The influence of the genotype and respiratory tract microflora on lung function and nutritional status in adult cystic fibrosis patients in long-term follow-up

Q4 Medicine Pulmonologiya Pub Date : 2023-06-08 DOI:10.18093/0869-0189-2023-33-3-366-373
O. Titova, V. Makhmutova, T. Gembitskaya, A. G. Chermensky, T. Stepanenko, N. A. Shklyarevich
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Abstract

In recent years, an increase in the number of patients with chronic infection with nonfermenting gram-negative bacteria (NFGNB) in adult patients with cystic fibrosis (CF) has increased. The genotype and phenotype characteristics, NFGNB structure, changes in sensitivity and the development of antibiotic resistance in adult patients have not been adequately studied.Aim. To determine the impact of genotype severity and Achromobacter xylosoxidans sensitivity to carbapenems on the functional and nutritional status of adult cystic fibrosis patients over a period 2016 – 2021.Materials. Retrospective analysis of genotypic and microbiological data from 54 adult CF patients and their effects on FEV1 and BMI over a period 2016 – 2021. Sputum cultures were confirmed by MALDI-TOF mass spectrometer. Depending on the severity of the mutation, the patients were divided into 2 groups: group 1 (“severe” genotype) – patients who had 2 mutations of class I – III; group 2 (“soft” genotype) – at least 1 class IV – VI mutation.Results. The group of patients with “mild” mutations had a higher BMI (kg / m2) than the group with severe mutations for a longer period of follow-up from 2018 – 2021 than in the group with severe mutations: BMI (2016) – 21.14 ± 3.55 / 19.28 ± 3.13 (p = 0.163); BMI (2017) – 21.27 ± 3.43 / 18.31 ± 2.05 (p = 0.123); BMI (2018) – 21.17 ± 4.00 / 18.80 ± 2.12 (p = 0.025); BMI (2019) – 21.01 ± 4.20 / 18.55 ± 2.53 (p = 0.049); BMI (2020) – 20.94 ± 4.12 / 18.41 ± 2.15 (p = 0.050). Age at diagnosis was 20.36 ± 2.18 years for “mild” genotypes and was higher (p = 0.042) than for “severe” genotypes (6.27 ± 1.53 years). All 7 patients who died (100%) were in the “severe” genotype group (23.3%). Functional status assessment showed no differences in FEV1 over 6 years between the “severe” and “mild” genotype groups: FEV1 (2016) – p = 0.51; FEV1 (2017) – p = 0.39; FEV1 (2018) – p = 0.51; FEV1 (2019) – p = 0.35; FEV1 (2020) – p = 0.48. Nonfermenting Gram-negative bacteria accounted for 49.9% of the isolated microorganisms. The group of carbapenem-resistant Achromobacter xylosoxidans lost the FEV1 level faster every year for 6 years (p < 0.05) compared to the group of the sensitive variant.Conclusion. In general, patients with the “mild” genotype have higher nutritional status and do not differ from patients with the “severe” genotype in terms of FEV1. The survival rate of patients with the “mild” genotype patients survival rate is higher, despite the later diagnosis and start of treatment. Development of carbаpenem resistance in Achromobacter xylosoxidans is associated with an unfavorable prognosis of the functional status decline.
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基因型及呼吸道菌群对成人囊性纤维化患者肺功能及营养状况的影响
近年来,囊性纤维化(CF)成人患者中非发酵革兰氏阴性菌(NFGNB)慢性感染的患者数量有所增加。成人患者的基因型和表型特征、NFGNB结构、敏感性变化和抗生素耐药性发展尚未得到充分研究。确定基因型严重程度和木氧化无色杆菌对碳青霉烯类药物敏感性对2016 - 2021年成人囊性纤维化患者功能和营养状况的影响。回顾性分析2016 - 2021年间54例成年CF患者的基因型和微生物数据及其对FEV1和BMI的影响。痰培养用MALDI-TOF质谱仪证实。根据突变的严重程度,将患者分为两组:1组(“严重”基因型)-患者有2个I - III类突变;第2组(“软”基因型)-至少1个IV - VI类突变。2018 - 2021年随访时间较长,“轻度”突变组BMI (kg / m2)高于重度突变组:BMI(2016) - 21.14±3.55 / 19.28±3.13 (p = 0.163);BMI(2017) - 21.27±3.43 / 18.31±2.05 (p = 0.123);BMI(2018) - 21.17±4.00 / 18.80±2.12 (p = 0.025);BMI(2019) - 21.01±4.20 / 18.55±2.53 (p = 0.049);BMI(2020) - 20.94±4.12 / 18.41±2.15 (p = 0.050)。“轻度”基因型患者的诊断年龄为20.36±2.18岁(p = 0.042),高于“重度”基因型患者(6.27±1.53岁)。7例死亡(100%)均为“重度”基因型组(23.3%)。功能状态评估显示,“重度”和“轻度”基因型组6年内FEV1无差异:FEV1 (2016) - p = 0.51;FEV1 (2017) - p = 0.39;FEV1 (2018) - p = 0.51;FEV1 (2019) - p = 0.35;FEV1 (2020) - p = 0.48。非发酵革兰氏阴性菌占分离微生物的49.9%。耐碳青霉烯木糖氧化无色杆菌组6年FEV1下降速度比敏感变异体组快(p < 0.05)。一般来说,“轻度”基因型患者的营养状况较高,在FEV1方面与“重度”基因型患者没有区别。“轻度”基因型患者的生存率较高,尽管诊断和开始治疗较晚。木糖氧化无色杆菌对碳霉烯耐药的发展与功能状态下降的不良预后有关。
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来源期刊
Pulmonologiya
Pulmonologiya Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.40
自引率
0.00%
发文量
70
期刊介绍: The aim of this journal is to state a scientific position of the Russian Respiratory Society (RRS) on diagnosis and treatment of respiratory diseases based on recent evidence-based clinical trial publications and international consensuses. The most important tasks of the journal are: -improvement proficiency qualifications of respiratory specialists; -education in pulmonology; -prompt publication of original studies on diagnosis and treatment of respiratory diseases; -sharing clinical experience and information about pulmonology service organization in different regions of Russia; -information on current protocols, standards and recommendations of international respiratory societies; -discussion and consequent publication Russian consensus documents and announcement of RRS activities; -publication and comments of regulatory documents of Russian Ministry of Health; -historical review of Russian pulmonology development. The scientific concept of the journal includes publication of current evidence-based studies on respiratory medicine and their discussion with the participation of Russian and foreign experts and development of national consensus documents on respiratory medicine. Russian and foreign respiratory specialists including pneumologists, TB specialists, thoracic surgeons, allergists, clinical immunologists, pediatricians, oncologists, physiologists, and therapeutists are invited to publish article in the journal.
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