Fetal Exposure to Secondhand Tobacco Smoke Assessed by Maternal Self-reports and Cord Blood Cotinine: Prospective Cohort Study in Krakow

2008 ◽  
Vol 13 (3) ◽  
pp. 415-423 ◽  
Author(s):  
Wieslaw Jedrychowski ◽  
Frederica Perera ◽  
Elzbieta Mroz ◽  
Susan Edwards ◽  
Elzbieta Flak ◽  
...  
2018 ◽  
Vol 5 (suppl_1) ◽  
pp. S39-S40
Author(s):  
Larry Kociolek ◽  
Ciaran P Kelly ◽  
Robyn Espinosa ◽  
Maria Budz ◽  
Aakash Balaji ◽  
...  

Abstract Background Infant C. difficile colonization is common, but the molecular epidemiology and immunologic consequences of colonization are poorly understood. Methods In this prospective cohort study of healthy infants, serial stools collected between 1–2 and 9–12 month olds were tested for glutamate dehydrogenase (detects nontoxigenic or toxigenic C. difficile [TCD]), tcdB PCR (detects TCD), and cultured for C. difficile. Isolates underwent whole genome sequencing and multilocus sequence typing (MLST). Clonal strains were identified by single nucleotide variant (SNV) analysis. TCD was confirmed by BLAST identification of tcdA/tcdB. Serum collected at 9–12 month olds underwent ELISA for measurement of IgA, IgG, and IgM against TCD toxins A and B. For comparison, anti-toxin IgG was measured in cord blood of 50 consecutive full-term deliveries (unrelated to study infants). Arbitrary ELISA units were compared by Wilcoxon rank-sum test. Results Among 32 infants, 16 (50%) had at least one TCD+ stool, 12 of whom were colonized at least 1 m prior to serology measurements (Figures 1 and 2). A variety of STs were identified, and evidence of putative in-home (enrolled siblings) and outpatient clinic transmission was identified (Figure 3). Infants with TCD colonization had significantly greater levels of anti-toxin IgA and IgG compared with non-colonized infants and IgG compared with unrelated cord blood (Table 1). Conclusion Infant C. difficile colonization is a dynamic process with variable strain types and duration. Outpatient clinics may be a C. difficile reservoir for some patients. TCD colonization is associated with a humoral immune response against toxins A and B, but whether natural TCD immunization protects against CDI later in life requires further investigation. Disclosures L. Kociolek, Alere/Techlab: Investigator, Research support. C. P. Kelly, Actelion: Consultant, Consulting fee. Artugen: Consultant, Consulting fee. Facile: Consultant, Consulting fee. GSK: Consultant, Consulting fee. MSD: Consultant, Consulting fee. Seres: Consultant, Consulting fee. Summit: Consultant, Consulting fee. Vedanta: Consultant, Consulting fee. D. N. Gerding, Merck: Scientific Advisor, Consulting fee. Actelion: Scientific Advisor, Consulting fee. DaVolterra: Scientific Advisor, Consulting fee. Summit: Scientific Advisor, Consulting fee. Rebiotix: Medical Officer and Scientific Advisor, Consulting fee. Pfizer: Consultant, Consulting fee. MGB Pharma: Consultant, Consulting fee. sanofi pasteur: Consultant, Consulting fee. Seres: Investigator, Research grant. CDC: Investigator, Research grant. US Dept VA: Investigator, Research grant. Treatment/Prevention of C. difficile: Patent Holder, no license or royalties.


BMJ ◽  
2006 ◽  
Vol 333 (7564) ◽  
pp. 376 ◽  
Author(s):  
Wanqing Wen ◽  
Xiao Ou Shu ◽  
Yu-Tang Gao ◽  
Gong Yang ◽  
Qi Li ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (7) ◽  
pp. e22425 ◽  
Author(s):  
Malcolm G. Semple ◽  
David C. Taylor-Robinson ◽  
Steven Lane ◽  
Rosalind L. Smyth

2020 ◽  
Vol 186 ◽  
pp. 109602
Author(s):  
Charissa van Zwol - Janssens ◽  
Leonardo Trasande ◽  
Alexandros G. Asimakopoulos ◽  
Maria-Pilar Martinez-Moral ◽  
Kurunthachalam Kannan ◽  
...  

2020 ◽  
Vol 44 (11) ◽  
pp. 2225-2235
Author(s):  
Chalana M. Sol ◽  
Susana Santos ◽  
Liesbeth Duijts ◽  
Alexandros G. Asimakopoulos ◽  
Maria-Pilar Martinez-Moral ◽  
...  

PEDIATRICS ◽  
2009 ◽  
Vol 123 (2) ◽  
pp. 682-689 ◽  
Author(s):  
C. S. Mantzoros ◽  
S. L. Rifas-Shiman ◽  
C. J. Williams ◽  
J. L. Fargnoli ◽  
T. Kelesidis ◽  
...  

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