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Dive into the research topics where Lone Skov is active.

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Featured researches published by Lone Skov.


Journal of Internal Medicine | 2011

Psoriasis is associated with clinically significant cardiovascular risk: a Danish nationwide cohort study

Ole Ahlehoff; Gunnar H. Gislason; Mette Charlot; Casper H. Jørgensen; Jesper Lindhardsen; Jonas Bjerring Olesen; Steen Z. Abildstrom; Lone Skov; Christian Torp-Pedersen; Peter Riis Hansen

Abstract.  Ahlehoff O, Gislason GH, Charlot M, Jørgensen CH, Lindhardsen J, Olesen JB, Abildstrøm SZ, Skov L, Torp‐Pedersen C, Hansen PR. (Copenhagen University Hospital Gentofte, Hellerup; Copenhagen University Hospital Bispebjerg, Copenhagen; National Institute of Public Health, University of Southern Denmark, Copenhagen; Copenhagen University Hospital Gentofte, Hellerup; University of Copenhagen, Copenhagen, Denmark) Psoriasis is associated with clinically significant cardiovascular risk: a Danish nationwide cohort study. J Intern Med2011; 270: 147–157.


British Journal of Dermatology | 2007

Dermal inorganic gadolinium concentrations: evidence for in vivo transmetallation and long-term persistence in nephrogenic systemic fibrosis.

Jerrold L. Abraham; C. Thakral; Lone Skov; K. Rossen; P. Marckmann

Background  Gadolinium (Gd)‐based magnetic resonance contrast agents (GBMCA), including gadodiamide, have been identified as the probable causative agents of the serious disease, nephrogenic systemic fibrosis (NSF).


European Heart Journal | 2012

Psoriasis and risk of atrial fibrillation and ischaemic stroke: a Danish Nationwide Cohort Study

Ole Ahlehoff; Gunnar H. Gislason; Casper H. Jørgensen; Jesper Lindhardsen; Mette Charlot; Jonas Bjerring Olesen; Steen Z. Abildstrom; Lone Skov; Christian Torp-Pedersen; Peter Riis Hansen

AIMS Psoriasis is a chronic inflammatory disease and inflammation contributes to the pathogenesis of atrial fibrillation (AF) and ischaemic stroke. We therefore investigated the risk of these endpoints in patients with psoriasis. METHODS AND RESULTS Cohort study of the entire Danish population followed from 1997 to 2006 by individual-level-linkage of nationwide prospectively recorded registers. Multivariable Poissons regression and sensitivity analyses were used to assess the psoriasis-related risk of AF and ischaemic stroke. A total of 36 765 patients with mild psoriasis and 2793 with severe psoriasis were compared with 4 478 926 individuals, i.e., the reference population. In patients with mild psoriasis, the adjusted rate ratios (RRs) for AF were 1.50 (1.21-1.86) and 1.16 (1.08-1.24) in patients aged <50 and ≥50 years, respectively. Patients with severe psoriasis had a higher risk of AF with RRs 2.98 (1.80-4.92) in patients aged <50 years and 1.29 (1.01-1.65) in patients aged ≥50 years. Patients with psoriasis also demonstrated a disease severity-dependent increased risk of ischaemic stroke, i.e. RRs 1.97 (1.66-2.34) and 2.80 (1.81-4.34) in patients aged <50 years with mild and severe psoriasis, and RRs 1.13 (1.04-1.21) and 1.34 (1.04-1.71) in patients aged ≥50 years with mild and severe psoriasis, respectively. A range of sensitivity analyses yielded comparable results. CONCLUSION Psoriasis is associated with increased risk of AF and ischaemic stroke. These novel results add to a growing body of evidence, suggesting that patients with psoriasis could be considered at increased cardiovascular risk.


Journal of Internal Medicine | 2013

Cardiovascular disease event rates in patients with severe psoriasis treated with systemic anti-inflammatory drugs: a Danish real-world cohort study.

Ole Ahlehoff; Lone Skov; Gunnar H. Gislason; Jesper Lindhardsen; Søren Lund Kristensen; Lars Iversen; Stine Lasthein; Robert Gniadecki; Tomas Norman Dam; Christian Torp-Pedersen; Peter Riis Hansen

Psoriasis is a chronic inflammatory disorder associated with cardiovascular morbidity and mortality. Systemic anti‐inflammatory drugs, including biological agents, are widely used in the treatment of patients with moderate to severe psoriasis and may attenuate the risk of cardiovascular disease events. We therefore examined the rate of cardiovascular disease events in patients with severe psoriasis treated with systemic anti‐inflammatory drugs.


JAMA Dermatology | 2013

Effect of Weight Loss on the Severity of Psoriasis: A Randomized Clinical Study

Peter Buhl Jensen; Claus Zachariae; Robin Christensen; Nina Rica Wium Geiker; Bente Krogsgaard Schaadt; Steen Stender; Peter Riis Hansen; Arne Astrup; Lone Skov

IMPORTANCE Psoriasis is associated with adiposity and weight gain increases the severity of psoriasis and the risk of incident psoriasis. Therefore, we aimed to measure the effect of weight reduction on the severity of psoriasis in obese patients with psoriasis. OBJECTIVE To assess the effect of weight reduction on the severity of psoriasis in overweight patients. DESIGN Sixty obese patients with psoriasis from our dermatology outpatient clinic were enrolled in a prospective randomized clinical trial in which they were allocated to a control group or an intervention group. SETTING University hospital outpatient dermatology clinic. PARTICIPANTS We included 60 of 69 eligible overweight patients with psoriasis (body mass index [calculated as weight in kilograms divided by height in meters squared], 27-40; aged 25-71 years). INTERVENTIONS The intervention group received a low-energy diet (LED) (800-1000 kcal/d) for 8 weeks to induce weight loss, followed by 8 weeks of reintroduction of normal food intake, reaching 1200 kcal/d. The control group was instructed to continue eating ordinary healthy foods. MAIN OUTCOMES AND MEASURES Psoriasis Area and Severity Index (PASI) after 16 weeks, with Dermatology Life Quality Index (DLQI) as a secondary end point. RESULTS The median PASI for all patients was 5.4 (interquartile range, 3.8-7.6) at baseline. At week 16, the mean body weight loss was 15.4 kg (95% CI, 12.3-18.5 kg; P < .001) greater in the intervention group than in the control group. The corresponding mean differences in PASI and DLQI, also in favor of the LED group, were -2.0 (95% CI, 4.1 to -0.1; P = .06) and -2.0 (95% CI, -3.6 to -0.3; P = .02), respectively. CONCLUSIONS AND RELEVANCE Treatment with an LED showed a trend in favor of clinically important PASI improvement and a significant reduction in DLQI in overweight patients with psoriasis. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT01137188.


Journal of Immunology | 2008

IL-8 as antibody therapeutic target in inflammatory diseases: Reduction of clinical activity in palmoplantar pustulosis

Lone Skov; Frank J. Beurskens; Claus Zachariae; Sakari Reitamo; Jessica L. Teeling; David Satijn; Kim M. Knudsen; Elmieke Pj Boot; Debra Hudson; Ole Baadsgaard; Paul Parren; Jan G. J. van de Winkel

IL-8 is a chemokine that has been implicated in a number of inflammatory diseases involving neutrophil activation. HuMab 10F8 is a novel fully human mAb against IL-8, which binds a discontinuous epitope on IL-8 overlapping the receptor binding site, and which effectively neutralizes IL-8-dependent human neutrophil activation and migration. We investigated whether interference in the cytokine network by HuMab 10F8 might benefit patients suffering from palmoplantar pustulosis, a chronic inflammatory skin disease. Treatment of patients with HuMab 10F8 was well tolerated and significantly reduced clinical disease activity at all five endpoints, which included a ≥50% reduction in the formation of fresh pustules. IL-8 neutralization was monitored at the site of inflammation by assessing exudates of palmoplantar pustulosis lesions. HuMab 10F8 sequestered IL-8 in situ, as observed by rapid dose-dependent decreases of IL-8 concentrations immediately following Ab infusion. These data demonstrate a critical role for IL-8 in the pathophysiology of palmoplantar pustulosis. HuMab 10F8 is capable of interrupting IL-8 activity in vivo and represents a candidate for treatment of inflammatory diseases and other pathological conditions associated with IL-8 overproduction.


British Journal of Dermatology | 1998

Allergens in combination have a synergistic effect on the elicitation response: a study of fragrance-sensitized individuals

J.D. Johansen; Lone Skov; Aage Vølund; Klaus Ejner Andersen; Torkil Menné

Perfume ingredients were chosen as model substances to study the effect of allergens in combination on the elicitation response. Two groups of eczema patients were studied. One consisted of 18 subjects with a contact allergy to two fragrance substances and the other was a control group of 15 subjects allergic to only one of the same two fragrance substances. The test and matched control subject were patch tested in exactly the same way with two allergens applied in serial dilution in separate chambers on one side and combined in one chamber on the other side of the upper back. The assessment of reactions was carried out on day 3 by clinical grading and laser Doppler flowmetry, and the extent of the reaction was measured in millimetres. The data were analysed by logistic dose–response models. It was found that the combination of two allergens in individuals allergic to both substances had a synergistic effect on the elicitation response evaluated by all three methods. The 1 : 1 mixtures of the two allergens elicited responses as if the doses were three to four times higher than those actually used, which is significantly more than expected if an additive effect had been present. In the control group, no increased response was seen to the combined allergens compared with the allergens tested separately. The synergistic effect demonstrated is likely to apply to other contact allergens as well and should be taken into account in designing diagnostic tests and performing safety assessments.


British Journal of Dermatology | 2014

Increased number and frequency of group 3 innate lymphoid cells in nonlesional psoriatic skin

Beatrice Dyring-Andersen; Carsten Geisler; C. Agerbeck; J.P.H. Lauritsen; S.D. Gúdjonsdottir; Lone Skov; Charlotte M. Bonefeld

Psoriasis is a common immune‐mediated inflammatory disease that affects the skin and joints. The interleukin (IL)‐23/IL‐17A axis and IL‐22 play key roles in the pathogenesis of psoriasis. IL‐23‐responsive innate lymphoid cells (ILCs) with a high capacity to produce IL‐17 and/or IL‐22 have recently been identified and associated with inflammatory bowel diseases. The occurrence and role of ILCs in human skin are poorly understood.


Journal of Internal Medicine | 2011

Prognosis following first‐time myocardial infarction in patients with psoriasis: a Danish nationwide cohort study

Ole Ahlehoff; Gunnar H. Gislason; Jesper Lindhardsen; Jonas Bjerring Olesen; Mette Charlot; Lone Skov; Christian Torp-Pedersen; Peter Riis Hansen

Abstract.  Ahlehoff O, Gislason GH, Lindhardsen J, Olesen JB, Charlot M, Skov L, Torp‐Pedersen C, Hansen PR. (Copenhagen University Hospital Gentofte, Hellerup; Copenhagen University Hospital Roskilde, Roskilde, Denmark). Prognosis following first‐time myocardial infarction in patients with psoriasis: a Danish nationwide cohort study. J Intern Med 2011; 270: 237–244.


Contact Dermatitis | 2013

CD4+ T cells producing interleukin (IL)‐17, IL‐22 and interferon‐γ are major effector T cells in nickel allergy

Beatrice Dyring-Andersen; Lone Skov; Marianne B. Løvendorf; Michael Bzorek; Knud Søndergaard; Jens-Peter H. Lauritsen; Sally Dabelsteen; Carsten Geisler; Charlotte M. Bonefeld

Background It has been suggested that interleukin (IL)‐17 and IL‐22 play important roles in the elicitation of human allergic contact dermatitis; however, the frequencies of T cell subtypes producing IL‐17 and IL‐22 in human allergic contact dermatitis are unknown.

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Gunnar H. Gislason

National Heart Foundation of Australia

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Ole Ahlehoff

Copenhagen University Hospital

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Jesper Lindhardsen

Copenhagen University Hospital

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Peter Marckmann

Odense University Hospital

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