Remuzgo-Martínez Sara, Atienza-Mateo Belén, Ocejo-Vinyals J Gonzalo, Genre Fernanda, Pulito-Cueto Verónica, Mora-Cuesta Víctor M, Iturbe-Fernández David, Lera-Gómez Leticia, Pérez-Fernández Raquel, Prieto-Peña Diana, Irure Juan, Romero-Bueno Fredeswinda, Sanchez-Pernaute Olga, Alonso-Moralejo Rodrigo, Nuño Laura, Bonilla Gema, Vicente-Rabaneda Esther F, Grafia Ignacio, Prieto-González Sergio, Narvaez Javier, Trallero-Araguas Ernesto, Selva-O'Callaghan Albert, Gualillo Oreste, Cavagna Lorenzo, Cifrián José M, Renzoni Elisabetta A, Castañeda Santos, López-Mejías Raquel, González-Gay Miguel A
Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, Avenida Cardenal Herrera Oria s/n, Lab. 201/202, 39011, Santander, Spain.
López Albo' Post-Residency Programme, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Sci Rep. 2021 Nov 19;11(1):22574. doi: 10.1038/s41598-021-01992-y.
Mucin 1/Krebs von den Lungen-6 (KL-6) is proposed as a serum biomarker of several interstitial lung diseases (ILDs), including connective tissue disorders associated with ILD. However, it has not been studied in a large cohort of Caucasian antisynthetase syndrome (ASSD) patients. Consequently, we assessed the role of MUC1 rs4072037 and serum KL-6 levels as a potential biomarker of ASSD susceptibility and for the differential diagnosis between patients with ILD associated with ASSD (ASSD-ILD +) and idiopathic pulmonary fibrosis (IPF). 168 ASSD patients (149 ASSD-ILD +), 174 IPF patients and 523 healthy controls were genotyped for MUC1 rs4072037 T > C. Serum KL-6 levels were determined in a subgroup of individuals. A significant increase of MUC1 rs4072037 CC genotype and C allele frequencies was observed in ASSD patients compared to healthy controls. Likewise, MUC1 rs4072037 TC and CC genotypes and C allele frequencies were significantly different between ASSD-ILD+ and IPF patients. Additionally, serum KL-6 levels were significantly higher in ASSD patients compared to healthy controls. Nevertheless, no differences in serum KL-6 levels were found between ASSD-ILD+ and IPF patients. Our results suggest that the presence of MUC1 rs4072037 C allele increases the risk of ASSD and it could be a useful genetic biomarker for the differential diagnosis between ASSD-ILD+ and IPF patients.
粘蛋白1/克雷布斯肺-6(KL-6)被提议作为几种间质性肺疾病(ILD)的血清生物标志物,包括与ILD相关的结缔组织疾病。然而,尚未在大量白种人抗合成酶综合征(ASSD)患者队列中进行研究。因此,我们评估了MUC1 rs4072037和血清KL-6水平作为ASSD易感性的潜在生物标志物以及用于鉴别与ASSD相关的ILD患者(ASSD-ILD +)和特发性肺纤维化(IPF)的作用。对168例ASSD患者(149例ASSD-ILD +)、174例IPF患者和523例健康对照进行MUC1 rs4072037 T>C基因分型。在一部分个体中测定血清KL-6水平。与健康对照相比,ASSD患者中观察到MUC1 rs4072037 CC基因型和C等位基因频率显著增加。同样,ASSD-ILD +和IPF患者之间MUC1 rs4072037 TC和CC基因型以及C等位基因频率存在显著差异。此外,ASSD患者的血清KL-6水平显著高于健康对照。然而,ASSD-ILD +和IPF患者之间未发现血清KL-6水平存在差异。我们的结果表明,MUC1 rs4072037 C等位基因的存在增加了ASSD的风险,并且它可能是用于鉴别ASSD-ILD +和IPF患者的有用遗传生物标志物。