自己免疫疾患は共通する遺伝的パターンを持つ(Autoimmune diseases share genetic patterns)

ad

2026-09-04 カロリンスカ研究所(KI)

カロリンスカ研究所などの研究チームは、自己免疫疾患には広く共通する単一の遺伝的基盤があるのではなく、罹患する組織・臓器に対応した遺伝的クラスターが形成されることを明らかにした。スウェーデンの全国登録データから、1932~1983年生まれの630万人超、約384万組のきょうだいを対象に、1969~2013年の22種類の自己免疫疾患を解析した。70万7,000人超(11.2%)に少なくとも1つの自己免疫疾患があり、複数疾患の併発は約1.3%だった。きょうだい間の疾患発生を比較した結果、結合組織疾患、内分泌系自己免疫疾患、消化器系自己免疫疾患などは、それぞれ明瞭な遺伝的関連群を形成した。一方、神経系疾患同士の遺伝的関連は比較的弱かった。乾癬と乾癬性関節炎などでは特に強い関連が確認された。本研究は、自己免疫疾患の遺伝的関係を臓器・組織別に理解する新たな枠組みを示す一方、きょうだい研究では遺伝要因と共有環境要因を完全には分離できないという限界もある。

<関連情報>

全国規模の兄弟姉妹研究における自己免疫疾患間の遺伝的相関の組織特異的クラスター化 Tissue-specific clustering of genetic correlations across autoimmune diseases in a nationwide sibling study

Daniel Eriksson, Ralf Kuja-Halkola, Marie E. Holmqvist, Henrik Larsson, Agnieszka Butwicka, Soffia Gudbjörnsdottir, Olle Kämpe, Sophie Bensing, and Jakob Skov
Journal of Clinical Investigation  Published: August 3, 2026

自己免疫疾患は共通する遺伝的パターンを持つ(Autoimmune diseases share genetic patterns)

Abstract

Background Autoimmune diseases (ADs) often co-occur within individuals and families, indicating shared genetic risk factors. However, the composition of genetic overlap across autoimmunity is largely unknown. Methods This nationwide study included 6,336,615 individuals born in Sweden between 1932 and 1983, comprising 3,839,400 full-sibling pairs. Based on national heath-registers, 22 ADs were identified from 1969-2013. Aggregation and co-aggregation of ADs among siblings was used to estimate pairwise genetic correlations of ADs under a liability-threshold model. Network analysis and principal component analysis was used to characterize the structure of shared genetic risk across ADs. Results A total of 707,995 individuals (11.2%) were diagnosed with at least one AD. The studied ADs formed a network of significant genetic correlations (mean rg = 0.24, range 0.08-0.84) with clusters of more closely related ADs (rg ≥ 0.3). We found no evidence of a significant universal factor predisposing to autoimmunity. Conclusions This study demonstrates that ADs share substantial cluster-specific genetic overlap that largely aligns with affected tissue types, leading to distinct groupings of connective tissue diseases, gastrointestinal disorders, and endocrinopathies, whereas diseases of the nervous system show limited genetic cohesion. This suggests that shared biological mechanisms may drive coaggregation within disease groups. Clinically, these insights highlight the importance of monitoring patients and their relatives for related autoimmune disorders. Funding The Swedish Society of Medicine, Region Värmland’s County Research Council, The Swedish Research Council, the Knut and Alice Wallenberg Foundation, The Regional Agreement on medical training and Clinical research (ALF) between Stockholm County Council and Karolinska Institutet

細胞遺伝子工学
ad
ad
Follow
ad
タイトルとURLをコピーしました