Table 5.
Geographic area | Study population | Source of the outcome N=number of cases |
Source of socioeconomic status | Main findings | |
---|---|---|---|---|---|
Diagnosed CD (serology and/or biopsy-positive cases) within medical settings | |||||
Burger et al12 | Netherlands | Subjects identified into the Dutch Pathology Registry, which covers all pathology labs in Netherlands 1995–2010 N= 6444 |
CD diagnosis according to biopsy reports N=4014 |
The socioeconomic status scores based on income, level of education and employment | Patients diagnosed with CD during childhood were more often from an area with a higher socioeconomic status compared with patients diagnosed later in life (p<0.001) |
West et al13 | The UK | All ages UK population registered with the Clinical Practice Research Datalink—1990–2011 N=65 856 848 person-years |
People with Read codes representing CD (J690.00; J690.13; J690z00; J690100; J690.14; J690000) N=9087 |
Indices of Multiple Deprivation | The CD incidence was 27% lower in people from the most-deprived areas than in people from the least-deprived ones (IRR 0.83, 95% CI 0.77 to 0.89) |
Whyte et al14 | Cardiff, Newport and Powys (South Wales) | The total paediatric population (age <16) in South Wales (UK national census 2008) N=298 530 children |
CD diagnosis according to ESPGHAN 1990 criteria in the same tertiary medical centre between 1995 and 2012 N=232 |
Welsh Index of Multiple Deprivation | The prevalence of CD in the lowest deprivation level was 1.16/1000 and 0.49/1000 in the highest deprivation level |
White et al15 | Southeast Scotland | The total paediatric population (age <16) in Southeast Scotland—1990–2009 (Scotland census) N=∼225 000 children |
CD diagnosis according to ESPGHAN 1990 criteria. Data from hospital records (ICD codes of CD), paediatric pathology records, regional clinical database, regional serology database and the electronic hospital record N=266 |
The Scottish government data for the Standard Index of Multiple Deprivation and urban/rural indices | The median of the Standard Index of Multiple Deprivation score and urban–rural classification indices of patients with CD were comparable to the general population of southeastern Scotland |
Olén et al16 | Sweden | Individuals aged 16–64 years using the Total Population Register 1969–2008 N=174 186 subjects |
CD diagnosis according to biopsy reports collected from all Swedish pathology departments N=29 096 |
European Socioeconomic Classification based on occupation. Data collected using The Swedish Occupational Register |
Individuals from the lowest social class were 11% less likely to be diagnosed with CD (OR 0.89, 95% CI 0.84 to 0.94) |
Wingren et al17 | Sweden | Prospective evaluation of babies born in Sweden between 1987 and 1993 (follow-up 2 years) N=392 568 men and 372 112 women |
The Swedish National Hospital Discharge Registry according to ICD codes of CD N=845 in men and 1401 in women |
Information on the mothers’ pre-tax equalised household income and social allowance for the year before delivery (five classes) | Boys born to mothers in an overt low socioeconomic position had a higher risk of CD (OR 1.37, 95% CI 1.03 to 1.82) than those with mothers with high income and no social allowance |
Robert et al18 | South East England | Babies born in the south east of England between 1970 and 1999 (mean follow-up duration 18 years) using the Oxford record linkage study database having linked maternity data in the same dataset N=248 521 |
Children with both a maternity record and a subsequent admission for CD (ICD codes of CD) in the Oxford record linkage study database N=90 |
Information collected from maternal records in the Oxford record linkage study database | Children from manual social classes IV and V had a 4.02 increased risk of coeliac disease (95% CI1.96 to 8.25) compared with those from professional social classes I and II |
Ludvigsson19 | Sweden | Babies born in southeast Sweden between 1997 and 1999 (follow-up 15 years) N=15 875 single births |
Coeliac cases reported by eight paediatric departments A case was included if he had intestinal biopsy suggesting CD, no symptoms after the introduction of a gluten-free diet and/or no or only minor histopathological abnormalities consistent with CD at the control biopsy under treatment with gluten-free diet N=45 |
Information collected in questionnaire completed by the mothers shortly after childbirth on: place of living 1 year before conception, maternal employed during pregnancy, paternal employed the year before the conception, family crowed living | CD was less common in mothers who had worked <3 months during pregnancy (OR=0.29; 95% CI 0.09 to 0.94; p=0.039). The other socioeconomic factors were not associated |
Screening detected CD in the general population | |||||
Kondrashova et al20 | Finland and Russia | Schoolchildren Russia Karelia: age ranged 6.2–18.3 years (1997–2001) N=1988 children Northern Finland: age ranged 7–18 years (1994) N= 3654 children |
Serological screening by tTGA All subjects who were positive were offered an intestinal biopsy to confirm CD diagnosis. N=4 in Russia and 34 in Finland |
Comparison between two areas with opposite socioeconomic condition (poor Russia vs rich Finland). | 0.6% of the children (12/1988; CI 0.3% to 1.1%) in Russian Karelia tested positive for tTGA compared with 1.4% (52/3654; CI 1.1% to 1.9%) in the Finnish cohort. Biopsy-proven CD: N=4 in Russia and 34 in Finland (no biopsy in 13 subjects) |
West et al21 | Cambridge | Participants, age 45–76 years registered with a general practice in Cambridge, England (1990–1995) N=7527 |
Serological screening by EMA N=87 |
Participant-reported occupation categorised as professional, skilled, unskilled/partly skilled | EMA positivity less common in partly skilled or unskilled workers, as compared to professionals (OR 0.51, 95% CI 0.18 to 1.43) |
CD, coeliac disease; EMA, antiendomisial antibody; ESPGHAN, European Society of Paediatric Gastroenterology, Hepatology and Nutrition; ICD, international classification of disease; IRR, incident rate ratio; tTGA, IgA antitransglutaminase.