Association between phenotypic and genotypic characteristics and disease severity in individuals with cystic fibrosis

被引:0
|
作者
Carneiro, Gabriella Vieira [1 ]
de Oliveira, Fabiana Sodre [1 ]
Pereira, Leandro Alves [1 ]
Rezende, Erica Rodrigues Mariano de Almeida [1 ]
Goncalves, Luciana Carneiro Pereira [1 ]
Azevedo, Vivian Mara Goncalves de Oliveira [1 ]
机构
[1] Univ Fed Uberlandia, Uberlandia, MG, Brazil
关键词
Cystic fibrosis; Genotype; Phenotype; transmembrane conductance regulator; EPIDEMIOLOGY; DIAGNOSIS; CHILDREN; SCORE; GENE;
D O I
10.1590/1984-0462/2023/41/2021286
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: To analyze the association between phenotypic and genotypic characteristics and disease severity in individuals with cystic fibrosis treated at a reference center in Minas Gerais, Brazil. Methods: This is a retrospective study that collected clinical and laboratory data, respiratory and gastrointestinal manifestations, type of treatment, Shwachman-Kulczycki score, and mutations from the patients' medical records.Results: The sample included 50 participants aged one to 33 years, 50% of whom were female. Out of the one hundred gene, the most prevalent mutations were DeltaF508 (45%) and S4X (18%). Mutation groups were only associated with pancreatic insufficiency (p=0.013) and not with disease severity (p=0.073). The latter presented an association with colonization by Pseudomonas aeruginosa and Staphylococcus aureus (p=0.007) and with underweight (p=0.036). Death was associated with age at diagnosis (p=0.016), respiratory symptomatology (p=0.013), colonization (p=0.024), underweight (p=0.017), and hospitalization (p=0.003).Conclusions: We could identify the association of mutations with pancreatic insufficiency; the association of Staphylococcus aureus colonization and underweight with disease severity; and the lack of association between mutations and disease severity. Environmental factors should be investigated more thoroughly since they seem to have an important effect on disease severity.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] The association between leptin and insulin levels in adults with cystic fibrosis
    Ziai, S.
    Belson, L.
    Malet, A.
    Tardif, A.
    Berthiaume, Y.
    Coderre, L.
    Rabasa-Lhoret, R.
    DIABETES & METABOLISM, 2012, 38 (01) : 34 - 39
  • [42] Phenotypic and genotypic caracteristics of non fermenting atypical strains recovered from cystic fibrosis patients
    Ferroni, A
    Sermet-Gaudelus, I
    Abachin, E
    Quesnes, G
    Lenoir, G
    Berche, P
    Gaillard, JL
    PATHOLOGIE BIOLOGIE, 2003, 51 (07): : 405 - 411
  • [43] Analysis of the genotypic profile and its relationship with the clinical manifestations in people with cystic fibrosis: study from a rare disease registry
    Rueda-Nieto, Senay
    Mondejar-Lopez, Pedro
    Mira-Escolano, Maria-Pilar
    Cutillas-Tolin, Ana
    Alberto Maceda-Roldan, Luis
    Jesus Arense-Gonzalo, Julian
    Palomar-Rodriguez, Joaquin A.
    ORPHANET JOURNAL OF RARE DISEASES, 2022, 17 (01)
  • [44] Evaluation of Phenotypic Characteristics of Microorganisms Isolated From Respiratory Tract of the Patients With Cystic Fibrosis
    Budeyri, Selin
    Zer, Yasemin
    Keskin, Ozlem
    Bilgic-Ertan, Sevgi
    KLIMIK JOURNAL, 2019, 32 (02) : 178 - 181
  • [45] Is There any Association between Fecal Calprotectin Levels and Cystic Fibrosis?
    Rafeey, Mandana
    Jafari-Rouhi, Amir Hossein
    Hejrati, Suzan
    Yasari, Sepideh
    Sarmadi, Maryam Hosseinpour
    Farhadi, Ebrahim
    IRANIAN RED CRESCENT MEDICAL JOURNAL, 2022, 24 (11)
  • [46] The association between gut microbiome and growth in infants with cystic fibrosis
    Deschamp, A. R.
    Chen, Y.
    Wang, W. F.
    Rasic, M.
    Hatch, J.
    Sanders, D. B.
    Ranganathan, S. C.
    Ferkol, T.
    Perkins, D.
    Finn, P.
    Davis, S. D.
    JOURNAL OF CYSTIC FIBROSIS, 2023, 22 (06) : 1010 - 1016
  • [47] Cystic Fibrosis Foundation consensus guidelines for the care of individuals with advanced cystic fibrosis lung disease
    Kapnadak, Siddhartha G.
    Dimango, Emily
    Hadjiliadis, Denis
    Hempstead, Sarah E.
    Tallarico, Erin
    Pilewski, Joseph M.
    Faro, Albert
    Albright, James
    Benden, Christian
    Blair, Shaina
    Dellon, Elisabeth P.
    Gochenour, Daniel
    Michelson, Peter
    Moshiree, Baharak
    Neuringer, Isabel
    Riedy, Carl
    Schindler, Teresa
    Singer, Lianne G.
    Young, Dave
    Vignola, Lauren
    Zukosky, Joan
    Simon, Richard H.
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (03) : 344 - 354
  • [48] Association of lung clearance index with survival in individuals with cystic fibrosis
    Kurz, Johanna Manuela
    Ramsey, Kathryn Angela
    Rodriguez, Romy
    Spycher, Ben
    Biner, Reta Fischer
    Latzin, Philipp
    Singer, Florian
    EUROPEAN RESPIRATORY JOURNAL, 2022, 59 (03)
  • [49] Genotypic and Phenotypic Diversity of Staphylococcus aureus Isolates from Cystic Fibrosis Patient Lung Infections and Their Interactions with Pseudomonas aeruginosa
    Bernardy, Eryn E.
    Petit, Robert A., III
    Raghuram, Vishnu
    Alexander, Ashley M.
    Read, Timothy D.
    Goldberg, Joanna B.
    MBIO, 2020, 11 (03): : 1 - 18
  • [50] Association between hematological profile and serum 25-hydroxyvitamin D levels and Fokl polymorphism in individuals with cystic fibrosis
    Coelho de Assisi, Milena Juana
    Braga Cartaxo, Constantino Giovanni
    de Carvalho Costa, Maria Jose
    Marques Queiroz, Dayanna Joyce
    Persuhn, Darlene Carmati
    Rodrigues Goncalves, Maria da Conceicao
    REVISTA DE NUTRICAO-BRAZILIAN JOURNAL OF NUTRITION, 2018, 31 (02): : 211 - 220