PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of bmcendiBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Endocrine Disorders
 
BMC Endocr Disord. 2017; 17: 19.
Published online 2017 March 23. doi:  10.1186/s12902-017-0170-x
PMCID: PMC5364612

The incidence of diabetes mellitus and diabetic retinopathy in a population-based cohort study of people age 50 years and over in Nakuru, Kenya

Abstract

Background

The epidemic rise of diabetes carries major negative public health and economic consequences particularly for low and middle-income countries. The highest predicted percentage growth in diabetes is in the sub-Saharan Africa (SSA) region where to date there has been no data on the incidence of diabetic retinopathy from population-based cohort studies and minimal data on incident diabetes. The primary aims of this study were to estimate the cumulative six-year incidence of Diabetes Mellitus (DM) and DR (Diabetic Retinopathy), respectively, among people aged ≥50 years in Kenya.

Methods

Random cluster sampling with probability proportionate to size were used to select a representative cross-sectional sample of adults aged ≥50 years in 2007-8 in Nakuru District, Kenya. A six-year follow-up was undertaken in 2013–14. On both occasions a comprehensive ophthalmic examination was performed including LogMAR visual acuity, digital retinal photography and independent grading of images. Data were collected on general health and risk factors. The primary outcomes were the incidence of diabetes mellitus and the incidence of diabetic retinopathy, which were calculated by dividing the number of events identified at 6-year follow-up by the number of people at risk at the beginning of follow-up. Age-adjusted risk ratios of the outcomes (DM and DR respectively) were estimated for each covariate using a Poisson regression model with robust error variance to allow for the clustered design and including inverse-probability weighting.

Results

At baseline, 4414 participants aged ≥50 years underwent complete examination. Of the 4104 non-diabetic participants, 2059 were followed-up at six-years (50 · 2%). The cumulative incidence of DM was estimated at 61 · 0 per 1000 (95% CI: 50 · 3–73 · 7) in people aged ≥50 years. The cumulative incidence of DR in the sample population was estimated at 15 · 8 per 1000 (95% CI: 9 · 5–26 · 3) among those without DM at baseline, and 224 · 7 per 1000 (116.9–388.2) among participants with known DM at baseline. A multivariable risk factor analysis demonstrated increasing age and higher body mass index to be associated with incident DM. DR incidence was strongly associated with increasing age, and with higher BMI, urban dwelling and higher socioeconomic status.

Conclusions

Diabetes Mellitus is a growing public health concern with a major complication of diabetic retinopathy. In a population of 1 · 6 million, of whom 150,000 are ≥50 years, we estimated that 1650 people aged ≥50 develop DM per year, and 450 develop DR. Strengthening of health systems is necessary to reduce incident diabetes and its complications in this and similar settings.

Background

The number of adults with Diabetes Mellitus (DM) in Africa is predicted to double from 12 · 1 million in 2010 to 23 · 9 million in 2030 based on projections from prevalence data [1]. The epidemic rise of DM carries major public health and economic consequences for the continent, particularly given it is home to some of the fastest growing economies and most rapid transitions in lifestyles conducive to DM ([http://unstats.un.org/unsd/methods/m49/m49regin.htm - least]). Currently, there are few incidence data from low and middle-income settings, particularly sub-Saharan Africa (SSA), making it difficult to plan screening and treatment services [2, 3].

DM causes visual impairment through cataract and diabetic retinopathy (DR) [4], a progressive disease of the retinal microvasculature. DR is not yet a leading cause of blindness in sub-Saharan Africa, responsible for just 2.8% of blindness [5]. However, it is likely to become an increasingly important cause of blindness and visual impairment, with the increasing prevalence of DM in SSA, and improving control of other leading causes of visual impairment such as cataract, uncorrected refractive error and trachoma. Population-based incidence data for DR are lacking for SSA, although some clinical follow-up data are available [6].

Current strategies to control DM in SSA focus on health system strengthening to enable a public health approach to both prevent the onset of DM and create awareness of the consequences of DM, including sight loss [7]. In addition, efforts are also being scaled-up for the identification of people with DM , and their enrolment in treatment programmes [8]. Systematic DR screening in SSA is currently very limited, with only a small number of locations having an active programme [9].

Data on the incidence and progression of DM and DR are needed to estimate the current and future burden of these conditions in order to inform service development, and future research. The primary aims of this study were to estimate the cumulative six-year incidence of DM and DR in people aged ≥50 years in Kenya. A secondary aim was to identify risk factors for each of these outcomes.

Methods

The fieldwork was carried out in Nakuru district, Kenya, which has a population of 1.6 million [accurate as of 2009], one third of which is urban. Nakuru is broadly representative of Kenya in terms of ethnic diversity and economic activities. The baseline survey took place from January 2007 to November 2008, and the follow-up survey from November 2012 to March 2014. Full details of the methods at baseline and follow-up are presented elsewhere [1012].

Sampling strategy and recruitment at baseline

We selected 100 clusters of 50 people aged ≥50 years through probability proportionate to size sampling, using the electoral roll as the sampling frame. Households were selected within clusters using a modified compact segment sampling method [13]. The village leaders produced a sketch map of the polling area. The polling area was divided into segments each including approximately 50 people aged ≥50 years. One segment was chosen at random by drawing lots and all households in the segment were included in the sample sequentially, until 50 people aged ≥50 years were identified. If the segment did not include 50 people aged ≥50 years then an additional segment was chosen at random and sampling continued.

The enumeration team visited households, assisted by a village guide, and invited all eligible participants aged ≥50 years to the examination clinic, held at a convenient place in the cluster over the subsequent two days. Eligible participants were defined as those aged ≥50 years resident in the cluster (i.e. living there at least 6 months per year) who had slept in the house either the night before or were planning on sleeping in the house that night. If an eligible person was absent then the survey team revisited the household at least twice.

The six-year follow-up assessment was initiated by an Advance Team who visited homes of baseline participants and confirmed their identity using National Identity cards. The two advance teams comprised of one nurse, one field officer and a driver or public transport. During this visit they located individuals with assistance from the guide, phone numbers when available and previously recorded GPS locations using a Garmin Oregon 450 Satellite Navigation device. In addition, the team explained details of the examination and obtained written/thumb print informed consent as well as informing participants about location and time of examination [11].

Data collection

Comprehensive data were collected at baseline and follow-up, using comparable methods, including slit lamp examination by an ophthalmologist at both time points. Details of data collection are available elsewhere [11, 14] with specific details provided here for the current analyses.

Diabetes mellitus

A single random finger-prick blood sample was taken to measure glucose (Accutrend GC system) at baseline and at follow-up. At follow-up, in addition, subjects with a random blood sugar greater than 11.1 mmol/L (International Diabetes Federation (IDF) guidance at time of baseline study), those with known DM (regardless of random measure), evidence of DR on retinal imaging and a subset (chosen randomly within each cluster) with random glucose between 7 and 11 mmol/L had an additional capillary blood HbA1C (A1C Now+, Bayer).

Visual acuity (VA)

Two ophthalmic nurses measured presenting VA, which was defined as the number of letters read correctly without glasses if the participant did not have glasses or with distance glasses if they had them. Each eye was tested separately at 4 m using a reduced Logarithm of the Minimal Angle of Resolution (LogMAR) tumbling ‘E’ chart [15] in a well illuminated area. If the subject’s vision was too poor to read any letters on the chart at four meters, then the subject was tested at one meter, then counting fingers, hand movements, light perception or no light perception.

Fundus photography

Pupil dilation was performed using one drop of tropicamide 1% and one drop of phenylephrine 2.5%. The participants had two non-stereoscopic digital 450 fundus photographs taken per eye by an ophthalmic clinical officer using a TRC-NW6S Non-Mydriatic Retinal Camera with 10 megapixel Nikon D80 (TopCon®) at baseline and a Haag-Streit DRS CentreVue + at follow-up. One image was centred on the optic disc while the other was centred on the macula.

Anthropometric data collection

At baseline and follow-up, a nurse recorded the blood pressure of participants three times on the right arm of the participant, at least five minutes apart after an initial period of five minutes of rest using the Omron digital automatic monitor (model HEM907). Weight was measured to the nearest kilogram using standard scales (Seca 761 scales) after the participant had removed all heavy clothing and shoes. Height was measured to the nearest centimetre while the participant stood without shoes using a standardized stadiometer (Leicester Height Measure). For weight and height the average of two readings was recorded. Waist and hip circumferences were measured with a tape to the nearest centimetre.

Interviews

Participants were interviewed by trained nurses. Information was collected on demographic data, education and asset ownership. People were asked whether their mother tongue was “Kikuyu”, “Kalenjin” (the two largest ethnic group in Nakuru County) or “other” to assign ethnicity. Information was also collected on health behaviour (smoking, alcohol use) and health status (diagnosis of diabetes or hypertension, family history and their treatment).

Grading of retinal images

Retinal images were forwarded to the Retinal Grading Centre at Moorfields Eye Hospital Reading Centre (MEHRC) London for grading DR. All images supplied by the Nakuru Eye Study Group, regardless of quality, were sent for grading. No manipulation of the images was allowed while grading, other than using grey-scale for viewing the images. All images were first categorized for quality as excellent, good, borderline and ungradeable.

Next, the photographs were graded for DR based on the UK National Guidelines on Screening for Diabetic Retinopathy [16]. Each eye was classified for all people with diabetes as: no DR, mild NPDR, moderate NPDR, severe NPDR or proliferative DR, based on the following criteria:

  • No DR - no changes characteristic of diabetic retinopathy visible on the images.
  • Mild non-proliferative DR (NPDR) - micro aneurysms (MAs) and retinal haemorrhages only were seen.
  • Moderate NPDR - in addition to MAs multiple deep, round or blot haemorrhages were noted.
  • Severe NPDR - the presence of features of NPDR plus cotton wool spots. In this scenario the grader was asked to search for vascular features of DR, such as venous loop, venous beading and Intra-retinal micro-vascular abnormality (IRMA). If these were found, severe NPDR was graded.
  • Proliferative DR (PDR) – as above, with new vessels on the disc (NVD) new vessels elsewhere (NVE), pre-retinal or vitreous haemorrhage or pre-retinal fibrosis ± tractional retinal detachment were seen.

All images were graded by the senior grader. In case of difficulties, the adjudicator (TP) adjudicated the images. The adjudicator also looked at a random selection of 5% of images to ensure quality control. Data were entered onto Excel and checked for consistency by a data monitor. Grading methods were the same at baseline and follow-up.

Data analysis

Definitions and statistical analyses

DM was defined as per WHO standards for population-based studies: reported current medication (tablets or insulin) or; diet control for diabetes or; random blood glucose level ≥11 · 1 mmol/L [17]. At follow up the definition included HbA1C when a result was possible. HbA1C of > =7 · 0 was taken as confirmation of DM and if <7 · 0 DM was excluded. An HbA1C result superseded other measures of DM apart from self-reported and on medication, in which case an HbA1C of <7 · 0 was taken as well controlled DM and HbA1C > =7 · 0 of poorly controlled DM.

A continuous socio-economic score (SES) was produced for each participant using principal component analysis based on asset ownership, household type and education [18]. The score was divided into quartiles to categorize the study participants into four socioeconomic groups with a higher score representing higher SES. Body Mass Index (BMI) was calculated as height (meters)/weight (kilograms)2. The clusters were defined as rural or urban according to the classification used by the District Health Statistics office [19].

All participants who had complete examinations at baseline who did not have DM or did not have DR were considered “at-risk” for incident DM or DR, respectively. Follow-up status at 6 years was categorised as i) Found and examined; ii) Found and not examined; iii) Deceased; iv) Moved away; or v) Unknown.

Statistical analysis was performed using STATA v13 (Stata Corp). All analysis accounted for the cluster survey design using Taylor linearized variance estimation to calculate standard errors.

Pearson chi-squared tests, corrected for the survey-design were used to calculate p-values in order to assess differences between participants seen and those lost to follow-up (LTFU), and between those known to have died and with unknown outcome status. Those who were deceased were then excluded. Those followed up but without complete records for all covariates at baseline were also excluded. An inverse probability-weighting (IPW) model [20] was developed to allow estimation of cumulative incidence while accounting for those LTFU. Multivariable logistic regression was used to identify independent baseline covariates associated with LTFU. Covariates for which there was evidence of univariable association with being LTFU (p < 0.1) were kept in a multivariable model. From this final model, the probability of being followed-up was estimated, based on the presence or absence of each of these baseline covariates. The inverse of this probability formed the weighting to be applied in order to account for those LTFU. The final step was to remove those individuals LTFU from the cohort, so that all subsequent analysis would be performed on only those with complete outcome records, with IPW applied to account for those LTFU. A sensitivity analyses for this approach involved a complete records analysis (i.e. only including those people who had complete records for outcome and all variables in the analysis).

The six-year cumulative incidence of each outcome was calculated by dividing the number of events identified at 6-year follow-up by the number of people at risk at the beginning of follow-up. 95% confidence intervals were estimated assuming a Poisson distribution of events. This analysis was done for the population overall, and stratified by key covariates. Age-adjusted risk ratios of the outcomes (DM and DR respectively) were estimated for each covariate using a Poisson regression model with robust error variance to allow for the clustered design and including IPW. For multivariable analysis, an initial model was fitted that included those variables associated with outcome in age-adjusted analysis (Wald p-value <0.05). A backward stepwise approach was applied to obtain a final multivariable model, removing variables with p > 0.05. Estimates were weighted to allow for any bias due to loss to follow up by weighting using inverse probability weights as described above. The six-year cumulative incidence was then used to estimate the expected number of new DR cases per year by multiplying the six-year incidence by the estimated Kenyan population and dividing by six, with the assumption that cumulative incidence was constant over time. Annual cumulative incidence was also estimated separately for men and women and in ten-year age categories (50–59, 60–69, 70–79 and 80 + .

Results

Diabetes mellitus

At baseline, 4414 participants aged ≥50 years underwent complete examination (response rate of 88 · 1%) and 4388 (99 · 4%) had DM status data available, of whom 287 (6 · 5%) were diagnosed with DM (Fig. 1). Of the 4,101who had no DM at baseline, 2059 (50 · 2%) were followed-up at six-years. Complete DM status data at follow-up were available on 2056 (99 · 9%) participants, of whom 123 (6 · 0%) were newly diagnosed with DM at six-year follow-up (Fig. 1).

Fig. 1
Flowcharts of participant Diabetes Mellitus status in the Nakuru Eye Disease Cohort Study

Baseline characteristics of individuals with known baseline DM status data who were re-examined at follow-up (participants) and those who were LTFU are shown in Table 1. There was strong evidence that those who were LTFU were less likely to be Kikuyu or Kalenjin speakers and more likely to be from urban areas (p < 0.001). The mean follow-up time of all participants was 5 · 6 (SD 0 · 6) years and the median was 5 · 5 (interquartile range (IQR): 5 · 0–6 · 1) years (referred to as “six-year cumulative incidence” from here on).

Table 1
Baseline characteristics of all individuals with a known baseline DM status subdivided by their follow-up category (participant, non-participant) at 6-year follow-up (N = 4388)

Of the 123 participants who developed incident DM by six-years, 64 diagnoses were self-reported and 59 were based on blood sugar readings. Of the 64 self-reported subjects with DM, 35 (54 · 7%) had random and HbA1C readings within normal limits and were considered “controlled DM”, and the remaining 29 were “uncontrolled DM” (10 had high HbA1C only, three had elevated random glucose data only (no HbA1C data) and 16 had both a high random glucose and HbA1C). Consequently, the cumulative incidence of DM was estimated at 61 · 0 per 1000 (95% CI: 50 · 3,73 · 7) in people aged ≥50 years when corrected for loss to follow-up. The incidence of DM decreased with age in both men and women, and was similar across the sexes (Table 2). Based on recent census data, the number of incident cases was estimated by extrapolating to the Kenyan population aged ≥50 years (Table 3), assuming an equal incidence per year over the study period. In the population of 1 · 6 million people in Nakuru, Kenya, approximately 150,000 individuals are aged ≥50 years, and of these approximately 1650 will develop DM each.

Table 2
Age-gender–specific 6-year cumulative incidence of diabetes mellitus among the Nakuru eye disease cohort study participants
Table 3
Extrapolated number of new adults, per year, aged 50 years and over in Kenya with diabetes mellitus and diabetic retinopathy based on incidence data (adjusted to take account of loss to follow up) and estimates of the population in Kenya by age ...

Of the 287 participants with known DM from baseline, 54 (18.8%) were known to have died, 110 (38.3%) were re-assessed and 123 (42.8%) were LTFU. All 110 people with known DM at baseline were defined as having known DM at follow-up regardless of self-report. Of these, 70 (63 · 6%) self-reported as DM at follow-up, of whom 20 (28 · 6%) were controlled. Of the 40 with known DM at baseline who did not report as having DM at follow-up, 32 (80 · 0%) were controlled. Of these, 25 had a normal random blood sugar at baseline but self-reported as DM, four did not self-report but had a high random blood sugar and three both self-reported and had a high blood sugar.

Increased risk of incident DM was associated with the following baseline variables: higher body mass index, urban dwelling, higher socioeconomic status, hypertension, and having no previous formal education (Table 4). A lower incidence was found with increasing age, former alcohol consumption and Kalenjin ethnicity. After adjustment for confounding, increasing age and higher body mass index remained associated with incident DM (Table 4).

Table 4
Age-adjusted and multivariable analysis of a number of baseline co-variables and incident diabetes mellitus in the Nakuru eye disease cohort study

Diabetic retinopathy

At baseline, 4414 participants aged ≥50 years underwent complete examination (response rate of 88 · 1%) and 3281 (74 · 3%) had DR image data available, of whom 195 (5 · 9%) were diagnosed with DM at baseline (Fig. 2). Of these 195 participants, 70 had DR at baseline. At follow-up, 78 (40 · 0%) of the 195 participants with baseline DM were seen, and 1562 (50 · 6%) of the 3086 participants without DM at baseline.

Fig. 2
Flowcharts of participant Diabetic Retinopathy status in the Nakuru Eye Disease Cohort Study. DM: Diabetes Mellitus, DR: Diabetic Retinopathy

The baseline characteristics of those with complete data for analysis (participants with a known DR status at follow-up, based on retinal images), and those for whom data was incomplete were similar. However a higher proportion of those who had impaired vision at baseline were not included in the DR incidence analysis, either due to LTFU or ungradeable retinal images (Table 5).

Table 5
Baseline characteristics of all individuals with a known baseline DR status, subdivided by their follow-up category (participant, non-participant) at 6-year follow-up (N = 3281)

Of the 1562 people without either DM or DR at baseline, 1377 (88 · 1%) had complete follow-up DR status data. Of these, 89/1377 (6 · 5%) were newly diagnosed with DM; and 9 (10 · 1%) had incident DR. A further 11 incident cases of DR were seen in the 44 participants with DM but no DR at baseline (Fig. 2). Therefore, in total, 20 participants developed DR during follow up, giving a corrected cumulative incidence of 15 · 8 per 1000 (95% CI: 9 · 5–26 · 3), Table 2. This equates 15,800 cases in the population aged ≥50 years per year per million. In the population of 1 · 6 million people in Nakuru, Kenya, approximately 150,000 individuals are aged ≥50 years, and of these approximately 1650 will develop DM each year and 450 will develop DR each year.

Among subjects with known DM at baseline, the corrected cumulative incidence of DR is 224 · 7 per 1000 (95% CI: 116 · 9–388 · 2) (Table 2). Similarly to DM, the incidence of DR decreased with increasing age (Table 2). Of the 20 incident cases of DR, seven had sight-threatening DR (STDR) of whom two cases were proliferative DR (five with severe retinopathy), four cases had moderate DR and nine mild DR (Table 2).

In total 23 participants with known DR at baseline were followed up and had a gradable retinal image. Of these, 15 still had signs of DR, while eight no longer had evidence of DR. Of nine with background DR at baseline, one progressed to pre-proliferative DR and the remainder either remained BDR (n = 2) or had no signs of DR at follow-up (n = 6). Of seven participants with moderate non-proliferative DR (NPDR) at baseline, three progressed to proliferative DR (PDR). One participant with severe NPDR at baseline developed PDR and one remained Severe NPDR. Of five with PDR at baseline, one regressed to Moderate NPDR (having undergone pan-retinal photocoagulation) and the other four remained PDR, of whom two had evidence of laser treatment.

Multivariable analysis of incident DR (Table 6) was not conducted due to the small number of participants in the category (n = 20). However, the age-adjusted risk ratio suggested a correlation between increasing incidence of DR and higher BMI, urban dwelling and higher socioeconomic status. No conclusions can be drawn from this due to the wide 95% confidence intervals.

Table 6
Age-adjusted analysis the association between a number of baseline co-variables and incident DR amongst those DR free at baseline in the Nakuru eye disease cohort study

Discussion

This population-based cohort study of people aged 50+ in rural Kenya is the first, to our knowledge, to assess the incidence of DM and DR in SSA. The six-year cumulative incidence of DM in this study was 61 cases per 1000, equating to approximately 10 new cases per 1000 of population aged ≥50 per year. Longo-Mbenza et al. investigated the incidence of type 2 DM in a prospective cohort of 807 subjects of Central Africans aged ≥40 years over a four-year period, all of whom had no DM at basline [2]. During the follow up, there were 93 incident DM cases (11 · 5%), corresponding to an incidence of 29 (95% CI 15-43) per 1000 persons per year, considerably higher than our estimated cumulative incidence. Motola et al. investigated the incidence of DM in a prospective cohort of 563 South African Indians with no-DM aged 15 years or greater over a ten-year period. During the follow up period there were 91 (16.2%) incident cases of DM, corresponding to an incidence (age and sex-adjusted) cumulative incidence of 8.3 per 1000 persons per year [21]. This latter estimate was more in line with ours, but included a much younger population.

The six-year cumulative incidence of DR among persons, 50 years and over, with known DM was 225 cases per 1000 (95%CI: 116 · 9388 · 2). There is minimal comparable data available for SSA. One systematic review of 62 studies that reported the prevalence or incidence of DR in SSA [6] found few high-quality population-based studies and the majority were hospital or clinic based surveys. Two cohort studies of DR have been conducted in SSA. Sixty-four patients with insulin-dependent (Type 1) DM (IDDM) in Soweto, South Africa were followed over a 10-year period between 1982 and 1992. In those subjects seen at 10 years, prevalence of DR had increased from 6 to 52% and PDR from 0 to 3%, but no incidence data was reported [22]. In a two-year prospective cohort study of DR in Malawi, 357 subjects were systematically sampled from two primary care diabetes clinics, and 295 participants were followed up. The incidence of any DR over the follow-up period was 380 per 1000 of population over two years [23]. Two of the leading cohort studies of eye disease from high-income settings, the Blue Mountains Study in Australia and The Wisconsin Epidemiologic Study of Diabetic Retinopathy (WESDR) in the United States in which comparable methodology was used show estimates of incident DR from Nakuru, Kenya are more than twice that of the findings from Wisconsin and three times that of the Blue Mountains Study. The Blue Mountains Study reported 222 cases per 1000 over five years (44 per 1000/year) and the WESDR study reported 327 cases per 1000 over a four-year period (82 per 1000/year).

In a prospective cohort in southern Malawi, sampled from two primary care diabetes clinics, the 2-year incidence of sight-threatening DR (STDR) amongst 357 subjects for subjects with no DR, BDR, and PDR at baseline was 2 · 7% (95% confidence interval [CI], 0 · 1–5 · 3), 27 · 3% (95% CI, 16 · 4–38 · 2), and 25 · 0% (95% CI, 0–67 · 4), respectively [23].

The sample of participants with DR at both study time points in the Nakuru cohort was too small to draw conclusions on the progression of DR. However, 23 participants over the six year follow up period had a DR assessment at baseline and follow-up, of whom four progressed from non-STDR to STDR and of five with STDR at baseline, one recovered to non-STDR and the other four remained with STDR [23].

Strengths

This study is one of the first reports of DM and DR from a population-based sample in SSA. The sampling methodology ensures that the data is representative for the population over 50 and minimised bias by sampling from the community rather than from hospitals or clinics. Retinal image data were collected for DR analysis and images were independently graded at Moorfields Eye Hospital Reading Centre.

Limitations

The definition of DM used in this study was based on a single, non-fasting, capillary blood sample and did not include fasting blood glucose samples and HbA1C measures were only available at follow-up. There was a high loss to follow-up which creates potential for selection bias however statistical methods were used to adjust for this. This high LTFU was largely due to post-election violence in the region between the two study time points which led to mass displacement. The population under observation were ≥50 years and therefore the study does not estimate the incidence of DM or DR in the population under age 50 years.

Implications

As the diabetes epidemic continues, a greater understanding is required of the resources needed and level of deployment of those resources within the health system to respond appropriately. This includes primary prevention of DM in the community, high treatment coverage of persons with DM in primary care, and inclusion of eye screening for people with DM as standard practice. With good prevalence data on DM available in many countries and regions in SSA and a growing understanding of the natural history of the diseases in different populations it should now be possible (within a wide range of confidence and based on several assumptions) to estimate the conversion in the over 50s of those without DM developing DM and DR.

Overall, DM is increasing in Africa probably related to environmental factors such as increased access to processed foods and more sedentary lifestyles; this is likely to increase in the next decade. The awareness of DM in the community is still low [3] and public campaigns to raise awareness as well as provide locally available DM screening and counselling facilities is needed. It is also important to consider detection of VTDR in the community and resourcing eye care providers with the knowledge and tools to manage patients with STDR is essential to ensure a high quality service and avoid sight loss from DM. Specific planning data for the region under investigation is provided in Table 7.

Table 7
Population summary for programme planning based on prevalence and incidence data from a Kenyan cohort over 50 years of age

Conclusions

In a population of 1 · 6 Million in Nakuru County, Kenya: 150,000 are 50 years and over, we estimated that 1650 people over the age of 50 develop DM per year, and 450 develop DR. The management of DM and DR is complex and requires different approaches at different levels of the healthcare system with considerable variation depending on location. For effective planning at any level, high quality information is required to effectively plan the services. This cohort provides some data to support planning and is indicative of areas that need further research.

Acknowledgements

Nil.

Funding

Medical Research Council [G1001934], Fight for Sight [1310], British Council for the Prevention of Blindness, International Glaucoma Association. MJB is supported by the Wellcome Trust (Grant Number 098481/Z/12/Z). HAW is supported by the MRC and DFID (Grant Number G0700837). TP was supported by NIHR BMRC at Moorfields Eye Hospital and UCL Institute of Ophthalmology.

Availability of data and materials

The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.

Authors’ contributions

AB Study design, Data collection, Analysis, wrote manuscript, reviewed/edit manuscript. WM Study design, Data collection, Analysis, reviewed/edit manuscript. KW Analysis, reviewed/edit manuscript. MB Study design, Data collection, Analysis, reviewed/edit manuscript. HR Data collection, reviewed/edit manuscript. HAW Study design, Analysis, reviewed/edit manuscript. DM Analysis, wrote manuscript, reviewed/edit manuscript. AF Study design, Analysis, reviewed/edit manuscript. TP Study design, Data collection, Analysis, reviewed/edit manuscript. PB Data collection, reviewed/edit manuscript. MB Study design, Data collection, Analysis, wrote manuscript, reviewed/edit manuscript. HK Study design, Data collection, Analysis, wrote manuscript, reviewed/edit manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

N/A.

Ethics approval and consent to participate

The London School of Hygiene & Tropical Medicine (LSHTM) Ethics committee and the African Medical Research Foundation (AMREF) granted ethical approval for the study. Approval was also granted by the Provincial Medical Officer for Nakuru County. Written approval was sought from the administrative heads in each cluster, usually the village chief. All participants gave written or thumbprint consent to participate. People requiring medical treatments were referred to the appropriate centre.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Abbreviations

BDR
Background diabetic retinopathy
DM
Diabetes mellitus
DR
Diabetic retinopathy
LTFU
Lost to follow up
NPDR
Non-proliferative diabetic retinopathy
PDR
Proliferative diabetic retinopathy
SSA
Sub Saharan Africa
VI
Visual impairment
VTDR
Vision threatening diabetic retinopathy

Contributor Information

Andrew Bastawrous, Phone: +44 (0)20 7958 8257, ku.ca.mthsl@suorwatsab.werdna.

Wanjiku Mathenge, moc.liame@ukic.

Kevin Wing, ku.ca.mthsl@gniw.nivek.

Madeleine Bastawrous, moc.liamg@suorwatsab.enieledam.

Hillary Rono, ku.ca.mthsl@onor.yrallih.

Helen A. Weiss, ku.ca.mthsl@ssiew.neleh.

David Macleod, ku.ca.mthsl@doelcam.divad.

Allen Foster, ku.ca.mthsl@retsof.nella.

Tunde Peto, ku.ca.buq@oteP.T.

Peter Blows, ku.shn.sdleifroom@swolB.reteP.

Matthew Burton, ku.ca.mthsl@notrub.wehttam.

Hannah Kuper, ku.ca.mthsl@repuk.hannah.

References

1. Shaw JE, Sicree RA, Zimmet PZ. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pract. 2010;87(1):4–14. doi: 10.1016/j.diabres.2009.10.007. [PubMed] [Cross Ref]
2. Longo-Mbenza B, On’kin JB, Okwe AN, Kabangu NK, Fuele SM. Metabolic syndrome, aging, physical inactivity, and incidence of type 2 diabetes in general African population. Diab Vasc Dis Res. 2010;7(1):28–39. doi: 10.1177/1479164109346362. [PubMed] [Cross Ref]
3. Hall V, Thomsen RW, Henriksen O, Lohse N. Diabetes in Sub Saharan Africa 1999–2011: epidemiology and public health implications. A systematic review. BMC Public Health. 2011;11:564. doi: 10.1186/1471-2458-11-564. [PMC free article] [PubMed] [Cross Ref]
4. Bourne RR, Stevens GA, White RA, Smith JL, Flaxman SR, Price H, Jonas JB, Keeffe J, Leasher J, Naidoo K, et al. Causes of vision loss worldwide, 1990–2010: a systematic analysis. Lancet Glob Health. 2013;1(6):e339–49. doi: 10.1016/S2214-109X(13)70113-X. [PubMed] [Cross Ref]
5. Naidoo K, Gichuhi S, Basanez MG, Flaxman SR, Jonas JB, Keeffe J, Leasher JL, Pesudovs K, Price H, Smith JL, et al. Prevalence and causes of vision loss in sub-Saharan Africa: 1990–2010. Br J Ophthalmol. 2014;98(5):612–8. doi: 10.1136/bjophthalmol-2013-304081. [PubMed] [Cross Ref]
6. Burgess PI, MacCormick IJ, Harding SP, Bastawrous A, Beare NA, Garner P. Epidemiology of diabetic retinopathy and maculopathy in Africa: a systematic review. Diabet Med. 2013;30(4):399–412. doi: 10.1111/j.1464-5491.2012.03756.x. [PMC free article] [PubMed] [Cross Ref]
7. Mbanya JC, Motala AA, Sobngwi E, Assah FK, Enoru ST. Diabetes in sub-Saharan Africa. Lancet. 2010;375(9733):2254–66. doi: 10.1016/S0140-6736(10)60550-8. [PubMed] [Cross Ref]
8. Atun R, Gale EA. The challenge of diabetes in sub-Saharan Africa. Lancet Diabetes Endocrinol. 2015;3(9):675–7. doi: 10.1016/S2213-8587(15)00236-3. [PubMed] [Cross Ref]
9. Poore S, Foster A, Zondervan M, Blanchet K. Planning and developing services for diabetic retinopathy in Sub-Saharan Africa. Int J Health Policy Manag. 2015;4(1):19–28. doi: 10.15171/ijhpm.2015.04. [PMC free article] [PubMed] [Cross Ref]
10. Mathenge W, Bastawrous A, Foster A, Kuper H. The Nakuru posterior segment eye disease study: methods and prevalence of blindness and visual impairment in Nakuru, Kenya. Ophthalmology. 2012;119(10):2033-9. doi:10.1016/j.ophtha.2012.04.019. [PubMed]
11. Bastawrous A, Mathenge W, Peto T, Weiss HA, Rono H, Foster A, Burton M, Kuper H. The Nakuru eye disease cohort study: methodology & rationale. BMC Ophthalmol. 2014;14:60. doi: 10.1186/1471-2415-14-60. [PMC free article] [PubMed] [Cross Ref]
12. Mathenge W, Bastawrous A, Peto T, Leung I, Yorston D, Foster A, Kuper H. Prevalence and correlates of diabetic retinopathy in a population-based survey of older people in Nakuru, Kenya. Ophthalmic Epidemiol. 2014;21(3):169–77. doi: 10.3109/09286586.2014.903982. [PubMed] [Cross Ref]
13. Turner AG, Magnani RJ, Shuaib M. A not quite as quick but much cleaner alternative to the Expanded Programme on Immunization (EPI) Cluster Survey design. Int J Epidemiol. 1996;25(1):198–203. doi: 10.1093/ije/25.1.198. [PubMed] [Cross Ref]
14. Mathenge W, Bastawrous A, Foster A, Kuper H. The Nakuru posterior segment eye disease study: methods and prevalence of blindness and visual impairment in Nakuru, Kenya. Ophthalmology. 2012;119(10):2033–9. doi: 10.1016/j.ophtha.2012.04.019. [PubMed] [Cross Ref]
15. Rosser DA, Laidlaw DA, Murdoch IE. The development of a “reduced logMAR” visual acuity chart for use in routine clinical practice. Br J Ophthalmol. 2001;85(4):432–6. doi: 10.1136/bjo.85.4.432. [PMC free article] [PubMed] [Cross Ref]
16. Taylor D. Diabetic eye screening revised grading definitions. In: To provide guidance on revised grading definitions for the NHS diabetic eye screening programme. Sandwell and West Birmingham Hospitals NHS Trust: NHS; 2012. p. 22.
17. Organization WH . Diabetes mellitus. Report of a WHO study group technical report series 727. Geneva: World Health Organization; 1985. [PubMed]
18. Kuper H, Polack S, Eusebio C, Mathenge W, Wadud Z, Foster A. A case-control study to assess the relationship between poverty and visual impairment from cataract in Kenya, the Philippines, and Bangladesh. PLoS Med. 2008;5(12):e244. doi: 10.1371/journal.pmed.0050244. [PubMed] [Cross Ref]
19. Office DS. Nakuru demographic data. In: Office DS, editor. Nakuru: Districts Statistics Office; 2001.
20. Seaman SR, White IR. Review of inverse probability weighting for dealing with missing data. Stat Methods Med Res. 2013;22(3):278–95. doi: 10.1177/0962280210395740. [PubMed] [Cross Ref]
21. Motala AA, Pirie FJ, Gouws E, Amod A, Omar MA. High incidence of Type 2 diabetes mellitus in South African Indians: a 10-year follow-up study. Diabet Med. 2003;20(1):23–30. doi: 10.1046/j.1464-5491.2003.00782.x. [PubMed] [Cross Ref]
22. Gill GV, Huddle KR, Rolfe M. Mortality and outcome of insulin-dependent diabetes in Soweto, South Africa. Diabet Med. 1995;12(6):546–50. doi: 10.1111/j.1464-5491.1995.tb00539.x. [PubMed] [Cross Ref]
23. Bastawrous A, Burgess PI, Mahdi AM, Kyari F, Burton MJ, Kuper H. First prospective cohort study of diabetic retinopathy from Sub-Saharan Africa: high incidence and progression of retinopathy and relationship to human immunodeficiency virus infection. Trop Med Int Health. 2014;19(5):600-9. doi:10.1111/tmi.12276. Review.

Articles from BMC Endocrine Disorders are provided here courtesy of BioMed Central