Trends in incidence of total or type 2 diabetes: systematic review.
Review
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Abstract
Objective
To assess what proportions of studies reported increasing, stable, or declining trends in the incidence of diagnosed diabetes.Design
Systematic review of studies reporting trends of diabetes incidence in adults from 1980 to 2017 according to PRISMA guidelines.Data sources
Medline, Embase, CINAHL, and reference lists of relevant publications.Eligibility criteria
Studies of open population based cohorts, diabetes registries, and administrative and health insurance databases on secular trends in the incidence of total diabetes or type 2 diabetes in adults were included. Poisson regression was used to model data by age group and year.Results
Among the 22 833 screened abstracts, 47 studies were included, providing data on 121 separate sex specific or ethnicity specific populations; 42 (89%) of the included studies reported on diagnosed diabetes. In 1960-89, 36% (8/22) of the populations studied had increasing trends in incidence of diabetes, 55% (12/22) had stable trends, and 9% (2/22) had decreasing trends. In 1990-2005, diabetes incidence increased in 66% (33/50) of populations, was stable in 32% (16/50), and decreased in 2% (1/50). In 2006-14, increasing trends were reported in only 33% (11/33) of populations, whereas 30% (10/33) and 36% (12/33) had stable or declining incidence, respectively.Conclusions
The incidence of clinically diagnosed diabetes has continued to rise in only a minority of populations studied since 2006, with over a third of populations having a fall in incidence in this time period. Preventive strategies could have contributed to the fall in diabetes incidence in recent years. Data are limited in low and middle income countries, where trends in diabetes incidence could be different.Systematic review registration
Prospero CRD42018092287.Free full text
Trends in incidence of total or type 2 diabetes: systematic review
Associated Data
Abstract
Objective
To assess what proportions of studies reported increasing, stable, or declining trends in the incidence of diagnosed diabetes.
Design
Systematic review of studies reporting trends of diabetes incidence in adults from 1980 to 2017 according to PRISMA guidelines.
Data sources
Medline, Embase, CINAHL, and reference lists of relevant publications.
Eligibility criteria
Studies of open population based cohorts, diabetes registries, and administrative and health insurance databases on secular trends in the incidence of total diabetes or type 2 diabetes in adults were included. Poisson regression was used to model data by age group and year.
Results
Among the 22
833 screened abstracts, 47 studies were included, providing data on 121 separate sex specific or ethnicity specific populations; 42 (89%) of the included studies reported on diagnosed diabetes. In 1960-89, 36% (8/22) of the populations studied had increasing trends in incidence of diabetes, 55% (12/22) had stable trends, and 9% (2/22) had decreasing trends. In 1990-2005, diabetes incidence increased in 66% (33/50) of populations, was stable in 32% (16/50), and decreased in 2% (1/50). In 2006-14, increasing trends were reported in only 33% (11/33) of populations, whereas 30% (10/33) and 36% (12/33) had stable or declining incidence, respectively.
Conclusions
The incidence of clinically diagnosed diabetes has continued to rise in only a minority of populations studied since 2006, with over a third of populations having a fall in incidence in this time period. Preventive strategies could have contributed to the fall in diabetes incidence in recent years. Data are limited in low and middle income countries, where trends in diabetes incidence could be different.
Systematic review registration
Prospero CRD42018092287.
Introduction
Over the past few decades, the prevalence of diabetes in developed and developing countries has risen substantially, making diabetes a key health priority globally.1 Examination of trends in total burden of diabetes is an essential part of the monitoring of this health priority area, but, to date, it has consisted primarily of studies looking at diabetes prevalence.1 2 3 4 5 Prevalence estimates suggest that the diabetes burden is still rising in most countries, and this is often interpreted as evidence of increasing risk in the population. However, selective incidence studies6 7 and some accompanying risk factor data8 suggest otherwise. Prevalence can be a crude and misleading metric of the trajectory of an epidemic, because increasing prevalence of a disease might be due to either increasing incidence or to improved survival. Furthermore, prevalence cannot be reliably used to study the effects of changes in population risk factors, because their effects are detected earlier with incidence trends than with prevalence trends, and incidence is not affected by changes in survival.
Incidence measures the proportion of people who develop diabetes over a period of time among the population at risk. It is the appropriate measure of population risk, and a valuable way of assessing whether public health campaigns for diabetes prevention are succeeding. While prevalence can rise simply because mortality falls, incidence of diagnosed diabetes is affected only by the risk of the population and the amount of screening undertaken. Changes in prevalence might be an inadequate guide to the effects of prevention activities, and could lead to the inappropriate rejection of effective interventions. It is only by measuring both incidence and prevalence that a better understanding of the extent of diabetes can be achieved.
Among existing diabetes incidence data, a few studies suggest that diabetes incidence could be falling despite rising or stable prevalence,6 7 9 but not all data are consistently showing the same trends. For example, studies from England and Wales (1994-98),10 Portugal (1992-2015),11 and Canada (1995-2007)12 are reporting increases in diabetes incidence. To understand what is happening at a global level over time, a systematic approach to review all incidence trend data should be undertaken to study patterns and distributions of incidence trends by time, age, and sex. So far, no systematic reviews have reported on trends in the incidence of diabetes. Therefore, we conducted a systematic review of the literature reporting diabetes incidence trends.
Methods
Data sources and searches
We conducted a systematic review in accordance with PRISMA guidelines.13 We searched Medline, Embase, and CINAHL from January 1980 to December 2017 without language restrictions. The full search strategy is available in supplementary table 1.
Study selection
Inclusion and exclusion criteria
Eligible studies needed to report diabetes incidence in two or more time periods. Study populations derived from open, population based cohort studies (that is, with ongoing recruitment over time), diabetes registries, or administrative or health insurance databases based mainly or wholly in primary care (electronic medical records, health insurance databases, or health maintenance organisations). We also included serial, cross sectional, population based studies where incidence was defined as a person reporting the development of diabetes in the 12 months before the survey. Studies were required to report on the incidence of either total diabetes or type 2 diabetes. We excluded studies reporting incidence restricted to select groups (eg, people with heart failure) and studies reporting only on children or youth.
Each title and abstract was screened by at least two authors (DJM, JES, DNK, JLH, and MT) and discrepancies were resolved by discussion. We aimed to avoid overlap of populations between studies. Therefore, if national data and regional data were available from the same country over the same time period, we only included the national data. If multiple publications used the same data source, over the same time period, we chose the publication that covered the longest time period.
Outcome measure
Our outcome was diabetes incidence using various methods of diabetes ascertainment including: blood glucose, glycated haemoglobin (HbA1c), linkage to drug treatment or reimbursement registries, clinical diagnosis by physicians, administrative data (ICD codes (international classification of diseases)), or self report. Several studies developed algorithms based on several of these elements to define diabetes. We categorised the definition of diabetes into one of five groups: clinical diagnosis, diabetes treatment, algorithm derived, glycaemia defined (blood glucose or HbA1c, with or without treatment), and self report.
Data extraction and quality of studies
We extracted crude and standardised incidence by year (including counts and denominators) and the reported pattern of the trends (increasing, decreasing, or stable, (that is, no statistically significant change)) in each time period as well as study and population characteristics. Age specific data were also extracted if available. Data reported only in graphs were extracted by DigitizeIt software (European Organisation for Nuclear Research, Germany). We assessed study quality using a modified Newcastle-Ottawa scale for assessing the risk of bias of cohort studies14 (supplementary material).
Statistical methods
Data were reported as incidence density (per person year) or yearly rates (percentage per year). From every study, we extracted data from every subpopulation reported, such that a study reporting incidence in men and women separately contributed two populations to this analysis. If studies reported two different trends over different time periods, we considered these as two populations. Further, if the study was over 10 years in duration, we treated these as two separate time periods. To avoid double counting, when the data were reported in the total population as well as by sex and ethnic groups, we only included data once and prioritised ethnicity specific data over sex specific data.
We extracted the age specific incidence data reported for every individual calendar year. These data were then categorised into four age bands (<40, 40-54, 55-69, and ≥70), and were plotted against calendar year. In studies where counts and denominators were reported by smaller age groups than we used, we recalculated incidence across our specified larger age groups. If we found multiple age groups within any of our broader age groups, but with insufficient information to combine the data into a new category, only data from one age group were used. To limit overcrowding on plots, if data were available for men, women, and the total population, only total population data were plotted. Data from populations with high diabetes incidence such as Mauritians15 and First Nation populations from Canada16 were plotted separately to allow the examination of most of the data more easily on a common scale (supplementary material). Furthermore, studies reporting data before 1991 or populations with fewer than three data points were not plotted. We also categorised studies into European and non-European populations on the basis of the predominant ethnicity of the population in which they were conducted. Studies conducted in Israel, Canada, and the United States were assigned to the European category.
We took two approaches to analyse trends of diabetes incidence over time. Firstly, we allocated the reported trend (increasing, decreasing, or stable (that is, no statistically significant change)) of each population to the mid-point of each study’s observational period, and then assigned this trend into one of five time periods (1960-79, 1980-89, 1990-99, 2000-05, and 2006-14). Where a test of significance of trends was not reported or when a time period was longer than 10 years, we performed Joinpoint trend analyses17 18 to observe any significant trends in the data (assuming a constant standard deviation). Joinpoint Trend Analysis Software (version 4.5.0.1) uses permutation tests to identify points where linear trends change significantly in direction or in magnitude, and calculates an annual percentage change for each time period identified. In sensitivity analyses we also tested different cut points in the last two time periods.
The second approach was used to more accurately allocate trends to the prespecified time periods. Among the studies that reported raw counts of diabetes cases and denominators, we examined the association between calendar year and incidence, using Poisson models with the log person years as offset. The midpoints of age and calendar period were used as continuous covariates, and the effects of these were taken as linear functions. We analysed each study separately by prespecified time periods, and reported annual percentage change when the number of data points in the time period was at least four. For studies that did not provide raw data but did report a sufficient number of points, we analysed the relation between year and incidence using Joinpoint regression across the time periods specified above and reported annual percentage change. Analyses were conducted with Stata software version 14.0 (Stata Corporation, College Station, TX, USA), and Joinpoint (Joinpoint Desktop Software Version 4.5.0.1).17 18
Patient and public involvement
No patients or members of the public were involved in setting the research question or the outcome measures for this study. No patients were asked to advise on interpretation or writing up of results. We intend to disseminate this research through press releases and at research meetings.
Results
We found 22833 unique abstracts from 1 January 1980 to the end of 2017. Among these, 80 described trends of diabetes incidence, of which 47 met all inclusion criteria. Articles describing trends were excluded for the following reasons: duplicated data (n=21), closed cohorts (n=5), populations included youth only (n=1), occupational cohorts (n=2), or no usable data presented (n=4; fig 1).
Flowchart of study selection
Table 1 and supplementary material table 2 describe the characteristics of the included studies. Only 19% (9/47) of studies were from predominantly non-Europid populations and 4% (2/47) of studies were from low or middle income countries (China25 and Mauritius15). Administrative datasets, health insurance data, registry data, survey data, and cohort studies accounted for 38% (n=18), 21% (n=10), 19% (n=9), 11% (n=5), and 11% (n=5) of the 47 data sources, respectively. Among the 47 studies, diabetes was defined by a clinical diagnosis, diabetes treatment (via linkage to drug treatment registers), an algorithm, blood glucose, and self report in 28% (n=13), 9% (n=4), 47% (n=22), 11% (n=5), and 6% (n=3) of studies, respectively. Sample sizes of the populations were greater than 10000 in every year in 85% (n=40) of the studies, and greater than 130 000 per year in 70% (n=33) of the studies. A total of 62% (n=29) of the 47 included studies exclusively reported on type 2 diabetes, and 38% (n=18) reported on total diabetes.
Table 1
Characteristics of 47 included studies reporting on diabetes incidence trends, by country
| Author, year | Years reported | Country | Origin of data | Type of data | Diabetes definition | Age range |
|---|---|---|---|---|---|---|
| CCDSS et al 201719 | 2000-11 | Canada | CCDSS (administrative data) | Administrative | Administrative algorithm | ≥0 |
| Dyck et al 201016 | 1980-2005 | Canada | Ministry of Health’s insurance registry | Administrative | Administrative algorithm | ≥20 |
| Oster et al 201112 | 1995-2007 | Canada, Alberta | Provincial administrative health records | Administrative | Administrative algorithm | ≥20 |
| Blanchard et al 1996*20 | 1986-91 | Canada, Manitoba | Manitoba Health Insurance, diabetes database | Health insurance | Administrative algorithm | ≥25 |
| Green et al 2003*21 | 1989, 1998† | Canada, Manitoba | Manitoba Health Insurance, diabetes database | Health insurance | Administrative algorithm | ≥20 |
| Alangh et al 201322 | 1996, 2001, 2003, 2005† | Canada, Ontario | Population health surveys linked to registry | Survey | Clinical diagnosis | ≥30 |
| Lipscombe et al 200723 | 1997-2003 | Canada, Ontario | Population based diabetes database | Administrative | Administrative algorithm | ≥20 |
| Horn et al 200724 | 1986-2003 | Canada, Quebec | KHMC diabetes registry | Registry | Clinical diagnosis | ≥18 |
| Liu et al 200725 | 1999-2005 | China, Harbin | Administrative health database | Administrative | Clinical diagnosis | ≥0 |
| Carstensen et al 2008*26 | 1995-2006 | Denmark | National diabetes register | Registry | Administrative algorithm | ≥0 ≥0 |
| Green et al 2015*27 | 2000-11 | Denmark | National diabetes register | Registry | Administrative algorithm | |
| Abouzeid et al 201528 | 1970s, 1980s, 1990s† | Finland | Finnrisk surveys linked to reimbursement database | Survey | Diabetes treatment | 30-59 |
| Laakso et al 199129 | 1970-87 | Finland | Medication database | Registry | Diabetes treatment | ≥30 |
| Michaeli et al 199330 | 1940-89 | Germany, East | National diabetes register | Registry | Clinical diagnosis | ≥0 |
| Boehme et al 201531 | 2007-10 | Germany, southwestern | Claims data AOK Baden, Wuerttemberg | Health insurance | Administrative algorithm | ≥0 |
| Quan et al 201732 | 2007-14 | Hong Kong, China | Hospital Authority clinical management system | Administrative | Administrative algorithm | ≥20 |
| Vilbergsson et al 199733 | 1968-71, 1972-75, 1976-79, 1980-85† | Iceland, Reykjavik | Reykjavik study | Cohort studies | Glucose (FBG, OGTT) plus treatment | 34-79 |
| Karpati et al 201434 | 2004-12 | Israel | Clalit health services | Health insurance | Administrative algorithm | >26 |
| Monesi et al 201135 | 2000-07 | Italy, Lombardy | Administrative health database | Administrative | Administrative algorithm | ≥0 |
| Song et al 201636 | 2004-12 | Korea | Korean national data health insurance | Health insurance | Administrative algorithm | ≥0 |
| Soderberg et al 200415 | 1987-92, 1992-98† | Mauritius | Non communicable disease survey | Cohort studies | Glucose (FBG, OGTT) plus treatment | 20-79 |
| Dowse et al 199137 | 1975/76-82, 1982-87† | Nauru | Non communicable disease survey | Survey | Glucose (FBG, OGTT) plus treatment | ≥20 |
| Ruwaard et al 199638 | 1980-83, 1990-92† | Netherlands | Dutch Sentinel Practice network | Administrative | Clinical diagnosis | ≥0 |
| Strom et al 201439 | 2006-11 | Norway | Norwegian prescription database | Administrative | Diabetes treatment | ≥0 |
| de Sousa-Uva et al 201611 | 1992-2015 | Portugal | General Practice Sentinel network | Administrative | Clinical diagnosis | ≥0 |
| Evans et al 200740 | 1993-2004 | Scotland | DARTS clinical system | Administrative | Administrative algorithm | >35 |
| Read et al 201641 | 2004-13 | Scotland | Diabetes register | Registry | Clinical diagnosis | 40-89 |
| Berger et al 199942 | 1991-95 | Sweden | Skaraborg Swedish diabetes registry | Registry | Clinical diagnosis | ≥0 |
| Jansson et al 201543 | 2006-12 | Sweden | Data from national Swedish registers | Registry | Diabetes treatment | ≥0 |
| Jansson et al 200744 | 1972-2001 | Sweden, Laxa | Diabetes register in primary care network | Administrative | Clinical diagnosis | ≥0 |
| Ringborg et al 200845 | 1996-2003 | Sweden, Uppsala | RECAP-DM (26 primary healthcare providers) | Administrative | Administrative algorithm | >30 |
| Huber et al 201446 | 2007, 2011† | Switzerland | Switzerland healthcare claims data | Health insurance | Administrative algorithm | ≥19 |
| Lin et al 201347 | 2000-07 | Taiwan | National insurance research database | Health insurance | Administrative algorithm | ≥20 |
| Tseng et al 200648 | 1992-96 | Taiwan | National insurance research database | Health insurance | Administrative algorithm | ≥0 |
| Holden et al 2013*49 | 1991-2010 | UK | Clinical Practice Research Datalink | Administrative | Clinical diagnosis | ≥0 |
| Zghebi et al 2017*50 | 2004-14 | UK | Clinical Practice Research Datalink | Administrative | Clinical diagnosis | ≥16 |
| Abraham et al 20158 | 1970s, 1980s, 1990s, 2000s† | US | FHS, FOS, population based, biennial exams | Cohort study | Glucose (FBG) plus treatment | 40-55 |
| Akushevich et al 201351 | 1993-2005 | US | Seer Medicare NLTCS Medicare | Administrative | Clinical diagnosis | >65 |
| Burke et al 200252 | 1970-74, 1975-79, 1990-84, 1985-89, 1990-94† | US | Rochester epidemiology project | Administrative | Administrative algorithm | ≥30 |
| CDC et al 200853 | 1995-97, 2005-07† | US | BFRSS | Survey | Self report | ≥18 |
| Geiss et al 20146 | 1980-2012 | US | NHIS | Survey | Self report | 20-79 |
| McBean et al 200454 | 1994-2001 | US | Medicare database | Administrative | Administrative algorithm | ≥65 |
| Narayanan et al 201055 | 1986-90, 1991-98, 1999-2001, 2001-06† | US | Alaska Native diabetes registry | Registry | Clinical diagnosis | ≥0 |
| Nichols et al 201556 | 2006-11 | US | Multicentre consortium SUPREME-DM | Health insurance | Administrative algorithm | ≥20 |
| Tabaei et al 201257 | 2002, 2004, 2008† | US | New York Community Health Survey | Cohort study | Self report | ≥18 |
| Weng et al 20169 | 2007, 2012† | US | Truven Health MarketScan | Health insurance | Administrative algorithm | ≥18 |
| Pavkov et al 200758 | 1965-77, 1978-90, 1991-2003†‡ | US, Pima | Cohort study with biennial exams | Cohort study | Glucose (FBG, OGTT) plus treatment | ≥5 |
BRFSS=Behavioural Risk Factor Surveillance System; CCDSS=Canadian chronic disease surveillance system; CDC=US Centre for Disease Control and Prevention; DARTS=Diabetes Audit and Research in Tayside Scotland; FBG=fasting blood glucose; FHS=Framingham Heart Study; FOS=Framingham Offspring Study; KMHC=Kateri Memorial Hospital Centre; NHIS=National Health Interview Survey; NLTCS=National Long Term Care Survey; OGTT=oral glucose tolerance test; RECAP-DM= Real-Life Effectiveness and Care Patterns in Diabetes Management; SUPREME- DM=Surveillance, Prevention and Management of Diabetes Mellitus study.
Table 2
Summary of patterns of diabetes incidence trends based on analyses reported in publications in 1960-99
| First author, year | Years included (range) | Mid-point | Country | Predominant ethnicity | Incidence trends (increasing, stable, or decreasing) | ||
|---|---|---|---|---|---|---|---|
| Men | Women | Total | |||||
| 1960-79 | |||||||
| Michaelis et al 1993*30 | 1960-69 | 1965 | Germany | Europid | Increase | ||
| Michaelis et al 1993*30 | 1970-79 | 1975 | Germany | Europid | Increase | ||
| Jansson et al 200744 | 1972-79 | 1976 | Sweden | Europid | Stable | Stable | |
| Vilbergsson et al 199733 | 1968-85 | 1977 | Iceland | Europid | Stable | Stable | |
| Burke et al 200252 | 1970-82 | 1976 | US | Europid | Increase | Increase | |
| Pavkov et al 200758 | 1971-84 | 1978 | US | Non-Europid (Pima) | Stable | ||
| 1980-89 | |||||||
| Abouzeid et al 201528 | 1975-85 | 1980 | Finland | Europid | Increase | Stable | |
| Abraham et al 20157 | 1970-89 | 1980 | US | Europid | Stable | ||
| Dowse et al 199137 | 1979-85 | 1982 | Nauru | Non-Europid | Stable | ||
| Abraham et al 20157 | 1970-97 | 1984 | US | Europid | Increase | ||
| Michaelis et al 1993*30 | 1980-89 | 1985 | Germany | Europid | Stable | ||
| Jansson et al 200744 | 1980-89 | 1985 | Sweden | Europid | Stable | Stable | |
| Geiss et al 20146 | 1980-89 | 1985 | US | Europid | Increase | Stable | |
| Ruwaard et al 199638 | 1980-92 | 1986 | Netherlands | Europid | Increase | ||
| Blanchard et al 199620 | 1986-91 | 1989 | Canada | Europid | Decrease | Decrease | |
| 1990-99 | |||||||
| Horn et al 2007†24 | 1986-94 | 1990 | Canada | Non-Europid (First Nation) | Decrease | ||
| Abouzeid et al 201528 | 1985-95 | 1990 | Finland | Europid | Increase | Stable | |
| Burke et al 200252 | 1987-92 | 1990 | US | Europid | Stable | Stable | |
| Pavkov et al 200758 | 1984-97 | 1991 | US | Non-Europid (Pima) | Stable | ||
| Soderberg et al 200415 | 1987-98 | 1993 | Mauritius | Non -Europid | Stable | Increase | |
| Berger et al 199942 | 1991-95 | 1993 | Sweden | Europid | Stable | ||
| Tseng et al 200648 | 1992-96 | 1994 | Taiwan | Non-Europid (Taiwan) | Increase | Increase | |
| Jansson et al 200744 | 1990-99 | 1995 | Sweden | Europid | Stable | Stable | |
| Holden et al 201349 | 1991-2000 | 1995 | UK | Europid | Increase | Increase | |
| Geiss et al 20146 | 1990-2000 | 1995 | US | Europid | Increase | Increase | |
| Cartensen et al 2008‡26 | 1989-2003 | 1996 | Denmark | Europid | Increase | Increase | |
| Narayanan et al 201055 | 1986-2006 | 1996 | US, Alaska | Non-Europid (Indian) | Increase | ||
| Narayanan et al 201055 | 1986-2006 | 1996 | US, Alaska | Non-Europid (Aleut) | Increase | ||
| Narayanan et al 201055 | 1986-2006 | 1996 | US, Alaska | Non-Europid (Eskimo) | Increase | ||
| de Sousa-Uva et al 201611 | 1992-2003 | 1998 | Portugal | Europid | Increase | Increase | |
| McBean et al 200454 | 1994-2001 | 1998 | US | Europid | Increase | ||
| McBean et al 200454 | 1994-2001 | 1998 | US | Non-Europid (White) | Increase | ||
| McBean et al 200454 | 1994-2001 | 1998 | US | Non-Europid (Black) | Increase | ||
| McBean et al 200454 | 1994-2001 | 1998 | US | Non-Europid (Hispanic) | Increase | ||
| Horn et al 2007†24 | 1994-2003 | 1999 | Canada | Non-Europid (First Nation) | Stable | ||
| Evans et al 200740 | 1993-2004 | 1999 | UK | Europid | Increase | Increase | |
| Akushevich et al 201351 | 1992-2005 | 1999 | US | Europid | Increase | ||
Empty cells in the table imply that the study did not report data through that decade.
Trends of diabetes incidence
Among the 47 studies, 16 provided information on incidence by age group. Of these 16 studies, 14 were plotted in figure 2, with those from high incidence countries plotted in supplementary figure 1. In these figures, incidence in most studies increased progressively until the mid-2000s in all age groups. Thereafter, most studies showed a stable or decreasing trend, apart from studies in Denmark26 27 and Germany31 and in a US health insurance population9 where the incidence inflected upwards in the later years for some age groups.
Incidence of diabetes over time for populations aged under 40, 40-54, 55-69, and 70 or more, among studies reporting age specific data. Only populations with at least three points were plotted. NHIS=National Health Interview Survey
Using the first approach to analyse trends of diabetes incidence over time, we separated the data into populations based on sex and ethnicity, and allocated a time period to each population, generating 105 populations for analysis. Seventy four and 31 populations were predominantly Europid and non-Europid, respectively. Table 2 and table 3 show the reported trend for each population. Table 4 summarises the findings in table 2 and table 3, and shows that the proportion of populations reporting increasing trends peaked in 1990-99 and fell progressively in the two later time periods. Between 1960 and 1989, 36% (8/22) of the populations studied had increasing trends in incidence of diabetes, 55% (12/22) had stable trends, and 9% (2/22) had decreasing trends. In 1990-2005, diabetes incidence increased in 66% (33/50) of populations, was stable in 32% (16/50), and decreased in 2% (1/50). In 2006-14, increasing trends were reported in 33% (11/33) of populations, whereas 30% (10/33) and 36% (12/33) had stable or declining incidence, respectively.
Table 3
Summary of patterns of diabetes incidence trends based on analyses reported in publications in 2000-14
| First author, year | Years reported (range) | Mid-point | Country | Predominant ethnicity | Incidence trends (increasing, stable, or decreasing) | ||
|---|---|---|---|---|---|---|---|
| Men | Women | Total | |||||
| 2000-05 | |||||||
| Lipscombe et al 200723 | 1997-2003 | 2000 | Canada | Europid | Increase | ||
| Ringborg et al 200845 | 1996-2003 | 2000 | Sweden | Europid | Stable | ||
| Abraham et al 20157 | 1990-2009 | 2000 | US | Europid | Stable | ||
| Oster et al 201112 | 1995-2007 | 2001 | Canada | Europid | Increase | Increase | |
| Oster et al 201112 | 1995-2007 | 2001 | Canada | Non-Europid (indigenous) | Increase | Stable | |
| CDC et al 200853 | 1995-2007 | 2001 | US | Europid | Increase | ||
| Liu et al 200725 | 1999-2005 | 2002 | China | Non-Europid (China) | Increase | ||
| Monesi et al 201135 | 2000-07 | 2004 | Italy | Europid | Stable | ||
| Lin et al 201347 | 2000-07 | 2004 | Taiwan | Non-Europid (Taiwan) | Stable | Stable | |
| CCDSS et al 201719 | 2000-06 | 2004 | Canada | Europid | Increase | Increase | |
| Cartensen et al 2008*26 27 | 2004-06 | 2005 | Denmark | Europid | Increase | ||
| Holden et al 2013*49 | 2001-10 | 2005 | UK | Europid | Increase | Increase | |
| Tabaei et al 201257 | 2002-08 | 2005 | US | Europid | Stable | ||
| 2006-14 | |||||||
| Song et al 201636 | 2004-09 | 2007 | Korea | Non-Europid (Korea) | Decrease | ||
| Karpati et al 201434 | 2004-12 | 2008 | Israel | Europid | Decrease | ||
| CCDSS et al 201719 | 2007-11 | 2009 | Canada | Europid | Stable | Stable | |
| Boehme et al 201531 | 2008-10 | 2009 | Germany | Europid | Increase | Increase | |
| Strom et al 201439 | 2006-11 | 2009 | Norway | Europid | Stable | Decrease | |
| de Sousa-Uva et al 201611 | 2004-15 | 2009 | Portugal | Europid | Increase | Increase | |
| Read et al 201641 | 2004-13 | 2009 | Scotland | Europid | Stable | Stable | |
| Huber et al 201446 | 2007-11 | 2009 | Switzerland | Europid | Decrease | Decrease | |
| Zghebi et al 2017*50 | 2004-14 | 2009 | UK | Europid | Stable | Stable | |
| Nichols et al 201556 | 2006-11 | 2009 | US | Europid (Non-Hispanic white) | Stable | Stable | |
| Nichols et al 201556 | 2006-11 | 2009 | US | Non-Europid (black) | Increase | ||
| Nichols et al 201556 | 2006-11 | 2009 | US | Non-Europid (Hispanic) | Increase | ||
| Nichols et al 201556 | 2006-11 | 2009 | US | Non-Europid (Asian) | Increase | ||
| Nichols et al 201556 | 2006-11 | 2009 | US | Non-Europid (Native American) | Increase | ||
| Nichols et al 201556 | 2006-11 | 2009 | US | Non-Europid (Hawaiian/Pacific) | Increase | ||
| Green et al 2015*27 | 2007-11 | 2009 | Denmark | Europid | Increase | Increase | |
| Jansson et al 201543 | 2006-13 | 2010 | Sweden | Europid | Decrease | Decrease | |
| Geiss et al 20146 | 2008-12 | 2010 | US | Europid | Decrease | Decrease | |
| Weng et al 21069 | 2007-12 | 2010 | US | Europid | Decrease | ||
| Quan et al 201732 | 2007-14 | 2011 | Hong Kong, China | Non-Europid (Hong Kong) | Decrease | Decrease | |
| Song et al 201636 | 2009-12 | 2011 | Korea | Non-Europid (Korea) | Stable | ||
Empty cells imply that the study did not report data through that decade. CDC=US Centre for Disease Control and Prevention; CCDSS=Canadian chronic disease surveillance system (published online only).
Table 4
Summary of incidence trends over time of total or type 2 diabetes
| Study years | No of populations | Distribution of populations (No (%)) | ||
|---|---|---|---|---|
| Increased | Stable | Decreased | ||
| 1960-79 | 9 | 4 (44) | 5 (56) | 0 |
| 1980-89 | 13 | 4 (31) | 7 (54) | 2 (15) |
| 1990-99 | 32 | 22 (69) | 9 (28) | 1 (3) |
| 2000-05 | 18 | 11 (61) | 7 (39) | 0 |
| 2006-14 | 33 | 11 (33) | 10 (30) | 12 (36) |
| Total | 105 | — | — | — |
Populations that reported a decrease in incidence after 2005 came from the US,6 9 Israel,34 Switzerland,46 Hong Kong,32 Sweden,43 and Korea.36 Populations reporting increasing incidence after 2005 included Portugal,11 Denmark,26 27 and Germany,31 while populations from Canada,19 Italy,35 Scotland,40 Norway,39 US (non-Hispanic white),56 and the United Kingdom50 showed stable incidence. For two studies (16 populations),16 29 we could not determine a direction of a trend (increasing, decreasing, or stable), because they showed three phases of change with the trend of the middle phase differing from the trend of the first and last phase. Across the total time period, we observed a higher proportion of populations reporting stable or decreasing trends in predominantly Europid than in non-Europid populations (52% v 41%).
Using the second approach to analyse trends of diabetes incidence over time, we modelled 21 studies (62 populations) that reported diabetes counts and denominators specifically within each time period (table 5). The percentage of populations with a decreased or stable incidence was highest in 1980-89 (88%; 7/8), but this proportion was based on only eight populations in three studies. From 1990 onwards, the percentage with decreasing or stable incidence increased progressively, reaching 83% (19/23) of populations in 2006-14. Eight studies (21 populations) that were analysed by Joinpoint had no data on counts or denominators (supplementary table 3). When these data were considered with the data in table 5, the percentage of populations in 2006-14 with decreasing or stable incidence fell to 70% (19/27), but this proportion was still the highest of all the time periods, whereas the percentage for 1990-99 remained the lowest at 31% (5/16).
Table 5
Annual percentage change in diabetes incidence in men (M), women (W), or total population (T) among studies that provided counts and denominators, by time period
| Author, year | Population | Country | Annual percentage change (%) in incidence, P value | ||||
|---|---|---|---|---|---|---|---|
| 1970-79 | 1980-89 | 1990-99 | 2000-05 | 2006-14 | |||
| CCDSS et al 201719 Canada | M | Canada | — | — | — | 0.8, 0.001 | −2.6, 0.001 |
| CCDSS et al 201719 Canada | F | Canada | — | — | — | 1.8, <0.001 | −2.8, <0.001 |
| Dyck et al 201016 (First Nation) | M | Canada | — | 2.2, 0.06 | 4.8, <0.001 | −0.3, 0.86 | — |
| Dyck et al 201016 (First Nation) | F | Canada | — | −2.4, 0.02 | −0.1, 0.90 | −6.03, <0.001 | — |
| Dyck et al 201016 (Non-First Nation) | M | Canada | — | −1.5, <0.001 | 3.6, <0.001 | −1.4, 0.006 | — |
| Dyck et al 201016 (Non-First Nation) | F | Canada | — | −2.5, <0.001 | 3.1, <0.001 | −1.0, 0.06 | — |
| Horn et al 200724 | M | Canada | — | — | −7.5, 0.08 | — | — |
| Horn et al 200724 | F | Canada | — | — | −7.5, 0.01 | — | — |
| Liu et al 200725 | T | China | 11.0, <0.001 | ||||
| Boehme et al 201531 | M | Germany | — | — | — | — | 1.6, <0.001 |
| Boehme et al 201531 | F | Germany | — | — | — | — | 2.9, <0.001 |
| Quan et al 201732 | M | Hong Kong, China | — | — | — | — | −1.70, <0.001 |
| Quan et al 201732 | F | Hong Kong, China | — | — | — | — | −1.27, <0.001 |
| Karpati et al 201434 | T | Israel | — | — | — | −5.3, <0.001 | −3.2, <0.001 |
| Song et al 201636 | M | Korea | — | — | — | 11.3, <0.001 | 1.3, <0.001 |
| Song et al 201636 | F | Korea | — | — | — | 17.2, <0.001 | −0.9, <0.001 |
| Strom et al 201439 | M | Norway | — | — | — | — | −0.5, 0.7 |
| Strom et al 201439 | F | Norway | — | — | — | — | −1.5, 0.1 |
| Read et al 201641 | M | Scotland | — | — | — | −5.5, <0.001 | −0.03, 0.86 |
| Read et al 201641 | F | Scotland | — | — | — | −9.2, <0.001 | −0.8, <0.001 |
| Jansson et al 201543 | M | Sweden | — | — | — | — | −0.3, <0.001 |
| Jansson et al 201543 | F | Sweden | — | — | — | — | −0.9, <0.001 |
| Ringborg et al 200845 | T | Sweden | — | — | −3.8, 0.01 | −4.8, 0.001 | — |
| Huber et al 201446 | M | Switzerland | — | — | — | — | −3.6, 0.001 |
| Huber et al 200446 | F | Switzerland | — | — | — | — | −3.5, 0.02 |
| Lin et al 201347 | T | Taiwan | — | — | — | −2.4, <0.001 | 3.9, <0.001 |
| Tseng et al 200648 | M | Taiwan | — | — | 15.4, <0.001 | — | — |
| Tseng et al 200648 | F | Taiwan | — | — | 8.1, <0.001 | — | — |
| Zghebi et al 201750 | M | UK | — | — | — | — | −4.1, 0.01 |
| Zghebi et al 201750 | F | UK | — | — | — | — | −3.0, <0.001 |
| Burke et al 200252 | M | US | 5.0, 0.04 | 5.0, 0.02 | — | — | — |
| Burke et al 200252 | F | US | −5.3, <0.02 | 2.2, 0.29 | — | — | — |
| McBean et al 200454 | T | US | — | — | 5.0 <0.001 | — | — |
| Nichols et al 201556 | T | US | — | — | — | — | −0.04, 0.91 |
| Geiss et al 2014*6 | M | US | — | 0.5, 0.81 | 13.6, <0.001 | 1.6, 0.5 | −4.1, <0.001 |
| Geiss et al 2014*6 | F | US | — | 1.8, 0.32 | 9.4, <0.001 | 4.7, 0.01 | −1.5, 0.07 |
| Weng et al 20169 | T | US | — | — | — | −8.0, <0.001 | — |
| Summary: Percentage (%) of populations that showed increasing incidence trends over time period | — | — | 50 | 12 | 66 | 31 | 17 |
| Summary: Percentage (%) of populations that showed decreasing or stable incidence trends over time period | — | — | 50 | 88 | 33 | 69 | 83 |
CCDSS=Canadian chronic disease surveillance system (published online only).
In a sensitivity analysis, we tested whether our selection of time periods was driving our results. When we defined the final time periods to be 2000-07 and 2008-14, our results were not altered, with 66% (21/32) of the populations in the last time period showing decreasing or stable trends. We also repeated the analysis in table 4 and excluded cohort studies and surveys, and found that the results were not materially altered, with 65% (20/31) of populations in the last time period (from 2006 onwards) showing decreasing or stable incidence of diabetes.
Quality of studies
The median score for study quality was 10 (interquartile range 8-11; supplementary table 4). We repeated the analyses reported in table 4 after excluding studies that had quality scores in the lowest quarter, and observed similar results to the main findings. For example, in 1960-89, 67% (10/15) of populations reported stable or decreasing incidence, while in the final time period, 67% (18/27) of populations reported stable or decreasing incidence of diagnosed diabetes.
Discussion
Principal findings
In this systematic review of population based studies on diabetes incidence, we show evidence that the incidence of diagnosed diabetes increased in most populations from the 1960s to the early 2000s, after which a pattern emerged of levelling trends in 30% and declining trends in 36% of the reported populations. Although the lack of data for non-Europid populations leaves global trends in incidence unclear, these findings suggest that trends in the diabetes epidemic in some high income countries have turned in a more encouraging direction compared with previous decades. It is important to note that these results apply predominantly to type 2 diabetes, as even though many studies did not accurately define diabetes type, the incidence of type 2 diabetes in adults is an order of magnitude greater than that of type 1 diabetes.
The countries that showed stable or decreasing trends in the last time period were from Europe and east Asia, with no obvious clustering or commonalities. For the countries showing decreasing or stable diabetes trends, if the prevalence data were used to understand the diabetes epidemic in that country, a different message would be obtained. For example, national data from Korea showed that the prevalence of diabetes increased from 2000 to 2010.59 Similarly in Sweden, the prevalence of pharmacologically treated diabetes increased moderately from 2006 to 2014.43 In the US, the prevalence of diabetes reached a plateau when incidence began to decrease. However, we lacked incidence data from many areas of the world where the most steady and substantial increases in prevalence have been reported, including the Pacific Islands, Middle East, and south Asia. Large increases in incidence could still be occurring in these areas. The lack of incidence data for much of the world, combined with the common observation of discordance between incidence and prevalence rates where such data exist, both underscore the importance of using incidence data to understand the direction of the diabetes epidemic.
Incidence could be starting to fall for several reasons. Firstly, we might be starting to benefit from prevention activities of type 2 diabetes, including increased awareness, education, and risk factor modification. These activities have involved both targeted prevention among high risk individuals, similar to that conducted in the Diabetes Prevention study60 and Diabetes Prevention Programme61 62 in many countries,63 and less intensive interventions with broader reach such as telephone counselling in the general community.64 65 67 Secondly, health awareness and education programmes have also been implemented in schools and work places, and many changes to the physical environment, such as the introduction of bike tracks and exercise parks, have occurred.68 Thirdly, favourable trends in selected risk factors of type 2 diabetes in some countries provide indirect evidence of positive changes to reduce diabetes incidence. Finally, in the US, there is some evidence in recent years of improved diets and related behaviours, which include reductions in intake of sugar sweetened beverages69 and fat,70 small declines in overall energy intake, and declines in some food purchases.8 71
Similar reduction in consumptions of sugar sweetened beverages have occurred in Norway72 and Australia73 and fast food intake has decreased in Korea.74 Some of these changes could be linked to a fall in diabetes incidence. Some places such as Scotland75 have also had a plateauing of obesity prevalence, but this is not universal. In the US, despite earlier studies suggesting that the rate of increase in obesity might be slowing down,76 77 more recent data show a small increase.78 79 While some evidence supports the hypothesis that these prevention activities for type 2 diabetes and an improved environment could trigger sufficient behaviour change to have an effect on diabetes incidence, other data, such as the continuing rising obesity prevalence in the US,79 casts some doubt over the explanations underpinning our findings on diabetes incidence trends.
Other factors might have also influenced reported diabetes incidence. Only 11% (n=5) of the studies reported here screened for undiagnosed diabetes, and therefore trends could have been influenced by secular changes in diagnostic behaviour. In 1997, the threshold for fasting plasma glucose for diagnosis of diabetes was reduced from 7.8 to 7.0 mmol/L, which could increase diagnosis of new cases of type 2 diabetes. In 2009-10, HbA1c was then introduced as an alternative way to diagnose diabetes.80 Evidence from some studies suggests that the HbA1c diagnostic threshold detects fewer people with diabetes than do the thresholds for fasting plasma blood glucose,80 81 potentially leading to a lowering of incidence estimates. However, across multiple studies, prevalence estimates based on fasting plasma glucose only versus HbA1c definitions are similar.82 Furthermore, because HbA1c can be measured in the non-fasting state (unlike the fasting blood glucose or oral glucose tolerance test), the number of people who actually undergo diagnostic testing could be higher with HbA1c. Nichols and colleagues56 reported that among seven million insured US adults, despite a shift towards HbA1c as the diagnostic test in 2010, the incidence of diabetes did not change from 2010 to 2011.
Another potential explanation for declining or stable diabetes incidence after the mid-2000s is a reduction in the pool of undiagnosed diabetes83 through the intensification of diagnostic and screening activities83 84 and changing diagnostic criteria during the previous decade.80 Data from Read and colleagues provide some evidence to support this notion.41
Among the included studies, two studies specifically examined clinical screening patterns in parallel with incidence trends. These studies reported that the proportion of the population screened for diabetes increased over time, and the incidence of diabetes remained stable56 or fell.34 While the Karpati study34 combined data for glucose testing with HbA1c testing, the study by Nichols and colleagues56 separated the two, and showed that both glucose testing and HbA1c testing increased over time. A third study, in Korea,36 also noted that the incidence of diabetes decreased in the setting of an increase in the uptake of the national health screening programme. Despite the introduction of HbA1c for diagnosis of diabetes by the World Health Organization, this practice has not been adopted everywhere. For example, neither Scotland nor Hong Kong have introduced the use of HbA1c for screening or diagnosis of diabetes, and studies in these areas showed a levelling of diabetes incidence trends and decreasing trends, respectively.
Our findings appear to contrast with data showing increasing global prevalence of diabetes.1 3 However, increasing prevalence could be influenced by improved survival of people with diabetes, because this increases the length of time that each individual remains within the diabetes population. As is shown in several studies in this review,23 41 mortality from diabetes and incidence of diabetes might both be falling but as long as mortality is lower than incidence, prevalence will rise. Therefore, we argue that prevalence alone is an insufficient measure to track the epidemic of diabetes and other non-communicable diseases.
Strengths and weaknesses of this study
A key strength of this work was the systematic approach and robust methodology to describe trends in diagnosed diabetes incidence. We also presented the reported trends allocated to approximate time periods, as well as conducting our own regression within exact time periods. The following limitations should also be considered. Firstly, we did not formally search the grey literature, because a preliminary grey literature search revealed only low quality studies, with inadequate methodological detail to provide confidence in any observed incidence trends, and thus review could be subject to publication bias. Secondly, we were not able to source age or sex specific data on all populations. Thirdly, it was not possible to adjust for different methods of diabetes diagnosis or ascertain trends by different definitions of diabetes. Fourthly, most data sources reported only on clinically diagnosed diabetes and so were subject to influence from diagnostic behaviour and coding practices. Fifthly, study type changed over time, with large administrative datasets becoming more common and cohort studies becoming less common over time. Nevertheless, the size and absence of volunteer bias in administrative datasets likely make them less biased. Finally, data were limited in low and middle income countries.
Conclusions and unanswered questions
This systematic review shows that in most countries for which data are available, the incidence of diagnosed diabetes was rising from the 1990s to the mid-2000s, but has been stable or falling since. Preventive strategies and public health education and awareness campaigns could have contributed to this recent trend. Data are limited in low and middle income countries where trends in diabetes incidence might be different. Improvement of the collection, availability, and analysis of incidence data will be important to effectively monitor the epidemic and guide prevention efforts into the future.
Acknowledgments
The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the US Centers for Disease Control and Prevention (CDC).
Web extra.
Extra material supplied by authors
Web appendix: Supplementary material
Web appendix: Visual summary
Notes
Contributors: MT, DNK, JLH, and RMI are postdoctoral fellows who screened abstracts for selection into the systematic review. JES and DJM also screened abstracts. ELMB applied the quality criteria to the selected articles. RMI extracted data, applied quality criteria to selected articles, and contributed to preparing the manuscript. DJM conceived the project, screened abstracts, extracted the data, analysed the data, and wrote the manuscript. JES, MEP, and EWG conceived the project, edited the manuscript, and provided intellectual input throughout the process. The funder of the study (CDC) was part of the study group and contributed to data collection, data analysis, data interpretation, and writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication. DJM is guarantor. The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted.
Funding: Funded by the CDC. The researchers were independent from the funders.
Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: support from the CDC for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
Ethical approval: Not required because this work was a systematic review.
Data sharing: Data are available from the corresponding author (dianna.magliano@baker.edu.au).
The lead author affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.
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