Data protection
Data protection statement
The data controller within the meaning of data protection laws, in particular the EU General Data Protection Regulation (GDPR), is:
Diabetes Center Berne
Martina Rothenbühler
Freiburgstrasse 3
3010 Bern
General notice
Based on Article 13 of the Swiss Federal Constitution and the data protection provisions of the Swiss Confederation (Swiss Data Protection Act [Datenschutzgesetz, DSG]), every person has the right to the protection of their privacy and to protection against the misuse of their personal data. The operator of this website takes the protection of your personal data very seriously. We handle all of your personal data confidentially and in accordance with legal requirements and with this data protection statement.
In cooperation with our hosting providers, we make every effort to protect databases from unauthorised access, data loss, misuse of data, and fraud.
We draw your attention to the fact that there can always be security vulnerabilities when you transmit data via the internet (for example through communication by e-mail). It is not possible to protect data from access by third parties with absolute certainty.
By using this website, you consent to the collection, processing, and use of data as described below. Anyone can access this website without needing to register. Data such as pages accessed and the names of files accessed, along with the date and time are stored on the server for statistical purposes, but this data does not make any direct reference to you. Personal data, in particular your name, address, or e-mail address can be gathered from you on a voluntary basis. None of this data will be passed on to third parties without your consent.
Privacy Policy in Clinical Studies
If you are a participant in a decentralized clinical trial, we will require your email and/or phone number.
The DCB uses your contact information exclusively for study-related communications.
Study-related information is stored securely for the duration of the trial and analysis periods specified in the respective ethics committee approved participant information sheets.
You can opt out of the messaging system at any time by withdrawing from the clinical study via text, study-specific link or email.
Your personal information will not be shared, sold, or rented to third parties for marketing or promotional purposes.
Processing of personal data
Personal data means all data that refers to a particular person or an identifiable person. The data subject is the person whose personal data is being processed. The term ‘processing’ covers almost any kind of handling of personal data, regardless of the methods or procedures used. In particular, it includes the storage, disclosure, procurement, deletion, saving, alteration, deletion, and use of personal data.
We process personal data in accordance with Swiss data protection legislation. In all other respects, we process personal data—insofar as and to the extent that the EU GDPR is applicable—in accordance with the following legal bases in connection with Art. 6, para. 1 of the GDPR:
- Sub-paragraph a) Processing of personal data with the consent of the data subject.
- Sub-paragraph b) Processing of personal data for the performance of a contract to which the data subject is party or in order to take steps at the request of the data subject prior to entering into a contract.
- Sub-paragraph c) Processing of personal data necessary for compliance with a legal obligation to which we are subject in accordance with applicable EU law or under any applicable law of a country in which the GDPR fully or partially applies.
- Sub-paragraph d) The processing of personal data necessary in order to protect the vital interests of the data subject or of another natural person.
- Sub-paragraph f) Processing of personal data necessary for the purposes of the legitimate interests pursued by us or by a third party, except where such interests are overridden by the interests or fundamental rights and freedoms of the data subject. Legitimate interests include in particular our economic interest in being able to provide our website, information security, the implementation of our own legal claims and compliance with Swiss law.
We process personal data for the duration that is necessary for the purpose or purposes in question. Where we are obligated to store data for a longer period due to legal or other obligations to which we are subject, we limit processing accordingly.
Data protection statement for cookies
This website uses cookies. These are small text files that make it possible for specific, user-related information to be stored on the user’s terminal device while they are using the website. Cookies make it possible to determine how frequently pages are used and how many people are using them, and to analyse how the pages are used. They also allow us to make our online offering more customer-friendly. Cookies are kept in storage after the end of a browsing session and can be called up again when the page is visited again. If you do not wish this to happen, you should configure your Internet browser so that it refuses to accept cookies.
It is possible to declare a general objection to the use of cookies for online marketing purposes for a large number of services, especially in the case of tracking, via the US website http://www.aboutads.info/choices/or the EU website http://www.youronlinechoices.com/. In addition, saving of cookies can be prevented by deactivating them in the browser settings. Please note that if you do this, you will not be able to use all of the functions of this website.
Data protection statement for SSL Encryption
This website uses SSL encryption for security reasons and in order to protect any confidential content that is transmitted, such as requests you send to us as a website operator. You can recognise an encrypted connection by the fact that the start of the address in the address bar of the browser changes from “http://” to “https://” and by the padlock symbol in your browser address bar.
If SSL encryption is activated, the data that you transmit to us cannot be read by third parties.
Data protection statement for the contact form
If you send us enquiries via the contact form, your details from the enquiry form, including the contact details you provided there, will be stored by us for the purpose of processing the enquiry and to resolve any follow-up questions. This data will not be passed on without your consent.
Data protection statement for newsletter data
If you wish to receive the newsletter offered on this website, we will need you to provide us with an e-mail address as well as information that allows us to verify that you are the owner of the e-mail address provided and that you agree to receiving the newsletter. No other data will be collected. We use this data exclusively for the purpose of sending the requested information and we do not pass it on to third parties.
You can revoke your consent to the storage of data, the e-mail address you provided and the use of these for the purpose of sending the newsletter at any time, for example by using the “Unsubscribe” link in the newsletter.
Data protection statement regarding the right to information, deletion, and blocking
At all times, you have the right to free-of-charge information about your stored personal data, about the origin and recipients of the data, and about the purpose of data processing as well as a right to have the data corrected, blocked, or deleted. You can contact us at any time regarding this or other questions on the subject of personal data at the address given in the legal notice.
Data protection statement for LinkedIn
This website uses features of the LinkedIn network. The provider of these features is LinkedIn Corporation, 2029 Stierlin Court, Mountain View, CA 94043, USA. Each time you access any of our web pages that contain LinkedIn features, you will be connected to LinkedIn servers. LinkedIn will be notified that you have visited our website with your IP address. If you click the LinkedIn “Recommend” button and are logged into your LinkedIn account, LinkedIn will be able to associate your visit to our website with your person and with your user account. We wish to draw your attention to the fact that we as the provider of the web pages have no knowledge of the content of the data transmitted to LinkedIn or of how it is used by LinkedIn.
Further information on this can be found in LinkedIn’s data protection statement at: https://www.linkedin.com/legal/privacy-policy
Plugins and Services from Third-party Providers
Our website uses plugins and services from third-party providers to recognize website visitors, evaluate their behavior and recognise preferences, as well as to make the functionality of the website as visitor-friendly as possible. Detailed information about the individual data processing can be found in the respective privacy statements of the third-party providers. Our website uses the following services and plugins:
Matomo Analytics
We use the service “Matomo Analytics”, which is offered by InnoCraft Ltd. The service uses “cookies” – text files that are stored on your terminal device. The information collected by the cookies is sent to a server hosted by us in Switzerland and stored there.
Changes
We reserve the right to change this data protection statement at any time without prior notice. The current version published on our website is the valid version. If this data protection statement is part of an agreement with you, we will notify you of any change to it by e-mail or via another appropriate avenue.
Questions for the Data Protection Officer
If you have any questions about data protection, please send us an e-mail or contact the person who is responsible for data protection at our organisation—their details are given at the beginning of this data protection statement.
Bern, 26.10.2023
Quelle: SwissAnwalt
But could the same data tell us much more about a person's health than we currently realise?
A new study published in npj Digital Medicine suggests that looking beyond individual glucose readings could reveal patterns associated with diabetes-related health risks. The findings point towards an interesting possibility: CGM technology may one day help us understand glucose levels, and also identify individual risk profiles and support more personalised diabetes care.
What did the researchers discover?
The researchers analysed CGM data from 90,757 participants in the iCanNet cohort, including people with normoglycemia, prediabetes, type 1 diabetes and type 2 diabetes. Rather than looking at individual glucose values alone, they examined 48 different CGM-derived metrics, including glucose variability and patterns over time. Their analysis revealed distinct glucose patterns across the different groups. Combining several metrics also improved the researchers' ability to distinguish between them.
Particularly interesting were the findings among people living with type 2 diabetes.
The researchers identified four distinct glycemic phenotypes – different patterns of glucose levels and fluctuations – associated with varying risks of diabetes-related complications.
For example:
- Sustained high glucose levels were associated with a 59% higher relative risk of acute complications.
- High glucose variability was associated with a 75% higher relative risk of acute complications and a 41% higher relative risk of chronic complications.
The researchers also developed a Digital Glycemic Risk Score (DGRS), combining multiple CGM metrics to identify people with potentially elevated risks.
Among participants with type 2 diabetes who had already achieved a Time in Range of at least 70%, the model reclassified 25% into a high-risk category for acute complications and 22.3% into a high-risk category for chronic complications. These were classifications generated by the model, not confirmed predictions of complications occurring in these individuals.
The findings suggest that combining different glucose patterns may reveal information about health risks that commonly used CGM metrics alone do not fully capture.
From CGM data to new insights. The study analysed 48 CGM-derived metrics from 90,757 participants and identified distinct glucose patterns across the diabetes spectrum. Among people with type 2 diabetes, four glycemic phenotypes were associated with
What could this mean for diabetes care?
Today, CGM systems primarily help people understand what is happening with their glucose levels and respond accordingly. But the enormous amount of data these devices generate may hold additional information that we are only beginning to explore.
By analysing glucose patterns over time, researchers may be able to develop digital biomarkers – measurable indicators derived from digital health data – that could help characterise individual metabolic profiles and identify potential health risks.
In the future, this could support healthcare professionals in recognising people who may benefit from closer monitoring or more personalised treatment approaches.
The Nordic region remains the global hotspot for childhood‑onset T1D. Finland has historically reported the highest incidence worldwide – around 60 per 100,000 children per year – although this rate appears to have stabilised or slightly declined since the early 2000s. Sweden, Norway and Denmark follow closely, and the IDF Diabetes Atlas 11 still places Finland, Sweden and Norway among the global top ten for published incidence.
A 2024 systematic review of European paediatric data (1994–2022) confirmed that the Nordic countries retain the highest absolute incidence in Europe, even as their rate of increase has slowed relative to the rapid rise in previously low‑incidence Central and Eastern European countries. A Swedish nationwide cohort study of 2.9 million children found that the heritability of childhood‑onset T1D has remained high and stable at around 0.83 over 30 years, implying that known environmental factors explain less than 10% of the observed rise.
In France, Santé publique France reports an annual T1D incidence increase of approximately 4%. Paediatric incidence rose from 15.4 to 19.1 per 100,000 person‑years between 2010 and 2015, with an overall rate of 19.5 per 100,000 in 2015–2017 and substantial regional variation. Sardinia (Italy) now reports the world’s highest published paediatric incidence at 76.3 per 100,000 (2022), having overtaken Finland, while the United Kingdom and Ireland also remain in the global top ten.
Projections to 2050
Two major modelling efforts suggest the same direction of travel. The GBD 2021 study projects that age‑standardised global type 1 diabetes prevalence will rise by about 23.9% between 2021 and 2050, a smaller relative increase than for type 2 diabetes, but a substantial absolute rise given the lifelong management burden of T1D. The IDF Diabetes Atlas 11 projects that overall adult diabetes prevalence (type 1 and type 2) will grow from 589 million in 2024 to around 853 million by 2050, a 46% absolute increase. While most of this growth is driven by type 2 diabetes, T1D contributes meaningfully through sustained or rising incidence in high‑income countries and improved survival, which increases prevalence even if incidence stabilises.
For the U.S., a modelling exercise based on SEARCH data suggests that, under a linear‑increase scenario, the number of young people with T1D could nearly triple by 2050, with the steepest relative growth among Hispanic and Black children.
Why is incidence rising?
T1D is a polygenic autoimmune disease in which environmental triggers act on a susceptible genetic background. Several, often overlapping, hypotheses are under investigation:
- Reduced early‑life exposure to common infections (“hygiene hypothesis”), with mixed evidence.
- Rising childhood adiposity and insulin resistance, which may accelerate the clinical presentation of existing islet autoimmunity (“accelerator hypothesis”).
- Viral triggers such as enteroviruses and, more recently, SARS‑CoV‑2, where meta‑analyses report a 14–27% increase in paediatric T1D incidence during the pandemic.
- Dietary and microbiome‑related factors, including early cow’s‑milk exposure, gluten timing and shifts in the infant gut microbiome.
- Vitamin D status and latitude, endocrine‑disrupting chemicals, pollution and perinatal factors such as higher maternal age, higher birth weight and Caesarean delivery.
The Swedish cohort study mentioned above is a stark reminder of how much remains unexplained: even with population‑wide data on several environmental exposures, less than 10% of the rise in T1D incidence in Sweden could be attributed to known factors. This underscores the need for long‑term birth cohorts, population‑level islet‑autoantibody screening and mechanistic immunology.
Implications for the next decade
Three practical implications stand out for health systems, innovators and the diabetes community:
- Health systems need to prepare for more people living with type 1 diabetes. Even under conservative assumptions, the number of people living with type 1 diabetes will continue to rise. This has practical consequences for insulin and sensor supply, reimbursement for diabetes technology, specialist care and clinical-trial infrastructure.
- Early detection is becoming more relevant. Type 1 diabetes can often be detected before symptoms appear, through markers of early autoimmune activity. With the first therapy now approved to delay clinical onset in people at an early disease stage, screening is no longer only a research question. Programmes such as Fr1da in Germany and the D1Ce trial in Italy show how early identification could inform future intervention strategies.
- We still need to understand why incidence is rising. Many environmental factors are being studied, but no single explanation is sufficient. Until we better understand the drivers behind the increase, true primary prevention will remain out of reach. This makes high-quality registries, long-term cohort studies and coordinated research more important than ever.
At DCB, we see these trends as both a warning and a call to action.
The rising incidence of type 1 diabetes will require sustained collaboration between clinicians, researchers, industry, policymakers and crucially people living with diabetes and their families.
Our work in innovation, clinical research infrastructure and community engagement aims to contribute to that collective effort.
Selected sources
GBD 2021 Diabetes Collaborators. Global, regional, and national burden of diabetes from 1990 to 2021, with projections of prevalence to 2050. The Lancet, 2023. https://www.thelancet.com/article/S0140-6736(23)01301-6/fulltext
International Diabetes Federation. IDF Diabetes Atlas, 11th edition. 2025. https://diabetesatlas.org/
Ogle GD, et al. Global type 1 diabetes prevalence, incidence, and mortality estimates 2025: Results from the IDF Atlas 11 and the T1D Index v3.0. Diabetes Research and Clinical Practice, 2025. https://www.sciencedirect.com/science/article/pii/S0168822725002918
Stahl-Pehe A, et al. Wave in Pediatric Type 1 Diabetes Incidence After the Emergence of COVID-19: Peak and Trough Patterns in German Youth — DPV Registry. Diabetes Care, 2025. https://diabetesjournals.org/care/article/48/4/e47/157803/
Buchmann M, et al. Type 1 diabetes incidence curves differ by age for girls and boys between 1996 and 2022: Results from the North Rhine-Westphalia Diabetes Registry. Diabetes Research and Clinical Practice, 2025. https://www.sciencedirect.com/science/article/pii/S0168822725000105
Nagl K, et al. Ongoing Increase in Incidence of Diabetes in Austrian Children and Adolescents 1989–2021. Pediatric Diabetes, 2023. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12017070/
Schoenle EJ, et al. Epidemiology of Type I diabetes mellitus in Switzerland: Steep rise in incidence in under-5 year old children in the past decade. Diabetologia, 2001. https://www.researchgate.net/publication/12017578
Santé publique France. Diabetes — Data. Updated 2024. https://www.santepubliquefrance.fr/en/diabete/data
Piffaretti C, et al. Trends in childhood type 1 diabetes incidence in France, 2010–2015. Diabetes Research and Clinical Practice, 2018. https://www.sciencedirect.com/science/article/abs/pii/S0168822718304662
Ruiz-Grao MC, et al. Trends in the Incidence of Type 1 Diabetes in European Children and Adolescents from 1994 to 2022: A Systematic Review and Meta-Analysis. Pediatric Diabetes, 2024. https://onlinelibrary.wiley.com/doi/10.1155/2024/2338922
Ji J, et al. Stable heritability of type 1 diabetes in a Swedish Nationwide Cohort Study. Nature Communications, 2024. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12174315/
D’Souza D, et al. Incidence of Diabetes in Children and Adolescents During the COVID-19 Pandemic: A Systematic Review and Meta-Analysis. JAMA Network Open, 2023. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314307/
Quinn LM, et al. Environmental Determinants of Type 1 Diabetes: From Association to Proving Causality. Frontiers in Immunology, 2021. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518604/
Esposito S, et al. Changes in the Global Epidemiology of Type 1 Diabetes in an Evolving Landscape of Environmental Factors. International Journal of Molecular Sciences, 2023. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141720/
Rogers MAM, et al. Fluctuations in the incidence of type 1 diabetes in the United States from 2001 to 2015: a longitudinal study. BMC Medicine, 2017. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688827/
Imperatore G, et al. Projections of Type 1 and Type 2 Diabetes Burden in the U.S. Population Aged <20 Years Through 2050. Diabetes Care, 2012. https://pmc.ncbi.nlm.nih.gov/articles/PMC3507562/
We hope this overview is helpful for your own work in diabetes care, research or advocacy. As always, we are grateful for your interest in and support of our activities and we look forward to continuing this conversation with you in future editions of our “DID YOU KNOW…” series.
An earlier version of this article was originally published in the private newsletter of our CEO, Derek Brandt here: Diabetes Technology News.
This post was previously published in Linkedin. Click here to see the original publication.
