the prevalence of diabetes complications and associated risk factors in pacific islands countries
TRANSCRIPT
The prevalence of diabetes complications andassociated risk factors in Pacific Islands countries
Si Thu Win Tin a,*, Geoffrey Kenilorea b, Eva Gadabu c, John Tasserei d,Ruth Colagiuri e
aHealth and Sustainability Unit, The Boden Institute of Obesity, Nutrition, Exercise & Eating Disorders, G82 Medical
Foundation Building K25, The University of Sydney, NSW 2006, AustraliabNon Communicable Diseases Unit, Ministry of Health and Medical Services, The Solomon IslandscPublic Health Centre, Ministry of Health and Medical Services, Republic of NaurudHealth Promotion Unit, Public Health Department, VanuatueHealth and Sustainability Unit, Menzies Centre for Health Policy, Victor Coppleson Building DO2, The University of
Sydney, NSW 2006, Australia
d i a b e t e s r e s e a r c h a n d c l i n i c a l p r a c t i c e 1 0 3 ( 2 0 1 4 ) 1 1 4 – 1 1 8
a r t i c l e i n f o
Article history:
Received 5 July 2013
Accepted 12 September 2013
Available online 9 November 2013
Keywords:
Type 2 diabetes
Complications
Risk factors
Pacific Island countries (PICs)
Diabetes care
a b s t r a c t
Aim: To determine the prevalence of diabetes complications and associated risk factors
among people with type 2 diabetes in three Pacific Island countries, Nauru, Solomon Islands
and Vanuatu.
Methods: This cross-sectional study was carried out on a sample of 459 people with diabetes.
Subjects were screened for complications using a standardised protocol which gathered
information on demographics, physical and biochemical parameters.
Results: Of the 459 subjects, 47% were female, mean age was 54 years and mean duration of
diabetes was eight years. The prevalence of diabetes complications was significantly higher
in Nauru compared with the Solomon Islands and Vanuatu – microalbuminuria 71%, 36%
and 51% respectively (P < 0.001), retinopathy 69%, 40% and 42% respectively (P < 0.001), and
abnormal foot sensation 30%, 23% and 19% respectively (P = 0.036). The prevalences of
hypertension, overweight/obesity and poor glycaemic control were high. The percentages of
subjects achieving recommended clinical targets were low. Microalbuminuria was signifi-
cantly associated with duration of diabetes, hypertension and glycaemic control. Diabetic
retinopathy was significantly associated with duration of diabetes whereas abnormal foot
sensation was significantly associated with duration of diabetes and glycaemic control.
Conclusions: This study found a high prevalence of diabetes complications and associated
risk factors, which indicate the need to improve diabetes care and strengthen preventive
efforts to reduce complications.
# 2013 Elsevier Ireland Ltd. All rights reserved.
Contents available at ScienceDirect
Diabetes Researchand Clinical Practice
journal homepage: www.elsevier .com/locate/diabres
1. Introduction
The magnitude of the global health burden of diabetes [1,2]
and its negative implications for human development and
* Corresponding author. Tel.: +61 424993595; fax: +61 290363176.E-mail addresses: [email protected], [email protected]
[email protected] (E. Gadabu), [email protected] (J. Tasse
0168-8227/$ – see front matter # 2013 Elsevier Ireland Ltd. All rights
http://dx.doi.org/10.1016/j.diabres.2013.09.017
achievement of global development goals [3,4] is well docu-
mented. The vast majority of this burden is due to compli-
cations of diabetes and accounts for substantial costs [5,6].
Many studies from a range of countries have reported the
prevalence of complications and related risk factors among
m (S.T. Win Tin), [email protected] (G. Kenilorea),rei), [email protected] (R. Colagiuri).
reserved.
d i a b e t e s r e s e a r c h a n d c l i n i c a l p r a c t i c e 1 0 3 ( 2 0 1 4 ) 1 1 4 – 1 1 8 115
people with diabetes. Diabetes complications can be pre-
vented through proven cost effective interventions [7,8].
Multi-risk factor interventions which include lifestyle changes
and pharmacological therapy have been shown to reduce the
risk of diabetes complications by up to 50% [9,10].
The risk of microvascular complications is reduced by
intensive glycaemic control [11] and tight blood pressure
control [12]. Regular risk factor assessment in the primary care
setting minimises hospitalisation due to diabetes complica-
tions [13], and improvements in systems of diabetes care,
screening and treatment programmes for diabetes improve
diabetes clinical outcomes [14,15].
Pacific Island countries (PICs) have a limited capacity to
deliver effective diabetes prevention and care [16,17] and the
proportion of people with diabetes who practice self care is
low [18]. Despite anecdotal reports of high rates of diabetes
complications in PICs, a formal literature search yielded no
recent peer-reviewed literature on the prevalence of diabetes
complications in these countries. Consequently, as part of a
larger capacity building project, we aimed to (i) determine the
prevalence of diabetes complications and associated risk
factors in people with diabetes in three PICs: Nauru, the
Solomon Islands and Vanuatu, and (ii) assess the control of
risk factors against recommended clinical targets.
2. Subjects, materials and methods
This cross-sectional study was carried out on a convenience
sample of 459 people with known diabetes (100 from Nauru,
160 from the Solomon Islands, and 199 from Vanuatu) to
determine the prevalence of diabetes complications and
associated risk factors. Subjects attending the diabetes clinics
in each country during a one week period, which co-incided
with a visit by an Australian diabetes team, were screened
using a standardised protocol. Data were collected on age,
gender, age at diagnosis, duration of diabetes and diabetes
treatment. Physical assessment included measurement of
weight and height and calculation of BMI with overweight
defined as a BMI � 25 and obese as a BMI � 30. The Omron
digital automatic blood pressure monitor was used to measure
resting blood pressure. Blood pressure was measured three
times and mean was used in the analysis. Hypertension was
defined as a systolic blood pressure �140 mmHg and/or
diastolic blood pressure �90 mmHg or taking blood pressure
lowering medications. Visual acuity was assessed and fundus
examination through dilated pupils was performed by an
experienced optometrist. Foot sensation was assessed using a
10 g monofilament by trained foot care nurses and loss of the
ability to detect this pressure (abnormal foot sensation) at one
or more anatomic sites on the plantar surface of the foot was
defined as neuropathy. Biochemical assessment included
measurement of HbA1c using a DCA Analyser; urinary
albumin/creatinine ratio (ACR) using a DCA Analyser and
microalbuminuria was defined as an ACR > 2.5 mg/mmol for
men or >3.5 mg/mmol for women; blood lipids (total choles-
terol, HDL cholesterol, LDL cholesterol and triglycerides) were
measured by Cholestech LDX analyser.
The clinical targets agreed for the overarching diabetes
project in the three PICs and specifically for this study were:
(i) HbA1c <7.0% (53 mmol/mol)
(ii) Blood pressure <130/85 mmHg
(iii) Total cholesterol <5.0 mmol/L
HDL cholesterol >1.0 mmol/L
LDL cholesterol <2.5 mmol/L
Triglycerides <2.0 mmol/L
The data were compiled and analysed using IBM SPSS
statistical package version 21. Country data are reported as
means � SEM and percentages, and compared using one way
ANOVA test and logistic regression model adjusted for age, sex
and duration of diabetes. Associations between diabetes
related complications and risk factors for complications were
assessed using logistic regression model adjusted for country.
Statistical significance was defined as P < 0.05.
This research was approved by the Human Research Ethics
Committee, the University of Sydney and the Research Ethics
Committees of the Nauru, Solomon Islands and Vanuatu.
3. Results
Table 1 shows the demographic details of the 459 people
(mean age 54 years, mean age at diagnosis 46 years, and mean
duration of diabetes eight years) screened for complications
and associated risk factors by country. Overall there were 244
(53%) males (mean age 53.9 years) and 215 (47%) females (mean
age 54.1 years). Subjects in Nauru were younger than those in
the Solomon Islands and Vanuatu but had the longest duration
of diabetes. The percentage treated with diet alone in Nauru,
Solomon Islands and Vanuatu was 41%, 13% and 11%
respectively, oral anti-diabetic agents 49%, 82% and 83%
respectively, and insulin 10%, 5% and 6% respectively.
Risk factors for diabetes complications were common but
the risk factor profile differed between the PICs. Nauru had the
highest mean BMI, HbA1c, ACR and LDL cholesterol while
Vanuatu had the highest mean blood pressure and triglycer-
ides. The percentage of people in Nauru, Solomon Islands and
Vanuatu achieving targets were 50%, 31% and 15% respectively
for blood pressure, 20%, 17% and 28% respectively for HbA1c,
47%, 55% and 49% respectively for total cholesterol, 29%, 29%,
and 11% respectively for HDL cholesterol, 16%, 24% and 42%
respectively for LDL cholesterol, and 54%, 50%, 45% respec-
tively for triglycerides.
Diabetes complications were common and the prevalence
also varied in the three PICs. The prevalence of microalbu-
minuria in Nauru, Solomon Island and Vanuatu was 71%, 36%
and 51% respectively, retinopathy 69%, 40% and 42% respec-
tively, and abnormal foot sensation 30%, 23% and 19%
respectively (Table 2).
The association between diabetes complications and risk
factors for complications was assessed using logistic regres-
sion models. Microalbuminuria was significantly associated
with longer duration of diabetes, hypertension and poorer
glycaemic control, abnormal foot sensation with longer
duration of diabetes and poor glycaemic control and diabetic
retinopathy with longer duration of diabetes. Although higher
rates of retinopathy were found in people with poor glycaemic
control and hypertension, the association was not statistically
significant.
Table 1 – Demographic details and risk factors for diabetes complications in the three Pacific Island countries.
Nauru (n = 100) Solomon Islands (n = 160) Vanuatu (n = 199) P value
Age (years)a 51.2 � 1.3 54.2 � 0.8 55.5 � 0.1 0.006
Genderb 0.340*
Male 41% 57% 42%
Female 59% 43% 58%
Age at diagnosis (years)c 39.5 � 1.3 44.9 � 0.8 50.2 � 0.6 <0.001
Duration of diabetes (years)d 11.8 � 0.9 9.2 � 0.7 5.2 � 0.4 <0.001
Diabetes treatmente <0.001*
Diet alone 41% 13% 11%
Oral anti-diabetic agents 49% 82% 83%
Insulin 10% 5% 6%
BMI (kg/m2) 31.1 � 0.6 28.6 � 0.4 28.8 � 0.4 <0.001
Overweight 90% 79% 78% 0.040*
Obese 53% 33% 38% 0.004*
Blood Pressure (mmHg) 127/74 141/81 151/85 <0.001
Hypertension 42% 55% 72% <0.001*
<130/85 mmHg 50% 31% 15% <0.001*
HbA1c (%) 10.0 � 0.3 9.5 � 0.2 8.0 � 0.1 <0.001
HbA1c (mmol/mol) 86 80 64
Glycemic control <0.001*
HbA1c <7.0 (<53 mmol/mol) 20% 17% 28%
HbA1c 7–7.9 (53–63 mmol/mol) 14% 11% 26%
HbA1c 8–8.9 (64–74 mmol/mol) 6% 20% 20%
HbA1c 9–9.9 (75–85 mmol/mol) 12% 11% 11%
HbA1c �10 (�86 mmol/mol) 48% 41% 15%
ACR (mg/mmol) 23.7 � 2.9 7.9 � 0.7 10.3 � 1.2 <0.001
Total cholesterol (mmol/L) 5.0 � 0.1 4.9 � 0.1 5.0 � 0.1 0.520
Total cholesterol <5.0 mmol/L 47% 55% 49% 0.783*
HDL cholesterol (mmol/L) 0.8 � 0.1 0.9 � 0.1 0.8 � 0.1 0.060
HDL >1.0 mmol/L 29% 29% 11% <0.001*
LDL cholesterol (mmol/L) 3.3 � 0.1 3.1 � 0.1 2.7 � 0.1 <0.001
LDL <2.5 mmol/L 16% 24% 42% 0.001*
Triglycerides (mmol/L) 2.0 � 0.1 2.0 � 0.1 2.8 � 0.1 <0.001
Triglycerides <2.0 mmol/L 54% 50% 45% 0.021*
Data are shown as mean � SEM or percentage. P values are derived from one way ANOVA test.a Overall mean = 54 years.b Overall male = 53%, female = 47%.c Overall mean = 46 years.d Overall mean = 8 years.e Overall diet alone = 18%, oral anti-diabetic agents = 76%, insulin = 6%.* P values are derived from logistic regression model adjusted for age, sex and duration of diabetes.
d i a b e t e s r e s e a r c h a n d c l i n i c a l p r a c t i c e 1 0 3 ( 2 0 1 4 ) 1 1 4 – 1 1 8116
4. Discussion
This study found a high prevalence of diabetes complications
and associated risk factors among people with diabetes, and a
low rate of subjects achieving standardised clinical targets in
all three PICs.
The prevalence of microalbuminuria, an indicator of future
nephropathy, found in this study was 71%, 36% and 51% in
Nauru, Solomon Islands and Vanuatu respectively which
overall was higher than in previous studies in PICs (23.4% in
Samoa [19], 33.3% in Pacific Islanders in South Auckland [20]
and 42.1% in Nauru [21]). These rates are also higher than in
western countries (24.9% in the UK [22] and 17.2% in the
Netherlands [23]). The prevalence of diabetic retinopathy was
also high. The highest rates were observed in Nauru (69%)
which are higher than previously reported in other PICs [19,24–
26] and western countries [23]. Similarly neuropathy and foot
problems were common, with Nauru again having the highest
prevalence of neuropathy (30%). These complications could
potentially be reduced or prevented with improved quality of
diabetes care in people with diabetes in PICs.
In this study microalbuminuria was significantly associat-
ed with duration of diabetes, hypertension and glycaemic
control, diabetic retinopathy with duration of diabetes, and
abnormal foot sensation with duration of diabetes and
glycaemic control. These findings are consistent with previous
studies [19,27]. Subjects in Nauru had longer duration of
diabetes and poorer glycaemic control and this finding may
explain why the Nauruan subjects had the highest prevalence
of diabetes complications. These factors together with the
highest prevalence of overweight/obesity in Nauru may
Table 2 – Prevalence of diabetes complications in the three Pacific Island countries.
Nauru N (%)(n = 100)
Solomon Islands N(%) (n = 160)
Vanuatu N (%)(n = 199)
P value
Microalbuminuria 71 (71%) 58 (36%) 102 (51%) <0.001
Diabetic retinopathy 69 (69%) 64 (40%) 83 (42%) <0.001
Abnormal foot sensation 30 (30%) 36 (23%) 38 (19%) 0.036
Abnormal digital foot pulse 24 (24%) 28 (18%) 3 (1.5%) <0.001
Foot ulcer 8 (8%) 13 (8%) 10 (5%) 0.870
Diabetes-related amputation 11 (11%) 17 (11%) 21 (11%) 0.520
P values are derived from logistic regression model adjusted for age, sex and duration of diabetes.
d i a b e t e s r e s e a r c h a n d c l i n i c a l p r a c t i c e 1 0 3 ( 2 0 1 4 ) 1 1 4 – 1 1 8 117
account for it having the highest prevalence of complications
of the three PICs. With regard to glycaemic control, Nauruan
subjects had the highest use of diet alone and the lowest use of
oral anti-diabetic agents. There is no evidence to explain this
and our study did not attempt to explore reasons for
differences in therapy.
Evidence from several studies has shown that diabetes
complications can be reduced by multi-risk factor interven-
tions [9,10], intensive glycaemic control [11] and tight blood
pressure control [12]. However this study found that the
percentage of subjects achieving the agreed clinical targets
in the three PICs was generally low. The glycaemic target
was achieved in 17–28% of individuals, blood pressure target
in 15–50% and LDL cholesterol target in 16–42%. Conse-
quently, this study confirms the need for better control of
risk factors which can prevent and minimise diabetes
complications.
Although our study has identified several key important
clinical findings, it has certain limitations. Cardiovascular
complications were not included in the analysis because this
information was poorly recorded in medical records and
appropriate diagnostic investigations were not available. The
potential causality of the associations observed between risk
factors and complications are limited by the cross-sectional
nature of this study. Although we used a standardised
protocol for biochemical assessment, methods and equip-
ment for assessing risk factors and complications, the
methods differed from previous studies and may have
impacted on direct comparisons. Notwithstanding these
limitations, our study has certain strengths including
comparable sample size for each country and use of a
standardised protocol to assess physical and biochemical
measures by experienced medical personnel. The findings in
PICs support current theories about complications of diabetes
and their associated risk factors.
In conclusion, this study found a high prevalence of
diabetes complications and associated risk factors in PICs,
and a low percentage of subjects achieving agreed standar-
dised clinical targets. This indicates the need to improve the
quality and accessibility of diabetes care and strengthen
preventive efforts to reduce diabetes complications. This will
require system changes to ensure the availability of essential
medicines, diagnostic and monitoring technologies, aware-
ness programmes and patient education services which still
remain a challenge in PICs. Further research is needed on
models and systems for reducing the diabetes burden in these
small developing Pacific nations.
Conflict of interest
None known or perceived.
Acknowledgements
The World Diabetes Foundation funded the overarching
diabetes capacity building projects in Nauru, Vanuatu and
the Solomon Islands under which this study was under-
taken. These projects were conducted in partnership with
the Ministries of Health of the Solomon Islands, Nauru
and Vanuatu, the International Centre for Eyecare Educa-
tion at the University of New South Wales, the Australia
and New Zealand Society of Nephrologists. Additional
support was provided by University of Sydney’s Medical
School Foundation.
r e f e r e n c e s
[1] Whiting DR, Guariguata L, Weil C, Shaw J. IDF diabetesatlas, global estimates of the prevalence of diabetes for2011 and 2030. Diabetes Res and Clin Pract 2011;94:311–21.
[2] Abegunde DO, Mathers CD, Adam T, Ortegon M, Strong K.The burden and costs of chronic diseases in low-incomeand middle-income countries. Lancet 2007;370:1929–37.
[3] International Diabetes Federation. A call to action ondiabetes. IDF Brussels; 2010, http://www.idf.org/webdata/Call-to-Action-on-Diabetes.pdf (retrieved 12.01.13).
[4] International Diabetes Federation. Global diabetes plan2011–2021. IDF Brussels; 2011, http://www.idf.org/sites/default/files/Global_Diabetes_Plan_Final.pdf (retrieved15.05.13).
[5] Lee CM, Colagiuri R, Magliano DJ, Cameron AJ, Shaw J,Zimmet P, et al. The cost of diabetes in adults in Australia.Diabetes Res Clin Pract 2013;99:385–90.
[6] Clarke P, Gray A, Legood R, Briggs A, Holman R. The impactof diabetes-related complications on healthcare costs:results from the United Kingdom prospective diabetesstudy (UKPDS 65). Diabet Med 2003;20:442–50.
[7] Gray A, Raikou M, McGuire A, Fenn P, Stevens R, Cull C,et al. Cost effectiveness of an intensive blood glucosecontrol policy in patients with type 2 diabetes: economicanalysis alongside randomised controlled trial (UKPDS 41).Br Med J 2000;320:1373–7.
[8] Raikou M, Gray A, Briggs A, Stevens R, Cull C, McGuire A,et al., UK prospective study group. Cost effectivenessanalysis of improved blood pressure control in
d i a b e t e s r e s e a r c h a n d c l i n i c a l p r a c t i c e 1 0 3 ( 2 0 1 4 ) 1 1 4 – 1 1 8118
hypertensive patients with type 2 diabetes (UKPDS 40). BrMed J 1998;17:720–6.
[9] Gaede P, Vedel P, Larsen N, Jensen GVH, Parving H,Pedersen O. Multifactorial intervention and cardiovasculardisease in patients with type 2 diabetes. N Engl J Med2003;348(5):383–93.
[10] Gæde P, Lund-Andersen H, Parving H-H, Pedersen O. Effectof a multifactorial intervention on mortality in type 2diabetes. N Engl J Med 2008;358:580–91.
[11] Patel A, MacMahon S, Chalmers J, Neal B, Billot L,Woodward M, et al., the ADVANCE Collaborative Group.Intensive blood glucose and vascular outcomes in patientswith type 2 diabetes. N Engl J Med 2008;358:2560–72.
[12] Tunner R, Holman R, Stratton I, Cull C, Frighi V, Manley S,et al., UK prospective diabetes study group. Tight bloodpressure control and risk of macrovascular andmicrovascular complications in type 2 diabetes (UKPDS 38).Br Med J 1998;317:703–13.
[13] Tomlin AM, Dovey SM, Tilyard MW. Risk factors forhospitalization due to diabetes complications. Diabetes ResClin Pract 2008;80:244–52.
[14] Bailie R, Si D, Dowden M, Donoghue L, Connors C, RobinsonG. Improving organizational systems for diabetes care inAustralian indigenous communities. BioMed Central2007;7:67. From http://www.biomedcentral.com/1472-6963/7/67 [retrieved 15.05.13].
[15] Lavery LA, Wunderlich R, Tredwell J. Disease managementfor the diabetic foot: Effectiveness of a diabetic footprevention program to reduce amputations andhospitalizations. Diabetes Res Clin Pract 2005;70:31–7.
[16] Colagiuri R. Building capacity to reduce diabetescomplications in the Pacific: the Vanuatu experience so far.Pract Diab Int 2006;23:343–6.
[17] Win Tin ST, Gadabu E, Iro G, Tasserei J, Colagiuri R.Diabetes related amputation in Pacific Islands countries: aroot cause analysis of precipitating events. Diabetes ResClin Pract 2013;100:230–4.
[18] Sugruitan G, McDuffie KY, Valdez R, Beckles G, Glover D,Benjamin S. Diabetes-related preventive-care practice –Guam, 2001–2003. Morb Mortal Wkly Rep 2005;54(13):333–5.
[19] Collins VR, Dowse GK, Plehwe WE, Imo TT, Toelupe PM,Taylor HR, et al. High prevalence of diabetic retinopathyand nephropathy in Polynesians of Western Samoa.Diabetes Care 1995;18:1140–9.
[20] Simmons D, Shaw LM, Scott DJ, Kenealy T, Scragg RK.Diabetic nephropathy and microalbuminuria in thecommunity, the South Auckland diabetes survey. DiabetesCare 1994;17:1404–14010.
[21] Collins VR, Dowse GK, Finch CF, Zimmet PZ, Linnane AW.Prevalence and risk factors for micro- and macro-albuminuria in diabetic subjects and entire population ofNauru. Diabetes 1989;38:1602–10.
[22] Adler AI, Stevens RJ, Manley SS, Bilous RW, Cull CA,Holman RR, et al. Development and progression ofnephropathy in type 2 diabetes: the United Kingdomprospective diabetes study (UKPDS 64). Kidney Int2003;63:225–32.
[23] Spijkerman AMW, Dekker JM, Nijpels G, Adriaanse MC,Kostense PJ, Ruwaard D, et al. Microvascular complicationsat time of diagnosis of type 2 are similar among diabeticpatients detected by targeted screening and patients newlydiagnosed in general practice. Diabetes Care 2003;26:2604–8.
[24] King H, Balkau B, Zimmet P, Taylor R, Raper LR, Borger J,et al. Diabetic reinopathy in Nauruans. Am J Epidemiol1983;117:659–67.
[25] Brooks B, Chong R, Ho I, Capstick F, Molyneaux L, Oo TT,et al. Diabetic retinopathy and nephropathy in Fiji:comparison with data from an Australian diabetes centre.Aust N Z J Ophthalmol 1999;27:9–13.
[26] Smith TST, Szetu J, Bourne RRA. The prevalence andseverity of diabetic retinopathy, associated risk factorsand vision loss in patients registered with type 2diabetes in Luganville, Vanuatu. Br J Ophthalmol2007;91:415–9.
[27] Stratton IM, Adler AI, Neil HAW, Matthews DR, Manley SE,Cull CA, et al. Association of glycaemia with macrovascularand microvascular complications of type 2 diabetes (UKPDS35): prospective observational study. Br Med J 2000;321:405–12.