Skip to main content
Erschienen in: Dermatology and Therapy 3/2019

Open Access 11.07.2019 | Original Research

ERAPSO: Revealing the High Burden of Obesity in German Psoriasis Patients

verfasst von: Peter E. H. Schwarz, Andreas Pinter, Nima Melzer, Philipp Barteczek, Maximilian Reinhardt

Erschienen in: Dermatology and Therapy | Ausgabe 3/2019

Abstract

Introduction

Plaque psoriasis is a chronic, systemic-inflammatory disease characterized by skin erythema, plaques and scaling, and is associated with different comorbidities like psoriatic arthritis, obesity, and cardiometabolic diseases. Obesity aggravates cardiovascular risk in psoriasis patients and can negatively affect psoriasis disease severity with proinflammatory adipocytokine production by adipocytes and infiltrated immune cells.

Methods

An online survey on nutrition and physical activity in psoriasis participants (ERAPSO) collected cross-sectional data about eating behavior, physical activity, and prevalence of obesity and metabolic syndrome components from 9940 psoriasis participants in Germany.

Results

ERAPSO revealed a high burden of obesity in German psoriasis participants with 66.9% overweight or obese (body mass index [BMI] ≥ 25 kg/m2), compared to approximately 50% of the German general population. Affected body surface area (BSA), cardiovascular risk factors, and cardiovascular event frequency increased with increasing BMI. Severe psoriasis was more frequent in overweight participants and impaired engagement in weight loss diets and physical activity. Most German psoriasis participants (90.2%) with BMI ≥ 25 kg/m2 perceived themselves as overweight. A minority (21.2%) were currently exercising with the aim of losing weight, and 12.6% were currently on a weight loss diet. In overweight participants, just 13.3% stated that their physicians and/or health insurance offered specific weight loss programs.

Conclusion

ERAPSO revealed inadequate medical care of obese psoriasis participants with insufficient support for weight loss through diet or increased physical activity. Although psoriasis participants showed an intact self-perception of obesity, they seemed to lack intrinsic motivation to lose weight, highlighting the need for external support in losing weight via tailored programs. Since psoriasis severity correlates with impairment in diets and sports, treating psoriasis adequately may allow participants to follow weight loss programs more successfully.

Funding

Novartis Pharma GmbH, Nuremberg, DE.
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s13555-019-0314-1) contains supplementary material, which is available to authorized users.
Peter E. H. Schwarz and Andreas Pinter contributed equally.

Enhanced Digital Features

To view enhanced digital features for this article go to https://​doi.​org/​10.​6084/​m9.​figshare.​8519390.

Introduction

Psoriasis is an inflammatory disease typically characterized by formation of erythema, plaques, and scaling of the skin. Proinflammatory cytokines including TNF-α, IL-23, or IL-17 are upregulated in psoriatic lesions and promote keratinocyte proliferation and inflammation in the skin [1, 2]. These proinflammatory cytokines also promote systemic inflammation, which is associated with a range of comorbidity including increased cardiovascular risk [3]. This includes risk factors such as hyperlipidemia, hypertension, type 2 diabetes mellitus, obesity [4], and metabolic syndrome [5], affecting around 40% of psoriasis patients, compared to 13–27% of the general population [6, 7]. Psoriasis patients are at increased risk of metabolic syndrome, which may be related to an increase in circulating adipocytokines [5, 8], mediating systemic proinflammatory effects [9].
The metabolic and cardiovascular comorbidity of psoriasis, such as obesity, is characterized by inflammatory processes, such as adipose tissue inflammation in obesity and insulin resistance or vascular inflammation in coronary artery disease [1014]. A cycle of feedback between psoriasis and obesity is postulated, in which psoriasis causes systemic inflammation that in turn stimulates adipocytes to secrete proinflammatory cytokines that can promote cutaneous inflammation (Fig. 1) [15]. Obesity and metabolic syndrome negatively impact psoriasis disease severity, treatment response, and also aggravate the cardiovascular risk in psoriasis patients [9, 1619]. Increased cutaneous inflammation is associated with vascular inflammation in psoriasis patients, which increases with psoriasis severity [20, 21].
A recent survey (PsoHealth) indicated that around 40% of German psoriasis patients are overweight, with an additional 30% classified as obese [2]. According to the World Health Organization (WHO) 2008, overweight is considered as BMI ≥ 25 kg/m2, whereas obesity is considered as BMI ≥ 30 kg/m2. To assess the relationship between psoriasis, obesity, patient behavior, and approach of care providers to weight management in individuals with psoriasis in the general population, a survey on health, nutrition, and physical activity was designed and conducted in German participants with self-reported psoriasis (hereafter referred to as participants) (Umfrage zu ERnährung und Aktivität bei PSOriasis-Patienten, or ERAPSO).

Methods

Study Objectives

The study aim was to collect representative cross-sectional data from approximately 10,000 participants (comprising around 0.5% of individuals with psoriasis in Germany) about eating behavior, physical activity, prevalence of obesity and other factors contributing to metabolic syndrome, as well as the extent to which care providers offered support with weight management. The data was then used to assess the association between psoriasis, obesity, and patient behavior. A second aim was to give insight into current treatment practices and identify the potential need for intervention.

Survey Execution and Analysis

ERAPSO was conducted with IT support from Clariness GmbH, Hamburg, Germany. The survey was online from 29 January to 21 March 2018. Completing the survey took approximately 10 min. ERAPSO was promoted in German language on German websites, search engines, and social media, targeting individuals with psoriasis and encouraging their participation by asking for help in developing a better understanding of psoriasis.
According to the European consensus on definition of psoriasis severity, mild psoriasis is defined as BSA ≤ 10% and moderate to severe disease is defined as BSA > 10% [22]. In this survey, BSA was self-assessed and entered online. To aid self-assessment of BSA, participants were shown a small graphic of a palm stating that the area of one palm is equal to 1.0% of the body surface.
For subgroup analyses, participants were divided into one group consisting of participants with mild disease (self-reported BSA ≤ 10%) and another group consisting of participants with moderate to severe disease (self-reported BSA > 10%). Participants reported data on (1) elevated cholesterol levels or other dyslipidemias, (2) impaired fasting glucose and/or diabetes mellitus, (3) arterial hypertension, and (4) waist circumference.
As a result of its observational and cross-sectional nature, the data restricted itself to purely descriptive methodology, and no statistical testing was performed. Furthermore, as a result of this survey’s self-reporting design, answers could not be confirmed.

Compliance with Ethics Guidelines

Ethics committee approval was not required because ERAPSO was conducted as an online survey. All the participants received explanations about the survey details. Informed consent was obtained from all participants for data storage, processing, and publication. This survey was performed in accordance with the Helsinki Declaration of 1964 and its later amendments.

Results

Demographic Data

Overall, 15,693 individuals participated in this survey (Fig. 2). Of those, 97.0% (n = 15,226) currently lived in Germany, and were included in the study. The study population comprised the 65.3% of the participants living in Germany who stated that they had been diagnosed with psoriasis (n = 9940, “true completers”), the 32.3% of participants who had never been diagnosed with psoriasis (n = 4923), and 2.4% who were not sure (n = 363), and were therefore excluded from the analysis. All of the following results describe only participants living in Germany with a confirmed diagnosis of psoriasis (n = 9940).
Within the study population, 55.1% (n = 5477) were female and 44.9% (n = 4463) were male, with a mean age at survey completion of 51.3 ± 14.0 years (Table 1). A majority (65.1%; n = 6474) were currently being treated for psoriasis by their dermatologist and 14.5% (n = 1439) were being treated by other physicians, for example general practitioners. A minority of participants (3.7%; n = 368) consulted a homeopath or alternative practitioner (multiple selections were possible). Nearly one-quarter of participants (25.3%; n = 2518) stated that they did not receive any treatment for psoriasis at all.
Table 1
Baseline characteristics
Characteristic
N = 9940
Age (years)
51.3 ± 14.0
Male gender
4463 (44.9%)
Body surface area (%)
12.7 ± 19.1
Mild psoriasis
7404 (74.5%)
Moderate to severe psoriasis
2536 (25.5%)
Time since diagnosis (years)
23.0 ± 16.0
Currently treated for psoriasis
7422 (83.3%)
Previous systemic treatment
4222 (42.5%)
Weight (kg)
83.8 ± 21.2
BMI (kg/m2)
28.5 ± 14.1
Waist circumference (male, cm)
92.7 ± 17.0
Of 15,693 total participants, 9940 currently live in Germany, have self-reported a diagnosis of psoriasis, and are included in this study. Mild psoriasis is defined as body surface area (BSA) ≤ 10% and moderate to severe disease is defined as BSA > 10%
BMI body mass index

Psoriasis Severity

In this survey, the mean BSA affected by psoriasis was 12.7 ± 19.1% (Table 1). The majority of participants (74.5%; n = 7404) had mild disease while 25.5% (n = 2536) were affected by moderate to severe psoriasis. Participants with mild psoriasis had a mean self-reported BSA of 4.0 ± 2.9% while participants with moderate to severe psoriasis had a mean self-reported BSA of 38.0 ± 23.5%. This is consistent with established prevalence of moderate to severe psoriasis.

Obesity

Mean participant body weight was 83.8 ± 21.2 kg. Mean BMI was 28.5 ± 14.1 kg/m2 (Table 1). Figure 3 shows the distribution of BMI in the overall study population. In this population, 66.9% (n = 6647) of all participants with psoriasis were overweight or obese (defined by the WHO 2008 as BMI ≥ 25 kg/m2). In comparison, approximately 50–60% of the general German population is overweight or obese [23]. Most participants (90.2%) with BMI ≥ 25 kg/m2 perceived themselves as being overweight. Figure 4 shows the association of BMI with psoriasis severity. Participants with high BMI tended to show increased reported BSA.

Cardiovascular Profile

Within the study population, 5.9% (n = 582) had reported coronary heart disease, 2.5% (n = 246) reported angina pectoris, 3.3% (n = 331) had signs of myocardial infarction, and 2.5% (n = 251) reported having had a stroke. On division by BMI subgroups, higher BMI was associated with increased prevalence of cardiovascular risk factors (CVRFs) and of cardiovascular events (CVEs) (Figs. S1 and S2, electronic supplementary material).
Of all the participants (n = 9940), 23.1% (n = 2297) reported high cholesterol or other dyslipidemias. Impaired fasting glucose was reported by 9.0% (n = 894) of participants and 9.5% (n = 940) had been diagnosed with diabetes mellitus. In total 34.4% (n = 3422) were diagnosed with arterial hypertension. Mean waist circumference in women was 88.4 + 16.5 cm and that in men was 92.7 + 17.0 cm. More women had elevated waist circumference (n = 3961/5477 [72.3%] above 78.7 cm) than men (n = 855/4463 [19.2%] above 100.0 cm). These are common cutoff values for elevated waist circumference [24].

Diet and Physical Activity

Among overweight participants, 12.6% (n = 836) were currently on a weight loss diet. The majority of overweight participants had tried weight loss diets already (60.7%, n = 4038) and 55.6% (n = 2244) had been successful (completed to participants’ satisfaction) with weight loss diets at least once.
Food was said to influence psoriasis severity by 25.9% (n = 1914) of participants with mild psoriasis and 31.0% (n = 785) of participants with moderate to severe psoriasis. Participants who stated that food can have positive or negative effects on their disease severity were asked to evaluate different types of food and how it affects their disease (Fig. 5). While vegetables, fish, potatoes, pasta, rice, and dairy products were perceived to have positive effects on psoriasis severity in many participants, convenience products, fast food, sweets, and alcohol appeared to have negative effects on psoriasis severity in approximately 50% of participants in the overall population. Within the ERAPSO population, 9.0% (n = 346) of participants with mild psoriasis say that psoriasis has prevented them from losing weight by diet, whereas 20.3% (n = 257) of participants with moderate to severe psoriasis say that their psoriasis has prevented them from losing weight by diet.
Only 21.2% (n = 1408) of overweight participants reported currently exercising to lose weight. Participants who were overweight reported greater discomfort with physical activity than those with BMI < 25 kg/m2 (Fig. 6a) when their psoriasis is active. One-quarter (25.6%; n = 904) of participants with mild psoriasis and 46.6% (n = 514) of participants with moderate to severe psoriasis said that psoriasis has prevented them from exercising at least once. Figure 6b illustrates how active psoriasis is associated with discomfort with physical activities in participants with increasing disease severity, to the extent of causing total abandonment of physical activity. Eighteen percent of participants with mild psoriasis and 25.8% of participants with moderate to severe psoriasis said that exercise can influence their disease severity. These participants were asked to evaluate different types of physical activity and how they affected their disease severity (Fig. 7). While walking, cycling, and endurance sports showed positive effects in 41.0%, 32.4%, and 26.6% of participants, respectively, housework showed a negative impact on psoriasis severity in 31.1% of participants.
Nearly one-third (35.7%; n = 2374) of overweight participants have been approached by their treating physician to lose weight by going on a diet or exercising. Only 13.3% (n = 887) of overweight participants stated that their physicians and health insurances offer specific programs to lose weight using diets or physical activity.

Discussion

ERAPSO identified a higher prevalence of overweight and obesity among participants than in the general German population, where around 50–60% are overweight or obese [23]. Rates of overweight and obesity in participants matched those determined in PsoHealth [2]. There is not only an objective burden of obesity but also a subjectively perceived burden of obesity, as participants show intact self-perception regarding overweight/obesity. Despite this, only a minority of overweight participants are currently attempting to lose weight by diet or exercise. This underlines the need for professional external support in multiple approaches.
Awareness of obesity or the necessity to treat obesity in psoriasis patients appears relatively low among physicians, as only a minority of participants were offered weight loss programs. Awareness of the negative impact of obesity and metabolic syndrome on psoriasis disease severity needs to be raised, and the efficacy of treatment options established. For example, weight loss combined with cyclosporine therapy improves psoriasis more than cyclosporine alone [25]. The combined efficacy of weight loss and secukinumab treatment for plaque psoriasis is under current investigation (METABOLYX trial, NCT03440736).
Compared to ERAPSO findings on the prevalence of CVRFs in participants, in Germany 28.1% of men and 27.1% of women overall have dyslipidemia, with a significant increase in prevalence with increasing age and with no significant differences between sexes [26]. Prevalence of arterial hypertension is around 40–50% in adults in Germany (Robert Koch Institut, Statistisches Bundesamt 2018). Type 2 diabetes occurs in 7–8% of the general German population (Deutsche Diabetes Gesellschaft 2018). ERAPSO participants showed a similar prevalence of dyslipidemia, arterial hypertension, and diabetes mellitus to the general German population. Increasing prevalence of CVRFs with growing BMI translated into increased incidence of CVEs.
Participants with moderate to severe psoriasis perceived stronger positive and negative influences of food and sports on their disease than participants with mild psoriasis. Psoriasis severity was identified by participants as a limiting factor for engaging in exercise, as might be expected given physical symptoms and concerns regarding outer appearance in sports clothing. Interestingly, some participants reported that severity of psoriasis also impacted their capacity to follow a specific diet. This suggests an intersection between the psychological effects of psoriasis, including depression and, potentially, emotional eating, and obesity, and may warrant further research. In addition, treating psoriasis and adequate control of skin symptoms could help participants to lose weight since psoriasis severity is associated with impairment in diets and exercise. Participants reported “healthy” foods such as vegetables having a positive effect on their psoriasis, whereas processed food, sweets, and alcohol were more frequently labelled as having negative effects. A perceptual effect cannot be ruled out, as for instance it is unclear whether increased alcohol consumption in psoriasis participants is a risk factor for the disease [27]. However, when giving advice on nutrition and diets for psoriasis patients, physicians can continue to recommend “healthy” food like fiber-rich vegetables and fish, which seems to have positive effects on participants’ perception of disease. In addition, when giving advice on physical exercise, physicians can continue to recommend daily physical activities like endurance sports, cycling, or walking. Furthermore, endurance sports, cycling, or walking are often more practical than resistance training to include as daily activities and they have a higher chance to burn body fat compared to resistance training. ERAPSO revealed participants’ perceptions of weight loss treatment as being limited. In terms of weight management, diet, and exercise, treatment offerings appeared to be insufficient.
Limitations of ERAPSO include the self-selecting patient population. For example, severely depressed participants may be less likely to complete online surveys. A further limitation is that all data collected, including psoriasis diagnosis, were based on participants self-reporting of their health information, not on physician’s records. Finally, differences in digital literacy between participants compared with the general population might be a further source of bias, with the ERAPSO participants being a self-selecting digitally literate subpopulation.

Conclusions

ERAPSO showed a high prevalence of overweight and obesity among participants in Germany, with psoriasis severity being associated with BMI. A relationship between obesity and CV risk factors or events was also apparent. Only a minority of overweight/obese participants were currently on a diet or exercising to lose weight, and few were approached by their physician with weight loss recommendations, indicating a lack of professional weight loss support for psoriasis patients. Psoriasis severity was associated with impairment in participation and success of diets and physical activity; therefore, optimal psoriasis disease control could in itself be a means to facilitate patients’ weight loss attempts. ERAPSO shows an unmet medical need in obese individuals with self-reported psoriasis, with insufficient offerings for professional support to lose weight or increase physical activity.

Acknowledgements

We thank the participants of the study.

Funding Sources

This research and article processing charges were funded by Novartis Pharma GmbH, Nuremberg, DE. The analyses presented here were funded by Novartis Pharma GmbH, Germany. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.

Medical Writing and/or Editorial Assistance

Medical writing assistance was provided by Evelyn Altemeyer and Jackie L. Johnson, Ph.D., Novartis Ireland Ltd, and funded by Novartis Pharma GmbH, Germany in line with GPP3.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Disclosures

Peter E. H. Schwarz has Grant/Research Support from Deutsches Zentrum für Diabetesforschung (DZD), European Commission, EU Directorate Public Health, BMBF; has served on the Speaker’s Bureau for the European Commission, AOKplus, Ascensia, Novartis, Lifescan, MERCK, Novo, Lilly, MSD, Boehringer, REHASAN, Sanofi; is a Consultant for AOKplus, Ascensia, TUMAINI Institut für Präventionsmanagement, REHASAN and is affiliated with TUMAINI Institut für Präventionsmanagement. Andreas Pinter has worked as an investigator and/or speaker and/or advisor for following pharmaceutical companies: AbbVie, Almirall-Hermal, Amgen, Biogen Idec, Boehringer-Ingelheim, Celgene, GSK, Eli-Lilly, Galderma, Hexal, Janssen, LEO-Pharma, Medac, Merck Serono, Mitsubishi, MSD, Novartis, Pascoe, Pfizer, Tigercat Pharma, Regeneron, Roche, Sandoz Biopharmaceuticals, Schering-Plough, and UCB Pharma. Nima Melzer is an employee of Novartis Pharma GmbH. Philipp Barteczek is an employee of Novartis Pharma GmbH. Maximilian Reinhardt is an employee of Novartis Pharma GmbH.

Compliance with Ethics Guidelines

Ethics committee approval was not required because ERAPSO was conducted as an online survey. All the participants received explanations about the survey details. Informed consent was obtained from all participants for data storage, processing, and publication. This survey was performed in accordance with the Helsinki Declaration of 1964 and its later amendments.

Data Availability

Novartis is committed to sharing with qualified external researchers, access to patient-level data, and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the survey in line with applicable laws and regulations.
Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( http://​creativecommons.​org/​licenses/​by-nc/​4.​0/​ ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Anhänge

Electronic supplementary material

Below is the link to the electronic supplementary material.
Literatur
1.
Zurück zum Zitat Chiricozzi A, Romanelli P, Volpe E, Borsellino G, Romanelli M. Scanning the immunopathogenesis of psoriasis. Int J Mol Sci. 2018;19(1):179. Chiricozzi A, Romanelli P, Volpe E, Borsellino G, Romanelli M. Scanning the immunopathogenesis of psoriasis. Int J Mol Sci. 2018;19(1):179.
2.
Zurück zum Zitat Jacobi A, Langenbruch A, Purwins S, Augustin M, Radtke MA. Prevalence of obesity in patients with psoriasis: results of the National Study PsoHealth3. Dermatology. 2015;231(3):231–8.CrossRefPubMed Jacobi A, Langenbruch A, Purwins S, Augustin M, Radtke MA. Prevalence of obesity in patients with psoriasis: results of the National Study PsoHealth3. Dermatology. 2015;231(3):231–8.CrossRefPubMed
3.
Zurück zum Zitat Griffiths CEM, Jo S-J, Naldi L, et al. A multidimensional assessment of the burden of psoriasis: results from a multinational dermatologist and patient survey. Br J Dermatol. 2018;179(1):173–81.CrossRefPubMed Griffiths CEM, Jo S-J, Naldi L, et al. A multidimensional assessment of the burden of psoriasis: results from a multinational dermatologist and patient survey. Br J Dermatol. 2018;179(1):173–81.CrossRefPubMed
4.
Zurück zum Zitat Shah K, Mellars L, Changolkar A, Feldman SR. Real-world burden of comorbidities in US patients with psoriasis. J Am Acad Dermatol. 2017;77(2):287–92.e4.CrossRef Shah K, Mellars L, Changolkar A, Feldman SR. Real-world burden of comorbidities in US patients with psoriasis. J Am Acad Dermatol. 2017;77(2):287–92.e4.CrossRef
5.
6.
Zurück zum Zitat Love TJ, Qureshi AA, Karlson EW, Gelfand JM, Choi HK. Prevalence of the metabolic syndrome in psoriasis: results from the National Health and Nutrition Examination Survey, 2003–2006. Arch Dermatol. 2011;147(4):419–24.CrossRefPubMed Love TJ, Qureshi AA, Karlson EW, Gelfand JM, Choi HK. Prevalence of the metabolic syndrome in psoriasis: results from the National Health and Nutrition Examination Survey, 2003–2006. Arch Dermatol. 2011;147(4):419–24.CrossRefPubMed
7.
Zurück zum Zitat Neuhauser H, Ellert U. Estimation of the metabolic syndrome prevalence in the general population in Germany. J Public Health. 2008;16(3):221–7.CrossRef Neuhauser H, Ellert U. Estimation of the metabolic syndrome prevalence in the general population in Germany. J Public Health. 2008;16(3):221–7.CrossRef
8.
Zurück zum Zitat Danielsen K, Wilsgaard T, Olsen AO, et al. Elevated odds of metabolic syndrome in psoriasis: a population-based study of age and sex differences. Br J Dermatol. 2015;172(2):419–27.CrossRefPubMed Danielsen K, Wilsgaard T, Olsen AO, et al. Elevated odds of metabolic syndrome in psoriasis: a population-based study of age and sex differences. Br J Dermatol. 2015;172(2):419–27.CrossRefPubMed
9.
Zurück zum Zitat Carrascosa JM, Rocamora V, Fernandez-Torres RM, et al. Obesity and psoriasis: inflammatory nature of obesity, relationship between psoriasis and obesity, and therapeutic implications. Actas Dermosifiliogr. 2014;105(1):31–44.CrossRefPubMed Carrascosa JM, Rocamora V, Fernandez-Torres RM, et al. Obesity and psoriasis: inflammatory nature of obesity, relationship between psoriasis and obesity, and therapeutic implications. Actas Dermosifiliogr. 2014;105(1):31–44.CrossRefPubMed
10.
Zurück zum Zitat Bluher M. Adipose tissue inflammation: a cause or consequence of obesity-related insulin resistance? Clin Sci. 2016;130(18):1603–14.CrossRef Bluher M. Adipose tissue inflammation: a cause or consequence of obesity-related insulin resistance? Clin Sci. 2016;130(18):1603–14.CrossRef
11.
Zurück zum Zitat Ali M, Girgis S, Hassan A, Rudick S, Becker RC. Inflammation and coronary artery disease: from pathophysiology to Canakinumab Anti-Inflammatory Thrombosis Outcomes Study (CANTOS). Coron Artery Dis. 2018;29(5):429–37. Ali M, Girgis S, Hassan A, Rudick S, Becker RC. Inflammation and coronary artery disease: from pathophysiology to Canakinumab Anti-Inflammatory Thrombosis Outcomes Study (CANTOS). Coron Artery Dis. 2018;29(5):429–37.
12.
13.
Zurück zum Zitat Prussick RB, Miele L. Nonalcoholic fatty liver disease in patients with psoriasis: a consequence of systemic inflammatory burden? Br J Dermatol. 2018;179(1):16–29. Prussick RB, Miele L. Nonalcoholic fatty liver disease in patients with psoriasis: a consequence of systemic inflammatory burden? Br J Dermatol. 2018;179(1):16–29.
14.
Zurück zum Zitat Xu X, Su L, Gao Y, Ding Y. The prevalence of nonalcoholic fatty liver disease and related metabolic comorbidities was associated with age at onset of moderate to severe plaque psoriasis: a cross-sectional study. PLoS One. 2017;12(1):e0169952.CrossRefPubMedPubMedCentral Xu X, Su L, Gao Y, Ding Y. The prevalence of nonalcoholic fatty liver disease and related metabolic comorbidities was associated with age at onset of moderate to severe plaque psoriasis: a cross-sectional study. PLoS One. 2017;12(1):e0169952.CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Reich K. The concept of psoriasis as a systemic inflammation: implications for disease management. J Eur Acad Dermatol Venereol. 2012;26(Suppl 2):3–11.CrossRefPubMed Reich K. The concept of psoriasis as a systemic inflammation: implications for disease management. J Eur Acad Dermatol Venereol. 2012;26(Suppl 2):3–11.CrossRefPubMed
16.
Zurück zum Zitat Versini M, Jeandel PY, Rosenthal E, Shoenfeld Y. Obesity in autoimmune diseases: not a passive bystander. Autoimmun Rev. 2014;13(9):981–1000.CrossRefPubMed Versini M, Jeandel PY, Rosenthal E, Shoenfeld Y. Obesity in autoimmune diseases: not a passive bystander. Autoimmun Rev. 2014;13(9):981–1000.CrossRefPubMed
17.
Zurück zum Zitat Yanaba K, Umezawa Y, Ito T, et al. Impact of obesity on the efficacy of ustekinumab in Japanese patients with psoriasis: a retrospective cohort study of 111 patients. Arch Dermatol Res. 2014;306(10):921–5.CrossRefPubMed Yanaba K, Umezawa Y, Ito T, et al. Impact of obesity on the efficacy of ustekinumab in Japanese patients with psoriasis: a retrospective cohort study of 111 patients. Arch Dermatol Res. 2014;306(10):921–5.CrossRefPubMed
18.
Zurück zum Zitat Gelfand JM, Neimann AL, Shin DB, Wang X, Margolis DJ, Troxel AB. Risk of myocardial infarction in patients with psoriasis. JAMA. 2006;296(14):1735–41.CrossRefPubMed Gelfand JM, Neimann AL, Shin DB, Wang X, Margolis DJ, Troxel AB. Risk of myocardial infarction in patients with psoriasis. JAMA. 2006;296(14):1735–41.CrossRefPubMed
19.
Zurück zum Zitat Hu SC, Lan CE. Psoriasis and cardiovascular comorbidities: focusing on severe vascular events, cardiovascular risk factors and implications for treatment. Int J Mol Sci. 2017;18(10):2211. Hu SC, Lan CE. Psoriasis and cardiovascular comorbidities: focusing on severe vascular events, cardiovascular risk factors and implications for treatment. Int J Mol Sci. 2017;18(10):2211.
20.
Zurück zum Zitat Gistera A, Hansson GK. The immunology of atherosclerosis. Nat Rev Nephrol. 2017;13(6):368–80.CrossRefPubMed Gistera A, Hansson GK. The immunology of atherosclerosis. Nat Rev Nephrol. 2017;13(6):368–80.CrossRefPubMed
21.
Zurück zum Zitat Jamasbi J, Ayabe K, Goto S, Nieswandt B, Peter K, Siess W. Platelet receptors as therapeutic targets: past, present and future. Thromb Haemost. 2017;117(7):1249–57.CrossRefPubMed Jamasbi J, Ayabe K, Goto S, Nieswandt B, Peter K, Siess W. Platelet receptors as therapeutic targets: past, present and future. Thromb Haemost. 2017;117(7):1249–57.CrossRefPubMed
22.
Zurück zum Zitat Mrowietz U, Kragballe K, Reich K, et al. Definition of treatment goals for moderate to severe psoriasis: a European consensus. Arch Dermatol Res. 2011;303(1):1–10.CrossRefPubMed Mrowietz U, Kragballe K, Reich K, et al. Definition of treatment goals for moderate to severe psoriasis: a European consensus. Arch Dermatol Res. 2011;303(1):1–10.CrossRefPubMed
24.
Zurück zum Zitat Alberti KG, Eckel RH, Grundy SM, et al. Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009;120(16):1640–5.CrossRefPubMed Alberti KG, Eckel RH, Grundy SM, et al. Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009;120(16):1640–5.CrossRefPubMed
25.
Zurück zum Zitat Gisondi P, Del Giglio M, Di Francesco V, Zamboni M, Girolomoni G. Weight loss improves the response of obese patients with moderate-to-severe plaque psoriasis to low-dose cyclosporine therapy: a randomized, controlled, investigator-blinded clinical trial. Am J Clin Nutr. 2008;88:1242–7.PubMed Gisondi P, Del Giglio M, Di Francesco V, Zamboni M, Girolomoni G. Weight loss improves the response of obese patients with moderate-to-severe plaque psoriasis to low-dose cyclosporine therapy: a randomized, controlled, investigator-blinded clinical trial. Am J Clin Nutr. 2008;88:1242–7.PubMed
26.
Zurück zum Zitat Scheidt-Nave C, Du Y, Knopf H, et al. Prevalence of dyslipidemia among adults in Germany: results of the German health interview and examination survey for adults (DEGS 1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;56(5–6):661–7.CrossRefPubMed Scheidt-Nave C, Du Y, Knopf H, et al. Prevalence of dyslipidemia among adults in Germany: results of the German health interview and examination survey for adults (DEGS 1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;56(5–6):661–7.CrossRefPubMed
27.
Zurück zum Zitat Brenaut E, Horreau C, Pouplard C, et al. Alcohol consumption and psoriasis: a systematic literature review. J Eur Acad Dermatol Venereol. 2013;27(Suppl 3):30–5.CrossRefPubMed Brenaut E, Horreau C, Pouplard C, et al. Alcohol consumption and psoriasis: a systematic literature review. J Eur Acad Dermatol Venereol. 2013;27(Suppl 3):30–5.CrossRefPubMed
Metadaten
Titel
ERAPSO: Revealing the High Burden of Obesity in German Psoriasis Patients
verfasst von
Peter E. H. Schwarz
Andreas Pinter
Nima Melzer
Philipp Barteczek
Maximilian Reinhardt
Publikationsdatum
11.07.2019
Verlag
Springer Healthcare
Erschienen in
Dermatology and Therapy / Ausgabe 3/2019
Print ISSN: 2193-8210
Elektronische ISSN: 2190-9172
DOI
https://doi.org/10.1007/s13555-019-0314-1

Weitere Artikel der Ausgabe 3/2019

Dermatology and Therapy 3/2019 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.