Subclinical intestinal inflammation: an inherited abnormality in Crohn's disease relatives?

2.50
Hdl Handle:
http://hdl.handle.net/2336/4502
Title:
Subclinical intestinal inflammation: an inherited abnormality in Crohn's disease relatives?
Authors:
Thjodleifsson, Bjarni; Sigthorsson, Gudmundur; Cariglia, Nick; Reynisdottir, Inga; Gudbjartsson, Daniel F; Kristjansson, Kristleifur; Meddings, Jonathan B; Gudnason, Vilmundur; Wandall, Johan H; Andersen, Leif Percival; Sherwood, Roy; Kjeld, Matthias; Oddsson, Einar; Gudjonsson, Hallgrimur; Bjarnason, Ingvar
Citation:
Gastroenterology 2003, 124(7):1728-37
Issue Date:
1-Jun-2003
Abstract:
BACKGROUND & AIMS: One approach to unraveling the genetics of complex inherited disease, such as Crohn's disease, is to search for subclinical disease markers among unaffected family members. We assessed the possible presence, prevalence, and inheritance pattern of subclinical intestinal inflammation in apparently healthy relatives of patients with Crohn's disease. METHODS: A total of 49 patients with Crohn's disease, 16 spouses, and 151 (58%) of 260 available first-degree relatives underwent a test for intestinal inflammation (fecal calprotectin concentration). The mode of inheritance was assessed from 36 index patients (by variance component analysis) when more than 50% of relatives were studied. RESULTS: Fecal calprotectin concentrations in patients with Crohn's disease (47 mg/L; confidence interval [CI], 27-95 mg/L) and relatives (11 mg/L; CI, 9-14 mg/L) differed significantly (P < 0.0001) from controls (4 mg/L; CI, 3-5 mg/L), whereas that of the spouses did not (4 mg/L; CI, 3-6 mg/L; P > 0.5). Fecal calprotectin concentration was increased in 49% of all relatives studied. The increased fecal calprotectin concentration among the relatives of the 36 index patients had an inheritance pattern that was most consistent with an additive inheritance pattern. CONCLUSIONS: There is a high prevalence of subclinical intestinal inflammation in first-degree relatives of patients with Crohn's disease that conforms best to an additive inheritance pattern. The genetic basis for this abnormality may represent a risk factor for Crohn's disease.
Additional Links:
http://www.sciencedirect.com/science/article/B6WFX-48TKRJT-H/2/d9547216e29f3b641e1d9a59b18a4bdc

Full metadata record

DC FieldValue Language
dc.contributor.authorThjodleifsson, Bjarni-
dc.contributor.authorSigthorsson, Gudmundur-
dc.contributor.authorCariglia, Nick-
dc.contributor.authorReynisdottir, Inga-
dc.contributor.authorGudbjartsson, Daniel F-
dc.contributor.authorKristjansson, Kristleifur-
dc.contributor.authorMeddings, Jonathan B-
dc.contributor.authorGudnason, Vilmundur-
dc.contributor.authorWandall, Johan H-
dc.contributor.authorAndersen, Leif Percival-
dc.contributor.authorSherwood, Roy-
dc.contributor.authorKjeld, Matthias-
dc.contributor.authorOddsson, Einar-
dc.contributor.authorGudjonsson, Hallgrimur-
dc.contributor.authorBjarnason, Ingvar-
dc.date.accessioned2006-09-20T08:50:58Z-
dc.date.available2006-09-20T08:50:58Z-
dc.date.issued2003-06-01-
dc.identifier.citationGastroenterology 2003, 124(7):1728-37en
dc.identifier.issn0016-5085-
dc.identifier.pmid12806605-
dc.identifier.doidoi:10.1016/S0016-5085(03)00383-4-
dc.identifier.otherGAS12-
dc.identifier.otherMAB12-
dc.identifier.urihttp://hdl.handle.net/2336/4502-
dc.description.abstractBACKGROUND & AIMS: One approach to unraveling the genetics of complex inherited disease, such as Crohn's disease, is to search for subclinical disease markers among unaffected family members. We assessed the possible presence, prevalence, and inheritance pattern of subclinical intestinal inflammation in apparently healthy relatives of patients with Crohn's disease. METHODS: A total of 49 patients with Crohn's disease, 16 spouses, and 151 (58%) of 260 available first-degree relatives underwent a test for intestinal inflammation (fecal calprotectin concentration). The mode of inheritance was assessed from 36 index patients (by variance component analysis) when more than 50% of relatives were studied. RESULTS: Fecal calprotectin concentrations in patients with Crohn's disease (47 mg/L; confidence interval [CI], 27-95 mg/L) and relatives (11 mg/L; CI, 9-14 mg/L) differed significantly (P < 0.0001) from controls (4 mg/L; CI, 3-5 mg/L), whereas that of the spouses did not (4 mg/L; CI, 3-6 mg/L; P > 0.5). Fecal calprotectin concentration was increased in 49% of all relatives studied. The increased fecal calprotectin concentration among the relatives of the 36 index patients had an inheritance pattern that was most consistent with an additive inheritance pattern. CONCLUSIONS: There is a high prevalence of subclinical intestinal inflammation in first-degree relatives of patients with Crohn's disease that conforms best to an additive inheritance pattern. The genetic basis for this abnormality may represent a risk factor for Crohn's disease.en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.urlhttp://www.sciencedirect.com/science/article/B6WFX-48TKRJT-H/2/d9547216e29f3b641e1d9a59b18a4bdcen
dc.subject.meshAdulten
dc.subject.meshAgeden
dc.subject.meshCrohn Diseaseen
dc.subject.meshFecesen
dc.subject.meshFemaleen
dc.subject.meshHumansen
dc.subject.meshLeukocyte L1 Antigen Complexen
dc.subject.meshMaleen
dc.subject.meshMiddle Ageden
dc.subject.meshPrevalenceen
dc.subject.meshResearch Support, Non-U.S. Gov'ten
dc.titleSubclinical intestinal inflammation: an inherited abnormality in Crohn's disease relatives?en
dc.typeArticleen
dc.identifier.journalGastroenterologyen
dc.format.digYES-

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