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. 2018 Feb;6(2):122-129.
doi: 10.1016/S2213-8587(17)30362-5. Epub 2017 Nov 30.

Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank

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Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank

Nicholas J Thomas et al. Lancet Diabetes Endocrinol. 2018 Feb.

Abstract

Background: Type 1 diabetes is typically considered a disease of children and young adults. Genetic susceptibility to young-onset type 1 diabetes is well defined and does not predispose to type 2 diabetes. It is not known how frequently genetic susceptibility to type 1 diabetes leads to a diagnosis of diabetes after age 30 years. We aimed to investigate the frequency and phenotype of type 1 diabetes resulting from high genetic susceptibility in the first six decades of life.

Methods: In this cross-sectional analysis, we used a type 1 diabetes genetic risk score based on 29 common variants to identify individuals of white European descent in UK Biobank in the half of the population with high or low genetic susceptibility to type 1 diabetes. We used Kaplan-Meier analysis to evaluate the number of cases of diabetes in both groups in the first six decades of life. We genetically defined type 1 diabetes as the additional cases of diabetes that occurred in the high genetic susceptibility group compared with the low genetic susceptibility group. All remaining cases were defined as type 2 diabetes. We assessed the clinical characteristics of the groups with genetically defined type 1 or type 2 diabetes.

Findings: 13 250 (3·5%) of 379 511 white European individuals in UK Biobank had developed diabetes in the first six decades of life. 1286 more cases of diabetes were in the half of the population with high genetic susceptibility to type 1 diabetes than in the half of the population with low genetic susceptibility. These genetically defined cases of type 1 diabetes were distributed across all ages of diagnosis; 537 (42%) were in individuals diagnosed when aged 31-60 years, representing 4% (537/12 233) of all diabetes cases diagnosed after age 30 years. The clinical characteristics of the group diagnosed with type 1 diabetes when aged 31-60 years were similar to the clinical characteristics of the group diagnosed with type 1 diabetes when aged 30 years or younger. For individuals diagnosed with diabetes when aged 31-60 years, the clinical characteristics of type 1 diabetes differed from those of type 2 diabetes: they had a lower BMI (27·4 kg/m2 [95% CI 26·7-28·0] vs 32·4 kg/m2 [32·2-32·5]; p<0·0001), were more likely to use insulin in the first year after diagnosis (89% [476/537] vs 6% [648/11 696]; p<0·0001), and were more likely to have diabetic ketoacidosis (11% [61/537] vs 0·3% [30/11 696]; p<0·0001).

Interpretation: Genetic susceptibility to type 1 diabetes results in non-obesity-related, insulin-dependent diabetes, which presents throughout the first six decades of life. Our results highlight the difficulty of identifying type 1 diabetes after age 30 years because of the increasing background prevalence of type 2 diabetes. Failure to diagnose late-onset type 1 diabetes can have serious consequences because these patients rapidly develop insulin dependency.

Funding: Wellcome Trust and Diabetes UK.

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Figures

Figure 1
Figure 1
Use of a type 1 diabetes genetic risk score to establish the proportion of population with genetically defined type 1 diabetes (A) Distribution of type 1 genetic risk score in the Wellcome Trust Case Control Consortium type 1 diabetes and type 2 diabetes cohorts. Type 1 diabetes is restricted to high type 1 diabetes genetic risk scores. Numbers of individuals with type 2 diabetes above and below the 50th centile (dotted line; fifth centile for type 1 diabetes) will be the same; thus, any excess in the top 50% will be cases of type 1 diabetes. In a population where the proportions of type 1 diabetes and type 2 diabetes are unknown, this method can be used to determine the proportion of type 1 diabetes cases. (B) Schematic showing that the high type 1 diabetes genetic risk group will have the same amount of type 2 diabetes as the low type 1 diabetes genetic risk group in addition to an excess of diabetes contributed by type 1 diabetes.
Figure 2
Figure 2
Kaplan-Meier curve of diabetes-free survival in the high and low genetic susceptibility groups Graph shows that diabetes was more likely in the high genetic susceptibility group. HR=hazard ratio.
Figure 3
Figure 3
Cumulative excess of genetically defined cases of type 1 diabetes occurring throughout the first six decades of life 58% (749/1286) of type 1 diabetes cases were diagnosed when individuals were aged 30 years or younger; 42% (537/1286) were diagnosed when individuals were aged 31–60 years.
Figure 4
Figure 4
Incidence of genetically defined type 1 and type 2 diabetes in the first six decades of life Cases of type 1 diabetes were distributed across all ages of diagnosis, whereas cases of type 2 diabetes increased substantially with increasing age.

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