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1.
Dermatitis ; 24(1): 29-32, 2013.
Article in English | MEDLINE | ID: mdl-23340396

ABSTRACT

BACKGROUND: Photoallergic contact dermatitis (PACD) is a hypersensitivity reaction that occurs when a previously photosensitized exogenous agent comes into contact with UV radiation. Currently, there are no studies profiling photoallergic reactions in Canada. Because the photoallergen profile changes over time, it is necessary to continually update our knowledge to ensure proper recognition of allergens and appropriate treatment of patients. OBJECTIVE: This study aimed to profile photoallergic reactions in Canada. METHODS: A retrospective chart review of all patients who underwent photopatch testing at Toronto Western Hospital between January 2001 and December 2010 was completed. Photoallergic, allergic, and irritant reactions were recorded for 26 common allergens. RESULTS: Ninety-nine patients (61.9%) had at least 1 positive reaction to the test allergens. Fifty-four patients (33.8%) had at least 1 photoallergic reaction. All 26 allergens produced at least 1 allergic or photoallergic reaction. The most common relevant photoallergens were benzophenone-3, octyl dimethyl para-aminobenzoic acid (PABA) in 5% alcohol, and butylmethoxy-dibenzoylmethane. CONCLUSIONS: This study is the first to profile photoallergic contact reactions in Canada. It is clear that the culprit photoallergen in PACD can often be identified in a properly selected population. Future surveillance is necessary to continue to characterize PACD trends in Canada and to help better treat and screen this patient population.


Subject(s)
Allergens/adverse effects , Dermatitis, Allergic Contact/etiology , Dermatitis, Photoallergic/etiology , Sunscreening Agents/adverse effects , Adolescent , Adult , Aged , Canada/epidemiology , Dermatitis, Allergic Contact/epidemiology , Dermatitis, Photoallergic/epidemiology , Female , Humans , Male , Middle Aged , Patch Tests/methods , Photosensitizing Agents/adverse effects , Retrospective Studies , Ultraviolet Rays/adverse effects , Young Adult
2.
J Matern Fetal Neonatal Med ; 25(11): 2470-4, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22506729

ABSTRACT

OBJECTIVES: To establish gender-specific differences in maternal and fetal immune response in healthy human fetuses at term. METHODS: Forty-five women with elective caesarean sections for uncomplicated singleton pregnancies were recruited for two studies. Using a multiplex biomarker immunoassay system, unstimulated maternal and fetal plasma concentrations of interleukin (IL)-1ß, IL-1ra, IL-6, IL-8, macrophage inflammatory protein (MIP)-1α, and tumor necrosis factor (TNF)-α were measured from one study population. Lipopolysaccharide (LPS)-stimulated cytokine response was measured in a second study. RESULTS: There were no significant gender differences in either maternal or fetal unstimulated plasma cytokine concentrations, but concentrations of the proinflammatory cytokines IL-1ß and IL-6 were significantly greater in male fetal LPS-stimulated samples than in female fetal samples. CONCLUSIONS: Blood of male fetuses mounts a larger pro-inflammatory response to lipopolysaccharide (LPS). This heightened response could be a critical pathway in promoting premature rupture of membranes (PPROM) and may be associated with life long differential gender response to infection.


Subject(s)
Fetal Blood/drug effects , Inflammation/blood , Inflammation/chemically induced , Lipopolysaccharides/pharmacology , Sex Characteristics , Adult , Cytokines/blood , Female , Fetal Blood/immunology , Fetal Blood/metabolism , Humans , In Vitro Techniques , Infant, Newborn , Male , Mothers , Osmolar Concentration , Pregnancy/blood , Umbilical Veins/chemistry , Umbilical Veins/drug effects , Umbilical Veins/immunology , Umbilical Veins/metabolism
3.
CNS Drugs ; 25(7): 575-83, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21623641

ABSTRACT

Alzheimer's disease is a chronic neurodegenerative disorder resulting in part from the degeneration of cholinergic neurons in the brain. Rivastigmine, a cholinesterase inhibitor, is commonly used as a treatment for dementia due to its ability to moderate cholinergic neurotransmission; however, treatment with oral rivastigmine can lead to gastrointestinal adverse effects such as nausea and vomiting. Transdermal administration of rivastigmine can minimize these adverse effects by providing continuous delivery of the medication, while maintaining the effectiveness of the oral treatment. While the transdermal form of rivastigmine has been found to have fewer systemic adverse effects compared with the oral form, cutaneous reactions, such as contact dermatitis, can lead to discontinuation of the drug in its transdermal form. Lack of patient compliance with regard to applying the patch to the designated site, applying the patch for the correct length of time or rotating patch application sites increases the risk of cutaneous adverse reactions. This article outlines the diagnosis and management of irritant contact dermatitis and allergic contact dermatitis secondary to transdermal rivastigmine. The large majority of reactions to transdermal patches are of an irritant type, which can be diagnosed clinically by the presence of a pruritic, erythematous, eczematous plaque strictly confined to the borders of the patch. In contrast, an allergic reaction can be differentiated by the presence of vesicles and/or oedema, erythema beyond the boundaries of the transdermal patch and lack of improvement of the lesion 48 hours after removal of the offending treatment. By encouraging the patient to follow a regular rotation schedule for the patch, and using lipid-based emollients for irritant dermatitis and pre- and post-treatment topical corticosteroids for allergic dermatitis, cutaneous reactions can often be alleviated and patients can continue with their medication regimen. Other simple changes to a patient's treatment routine, including minimizing the use of harsh soaps, avoiding recently shaven or damaged areas of skin and carefully removing the patch after use, can help to further decrease the risk of dermatitis development.


Subject(s)
Alzheimer Disease/drug therapy , Cholinesterase Inhibitors/adverse effects , Phenylcarbamates/adverse effects , Administration, Cutaneous , Cholinesterase Inhibitors/administration & dosage , Cholinesterase Inhibitors/therapeutic use , Dermatitis, Allergic Contact/drug therapy , Dermatitis, Allergic Contact/etiology , Dermatitis, Allergic Contact/prevention & control , Dermatitis, Contact/drug therapy , Dermatitis, Contact/etiology , Dermatitis, Contact/prevention & control , Humans , Medication Adherence , Phenylcarbamates/administration & dosage , Phenylcarbamates/therapeutic use , Rivastigmine , Transdermal Patch
4.
J Cell Commun Signal ; 2(1-2): 19-23, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18649016

ABSTRACT

Connective tissue growth factor (CTGF, CCN2) is induced in response to TGFbeta in fibroblasts. In this report, we show that C2 ceramide reduced the ability of TGFbeta to induce CCN2 protein, mRNA and promoter activity in fibroblasts. C2 ceramide reduced the ability of TGFbeta to induce the generic Smad responsive promoter/reporter construct SBE-luciferase. These results suggest that C2 ceramide reduces the action of TGFbeta in fibroblasts via Smad antagonism.

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