TY - JOUR
T1 - Infant nasopharyngeal microbiota subphenotypes and early childhood lung function
T2 - Evidence from a rural ghanaian pregnancy cohort
AU - Dubowski, Kathryn
AU - Kaali, Seyram
AU - Jack, Darby
AU - Prah, Rebecca Kyerewaa Dwommoh
AU - Clemente, Jose C.
AU - Tawiah, Theresa
AU - Mujtaba, Mohammed
AU - Iddrisu, Louisa
AU - Carrión, Daniel
AU - Konadu, Dennis Gyasi
AU - Agyei, Oscar
AU - Kornu, Francis Mensah
AU - Osei-Owusu, Samuel
AU - Lee, Alison G.
AU - Asante, Kwaku Poku
N1 - Funding Information:
Funding: The GRAPHS cohort is supported by R01 ES026991, R01 ES019547, R21 TW010957, a Mailman School of Public Health Dean’s Pilot Award and a child survival grant from the Clean Cooking Alliance. AGL was supported by K23 HL135349.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/7/2
Y1 - 2021/7/2
N2 - Early life respiratory microbiota may increase risk for future pulmonary disease. Associations between respiratory microbiota and lung health in children from low-and middle-income countries are not well-described. Leveraging the Ghana Randomized Air Pollution and Health Study (GRAPHS) prospective pregnancy cohort in Kintampo, Ghana, we collected nasopharyngeal swabs in 112 asymptomatic children aged median 4.3 months (interquartile range (IQR) 2.9, 7.1) and analyzed 22 common bacterial and viral pathogens with MassTag polymerase chain reaction (PCR). We prospectively followed the cohort and measured lung function at age four years by impulse oscillometry. First, we employed latent class analysis (LCA) to identify nasopharyngeal microbiota (NPM) subphenotypes. Then, we used linear regression to analyze associations between subpheno-type assignment and lung function. LCA suggest that a two-class model best described the infant NPM. We identified a higher diversity subphenotype (N = 38, 34%) with more pathogens (median 4; IQR 3.25, 4.75) and a lower diversity subphenotype (N = 74, 66%) with fewer pathogens (median 1; IQR 1, 2). In multivariable linear regression models, the less diverse NPM subphenotype had higher small airway resistance (R5-R20 β = 17.9%, 95% CI 35.6, 0.23; p = 0.047) compared with the more diverse subphenotype. Further studies are required to understand the role of the microbiota in future lung health.
AB - Early life respiratory microbiota may increase risk for future pulmonary disease. Associations between respiratory microbiota and lung health in children from low-and middle-income countries are not well-described. Leveraging the Ghana Randomized Air Pollution and Health Study (GRAPHS) prospective pregnancy cohort in Kintampo, Ghana, we collected nasopharyngeal swabs in 112 asymptomatic children aged median 4.3 months (interquartile range (IQR) 2.9, 7.1) and analyzed 22 common bacterial and viral pathogens with MassTag polymerase chain reaction (PCR). We prospectively followed the cohort and measured lung function at age four years by impulse oscillometry. First, we employed latent class analysis (LCA) to identify nasopharyngeal microbiota (NPM) subphenotypes. Then, we used linear regression to analyze associations between subpheno-type assignment and lung function. LCA suggest that a two-class model best described the infant NPM. We identified a higher diversity subphenotype (N = 38, 34%) with more pathogens (median 4; IQR 3.25, 4.75) and a lower diversity subphenotype (N = 74, 66%) with fewer pathogens (median 1; IQR 1, 2). In multivariable linear regression models, the less diverse NPM subphenotype had higher small airway resistance (R5-R20 β = 17.9%, 95% CI 35.6, 0.23; p = 0.047) compared with the more diverse subphenotype. Further studies are required to understand the role of the microbiota in future lung health.
KW - Global health
KW - Impulse oscillometry
KW - Nasopharyngeal microbiota
UR - http://www.scopus.com/inward/record.url?scp=85109068212&partnerID=8YFLogxK
U2 - 10.3390/ijerph18147276
DO - 10.3390/ijerph18147276
M3 - Article
C2 - 34299726
AN - SCOPUS:85109068212
VL - 18
JO - International Journal of Environmental Research and Public Health
JF - International Journal of Environmental Research and Public Health
SN - 1661-7827
IS - 14
M1 - 7276
ER -