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1.
Epidemiol Infect ; 144(15): 3226-3236, 2016 11.
Article in English | MEDLINE | ID: mdl-27405603

ABSTRACT

The incidence of childhood respiratory infections in Greenland is among the highest globally. We performed a population-based study of 352 Greenlandic children aged 0-6 years aiming to describe rates and risk factors for carriage of four key bacteria associated with respiratory infections, their antimicrobial susceptibility and inter-bacterial associations. Nasopharyngeal swabs were tested for Streptococcus pneumoniae grouped by serotypes included (VT) or not included (NVT) in the 13-valent pneumococcal conjugate vaccine, non-typable Haemophilus influenzae (NTHi), Staphylococcus aureus and Moraxella catarrhalis. S. pneumoniae was detected from age 2 weeks with a peak carriage rate of 60% in 2-year-olds. Young age and having siblings attending a daycare institution were associated with pneumococcal carriage. Overall co-colonization with ⩾2 of the studied bacteria was 52%. NTHi showed a positive association with NVT pneumococci and M. catarrhalis, respectively, M. catarrhalis was positively associated with S. pneumoniae, particular VT pneumococci, whereas S. aureus were negatively associated with NTHi and M. catarrhalis. Nasopharyngeal bacterial carriage was present unusually early in life and with frequent co-colonization. Domestic crowding increased odds of carriage. Due to important bacterial associations we suggest future surveillance of pneumococcal conjugate vaccine's impact on carriage in Greenland to also include other pathogens.


Subject(s)
Carrier State/epidemiology , Nasopharynx/microbiology , Respiratory Tract Infections/epidemiology , Carrier State/microbiology , Child , Child, Preschool , Cross-Sectional Studies , Drug Resistance, Bacterial , Female , Greenland/epidemiology , Haemophilus Infections/epidemiology , Haemophilus Infections/microbiology , Haemophilus influenzae/drug effects , Haemophilus influenzae/physiology , Humans , Infant , Infant, Newborn , Male , Moraxella catarrhalis/drug effects , Moraxella catarrhalis/physiology , Moraxellaceae Infections/epidemiology , Moraxellaceae Infections/microbiology , Pneumococcal Infections/epidemiology , Pneumococcal Infections/microbiology , Pneumococcal Vaccines/therapeutic use , Population Surveillance , Prevalence , Respiratory Tract Infections/microbiology , Risk Factors , Staphylococcal Infections/epidemiology , Staphylococcal Infections/microbiology , Staphylococcus aureus/drug effects , Staphylococcus aureus/physiology , Streptococcus pneumoniae/drug effects , Streptococcus pneumoniae/physiology
2.
Epidemiol Infect ; 144(2): 225-33, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26094936

ABSTRACT

Helicobacter pylori infection is a major cause of peptic ulcer and is also associated with chronic gastritis, mucosa-associated lymphoid tissue (MALT) lymphoma, and adenocarcinoma of the stomach. Guidelines have been developed in the United States and Europe (areas with low prevalence) for the diagnosis and management of this infection, including the recommendation to 'test and treat' those with dyspepsia. A group of international experts performed a targeted literature review and formulated an expert opinion for evidenced-based benefits and harms for screening and treatment of H. pylori in high-prevalence countries. They concluded that in Arctic countries where H. pylori prevalence exceeds 60%, treatment of persons with H. pylori infection should be limited only to instances where there is strong evidence of direct benefit in reduction of morbidity and mortality, associated peptic ulcer disease and MALT lymphoma and that the test-and-treat strategy may not be beneficial for those with dyspepsia.


Subject(s)
Helicobacter Infections/diagnosis , Helicobacter Infections/drug therapy , Helicobacter pylori/physiology , Arctic Regions/epidemiology , Dyspepsia/diagnosis , Dyspepsia/drug therapy , Dyspepsia/microbiology , Guidelines as Topic , Helicobacter Infections/epidemiology , Helicobacter Infections/microbiology , Humans , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/drug therapy , Lymphoma, B-Cell, Marginal Zone/microbiology , Peptic Ulcer/diagnosis , Peptic Ulcer/drug therapy , Peptic Ulcer/microbiology , Prevalence
3.
J Viral Hepat ; 20(2): 122-30, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23301547

ABSTRACT

Hepatitis B virus (HBV) infection is highly prevalent in circumpolar indigenous peoples. However, the clinical outcome is extremely variable, such that while hepatocellular carcinoma (HCC) is uncommon in Canadian Inuit, the incidence of HCC is slightly higher in Greenlanders than in Danes, and it is especially high in Alaskan Native people infected with HBV genotypes F (HBV/F) and C (HBV/C). These differences may be associated with the genomic variability of the predominant HBV genotype in each group. The purpose of this study was to determine the rate, nature and regional susceptibility of HBV genomic mutations among circumpolar indigenous individuals. Paired serum samples, separated by 5-6 years, were analysed from Canadian and Greenlandic Inuit infected with HBV genotype B6 (HBV/B6) and HBV/D, respectively, and from Alaskan Native people infected with HBV/F, each having subsequently developed HCC. Phylogenetic and mutational analyses were performed on full-genome sequences, and the dynamic evolution within the quasispecies population of each patient group was determined by clonal analysis of the non-overlapping core coding region. Mutations associated with severe outcomes predominated in HBV/F, mostly within the precore/core and PreS1 region. HBV/B6 genomes exhibited higher diversity compared to HBV/D and HBV/F, particularly within the core coding region. Thus, differing mutational profiles and genetic variability were observed among different HBV genotypes predominating in circumpolar indigenous patients. The unusual observation of persistently high genetic variability with HBV/B6 despite clinical inactivity could be due to the evolution of a host-pathogen balance, but other possible factors also need to be explored.


Subject(s)
Genetic Variation , Hepatitis B virus/genetics , Hepatitis B, Chronic/virology , Inuit , Adolescent , Adult , Aged , Aged, 80 and over , Arctic Regions , Canada , Child , DNA Mutational Analysis , Evolution, Molecular , Female , Genome, Viral , Genotype , Greenland , Humans , Male , Middle Aged , Phylogeny , Young Adult
4.
J Viral Hepat ; 17(3): 162-70, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19780937

ABSTRACT

Hepatitis B virus (HBV) infection is endemic in Greenland with 5-10% of the population being HBsAg-positive (chronic carriers). Surprisingly, despite of the high prevalence of HBV infection, acute and chronic hepatitis B, liver cirrhosis and primary hepatocellular carcinoma appear much less frequently than expected. The reasons for the low frequencies are unknown, but as a consequence implementation of a childhood HBV vaccination programme, though debated for years, has never been instituted. We describe an outbreak of hepatitis D (HDV) infection among children in a hepatitis B hyper-endemic settlement of 133 inhabitants on the west coast of Greenland. In 2006 a total of 27% of the inhabitants were HBsAg-positive (chronic carriers) and 83% were HBcAb-positive (previously exposed). Forty-six percent of the HBsAg-positive persons were below 20 years of age. On follow-up 1 year later a total of 68% of the HBsAg-positive persons were HDV-IgG positive. Five children, who were HBsAg-positive in 2006, had HDV-seroconverted from 2006 to 2007, indicating a HDV-super-infection. Most of the HDV-IgG positive children had markedly elevated liver enzymes. In the multivariate analysis, among the HBV and HDV markers, presence of HDV-IgG was most strongly associated with elevation of liver enzymes. In conclusion, the HBV-HDV super-infection and presumed HDV outbreak in this settlement challenges the notion that HBV infection may not be as harmless in Greenland as previously anticipated. The findings strongly suggest that HBV vaccination should be included in the child-immunization program in Greenland.


Subject(s)
Disease Outbreaks , Endemic Diseases , Hepatitis B/epidemiology , Hepatitis D/epidemiology , Adolescent , Adult , Child , Child, Preschool , Enzymes/blood , Female , Greenland/epidemiology , Hepatitis Antibodies/blood , Hepatitis B/complications , Hepatitis B Surface Antigens/blood , Hepatitis D/complications , Humans , Immunoglobulin G/blood , Liver Function Tests , Male , Middle Aged , Young Adult
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