Maimysheva Saule, Karazhanova Lyudmila, Orekhov Andrey, Chinybayeva Assel, Ashirov Bolat
Department of Internal Medicine, Semey Medical University, Semey 071400, Kazakhstan.
Cardiology Department, Astana Medical University, Astana 010000, Kazakhstan.
Diagnostics (Basel). 2025 May 1;15(9):1154. doi: 10.3390/diagnostics15091154.
: Severe and difficult-to-control asthma occurs in 3-10% of patients in developed countries. The aim of our study was to investigate the association of the prognostic role of leptin and adiponectin, as well as the leptin receptor gene polymorphism Gln223Arg, in patients with difficult-to-control and severe asthma. : The present study included 200 patients with asthma hospitalized in the Department of Pulmonology between January 2018 and December 2021. In all patients, in addition to routine clinical investigations, adiponectin, leptin and their ratio were analyzed, as well as levels of pro-inflammatory cytokines (IL-6, IL-8 and TNF-alpha). External respiratory function was also assessed. LEPR Gln223Arg single-nucleotide polymorphisms were genotyped by real-time PCR method. : Patients were randomized into two groups, depending on the severity of asthma: an uncontrolled asthma group and a controlled asthma group, according to the GINA criteria. Among patients with uncontrolled asthma, 101 subjects (74.3%) had metabolic syndrome ( < 0.001). There was an inverse association of the adiponectin/leptin ratio with the eosinophil count (B = -0.305, < 0.001), IL-6 (B = -0.026, < 0.001), IL-8 (B = -0.062, < 0.001) and TNF-alpha (B = -0.047, < 0.001) and a direct correlation with the level of FEV1 (B = 0.121, < 0.001) and FVC (B = 0.104, < 0.001). A probable association of homozygous A/A allele with increased risk of uncontrolled asthma was shown ( = 0.007). : Leptin receptor polymorphism with A/A genotype may be associated with a higher probability of developing severe and difficult-to-control asthma.
在发达国家,3%至10%的患者会出现严重且难以控制的哮喘。我们研究的目的是调查瘦素和脂联素的预后作用以及瘦素受体基因多态性Gln223Arg与难以控制的严重哮喘患者之间的关联。
本研究纳入了2018年1月至2021年12月在肺病科住院的200例哮喘患者。所有患者除了进行常规临床检查外,还分析了脂联素、瘦素及其比值,以及促炎细胞因子(IL-6、IL-8和TNF-α)的水平。还评估了肺外呼吸功能。通过实时PCR方法对LEPR Gln223Arg单核苷酸多态性进行基因分型。
根据哮喘严重程度,患者被随机分为两组:根据GINA标准分为未控制哮喘组和控制哮喘组。在未控制哮喘患者中,101名受试者(74.3%)患有代谢综合征(P<0.001)。脂联素/瘦素比值与嗜酸性粒细胞计数(B=-0.305,P<0.001)、IL-6(B=-0.026,P<0.001)、IL-8(B=-0.062,P<0.001)和TNF-α(B=-0.047,P<0.001)呈负相关,与FEV1水平(B=0.121,P<0.001)和FVC(B=0.104,P<0.001)呈正相关。显示纯合A/A等位基因与未控制哮喘风险增加可能存在关联(P=0.007)。
A/A基因型的瘦素受体多态性可能与发生严重且难以控制的哮喘的较高概率相关。