and ASMR were analyzed using Joinpoint regression to calculate annual percentage change (APC) and average APC (AAPC).
View Article and Find Full Text PDFBMJ Open
January 2025
Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark.
Introduction: Omalizumab, an anti-IgE monoclonal antibody, is effective in treating antihistamine-refractory chronic spontaneous urticaria (CSU). However, tapering strategies for omalizumab are currently not well-studied, and patients may be treated longer than needed. Here, we present the rationale and design of the EXtending Omalizumab Treatment Intervals in patients with Chronic spontaneous urticaria trial, a multicentre, randomised, open-label, non-inferiority clinical trial.
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