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Analysis of phenotypic variation in psoriasis as a function of age at onset and family history

dc.contributor.authorHenseler, Tiloen_US
dc.contributor.authorLim, Henry W.en_US
dc.contributor.authorElder, James T.en_US
dc.contributor.authorChristophers, Ennoen_US
dc.contributor.authorJenisch, Stefanen_US
dc.contributor.authorNair, Rajan P.en_US
dc.contributor.authorMalick, Farahen_US
dc.contributor.authorStuart, Philipen_US
dc.contributor.authorVoorhees, John J.en_US
dc.date.accessioned2006-09-08T20:05:34Z
dc.date.available2006-09-08T20:05:34Z
dc.date.issued2002-07en_US
dc.identifier.citationStuart, Philip; Malick, Farah; Nair, Rajan P.; Henseler, Tilo; Lim, Henry W.; Jenisch, Stefan; Voorhees, John; Christophers, Enno; Elder, James T.; (2002). "Analysis of phenotypic variation in psoriasis as a function of age at onset and family history." Archives of Dermatological Research 294(5): 207-213. <http://hdl.handle.net/2027.42/42214>en_US
dc.identifier.issn0340-3696en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42214
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12115023&dopt=citationen_US
dc.description.abstractTo evaluate the relationship between psoriasis disease severity, age at onset, and family history, we analyzed 537 US psoriatics, most of whom were from Michigan. Total body surface area involvement (%TBSA), presence or absence of joint complaints, and nail involvement were measured. Analysis of familial psoriatics revealed that %TBSA was 15.1% when onset was early, but only 8.7% when onset was late ( P =0.00003). The opposite trend was seen when psoriasis was sporadic: %TBSA was 14.3% when onset was early (≤40 years of age) compared to 28.0% when onset was late ( P =0.0034). However, the sporadic group was small and ascertainment of the sporadic group was biased for severe involvement. As determined by log-linear analysis, joint complaints and age at onset were not significantly associated after controlling for age at examination, nor were joint complaints and familial status. Psoriatic nail changes were conditionally independent of familial status, given age at onset; nail changes were more frequently encountered in early-onset patients. There was no significant difference in the frequency of carriage of the MHC psoriasis risk determinant in the familial vs sporadic groups. Early-onset psoriatics did carry this determinant significantly more frequently, as expected. These results demonstrate increased severity of skin and nail disease in early-onset psoriasis, when psoriasis is familial. The lack of clinical differences between "familial" and "sporadic" psoriasis may reflect a similar genetic basis for both conditions, at least when onset is early.en_US
dc.format.extent55454 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherLegacyen_US
dc.subject.otherPsoriasis Psoriatic Arthritis Nail Diseases Genetic Variationen_US
dc.titleAnalysis of phenotypic variation in psoriasis as a function of age at onset and family historyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDermatologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA,en_US
dc.contributor.affiliationumDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA,en_US
dc.contributor.affiliationumDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA,en_US
dc.contributor.affiliationumDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA,en_US
dc.contributor.affiliationotherDepartment of Dermatology, Henry Ford Health System, Detroit, Michigan, USA,en_US
dc.contributor.affiliationotherDepartment of Dermatology, University of Kiel, Kiel, Germany,en_US
dc.contributor.affiliationotherDepartment of Dermatology, University of Kiel, Kiel, Germany,en_US
dc.contributor.affiliationotherDepartment of Dermatology, University of Kiel, Kiel, Germany,en_US
dc.contributor.affiliationotherDepartment of Dermatology, Henry Ford Health System, Detroit, Michigan, USA,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12115023en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42214/1/403-294-5-207_s00403-002-0321-3.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00403-002-0321-3en_US
dc.identifier.sourceArchives of Dermatological Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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