Abstract
Psoriasis is an immune-mediated systemic disease with associated comorbidities, including metabolic syndrome (MetS) which contributes substantially to premature mortality in patients with psoriasis. However, the pathological mechanisms underlying this comorbidity are unclear. Studies have shown that the pathological parameters of psoriasis mediate the development of MetS. We reviewed the potential mechanisms which mediate the association between psoriasis and MetS, including endoplasmic reticulum stress, pro-inflammatory cytokine releases, excess production of reactive oxygen species, alterations in adipocytokine levels and gut microbiota dysbiosis. Here, we highlight important research questions regarding this association and offer insights into MetS research and treatment.
Keywords: psoriasis, metabolic syndrome, gut microbiota, insulin resistance, autoimmunity, obesity
Introduction
Psoriasis, one of the most common chronic, recurrent, and inflammatory skin diseases, affects 2~3% of the total world population (1). There are several clinical cutaneous manifestations of psoriasis. The disease most commonly presents as chronic, symmetrical, erythematous, scaling papules and plaques (2). Pathologically, epidermal hyperproliferation and parakeratosis are the main histological features of psoriasis. Notably, increased release of pro-inflammatory cytokines and the chronic activation of innate and adaptive immune systems result in long-term damage to multiple tissues and organs of patients with psoriasis (3). Psoriasis is a systemic disease that is associated with multiple comorbidities, such as psoriatic arthritis, Crohn’s disease, cancer, depression, cardiovascular disease (CVD) (4), and metabolic syndrome (MetS). Among these, MetS is one of the most common and important comorbidities (5–8). An increasing number of clinical studies have confirmed that psoriasis is often related with MetS, such as obesity, hypertension, diabetes mellitus, hyperlipidemia, and obesity-associated non-alcoholic fatty liver disease (NAFLD) ( Figure 1 ) (9–15). Another study views that compared to patients with milder psoriasis, those with more severe psoriasis have greater hazard of MetS (16). MetS directly increases the risk of CVD and premature mortality in patients with psoriasis (17), thus substantially reducing their life expectancy. Therefore, it is critical to understand the exact mechanisms underlying the relationship between psoriasis and MetS.
Figure 1.
Metabolic diseases which frequently occur in patients with psoriasis. Psoriasis is often associated with obesity, hypertension, diabetes mellitus, hyperlipidemia, and obesity-associated non-alcoholic fatty liver disease, all of which belong to metabolic syndrome.
Recently, the prevalence of MetS in patients with psoriasis has attracted the attention of researchers. The precise mechanisms underlying the association between psoriasis and MetS remain unknown. Therefore, in this review, we have discussed these mechanisms, particularly, the pathogenic factors possibly involved, including endoplasmic reticulum (ER) stress in multiple cells, pro-inflammatory cytokine profiles, excess production of reactive oxygen species (ROS), alterations in adipocytokine levels, and gut microbiota dysbiosis. This review highlights the previously established and the emerging important mechanisms that link psoriasis with MetS.
Pro-Inflammatory Cytokines Linking Psoriasis and MetS
The hallmark of psoriasis is sustained inflammation (18). The pathogenesis of psoriasis has involvement of dynamic interactions between multiple cell types and cytokines (19). Th17 cells produce several cytokines, such as IL-17 (IL-17A/IL-17F), tumor necrosis factor-α (TNF-α), and IL-22 (4), which induce altered differentiation and hyperproliferation of keratinocytes. Therefore, Th17 cells play a predominant role in the pathogenesis of psoriasis and are indicators of an increased risk of psoriasis. Moreover, pro-inflammatory cytokines are implicated in many diseases, including obesity, diabetes mellitus, hypertension, NAFLD, and hyperlipidemia (20–23). It is well-known that tissue inflammation plays a critical role in insulin resistance (IR) (24–26). IR is the key primary defect underlying the development of type 2 diabetes (T2D), and it is also a central component of MetS (27).
IL-17 plays a crucial role in inflammation, IR, and T2D, indicating that it is a potential mediator linking MetS and psoriasis (28). It promotes a vascular inflammatory response and plays a critical role in angiotensin II-induced hypertension and vascular dysfunction (29). Previous studies reported that serum IL-17 levels were significantly elevated in subjects with MetS and Type 1 diabetes compared to health group (30, 31). Secukinumab, anti-IL-17A monoclonal antibody, is an effective biological agent for the treatment of plaque psoriasis. In patients with higher response for secukinumab, mean body weight, waist circumference, and BMI consistently decreased (32). Furthermore, combined administration of anti-IL-17A monoclonal antibody (secukinumab and ixekizumab) reduced fasting glucose levels in imiquimod treated mice and improved hyperglycemia in patients with psoriasis (33), suggesting that IL-17 may be a key cytokine linking psoriasis and hyperglycemia (34).
TNF is also closely associated with the pathogenesis of psoriasis. The Food and Drug Administration has approved efficacious TNF inhibitors for the treatment of moderate and severe plaque psoriasis, including infliximab, adalimumab, and etanercept (35). Patients with psoriasis who have administration of anti-TNF drugs often show an improvement in MetS. For patients with psoriasis, it has been demonstrated that the treatment with etanercept or adalimumab improved metabolic parameters including blood lipid and glucose levels and systolic and diastolic blood pressure (36). Another study further confirmed that anti-TNF treatment improves the metabolic profile of patients with psoriasis by downregulating their total cholesterol and low-density lipoprotein (LDL) levels (37). Mechanistically, TNF-α inhibits THP-1 cell uptake of oxidized LDL, thus increasing the extracellular accumulation of oxidized LDL (38). Additionally, the treatment with adalimumab significantly improves insulin sensitivity in patients with moderate-to-severe plaque psoriasis (39). TNF-α directly contributes to IR (40, 41) by activating stress kinases, such as IκB kinase, c-Jun N-terminal kinase, and p38 mitogen-activated protein kinase in muscle and fat cells, thereby blocking insulin signal transduction (42, 43). In some views, anti-TNF-α antibody is supposed as the first-line treatment for psoriasis with metabolic syndrome (44). In contrast, a view points out that the treatment with anti-TNF (infliximab and adalimumab) leads to no significant changes in insulin sensitivity or fasting glucose levels, but increased body fat (45). This may be due to the limited studied population, and only men were included.
Moreover, serum IL-1β, IL-6, and IL-22 levels were significantly upregulated in patients with T2D (46) and obese individuals (47, 48). Notably, deletion of IFN-γ improves IR and metabolic parameters in diet-induced obesity models (49). The above-mentioned studies have demonstrated that the immune system is closely linked to metabolic disorders. Pro-inflammatory cytokines may link psoriasis with MetS ( Figure 2 ).
Figure 2.
Possible mechanisms linking psoriasis and metabolic syndrome (MetS). The increased release of pro-inflammatory cytokines, adipose tissue secretory adipocytokines, activation of oxidative stress states, increased endoplasmic reticulum (ER) stress, and gut microbiota dysbiosis observed in psoriasis contribute to the development of MetS.
Adipocytokines Linking Psoriasis and MetS
Adipose tissues secrete adipocytokines that modulate organ functions and lipid metabolism. Leptin and adiponectin, two classical adipokines, are well-established endocrine hormones that act on specific receptors of remote target organs (50). Adiponectin is an insulin sensitizer that ameliorates IR and regulates glucose and lipid metabolism by binding to its receptors, AdipoR1 and AdipoR2 (51). This might be due to reduction in ectopic lipids in the liver and muscle (52). Adiponectin induces an increase in serum high-density lipoprotein (HDL) and down-regulates serum triglycerides through enhanced catabolism of triglyceride-rich lipoproteins (53). Adiponectin ameliorates obesity-induced NAFLD by interacting with hepatic peroxisome proliferator-activated receptors (54).
Several studies have demonstrated that low adiponectin concentrations in patients with psoriasis may contribute to the development of MetS. Of note, the serum adiponectin level is negatively associated with the TNF-α and IL-6 levels (55). TNF-α can impair adiponectin multimerization, consequently decreasing adiponectin secretion (56, 57). This might be a reasonable explanation for the lower adiponectin concentrations in patients with psoriasis compared to those of controls. Moreover, multiple studies postulate that adiponectin links the pathological processes of psoriasis and obesity (58). A meta-analysis has shown that patients with psoriasis exhibit low levels of adiponectin (59). Compared to patients with psoriasis without metabolic abnormalities, patients with psoriasis and MetS or high body mass index have significantly lower adiponectin levels. The psoriasis area and severity index (PASI) score (60) are negatively correlated with adiponectin levels (61, 62). Overall, low serum adiponectin levels in patients with psoriasis may be the link to MetS.
Leptin is a critical hormonal regulator of metabolism, and leptin concentrations are directly associated with the subsequent development of metabolic disorders such as IR, T2D, and CVD (63, 64). The reduction of plasma leptin levels in obese individuals can restore hypothalamic leptin sensitivity, then effectively enhancing insulin sensitivity, reduces weight gain (65). Increased leptin levels are observed in obese people and in patients with psoriasis (66), and are positively correlated with severity of psoriasis (67). The systemic anti-inflammatory drug, acitretin, used to treat psoriasis, reduces leptin levels (68). In addition, leptin is an important signaling transducer which may link obesity and psoriasis (69). One study reported that leptin levels were higher in obese patients with psoriasis than those of normal-weight patients (70). Moreover, leptin level is affected by IL-17 (71), which might explain the higher leptin concentrations observed in patients with psoriasis than controls. These studies suggest that high leptin levels may be an important factor in psoriasis-associated metabolic diseases.
Moreover, recent studies have hypothesized that several other important adipokines, such as retinol-binding protein 4, fetuin-A, and lipocalin-2 are mediators of obesity in psoriasis (58). Adipokines could serve as a crucial link in the causal relationship between psoriasis and MetS ( Figure 2 ) and may serve as biomarkers for determining the risk of developing psoriasis comorbidities.
Oxidative Stress Status in Patients with Psoriasis and the Association with MetS
Oxidative stress is the dysregulation between the production of ROS and endogenous antioxidant defense mechanisms, which causes protein and lipid peroxidation, DNA damage, and cellular dysfunction, eventually leading to cell death (72). Increased oxidative stress in adipocytes is one of pathological mechanisms of obesity-associated metabolic diseases (73, 74). Thus, reducing ROS production can increase insulin sensitivity and alleviate hyperlipidemia, hepatic steatosis, and IR (75, 76). Additionally, a positive correlation has been established between oxidative stress and low HDL levels (77). Furthermore, LDL-related dyslipidemia and impaired fasting glucose are associated with increased oxidative stress (78). Quantitative combination of natural antioxidants (vitamins C and E) prevents MetS by reducing oxidative stress (79). These results indicate that a pro-oxidant/antioxidant imbalance plays an important role in MetS development (80).
Numerous evidences support that increased ROS production and oxidative stress status are implicated in the progression of psoriasis. Studies have revealed that in the serum/plasma and blood cells of patients with psoriasis, oxidative damage markers increased (81–87). In addition, oxidative stress markers and PASI score have a positive correlation (88). The salivary total oxidative status and oxidative stress index may serve as potential diagnostic biomarkers for plaque psoriasis (89). Of note, the activated neutrophils/monocytes that generate oxidative damage may be the main source of oxidative stress in psoriasis. Increased oxidative stress in psoriasis may be caused by an insufficient antioxidant system (90). These evidences suggest that oxidative stress may contribute to the development of MetS in patients with psoriasis ( Figure 2 ).
Endoplasmic Reticulum Stress Links Psoriasis with MetS
ER is an important organelle with a vast membranous network in eukaryotic cells (91, 92). The ER has many cellular functions, including protein synthesis, folding, and transport, lipid and steroid synthesis, carbohydrate metabolism and calcium storage (93–96). The altered functions of ER can result in the accumulation of unfolded or misfolded proteins, which is a cellular condition named ER stress (97). Prolonged ER stress is a critical factor in the pathogenesis of MetS (98, 99). Inositol-requiring enzyme 1, an ER stress sensor, induces malfunction in both brown and beige fat, eventually leading to obesity (100). Treatment with the ER stress inhibitor (tauroursodeoxycholate) can improve metabolic parameters in MetS rat and mitigate the MetS-induced cardiovascular complications (101). Reducing ER stress can alleviate IR (102–105). Specifically, the interfered transport of newly synthesized insulin proreceptors from ER to the plasma membrane can inhibit the proteolytic maturation of insulin proreceptors. Consequently, the insulin signaling was broken by consuming the insulin receptors on cell surface (106).
Studies have shown that pro-inflammatory mediators such as TNF-α, IL-1β, IL-17A, and IFN-γ contribute to the induction of ER stress in multiple immunocytes such as macrophages and T cells (107–110). ER stress can be found in patients with psoriasis. Moreover, the over-expressed ER stress-associated proteins, including binding immunoglobulin heavy-chain protein, C/EBP homologous protein, and X-box binding protein 1 in the epidermis of patients with psoriasis vulgaris suggests that ER stress is increased in the keratinocytes of these patients (111). One study reported increased expression of ER stress marker GRP78/BIP in the subcutaneous fat tissues of imiquimod-induced psoriasiform in diabetic obese mice (112). Above evidences show increased ER stress is involved in psoriasis.
Overall, due to the common emergence of ER stress in both MetS and psoriasis, we may speculate that ER stress mediates their frequent co-occurrence ( Figure 2 ). However, there is less evidence on ER stress in the association between MetS and psoriasis. The ER stress in psoriasis that promotes MetS is expected to elucidate in further research.
Gut Microbiota in Patients with Psoriasis and its Association with MetS
In the bodies of adult mammals, skin, oral mucosa and gastrointestinal tract are heavily colonized by microbiota, with the largest population found in the colon. Microorganisms have variable relationships with their hosts and exist as mutualists, symbionts, or pathobionts (113). The gut microbiome plays important roles in host immunity, metabolism, and the production of numerous compounds that influence the host (114, 115). There is an emerging interest in metabolic health and gut microbiome dysbiosis. After the transplantation of metformin-treated human microbiome into germ-free mice with glucose intolerance, the glucose defects were corrected (116). Moreover, gut microbiota specifically controlled the expression of microRNAs in white adipocytes, controlling adiposity and insulin sensitivity in mice (117). Overall, these studies suggest that the gut microbiota regulates host metabolism and obesity.
Numerous studies have demonstrated the role of Akkermansia muciniphila in preventing obesity-associated metabolic disorders in both humans and animal models (118–121). Importantly, the intestinal microbes of patients with psoriasis show significant differences from those of healthy subjects (122–124). Notably, a previous study found that the abundance of A. muciniphila was significantly decreased in patients with psoriasis (125). Overall, compared with healthy controls, patients with psoriasis have a different specific intestinal microbiome. Therefore, we hypothesize that MetS in patients with psoriasis may be related to changes in the richness of specific flora ( Figure 2 ).
The intestinal microbiota plays critical roles in preserving epithelial barrier integrity, forming a mucosal immune system to battle with exogenous pathogens (126, 127). There are differences in intestinal permeability between individuals with and without T2D (128, 129). The disruption of barrier integrity is closely related with the emergence of metabolic disorder, such as obesity and T2D (127–130). Alleviated metabolic endotoxemia and enhanced intestinal barrier function causes significant weight loss and improves IR in diet-induced obese mice (131). The loss of intestinal barrier can cause the bacteria translocation and produce endotoxins or harmful metabolites, then induce systemic inflammation and aggravate MetS (132). For instance, elevated bacterial lipopolysaccharides in the circulation and organs activate the transcription of cytokines via toll-like receptor 4, promoting IR and metabolic diseases (133). Thus, the injured mucosal barrier induced by the gut microbiota involves in the development of MetS.
It has been found that barrier integrity injury and bacterial translocation are involved in the development of psoriasis (134). Bacterial DNA was detected in the peripheral blood of patients with psoriasis (135). In patients with moderate-to-severe psoriasis, serum markers of intestinal barrier integrity injury increased (136). For example, intestinal fatty acid binding protein, a biomarker of intestinal barrier damage, significantly elevated in patients with psoriasis compared to that in controls (137). From these studies, bacterial translocation may occur in psoriasis (138). Therefore, intestinal barrier impairment and bacterial translocation caused by dysbiosis of the gut microbiota may explain pathologically metabolic diseases in patients with psoriasis. Dysregulated gut microbiota in patients with psoriasis may be a novel therapeutic target in MetS.
Perspective
Accumulating evidence suggests there is a relationship between psoriasis and increased risks of MetS. However, major gaps in understanding of MetS in patients with psoriasis remain. In this review, we summarized numerous studies that links psoriasis and MetS. We assume that the emergence of some factors, including ER stress, pro-inflammatory cytokine releases, excess production of ROS, alterations in adipocytokine levels and gut microbiota dysbiosis, may be predictors of MetS in patients with psoriasis.
Specifically, it seems that the pathogenic pathways in psoriasis and MetS have considerable overlap. Thus, there is a possible interaction between the psoriasis and MetS. Psoriasis and MetS both show the chronic inflammatory state (139). Notably, some inflammatory factors, such as IL-17 and TNF, can both mediate the occurrence of psoriasis and MetS. Besides, adipocytokine, a vital meditator of MetS, can regulate body metabolism meanwhile contribute to the development of a pro-inflammatory state. Subsequent studies should focus on the causal relationship between the common pathogenic factors and psoriasis with MetS. Furthermore, the role of Th17-derived cytokines in the pathogenesis of psoriasis and MetS is both increasingly recognized. Anti-IL-17 agents or TNF inhibitors improved the metabolic disorder when treat psoriasis. Thus, further long-term and large-scale studies are warranted to identify whether anti-IL-17 agents or TNF inhibitors have benefits on psoriasis with MetS. Despite the pathological mechanism of MetS remains incompletely understood, oxidative stress and ER stress are considered as leading causes and can be therapeutically targeted (140, 141). In order to underly the pathophysiological mechanisms psoriasis and MetS, more connections from the complex molecular regulatory network should be established through muti-omics analysis. Future investigations should aim to determine the elaborate upstream and downstream signaling pathways that activate ER stress and oxidative stress in psoriasis complicated with MetS. What’s more, the dysregulated gut microbiota may become a novel therapeutic target in patients with psoriasis. The oral supplementation with A. muciniphila should be applied to investigate the effects on metabolic abnormalities in patients and or animal models with psoriasis. In addition, other possible targeted microbiotas should be screened in psoriasis and MetS through genomics and metabolomics. These selected microbiotas could be used as a biological marker for monitoring the MetS in psoriasis.
Collectively, our review implies that administration of MetS is of importance in clinical management of patients with psoriasis in the future. Elucidating the mechanisms linking MetS and psoriasis could provide potential new therapeutic targets and specific strategies to combat MetS in psoriasis, even other autoimmune disease, such as systemic lupus erythematosus and psoriatic arthritis.
Author Contributions
YH collected and reviewed the literature and wrote the manuscript. SZ and Y-jZ wrote and revised the manuscript. PZ rechecked the manuscript and put forward meaningful comments on it. Q-xZ and Y-wH assisted in drawing. Y-wH, L-nG and H-zZ revised the manuscript. ZW and JL designed the main study and reviewedthis manuscript. All authors have read and approved the final submitted manuscript.
Funding
This work was supported by the National Natural Science Foundation of China (81673061 to J. Li, 81472650 to J. Li, 31271483 to J. Li, 81703132 to Z. Wang), the National Science and Technology Major Project (2018ZX09303006-001-006 to J. Li and 2019ZX09201004-003 to J. Li), the Key Research and Development Program of Sichuan Province [2020YFS0271], the Applied Basic Research Program of Sichuan Province [2021YJ0420], the Postdoctoral Fund for West China Hospital [2019HXBH075], the Fundamental Research Funds for the Central Universities [2019SCU12041, the Postdoctoral Foundation of Sichuan University].
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
We appreciate Taylor & Francis Editing Services for their help on the language polishing and manuscript editing.
References
- 1. Scher JU, Ogdie A, Merola JF, Ritchlin C. Preventing Psoriatic Arthritis: Focusing on Patients With Psoriasis at Increased Risk of Transition. Nat Rev Rheumatol (2019) 15:153–66. 10.1038/s41584-019-0175-0 [DOI] [PubMed] [Google Scholar]
- 2. Mahil SK, Capon F, Barker JN. Update on Psoriasis Immunopathogenesis and Targeted Immunotherapy. Semin Immunopathol (2016) 38:11–27. 10.1007/s00281-015-0539-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Deng Y, Chang C, Lu Q. The Inflammatory Response in Psoriasis: A Comprehensive Review. Clin Rev Allergy Immunol (2016) 50:377–89. 10.1007/s12016-016-8535-x [DOI] [PubMed] [Google Scholar]
- 4. Boehncke WH, Schon MP. Psoriasis. Lancet (2015) 386:983–94. 10.1016/S0140-6736(14)61909-7 [DOI] [PubMed] [Google Scholar]
- 5. Takeshita J, Grewal S, Langan SM, Mehta NN, Ogdie A, Van Voorhees AS, et al. Psoriasis and Comorbid Diseases: Epidemiology. J Am Acad Dermatol (2017) 76:377–90. 10.1016/j.jaad.2016.07.064 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Peralta C, Hamid P, Batool H, Al Achkar Z, Maximus P. Psoriasis and Metabolic Syndrome: Comorbidities and Environmental and Therapeutic Implications. Cureus (2019) 11:e6369. 10.7759/cureus.6369 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Voiculescu VM, Lupu M, Papagheorghe L, Giurcaneanu C, Micu E. Psoriasis and Metabolic Syndrome–Scientific Evidence and Therapeutic Implications. J Med Life (2014) 7:468–71. [PMC free article] [PubMed] [Google Scholar]
- 8. Cohen AD, Gilutz H, Henkin Y, Zahger D, Shapiro J, Bonneh DY, et al. Psoriasis and the Metabolic Syndrome. Acta Derm Venereol (2007) 87:506–9. 10.2340/00015555-0297 [DOI] [PubMed] [Google Scholar]
- 9. Choudhary S, Pradhan D, Pandey A, Khan MK, Lall R, Ramesh V, et al. The Association of Metabolic Syndrome and Psoriasis: A Systematic Review and Meta-Analysis of Observational Study. Endocr Metab Immune Disord Drug Targets (2020) 20:703–17. 10.2174/1871530319666191008170409 [DOI] [PubMed] [Google Scholar]
- 10. Coto-Segura P, Eiris-Salvado N, Gonzalez-Lara L, Queiro-Silva R, Martinez-Camblor P, Maldonado-Seral C, et al. Psoriasis, Psoriatic Arthritis and Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis. Br J Dermatol (2013) 169:783–93. 10.1111/bjd.12473 [DOI] [PubMed] [Google Scholar]
- 11. Armstrong AW, Harskamp CT, Armstrong EJ. The Association Between Psoriasis and Obesity: A Systematic Review and Meta-Analysis of Observational Studies. Nutr Diabetes (2012) 2:e54. 10.1038/nutd.2012.26 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Rodriguez-Zuniga MJM, Garcia-Perdomo HA. Systematic Review and Meta-Analysis of the Association Between Psoriasis and Metabolic Syndrome. J Am Acad Dermatol (2017) 77:657–66.e658. 10.1016/j.jaad.2017.04.1133 [DOI] [PubMed] [Google Scholar]
- 13. Candia R, Ruiz A, Torres-Robles R, Chavez-Tapia N, Mendez-Sanchez N, Arrese M. Risk of non-Alcoholic Fatty Liver Disease in Patients With Psoriasis: A Systematic Review and Meta-Analysis. J Eur Acad Dermatol Venereol: JEADV (2015) 29:656–62. 10.1111/jdv.12847 [DOI] [PubMed] [Google Scholar]
- 14. Caroppo F, Galderisi A, Moretti C, Ventura L, Fortina BA. Prevalence of Psoriasis in a Cohort of Children and Adolescents With Type 1 Diabetes. J Eur Acad Dermatol Venereol: JEADV (2021). 10.1111/jdv.17318 [DOI] [PubMed] [Google Scholar]
- 15. Di Costanzo L, Fattorusso V, Mozzillo E, Patrì A, Di Caprio R, De Nitto E, et al. Psoriasis in Children With Type 1 Diabetes: A New Comorbidity to be Considered? Acta Diabetologica (2017) 54:803–4. 10.1007/s00592-017-1000-3 [DOI] [PubMed] [Google Scholar]
- 16. Armstrong AW, Harskamp CT, Armstrong EJ. Psoriasis and Metabolic Syndrome: A Systematic Review and Meta-Analysis of Observation Studies. J Am Acad Dermatol (2013) 68:654–62. 10.1016/j.jaad.2012.08.015 [DOI] [PubMed] [Google Scholar]
- 17. Kastorini CM, Panagiotakos DB, Georgousopoulou EN, Laskaris A, Skourlis N, Zana A, et al. Metabolic Syndrome and 10-Year Cardiovascular Disease Incidence: The ATTICA Study. Nutr Metab Cardiovasc Dis (2016) 26:223–31. 10.1016/j.numecd.2015.12.010 [DOI] [PubMed] [Google Scholar]
- 18. Rendon A, Schakel K. Psoriasis Pathogenesis and Treatment. Int J Mol Sci (2019) 20:1–28. 10.3390/ijms20061475 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Boehncke WH. Etiology and Pathogenesis of Psoriasis. Rheum Dis Clin North Am (2015) 41:665–75. 10.1016/j.rdc.2015.07.013 [DOI] [PubMed] [Google Scholar]
- 20. Donath MY. Targeting Inflammation in the Treatment of Type 2 Diabetes: Time to Start. Nat Rev Drug Discov (2014) 13:465–76. 10.1038/nrd4275 [DOI] [PubMed] [Google Scholar]
- 21. Schaffler A, Buechler C. CTRP Family: Linking Immunity to Metabolism. Trends Endocrinol Metab (2012) 23:194–204. 10.1016/j.tem.2011.12.003 [DOI] [PubMed] [Google Scholar]
- 22. Odegaard JI, Chawla A. Pleiotropic Actions of Insulin Resistance and Inflammation in Metabolic Homeostasis. Science (2013) 339:172–7. 10.1126/science.1230721 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Chan KL, Cathomas F, Russo SJ. Central and Peripheral Inflammation Link Metabolic Syndrome and Major Depressive Disorder. Physiol (Bethesda) (2019) 34:123–33. 10.1152/physiol.00047.2018 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Mathis D. Immunological Goings-on in Visceral Adipose Tissue. Cell Metab (2013) 17:851–9. 10.1016/j.cmet.2013.05.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Lee YS, Wollam J, Olefsky JM. An Integrated View of Immunometabolism. Cell (2018) 172:22–40. 10.1016/j.cell.2017.12.025 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Donath MY, Meier DT, Boni-Schnetzler M. Inflammation in the Pathophysiology and Therapy of Cardiometabolic Disease. Endocr Rev (2019) 40:1080–91. 10.1210/er.2019-00002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Tilg H, Moschen AR. Inflammatory Mechanisms in the Regulation of Insulin Resistance. Mol Med (2008) 14:222–31. 10.2119/2007-00119.Tilg [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Abdel-Moneim A, Bakery HH, Allam G. The Potential Pathogenic Role of IL-17/Th17 Cells in Both Type 1 and Type 2 Diabetes Mellitus. BioMed Pharmacother (2018) 101:287–92. 10.1016/j.biopha.2018.02.103 [DOI] [PubMed] [Google Scholar]
- 29. Madhur MS, Lob HE, McCann LA, Iwakura Y, Blinder Y, Guzik TJ, et al. Interleukin 17 Promotes Angiotensin II-Induced Hypertension and Vascular Dysfunction. Hypertension (2010) 55:500–7. 10.1161/HYPERTENSIONAHA.109.145094 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Demir E, Harmankaya NO, Kirac Utku I, Aciksari G, Uygun T, Ozkan H, et al. The Relationship Between Epicardial Adipose Tissue Thickness and Serum Interleukin-17a Level in Patients With Isolated Metabolic Syndrome. Biomolecules (2019) 9:1–12. 10.3390/biom9030097 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Baharlou R, Ahmadi-Vasmehjani A, Davami MH, Faraji F, Atashzar MR, Karimipour F, et al. Elevated Levels of T-Helper 17-Associated Cytokines in Diabetes Type I Patients: Indicators for Following the Course of Disease. Immunol Invest (2016) 45:641–51. 10.1080/08820139.2016.1197243 [DOI] [PubMed] [Google Scholar]
- 32. Pinter A, Gerdes S, Papavassilis C, Reinhardt M. Characterization of Responder Groups to Secukinumab Treatment in Moderate to Severe Plaque Psoriasis. J Dermatolog Treat (2020) 31:769–75. 10.1080/09546634.2019.1626973 [DOI] [PubMed] [Google Scholar]
- 33. Ikumi K, Odanaka M, Shime H, Imai M, Osaga S, Taguchi O, et al. Hyperglycemia Is Associated With Psoriatic Inflammation in Both Humans and Mice. J Invest Dermatol (2019) 139:1329–38.e1327. 10.1016/j.jid.2019.01.029 [DOI] [PubMed] [Google Scholar]
- 34. Gardner LCS, Grantham HJ, Reynolds NJ. IL-17 May Be a Key Cytokine Linking Psoriasis and Hyperglycemia. J Invest Dermatol (2019) 139:1214–6. 10.1016/j.jid.2019.02.038 [DOI] [PubMed] [Google Scholar]
- 35. Chima M, Lebwohl M. TNF Inhibitors for Psoriasis. Semin Cutan Med Surg (2018) 37:134–42. 10.12788/j.sder.2018.039 [DOI] [PubMed] [Google Scholar]
- 36. Merlo G, Cozzani E, Burlando M, Calvieri S, Potenza C, Stingeni L, et al. Effects of Tnfalpha Inhibitors in Patients With Psoriasis and Metabolic Syndrome: A Preliminary Study. G Ital Dermatol Venereol (2020) 155:14–8. 10.23736/S0392-0488.17.05621-8 [DOI] [PubMed] [Google Scholar]
- 37. Botelho KP, Pontes MAA, Rodrigues CEM, Freitas MVC. Prevalence of Metabolic Syndrome Among Patients With Psoriasis Treated With TNF Inhibitors and the Effects of Anti-TNF Therapy on Their Lipid Profile: A Prospective Cohort Study. Metab Syndr Relat Disord (2020) 18:154–60. 10.1089/met.2019.0092 [DOI] [PubMed] [Google Scholar]
- 38. Arjuman A, Chandra NC. Differential Pro-Inflammatory Responses of TNF-Alpha Receptors (TNFR1 and TNFR2) on LOX-1 Signalling. Mol Biol Rep (2015) 42:1039–47. 10.1007/s11033-014-3841-y [DOI] [PubMed] [Google Scholar]
- 39. Pina T, Armesto S, Lopez-Mejias R, Genre F, Ubilla B, Gonzalez-Lopez MA, et al. Anti-TNF-Alpha; Therapy Improves Insulin Sensitivity in Non-Diabetic Patients With Psoriasis: A 6-Month Prospective Study. J Eur Acad Dermatol Venereol: JEADV (2015) 29:1325–30. 10.1111/jdv.12814 [DOI] [PubMed] [Google Scholar]
- 40. Antohe JL, Bili A, Sartorius JA, Kirchner HL, Morris SJ, Dancea S, et al. Diabetes Mellitus Risk in Rheumatoid Arthritis: Reduced Incidence With Anti-Tumor Necrosis Factor Alpha Therapy. Arthritis Care Res (Hoboken) (2012) 64:215–21. 10.1002/acr.20657 [DOI] [PubMed] [Google Scholar]
- 41. Solomon DH, Massarotti E, Garg R, Liu J, Canning C, Schneeweiss S. Association Between Disease-Modifying Antirheumatic Drugs and Diabetes Risk in Patients With Rheumatoid Arthritis and Psoriasis. JAMA (2011) 305:2525–31. 10.1001/jama.2011.878 [DOI] [PubMed] [Google Scholar]
- 42. Broussard SR, McCusker RH, Novakofski JE, Strle K, Shen WH, Johnson RW, et al. IL-1beta Impairs Insulin-Like Growth Factor I-Induced Differentiation and Downstream Activation Signals of the Insulin-Like Growth Factor I Receptor in Myoblasts. J Immunol (2004) 172:7713–20. 10.4049/jimmunol.172.12.7713 [DOI] [PubMed] [Google Scholar]
- 43. Rui L, Aguirre V, Kim JK, Shulman GI, Lee A, Corbould A, et al. Insulin/IGF-1 and TNF-Alpha Stimulate Phosphorylation of IRS-1 at Inhibitory Ser307 via Distinct Pathways. J Clin Invest (2001) 107:181–9. 10.1172/JCI10934 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44. Gisondi P, Fostini AC, Fossà I, Girolomoni G, Targher G. Psoriasis and the Metabolic Syndrome. Clinics Dermatol (2018) 36:21–8. 10.1016/j.clindermatol.2017.09.005 [DOI] [PubMed] [Google Scholar]
- 45. Kofoed K, Clemmensen A, Mikkelsen UR, Simonsen L, Andersen O, Gniadecki R. Effects of Anti-Tumor Necrosis Factor Therapy on Body Composition and Insulin Sensitivity in Patients With Psoriasis. Arch Dermatol (2012) 148:1089–91. 10.1001/archdermatol.2012.1753 [DOI] [PubMed] [Google Scholar]
- 46. Fatima N, Faisal SM, Zubair S, Siddiqui SS, Moin S, Owais M. Emerging Role of Interleukins IL-23/IL-17 Axis and Biochemical Markers in the Pathogenesis of Type 2 Diabetes: Association With Age and Gender in Human Subjects. Int J Biol Macromol (2017) 105:1279–88. 10.1016/j.ijbiomac.2017.07.155 [DOI] [PubMed] [Google Scholar]
- 47. Goyal R, Faizy AF, Siddiqui SS, Singhai M. Evaluation of TNF-Alpha and IL-6 Levels in Obese and Non-Obese Diabetics: Pre- and Postinsulin Effects. N Am J Med Sci (2012) 4:180–4. 10.4103/1947-2714.94944 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48. Schmidt FM, Weschenfelder J, Sander C, Minkwitz J, Thormann J, Chittka T, et al. Inflammatory Cytokines in General and Central Obesity and Modulating Effects of Physical Activity. PloS One (2015) 10:e0121971. 10.1371/journal.pone.0121971 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Wensveen FM, Jelencic V, Valentic S, Sestan M, Wensveen TT, Theurich S, et al. NK Cells Link Obesity-Induced Adipose Stress to Inflammation and Insulin Resistance. Nat Immunol (2015) 16:376–85. 10.1038/ni.3120 [DOI] [PubMed] [Google Scholar]
- 50. Scheja L, Heeren J. The Endocrine Function of Adipose Tissues in Health and Cardiometabolic Disease. Nat Rev Endocrinol (2019) 15:507–24. 10.1038/s41574-019-0230-6 [DOI] [PubMed] [Google Scholar]
- 51. Yamauchi T, Kamon J, Ito Y, Tsuchida A, Yokomizo T, Kita S, et al. Cloning of Adiponectin Receptors That Mediate Antidiabetic Metabolic Effects. Nature (2003) 423:762–9. 10.1038/nature01705 [DOI] [PubMed] [Google Scholar]
- 52. Li X, Zhang D, Vatner DF, Goedeke L, Hirabara SM, Zhang Y, et al. Mechanisms by Which Adiponectin Reverses High Fat Diet-Induced Insulin Resistance in Mice. Proc Natl Acad Sci USA (2020) 117:32584–93. 10.1073/pnas.1922169117 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53. Yanai H, Yoshida H. Beneficial Effects of Adiponectin on Glucose and Lipid Metabolism and Atherosclerotic Progression: Mechanisms and Perspectives. Int J Mol Sci (2019) 20:1–25. 10.3390/ijms20051190 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54. Ahmad A, Ali T, Kim MW, Khan A, Jo MH, Rehman SU, et al. Adiponectin Homolog Novel Osmotin Protects Obesity/Diabetes-Induced NAFLD by Upregulating AdipoRs/PPARalpha Signaling in Ob/Ob and Db/Db Transgenic Mouse Models. Metabolism (2019) 90:31–43. 10.1016/j.metabol.2018.10.004 [DOI] [PubMed] [Google Scholar]
- 55. Sereflican B, Goksugur N, Bugdayci G, Polat M, Parlak HA. Serum Visfatin, Adiponectin, and Tumor Necrosis Factor Alpha (TNF-Alpha) Levels in Patients With Psoriasis and Their Correlation With Disease Severity. Acta Dermatovenerol Croat (2016) 24:13–9. [PubMed] [Google Scholar]
- 56. He Y, Lu L, Wei X, Jin D, Qian T, Yu A, et al. The Multimerization and Secretion of Adiponectin Are Regulated by TNF-Alpha. Endocrine (2016) 51:456–68. 10.1007/s12020-015-0741-4 [DOI] [PubMed] [Google Scholar]
- 57. Morris EV, Suchacki KJ, Hocking J, Cartwright R, Sowman A, Gamez B, et al. Myeloma Cells Down-Regulate Adiponectin in Bone Marrow Adipocytes via TNF-Alpha. J Bone Miner Res (2020) 35:942–55. 10.1002/jbmr.3951 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58. Kong Y, Zhang S, Wu R, Su X, Peng D, Zhao M, et al. New Insights Into Different Adipokines in Linking the Pathophysiology of Obesity and Psoriasis. Lipids Health Dis (2019) 18:171. 10.1186/s12944-019-1115-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59. Bai F, Zheng W, Dong Y, Wang J, Garstka MA, Li R, et al. Serum Levels of Adipokines and Cytokines in Psoriasis Patients: A Systematic Review and Meta-Analysis. Oncotarget (2018) 9:1266–78. 10.18632/oncotarget.22260 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60. Langley RG, Ellis CN. Evaluating Psoriasis With Psoriasis Area and Severity Index, Psoriasis Global Assessment, and Lattice System Physician’s Global Assessment. J Am Acad Dermatol (2004) 51:563–9. 10.1016/j.jaad.2004.04.012 [DOI] [PubMed] [Google Scholar]
- 61. Gerdes S, Pinter A, Biermann M, Papavassilis C, Reinhardt M. Adiponectin Levels in a Large Pooled Plaque Psoriasis Study Population. J Dermatolog Treat (2020) 31:531–4. 10.1080/09546634.2019.1621979 [DOI] [PubMed] [Google Scholar]
- 62. Chan WSA, Liew CF, Theng CTS, Oon HH. Serum Adiponectin Levels and Their Association With Cardiometabolic Risk Factors in Patients With Psoriasis. Cureus (2020) 12:e8128. 10.7759/cureus.8128 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63. Landecho MF, Tuero C, Valenti V, Bilbao I, de la Higuera M, Fruhbeck G. Relevance of Leptin and Other Adipokines in Obesity-Associated Cardiovascular Risk. Nutrients (2019) 11:1–16. 10.3390/nu11112664 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64. Ghadge AA, Khaire AA. Leptin as a Predictive Marker for Metabolic Syndrome. Cytokine (2019) 121:154735. 10.1016/j.cyto.2019.154735 [DOI] [PubMed] [Google Scholar]
- 65. Zhao S, Zhu Y, Schultz RD, Li N, He Z, Zhang Z, et al. Partial Leptin Reduction as an Insulin Sensitization and Weight Loss Strategy. Cell Metab (2019) 30:706–19.e706. 10.1016/j.cmet.2019.08.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66. Kyriakou A, Patsatsi A, Sotiriadis D, Goulis DG. Serum Leptin, Resistin, and Adiponectin Concentrations in Psoriasis: A Meta-Analysis of Observational Studies. Dermatology (2017) 233:378–89. 10.1159/000481882 [DOI] [PubMed] [Google Scholar]
- 67. Coimbra S, Oliveira H, Reis F, Belo L, Rocha S, Quintanilha A, et al. Circulating Adipokine Levels in Portuguese Patients With Psoriasis Vulgaris According to Body Mass Index, Severity and Therapy. J Eur Acad Dermatol Venereol: JEADV (2010) 24:1386–94. 10.1111/j.1468-3083.2010.03647.x [DOI] [PubMed] [Google Scholar]
- 68. Karadag AS, Ertugrul DT, Kalkan G, Bilgili SG, Celik HT, Takci Z, et al. The Effect of Acitretin Treatment on Insulin Resistance, Retinol-Binding Protein-4, Leptin, and Adiponectin in Psoriasis Vulgaris: A Noncontrolled Study. Dermatology (2013) 227:103–8. 10.1159/000351769 [DOI] [PubMed] [Google Scholar]
- 69. Hwang J, Yoo JA, Yoon H, Han T, Yoon J, An S, et al. The Role of Leptin in the Association Between Obesity and Psoriasis. Biomol Ther (Seoul) (2021) 29:11–21. 10.4062/biomolther.2020.054 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70. Bavoso NC, Pinto JM, Soares MMS, Diniz MDS, Junior TAL. Psoriasis in Obesity: Comparison of Serum Levels of Leptin and Adiponectin in Obese Subjects - Cases and Controls. Bras Dermatol (2019) 94:192–7. 10.1590/abd1806-4841.20197716 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71. Liang L, Hur J, Kang JY, Rhee CK, Kim YK, Lee SY. Effect of the Anti-IL-17 Antibody on Allergic Inflammation in an Obesity-Related Asthma Model. Korean J Intern Med (2018) 33:1210–23. 10.3904/kjim.2017.207 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72. Finkel T. Signal Transduction by Reactive Oxygen Species. J Cell Biol (2011) 194:7–15. 10.1083/jcb.201102095 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73. Darroudi S, Fereydouni N, Tayefi M, Ahmadnezhad M, Zamani P, Tayefi B, et al. Oxidative Stress and Inflammation, Two Features Associated With a High Percentage Body Fat, and That May Lead to Diabetes Mellitus and Metabolic Syndrome. Biofactors (2019) 45:35–42. 10.1002/biof.1459 [DOI] [PubMed] [Google Scholar]
- 74. Furukawa S, Fujita T, Shimabukuro M, Iwaki M, Yamada Y, Nakajima Y, et al. Increased Oxidative Stress in Obesity and Its Impact on Metabolic Syndrome. J Clin Invest (2004) 114:1752–61. 10.1172/JCI21625 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75. Houstis N, Rosen ED, Lander ES. Reactive Oxygen Species Have a Causal Role in Multiple Forms of Insulin Resistance. Nature (2006) 440:944–8. 10.1038/nature04634 [DOI] [PubMed] [Google Scholar]
- 76. Onyango AN. Cellular Stresses and Stress Responses in the Pathogenesis of Insulin Resistance. Oxid Med Cell Longev (2018) 2018:4321714. 10.1155/2018/4321714 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77. Hofmanis J, Hofmane D, Svirskis S, Mackevics V, Tretjakovs P, Lejnieks A, et al. HDL-C Role in Acquired Aortic Valve Stenosis Patients and Its Relationship With Oxidative Stress. Medicina (Kaunas) (2019) 55:1–16. 10.3390/medicina55080416 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78. Bastard JP, Couffignal C, Fellahi S, Bard JM, Mentre F, Salmon D, et al. Diabetes and Dyslipidaemia Are Associated With Oxidative Stress Independently of Inflammation in Long-Term Antiretroviral-Treated HIV-Infected Patients. Diabetes Metab (2019) 45:573–81. 10.1016/j.diabet.2019.02.008 [DOI] [PubMed] [Google Scholar]
- 79. Gao M, Zhao Z, Lv P, Li Y, Gao J, Zhang M, et al. Quantitative Combination of Natural Anti-Oxidants Prevents Metabolic Syndrome by Reducing Oxidative Stress. Redox Biol (2015) 6:206–17. 10.1016/j.redox.2015.06.013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80. Vona R, Gambardella L, Cittadini C, Straface E, Pietraforte D. Biomarkers of Oxidative Stress in Metabolic Syndrome and Associated Diseases. Oxid Med Cell Longev (2019) 2019:8267234. 10.1155/2019/8267234 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81. Ferretti G, Bacchetti T, Campanati A, Simonetti O, Liberati G, Offidani A. Correlation Between Lipoprotein(a) and Lipid Peroxidation in Psoriasis: Role of the Enzyme Paraoxonase-1. Br J Dermatol (2012) 166:204–7. 10.1111/j.1365-2133.2011.10539.x [DOI] [PubMed] [Google Scholar]
- 82. Nemati H, Khodarahmi R, Sadeghi M, Ebrahimi A, Rezaei M, Vaisi-Raygani A. Antioxidant Status in Patients With Psoriasis. Cell Biochem Funct (2014) 32:268–73. 10.1002/cbf.3011 [DOI] [PubMed] [Google Scholar]
- 83. Sikar Akturk A, Ozdogan HK, Bayramgurler D, Cekmen MB, Bilen N, Kiran R. Nitric Oxide and Malondialdehyde Levels in Plasma and Tissue of Psoriasis Patients. J Eur Acad Dermatol Venereol: JEADV (2012) 26:833–7. 10.1111/j.1468-3083.2011.04164.x [DOI] [PubMed] [Google Scholar]
- 84. Ambrozewicz E, Wojcik P, Wronski A, Luczaj W, Jastrzab A, Zarkovic N, et al. Pathophysiological Alterations of Redox Signaling and Endocannabinoid System in Granulocytes and Plasma of Psoriatic Patients. Cells (2018) 7:1–18. 10.3390/cells7100159 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85. Wojcik P, Gegotek A, Wronski A, Jastrzab A, Zebrowska A, Skrzydlewska E. Effect of Redox Imbalance on Protein Modifications in Lymphocytes of Psoriatic Patients. J Biochem (2020) 167:323–31. 10.1093/jb/mvz096 [DOI] [PubMed] [Google Scholar]
- 86. Plenkowska J, Gabig-Ciminska M, Mozolewski P. Oxidative Stress as an Important Contributor to the Pathogenesis of Psoriasis. Int J Mol Sci (2020) 21:1–15. 10.3390/ijms21176206 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87. Oszukowska M, Kozlowska M, Kaszuba A. Paraoxonase-1 and Other Factors Related to Oxidative Stress in Psoriasis. Postepy Dermatol Alergol (2020) 37:92–6. 10.5114/ada.2020.93386 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88. Lin X, Huang T. Oxidative Stress in Psoriasis and Potential Therapeutic Use of Antioxidants. Free Radic Res (2016) 50:585–95. 10.3109/10715762.2016.1162301 [DOI] [PubMed] [Google Scholar]
- 89. Liu A, Zhao W, Zhang B, Tu Y, Wang Q, Li J. Cimifugin Ameliorates Imiquimod-Induced Psoriasis by Inhibiting Oxidative Stress and Inflammation via NF-KappaB/MAPK Pathway. Biosci Rep (2020) 40:1–11. 10.1042/BSR20200471 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90. Yazici C, Kose K, Utas S, Tanrikulu E, Taslidere N. A Novel Approach in Psoriasis: First Usage of Known Protein Oxidation Markers to Prove Oxidative Stress. Arch Dermatol Res (2016) 308:207–12. 10.1007/s00403-016-1624-0 [DOI] [PubMed] [Google Scholar]
- 91. Rowland AA, Voeltz GK. Endoplasmic Reticulum-Mitochondria Contacts: Function of the Junction. Nat Rev Mol Cell Biol (2012) 13:607–25. 10.1038/nrm3440 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92. Fewell SW, Travers KJ, Weissman JS, Brodsky JL. The Action of Molecular Chaperones in the Early Secretory Pathway. Annu Rev Genet (2001) 35:149–91. 10.1146/annurev.genet.35.102401.090313 [DOI] [PubMed] [Google Scholar]
- 93. S. Mohan PRMR, Brown L, Ayyappan P, K. G R. Endoplasmic Reticulum Stress: A Master Regulator of Metabolic Syndrome. Eur J Pharmacol (2019) 860:172553. 10.1016/j.ejphar.2019.172553 [DOI] [PubMed] [Google Scholar]
- 94. Reid DW, Nicchitta CV. Diversity and Selectivity in Mrna Translation on the Endoplasmic Reticulum. Nat Rev Mol Cell Biol (2015) 16:221–31. 10.1038/nrm3958 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95. Schwarz DS, Blower MD. The Endoplasmic Reticulum: Structure, Function and Response to Cellular Signaling. Cell Mol Life Sci (2016) 73:79–94. 10.1007/s00018-015-2052-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 96. Fagone P, Jackowski S. Membrane Phospholipid Synthesis and Endoplasmic Reticulum Function. J Lipid Res (2009) 50 Suppl:S311–6. 10.1194/jlr.R800049-JLR200 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 97. Hetz C. The Unfolded Protein Response: Controlling Cell Fate Decisions Under ER Stress and Beyond. Nat Rev Mol Cell Biol (2012) 13:89–102. 10.1038/nrm3270 [DOI] [PubMed] [Google Scholar]
- 98. Ozcan U, Cao Q, Yilmaz E, Lee AH, Iwakoshi NN, Ozdelen E, et al. Endoplasmic Reticulum Stress Links Obesity, Insulin Action, and Type 2 Diabetes. Science (2004) 306:457–61. 10.1126/science.1103160 [DOI] [PubMed] [Google Scholar]
- 99. Wang M, Kaufman RJ. Protein Misfolding in the Endoplasmic Reticulum as a Conduit to Human Disease. Nature (2016) 529:326–35. 10.1038/nature17041 [DOI] [PubMed] [Google Scholar]
- 100. Shan B, Wang X, Wu Y, Xu C, Xia Z, Dai J, et al. The Metabolic ER Stress Sensor IRE1alpha Suppresses Alternative Activation of Macrophages and Impairs Energy Expenditure in Obesity. Nat Immunol (2017) 18:519–29. 10.1038/ni.3709 [DOI] [PubMed] [Google Scholar]
- 101. Radwan E, Bakr MH, Taha S, Sayed SA, Farrag AA, Ali M. Inhibition of Endoplasmic Reticulum Stress Ameliorates Cardiovascular Injury in a Rat Model of Metabolic Syndrome. J Mol Cell Cardiol (2020) 143:15–25. 10.1016/j.yjmcc.2020.04.020 [DOI] [PubMed] [Google Scholar]
- 102. Liu F, Zhu S, Ni L, Huang L, Wang K, Zhou Y. Dexmedetomidine Alleviates Insulin Resistance in Hepatocytes by Reducing Endoplasmic Reticulum Stress. Endocrine (2020) 67:87–94. 10.1007/s12020-019-02118-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103. Jia B, Wang Y, Yu G, Cheng Y, Yang C, Cao F, et al. Naringenin Ameliorates Insulin Resistance by Modulating Endoplasmic Reticulum Stress in Hepatitis C Virus-Infected Liver. BioMed Pharmacother (2019) 115:108848. 10.1016/j.biopha.2019.108848 [DOI] [PubMed] [Google Scholar]
- 104. Zhao H, Zhang Y, Shu L, Song G, Ma H. Resveratrol Reduces Liver Endoplasmic Reticulum Stress and Improves Insulin Sensitivity in Vivo and in Vitro . Drug Des Devel Ther (2019) 13:1473–85. 10.2147/DDDT.S203833 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105. Liang B, Liu L, Huang H, Li L, Zhou J. High T3 Induces Beta-Cell Insulin Resistance via Endoplasmic Reticulum Stress. Mediators Inflammation (2020) 2020:5287108. 10.1155/2020/5287108 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106. Brown M, Dainty S, Strudwick N, Mihai AD, Watson JN, Dendooven R, et al. Endoplasmic Reticulum Stress Causes Insulin Resistance by Inhibiting Delivery of Newly Synthesized Insulin Receptors to the Cell Surface. Mol Biol Cell (2020) 31:2597–629. 10.1091/mbc.E18-01-0013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107. Xue X, Piao JH, Nakajima A, Sakon-Komazawa S, Kojima Y, Mori K, et al. Tumor Necrosis Factor Alpha (TNFalpha) Induces the Unfolded Protein Response (UPR) in a Reactive Oxygen Species (ROS)-Dependent Fashion, and the UPR Counteracts ROS Accumulation by TNFalpha. J Biol Chem (2005) 280:33917–25. 10.1074/jbc.M505818200 [DOI] [PubMed] [Google Scholar]
- 108. Hasnain SZ, Lourie R, Das I, Chen AC, McGuckin MA. The Interplay Between Endoplasmic Reticulum Stress and Inflammation. Immunol Cell Biol (2012) 90:260–70. 10.1038/icb.2011.112 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 109. Kim SR, Kim HJ, Kim DI, Lee KB, Park HJ, Jeong JS, et al. Blockade of Interplay Between IL-17A and Endoplasmic Reticulum Stress Attenuates LPS-Induced Lung Injury. Theranostics (2015) 5:1343–62. 10.7150/thno.11685 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110. Yang Z, Liu Q, Shi H, Jiang X, Wang S, Lu Y, et al. Interleukin 17A Exacerbates ER-Stress-Mediated Inflammation of Macrophages Following ICH. Mol Immunol (2018) 101:38–45. 10.1016/j.molimm.2018.05.020 [DOI] [PubMed] [Google Scholar]
- 111. Zhao M, Luo J, Xiao B, Tang H, Song F, Ding X, et al. Endoplasmic Reticulum Stress Links Psoriasis Vulgaris With Keratinocyte Inflammation. Postepy Dermatol Alergol (2020) 37:34–40. 10.5114/ada.2020.93382 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 112. Shimoura N, Nagai H, Fujiwara S, Jimbo H, Nishigori C. Exacerbation and Prolongation of Psoriasiform Inflammation in Diabetic Obese Mice: A Synergistic Role of CXCL5 and Endoplasmic Reticulum Stress. J Invest Dermatol (2018) 138:854–63. 10.1016/j.jid.2017.10.023 [DOI] [PubMed] [Google Scholar]
- 113. Ruff WE, Kriegel MA. Autoimmune Host-Microbiota Interactions at Barrier Sites and Beyond. Trends Mol Med (2015) 21:233–44. 10.1016/j.molmed.2015.02.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114. Cho I, Blaser MJ. The Human Microbiome: At the Interface of Health and Disease. Nat Rev Genet (2012) 13:260–70. 10.1038/nrg3182 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115. Lynch SV, Pedersen O. The Human Intestinal Microbiome in Health and Disease. N Engl J Med (2016) 375:2369–79. 10.1056/NEJMra1600266 [DOI] [PubMed] [Google Scholar]
- 116. Wu H, Esteve E, Tremaroli V, Khan MT, Caesar R, Manneras-Holm L, et al. Metformin Alters the Gut Microbiome of Individuals With Treatment-Naive Type 2 Diabetes, Contributing to the Therapeutic Effects of the Drug. Nat Med (2017) 23:850–8. 10.1038/nm.4345 [DOI] [PubMed] [Google Scholar]
- 117. Virtue AT, McCright SJ, Wright JM, Jimenez MT, Mowel WK, Kotzin JJ, et al. The Gut Microbiota Regulates White Adipose Tissue Inflammation and Obesity via a Family of MicroRNAs. Sci Transl Med (2019) 11:1–15. 10.1126/scitranslmed.aav1892 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 118. Macchione IG, Lopetuso LR, Ianiro G, Napoli M, Gibiino G, Rizzatti G, et al. Akkermansia Muciniphila: Key Player in Metabolic and Gastrointestinal Disorders. Eur Rev Med Pharmacol Sci (2019) 23:8075–83. 10.26355/eurrev_201909_19024 [DOI] [PubMed] [Google Scholar]
- 119. Zhang T, Li Q, Cheng L, Buch H, Zhang F. Akkermansia Muciniphila Is a Promising Probiotic. Microb Biotechnol (2019) 12:1109–25. 10.1111/1751-7915.13410 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 120. Cani PD, de Vos WM. Next-Generation Beneficial Microbes: The Case of Akkermansia Muciniphila. Front Microbiol (2017) 8:1765. 10.3389/fmicb.2017.01765 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 121. Depommier C, Everard A, Druart C, Plovier H, Van Hul M, Vieira-Silva S, et al. Supplementation With Akkermansia Muciniphila in Overweight and Obese Human Volunteers: A Proof-of-Concept Exploratory Study. Nat Med (2019) 25:1096–103. 10.1038/s41591-019-0495-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122. Codoner FM, Ramirez-Bosca A, Climent E, Carrion-Gutierrez M, Guerrero M, Perez-Orquin JM, et al. Gut Microbial Composition in Patients With Psoriasis. Sci Rep (2018) 8:3812. 10.1038/s41598-018-22125-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123. Chen YJ, Ho HJ, Tseng CH, Lai ZL, Shieh JJ, Wu CY. Intestinal Microbiota Profiling and Predicted Metabolic Dysregulation in Psoriasis Patients. Exp Dermatol (2018) 27:1336–43. 10.1111/exd.13786 [DOI] [PubMed] [Google Scholar]
- 124. Shapiro J, Cohen NA, Shalev V, Uzan A, Koren O, Maharshak N. Psoriatic Patients Have a Distinct Structural and Functional Fecal Microbiota Compared With Controls. J Dermatol (2019) 46:595–603. 10.1111/1346-8138.14933 [DOI] [PubMed] [Google Scholar]
- 125. Tan L, Zhao S, Zhu W, Wu L, Li J, Shen M, et al. The Akkermansia Muciniphila Is a Gut Microbiota Signature in Psoriasis. Exp Dermatol (2018) 27:144–9. 10.1111/exd.13463 [DOI] [PubMed] [Google Scholar]
- 126. Chen L, Li J, Zhu W, Kuang Y, Liu T, Zhang W, et al. Skin and Gut Microbiome in Psoriasis: Gaining Insight Into the Pathophysiology of It and Finding Novel Therapeutic Strategies. Front Microbiol (2020) 11:589726. 10.3389/fmicb.2020.589726 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 127. Chelakkot C, Ghim J, Ryu SH. Mechanisms Regulating Intestinal Barrier Integrity and Its Pathological Implications. Exp Mol Med (2018) 50:103. 10.1038/s12276-018-0126-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 128. Cox AJ, Zhang P, Bowden DW, Devereaux B, Davoren PM, Cripps AW, et al. Increased Intestinal Permeability as a Risk Factor for Type 2 Diabetes. Diabetes Metab (2017) 43:163–6. 10.1016/j.diabet.2016.09.004 [DOI] [PubMed] [Google Scholar]
- 129. Sorini C, Cosorich I, Lo Conte M, De Giorgi L, Facciotti F, Luciano R, et al. Loss of Gut Barrier Integrity Triggers Activation of Islet-Reactive T Cells and Autoimmune Diabetes. Proc Natl Acad Sci USA (2019) 116:15140–9. 10.1073/pnas.1814558116 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130. Damms-Machado A, Louis S, Schnitzer A, Volynets V, Rings A, Basrai M, et al. Gut Permeability Is Related to Body Weight, Fatty Liver Disease, and Insulin Resistance in Obese Individuals Undergoing Weight Reduction. Am J Clin Nutr (2017) 105:127–35. 10.3945/ajcn.116.131110 [DOI] [PubMed] [Google Scholar]
- 131. Ma L, Ni Y, Wang Z, Tu W, Ni L, Zhuge F, et al. Spermidine Improves Gut Barrier Integrity and Gut Microbiota Function in Diet-Induced Obese Mice. Gut Microbes (2020) 12:1–19. 10.1080/19490976.2020.1832857 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 132. Mirza A, Mao-Draayer Y. The Gut Microbiome and Microbial Translocation in Multiple Sclerosis. Clin Immunol (2017) 183:213–24. 10.1016/j.clim.2017.03.001 [DOI] [PubMed] [Google Scholar]
- 133. Boulange CL, Neves AL, Chilloux J, Nicholson JK, Dumas ME. Impact of the Gut Microbiota on Inflammation, Obesity, and Metabolic Disease. Genome Med (2016) 8:42. 10.1186/s13073-016-0303-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 134. Okubo Y, Oki N, Takeda H, Amaya M, Ito S, Osada M, et al. Increased Microorganisms DNA Levels in Peripheral Blood Monocytes From Psoriatic Patients Using PCR With Universal Ribosomal RNA Primers. J Dermatol (2002) 29:547–55. 10.1111/j.1346-8138.2002.tb00179.x [DOI] [PubMed] [Google Scholar]
- 135. Munz OH, Sela S, Baker BS, Griffiths CE, Powles AV, Fry L. Evidence for the Presence of Bacteria in the Blood of Psoriasis Patients. Arch Dermatol Res (2010) 302:495–8. 10.1007/s00403-010-1065-0 [DOI] [PubMed] [Google Scholar]
- 136. Sikora M, Chrabaszcz M, Maciejewski C, Zaremba M, Waskiel A, Olszewska M, et al. Intestinal Barrier Integrity in Patients With Plaque Psoriasis. J Dermatol (2018) 45:1468–70. 10.1111/1346-8138.14647 [DOI] [PubMed] [Google Scholar]
- 137. Sikora M, Stec A, Chrabaszcz M, Waskiel-Burnat A, Zaremba M, Olszewska M, et al. Intestinal Fatty Acid Binding Protein, a Biomarker of Intestinal Barrier, Is Associated With Severity of Psoriasis. J Clin Med (2019) 8:1–9. 10.3390/jcm8071021 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 138. Visser MJE, Kell DB, Pretorius E. Bacterial Dysbiosis and Translocation in Psoriasis Vulgaris. Front Cell Infect Microbiol (2019) 9:7. 10.3389/fcimb.2019.00007 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 139. Welty FK, Alfaddagh A, Elajami TK. Targeting Inflammation in Metabolic Syndrome. Trans research: J Lab Clin Med (2016) 167:257–80. 10.1016/j.trsl.2015.06.017 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 140. Ghemrawi R, Battaglia-Hsu SF, Arnold C. Endoplasmic Reticulum Stress in Metabolic Disorders. Cells (2018) 7:1–39. 10.3390/cells7060063 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 141. Rani V, Deep G, Singh RK, Palle K, Yadav UC. Oxidative Stress and Metabolic Disorders: Pathogenesis and Therapeutic Strategies. Life Sci (2016) 148:183–93. 10.1016/j.lfs.2016.02.002 [DOI] [PubMed] [Google Scholar]