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Geospatial clustering of T1DM in Sweden: a cohort study from birth to diagnosis. NDR. Diabetologia

Vol.:(0123456789)Diabetologia

https://doi.org/10.1007/s00125-026-06675-9

 

 

ARTICLE

Geospatial clustering of type 1 diabetes in Sweden: a cohort study based on all residential locations from birth to diagnosis

 

Samy Sebraoui 1 · Oskar Englund2 · Fredrik Nyberg3 · Annelie Carlsson4 · Olle Korsgren5 · Gun Forsander6 ·

Katarina Eeg‑Olofsson1 · Björn Eliasson7 · Hanne K. Carlsen8 · Karin Åkesson8,9 · Soffia Gudbjörnsdottir

 

Vol.:(0123456789)Diabetologia

https://doi.org/10.1007/s00125-026-06675-9

 

 

ABSTRACT

 

Aims/hypothesis

Type 1 diabetes develops gradually, and previous exposures may influence incidence. We aimed to assess

the geographical variation in type 1 diabetes incidence in Sweden by considering all residential locations from birth to

diagnosis in individuals aged 0–30 years, diagnosed between 2005 and 2022. Significant high- and low-risk clusters were

identified for different life stage exposure windows.

 

Methods

In 21,774 individuals with type 1 diabetes, all residential geographical locations from birth to diagnosis were

geocoded. Geostatistical analysis of the incidence of type 1 diabetes was conducted at the municipality level using the most

common residential location during four life stage-specific exposure windows (at diagnosis, the first 5 years after birth, 5

years prior to diagnosis, and from birth to diagnosis).

 

Spatial scan statistics were used to identify statistically significant

high- and low-risk clusters for each window. Land use and land cover within these clusters were also characterised.

 

 

Results

Significant geographical variation in the incidence of type 1 diabetes was observed.

 

The incidence was consistently higher in rural, low-population-density areas, particularly in central Sweden, and lower in major urban areas.

 

The largest number of spatial clusters of both high risk (RR 1.29–16.0) and low risk (RR 0.32–0.73) was identified when using the most

common residential location during the first 5 years after birth. High-risk clusters for this exposure window were charac-

terised by forested and agricultural land, while low-risk clusters were characterised by urban land and open land other than

agricultural land.

 

Conclusions/interpretation

Our findings suggest that the development of type 1 diabetes in Sweden varies geographically

and is associated with specific features of the local surroundings in early childhood.

 

This is important knowledge as a basis

for identifying possible environmental risk factors and the relationship with risk of type 1 diabetes in future studies.

 

 

 

From the article

Discussion

In this nationwide study of individuals diagnosed with type

1 diabetes in Sweden between 2005 and 2022 at the age

of 0–30 years, we identified a notable geographical varia-

tion in incidence. Using high-resolution geospatial analyses,

we observed that the incidence of type 1 diabetes was con-

sistently higher in rural and low-population-density areas

particularly in the central part of the country and lower in

major urban areas. These patterns were consistent using

various analytical approaches and between four different life

stage-specific exposure windows. The most striking find-

ings emerged when evaluating the most dominant residential

location in the first 5 years after birth, which revealed the

highest number of significant high-risk and low-risk spatial

clusters.

 

 

Nearly one in four individuals in this study relocated

between municipalities between birth and diagnosis,

underscoring the potential for exposure misinterpretation

in studies relying solely on residential location at the time

of diagnosis or even later [10, 13, 14, 17]. By incorporat-

ing longitudinal residential data and analysing different life

stage exposure windows, our approach captures critical

periods of the development of the disease, including early-

life exposure, which may contribute differently to type 1

diabetes pathogenesis. Patients in the high-risk clusters

were less likely to relocate to a different municipality com-

pared with those in the low-risk clusters, both from birth to

diagnosis (26.4% vs 38.7%) and during the first 5 years after

birth (25.1% vs 28.4%). This may have contributed to the

stronger association between place of birth and subsequent

incidence.

 

 

Across the 290 municipalities the incidence rate varied

more than sixfold from 13.8 to 91.1 per 100,000 person-

years. The highest incidence was found predominantly in

sparsely populated municipalities located in central Swe-

den, without a clear north-south gradient, in contrast to the

findings of previous studies [31]. Conversely, the lowes

risk was observed in urban areas around the largest cities.

These results are in line with previous data from the Nor-

dic countries of children 0–14 years old during 2006–2011

[32], as well as with an older study from Finland [33]. Our

study extends these findings across a wider age span and

over a longer period. Most importantly, our findings suggest

that the risk associated with geographical location is more

pronounced when considering early-life residential location

rather than location at diagnosis.

 

 

Both the risk of type 1 diabetes and the residential distri-

bution of individuals with non-Swedish ethnicity vary across

the country. A previous study showed that children in fami-

lies that have immigrated to Sweden have lower incidence

compared with Sweden-born children [34]. These factors

cannot explain our findings since separate analysis for indi-

viduals born in Sweden to two Sweden-born parents showed

the same general geographical patterns for all life stage

exposure windows when compared with the analysis with

all cases included.

 

However, municipalities that previously

demonstrated low incidence when all cases were included,

particularly in the southern regions of the country, showed

higher incidence when the non-native group was excluded.

This phenomenon could be explained by immigration.

The study of geographical variation based on munici-

palities is limited as some municipalities are very sparsely

populated and only a few cases might make a large differ-

ence, and the large number of municipalities implies a risk

of significance by chance. In addition, artificial boundaries

that do not account for geographical or environmental fac-

tors may result in overlooking accumulations of geographi-

cal influences that are spread across multiple municipalities.

To overcome these limitations, we also identified clusters

independently of any artificial boundaries. This approach

provided a more detailed analysis compared with methods

based on municipal boundaries and should result in more

accurate geographical patterns.

 

 

High-risk and low-risk clusters were analysed for the four

life stage exposure windows. Again, this approach is essen-

tial given that the disease takes years to develop [11] and

that one fourth of all individuals relocated between birth

and diagnosis. However, no earlier studies have assessed

geographical exposure at different life stages leading up to

the development of the disease.

 

 

The cluster analysis at diagnosis revealed four significant

high-risk clusters with an RR from 1.31 to 1.80 located in

the mid country, and five low-risk clusters in the largest cit-

ies, which largely mirrored the results from the municipal-

ity-based analysis. Country-specific incidence rate studies

have shown rural excess in some countries of type 1 diabetes

[10, 12, 15, 16, 35] but not all [13, 36–38]. These studies

vary in terms of methodology, and some studies only have

a few cases and small geographical units. The characteris-

tics of rural/urban environments also need to be considered.

Several studies have found a higher incidence of type 1 dia-

betes in areas with lower levels of deprivation [35, 39–42].

A study from Sweden has shown that low maternal educa-

tion increases the risk of the disease [43]. In the current

study, the observed differences in incidence between rural

and urban areas could be attributed to spatial patterns in the

population composition of individual-level socioeconomic

status, which may be related to differences in lifestyle, expo-

sure to infections or other exposures.

 

 

The LULC analyses revealed a distinct urban–rural con-

trast: high-risk clusters were largely in rural areas, with a

high proportion of forested and agricultural land; low-risk

clusters were dominated by urban land and open land other

than agriculture. Given that the highest number of significant

high-risk and low-risk spatial clusters were found for the

first 5 years after birth, this suggests that the risk for type

1 diabetes could be linked to specific features of the local

surroundings in early childhood, independently of the age

of diagnoses. These could be associated with environmental

risk factors specific to rural living or protective factors in

urban living during early childhood. Our results are consist-

ent with growing evidence suggesting that early-life events

including parental psychosocial stress, pregnancy-related

factors, infant growth patterns, infections, and environmen-

tal exposures may influence the later development of type

1 diabetes [8, 9, 44, 45]. This is important knowledge to be

able to identify possible early environmental risk factors of

type 1 diabetes in future studies. Our finding of lower risk

in urban areas is in line with a recent study from England,

which reported that air pollution, light at night, population

density, and overcrowding were negatively associated with

type 1 diabetes incidence [10].

 

 

Furthermore, day care attendance may be associated

with a reduced risk of type 1 diabetes [46]. Our findings

could imply the presence of a protective effect linked to

characteristics of the urban environment and might partly

be explained by the hygiene hypothesis, which posits that

children with low exposure to infectious agents at an early

stage after birth have an increased susceptibility for type 1

diabetes [44, 47–49].

 

 

It is unlikely that a difference in geographical distribu-

tion of high-risk HLA haplotypes could explain our finding,

especially given that less than 5% of individuals with these

haplotypes in the general population develop overt type 1

diabetes, strongly suggesting a second critical hit is needed

[50].

 

 

The strengths of this study are that it is a large nation-

wide study from a country with a high incidence of type

1 diabetes, covering both children and young adults. We

used precise geographical coordinates of all cases from

birth to the year of diagnosis. High-resolution geospatial

analyses were used to identify geographical incidence pat-

terns during different life stage exposure windows. This is

unique and has not been previously conducted in diabetes

epidemiology. All analyses were compared with those of

the mean population in the same age group, during the

study period, and thus, the individuals with type 1 diabetes

were consistently matched with those in the corresponding

population group. We have also quantitatively character-

ised all high- and low-risk clusters in terms of land use/

land cover.

 

 

The weaknesses of the study are that spatial analysis is

sensitive to sample size, which implies that areas with a

small number of type 1 diabetes cases may result in the iden-

tification of large areas as ‘hot spots’ or clusters. Given the

large study population and the long observation time, this

should not affect our conclusions. The coverage of NDR was

somewhat lower during the first 2 years of the study period.

However, NDR collects repeated registrations (including

date or year of diagnosis) at least annually; therefore, almost

all patients with type 1 diabetes diagnosed between 2005 and

2022 are eventually captured. We lacked access to gridded

population data for the period 2005–2014. Consequently,

it was necessary to interpolate population estimates based

on municipal population data from 2015–2022, which were

subsequently transferred to the grid cells. Municipal popu-

lation data over time exhibited minimal variation. Type 1

diabetes is a relatively rare disease, and robust cluster analy-

ses require large patient numbers to ensure statistical cer-

tainty. Subdivisions in time periods or age groups further

reduce numbers and power; thus, such data could be prone

to spurious findings. Furthermore, we did not assess whether

the results differed between male and female individuals or

explore gender-related factors, which limits generalisability

across all sexes and genders.

 

 

We deliberately chose to use crude incidence rate to

ensure methodological consistency and comparability across

the difference analyses. Sensitivity analyses did not show

any substantial differences between age- and sex-standard-

ised incidence rates and crude incidence. Thus, the methodi-

cal choice is highly unlikely to affect our conclusions (ESM

Fig. 4).

 

 

Conclusion

Type 1 diabetes incidence in Sweden shows

clear geographical variation, with higher rates in rural, low-

population-density areas, particularly in central Sweden,

and lower rates in major urban areas. The strongest spatial

patterns were linked to residence in early childhood, sug-

gesting that local environmental features – such as forested

and agricultural land – may influence disease risk. These

findings underscore the importance of investigating early-life

environmental exposures in future type 1 diabetes research.

 

 

 

Nyhetsinfo

 

Läs hela artrikeln open source pdf free

https://pubmed.ncbi.nlm.nih.gov/41692841/

 

 

AI

2026 Swedish cohort study found that type 1 diabetes (T1D) incidence is higher in rural areas and lower in major cities, with significant spatial clustering linked to residential location, especially during the first 5 years of life
. High-risk clusters (1.29–16.0 RR) were associated with forested/agricultural land, while low-risk clusters (0.32–0.73 RR) were in urban areas.  springermedicine.com +2

 

Key Findings:
Early Life Exposure: The highest number of high- and low-risk clusters were identified based on the first 5 years of life, suggesting environmental factors during early childhood strongly influence T1D development.
Urban-Rural Disparity: Significant high-risk clusters for T1D (30% to 80% higher than average) were found in rural, central Sweden.
Protective Urban Factors: Conversely, major cities like Stockholm, Gothenburg, and Malmö showed significant low-risk clusters.
Study Design: The study (2005–2022) analyzed T1D incidence in individuals aged 0–30, accounting for residential mobility, with 24% of patients having moved between municipalities.  springermedicine.com +3
These findings suggest that environmental factors, possibly associated with rural living, may trigger the development of T1D, while urban environments might offer protective, yet unidentified, factors.  springermedizin.de +1

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