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Assessment of vitamin D and its association with cardiovascular disease risk factors in an adult migrant population: an audit of patient records at a Community Health Centre in Kensington, Melbourne, Australia
BMC Cardiovascular Disorders volume 14, Article number: 157 (2014)
Vitamin D deficiency is a global public health problem associated with increased risk of cardio-metabolic diseases and osteoarthritis. Migrants with dark skin settled in temperate climates are at greater risk of both vitamin D deficiency and cardiovascular diseases. This study aims to identify the risk of vitamin D deficiency and associations with cardiovascular disease in a migrant population in Australia.
An audit was carried out at a Community Health Service in Kensington, Melbourne which, services a large migrant population. Data from the clinical records of all adults who visited the medical centre at least once during the period from 1st January 2010 to 31st December 2012 was extracted. The future (10 year) coronary heart disease risk was estimated using Framingham Risk Score.
The centre has given higher priority to vitamin D testing in migrants, those middle-aged, females and those with diabetes and osteoarthritis. Migrants from countries located in lower latitude regions (Latitude N230 to S230) were 1.48 (95% C.I. 1.32-1.65) times more likely to develop vitamin D deficiency post migration and 0.44 (95% C.I. 0.31-0.62) times less likely to have a >15% 10-year risk of coronary heart disease when compared to their Australian-born counterparts.
Adherence to a high risk strategy for vitamin D testing was observed in the centre. Pre-migration latitude is an important factor for vitamin D deficiency (lower the latitude higher the risk) and in predicting future risk of cardiovascular disease in migrants. These findings suggest that a targeted approach for vitamin D testing, including zone of origin might better identify individuals at higher risk of both vitamin D deficiency and cardiovascular disease.
Vitamin D deficiency (VDD) has been classified as a pandemic affecting more than one billion people across all ages and ethnic groups worldwide . An internationally standardised cut-off for deficiency is still under debate, but it is commonly defined as serum 25-hydroxyvitamin D (25(OH) D) levels less than 50 nmol/L, with levels of 50–75 nmol/L considered as borderline insufficiency [2, 3]. There are few rich sources of vitamin D in food and the main source for humans is the conversion of pro-vitamin D (7-dehydrocholesterol) to pre-vitamin D3 following skin exposure to ultraviolet B (UVB) radiation, which is subsequently converted to vitamin D3 via a heat dependant process . Most people can meet their vitamin D needs through exposure to sunlight , however synthesis of vitamin D varies by colour of the skin (determined by the amount and type of melanin) in addition to the extent of exposure.
Despite the fact that Australia has a relatively sunny climate the prevalence of VDD (mean serum 25(OH) D < 50 nmol/L) has been estimated as 31% (females - 39% males- 22%) and at high as 50% during winter-spring . Prevalence of vitamin D insufficiency (VDI) (mean serum 25(OH) D < 75 nmol/L) was reported to be 73%. Risk factors identified for VDD in Australia are older age, female gender, non-European origin, obesity, physical inactivity and higher level of education. In migrant populations risk factors included darker skin colour, Muslim religion, longer length of stay in Australia, full-covering clothing, decreased daylight exposure, testing vitamin D levels during winter or spring, living in an urban environment, coming from a socio-economically disadvantaged background and being an inpatient or institutionalised [5–7].
Migrants from low- and middle-income countries, particularly from South East Asia, the Middle East and Africa, constitute a significant segment of the Australian population. The latest Australian census showed that 27% of the resident Australian population was born overseas, an increase of 23.1% from 2001 . Studies elucidating the prevalence of VDD among these populations reported values as high as 88%  and an understanding of the burden of disease associated with VDD in these at-risk sub-populations are lacking. Migration from low- and middle-income countries to industrialised countries has been found to be associated with increased risk of many chronic diseases . While changes in lifestyles and acculturation are thought to be significant drivers of chronic disease risk, they do not solely explain the exponential risk of metabolic diseases in these sub-populations. It is possible that VDD plays a role in increasing risk of cardiovascular diseases (CVD).
Darker skin types of the some immigrant populations while offering protection against the intensity of sunlight in their countries of origin become a risk factor for VDD when relocating to countries further from the equator . The origin of migrants could be classified into three zones according to ability, to synthesize adequate vitamin D as identified by Arabi et al. . This has been developed using the country specific vitamin D levels.
● Zone 1 - sufficient Vitamin D production year-round
● (Latitude N23.5° to S23.5°)
● Zone 2 - insufficient Vitamin D production at least one month/year
● (Latitude N23.5° to N48° and > S23.5°)
● Zone 3 - insufficient Vitamin D production most of the months/year
● (Latitude > N48°)
VDD has been long been associated with bone diseases such as rickets, osteomalacia and osteoporosis, but recent studies also suggest a relationship between VDD and cardiovascular risk factors , including hypertension, diabetes, and metabolic syndromes . What pre-migration factors influence vitamin D status and chronic diseases post migration is not clear, however studies suggest that those who have Vitamin D levels less than 37 nmol/L and hypertension have double the risk of developing myocardial infarction, heart failure or stroke compared to those with Vitamin D levels more than 37 nmol/L .
A number of algorithms for estimating cardiovascular risk, however the Framingham risk score (FRS) is a widely accepted method to estimate the risk of coronary heart disease (CHD) . The method of calculation of FRS is given in detail elsewhere . FRS has been used in Australia by the National Vascular Disease Prevention Alliance to assess the absolute CVD risk , and Zomer and colleagues validated FRS to Australian population by using a large countrywide sample .
With a large and ethnically diverse population living in Australia, information on CHD risk factors in migrant sub-groups are limited . Therefore, we hypothesised that:
● Migrants will be more likely to be tested for vitamin D than Australian-born residents
● Migrants from sufficient vitamin D zones prior to migration will be at increased risk of VDD post-migration
● Migrants from sufficient vitamin D zones prior to migration will have reduced risk of CHD than Australian born residents
● VDD will be associated with a higher 10 year cardiovascular risk, and this association will vary by migration status
Setting and data collection
This cross sectional clinical audit was carried out in a Community Medical Centre in Kensington, Melbourne, Australia, which services a large migrant population and has a specific refugee health program. Moonee Valley and Melbourne City were the two main local government areas of this centre, and census data indicate that in those areas the proportion of residents born overseas is 28.8% and 49.4% respectively [21, 22]. Electronic medical records were accessed and the most recent laboratory test results for vitamin D levels, risk factors for CHD, and demographic data, including migrant status, county of origin were collected while maintaining patient anonymity. The blood pressure reading of the last visit to the clinic was used to identify the individuals as hypertensive (>140/90 mmHg).
Inclusion and exclusion criteria
Adults (19–99 years) (both migrants and non-migrants) who visited the medical centre at least once during the period from 1st January 2010 to 31st December 2012 (three years) were included in the study. The information in the last visit was used for those who visited more than once during the specified period. Data cleaning was undertaken and three population samples were drawn at different levels for different purposes. (Figure 1) Sample 1 was used to study the vitamin D testing pattern of the centre, while sample 2 was used to associate the country of origin latitude to the post migration VDD. The association between VDD and the FRS was assessed using the third sample. Steps were taken to eliminate the effect of supplementation on vitamin D test results in sample 2 and 3 (Figure 1).
The correction method (“log (vit D) + [overall mean log (vit D) – mean (log vit D) sampled in same month])” described by Tomson et al.  was used to adjust for seasonal variation of the vitamin D levels in the cohort. Serum vitamin D (25(OH) D) level < 50 nmol/L was considered as deficient. Data was summarised using descriptive statistics. Log binomial regression method was undertaken to test the association between VDD, cardiovascular risk factors, cardiovascular risk score, and the zone of origin of the migrants. Data were analysed using IBM SPSS version 21. The study was approved by the Monash University Ethics Committee (CF12/3788 – 2012001835).
Vitamin D testing pattern of the community medical centre (sample 1)
The total population (of whom 59% were migrants) was used to examine the vitamin D testing pattern of the centre. Data presented in Table 1 suggest that, after controlling for age and gender, the centre has given higher priority in testing vitamin D levels in migrants from zone 1 and 2, those who are middle-aged, females, and those with diabetes, or osteoarthritis.
Association between pre-migration latitude and post-migration VDD (sample 2)
Further analysis using a subset of the cohort (sample 2) was used to examine the associations between pre-migration latitude and VDD, eliminating those using vitamin D supplements. VDD in migrants from three identified pre-migration zones were compared to those born in Australia. As shown in Table 2, migrants from Zone 1 (sufficient Vitamin D production year round) were approximately 1.5 times, and those from Zone 2 (insufficient Vitamin D production at least one month per year) were almost 1.2 times, more likely to be VDD than Australian-born residents after adjusting for age and gender. This suggests that the lower latitude, the higher the prevalence of VDD in migrants relocating to Australia.
Association of zone of origin with cardiovascular risk
Migrants from Zone 1 showed lower smoking rates and higher cholesterol/HDL ratios, but were 0.44 likely to have a >15% risk of developing future (10 year) CHD events when compared to their Australian-born counterparts (Table 3).
Association between VDD and the risk of CHD by migration status
In those for whom 10-year Framingham risk score could be calculated, there was no association between VDD and cardiovascular risk in migrants or non-migrants (Table 4).
This study examined vitamin D testing patterns among a multicultural sample of Australian adults in north-east Melbourne, Australia and examined whether pre-migration latitude was a risk factor for vitamin D deficiency and cardiovascular risk post-migration. Migrants, especially those from Zone 1 and 2, were more likely to be tested for vitamin D than their Australian-born counterparts. However given the criteria set for data extraction by the audit it cannot be determined to what extent the decision to test for vitamin D testing is informed by clinical decisions. It is possible that the preferential vitamin D testing among migrants is simply driven by practitioners’ perceived risk of VDD among migrant populations. Current evidence suggests that the cost of vitamin D testing in Australia has increased from $1.02 million in 2000 to $95.6 million in 2010, representing a 94-fold increase over a 10-year period . Current Australian recommendations  are to test those at increased risk of VDD, such as elderly and those with darker skin. Formal guidelines that govern the timing of testing (diagnosis) and frequency (monitoring) of vitamin D testing and VDD treatment are urgently needed .
In the present study cohort vitamin D testing was also more frequently undertaken in middle-aged people, females and those with chronic disease indicative of a testing pattern adhering to the high risk approach . This finding is supported by previous analysis of data from the national health care provider, Medicare Australia, showing the majority of the vitamin D test had been performed in middle aged adults (30–64 years) and in females .
The findings of this study suggest that those migrating from a zone where sunlight is sufficient to achieve year-round vitamin D production (closer to the equator) are at increased risk of VDD post-migration. Migrants from Zone 1 generally have a darker skin which acts as a barrier for the skin penetration of the UVB rays and may reduce the production of Vitamin D . Our findings are consistent with the literature showing the higher risk of VDD in refugee population who migrated to Australia from countries closer to the equator . For example, studies done among immigrants from Africa to Australia reported a prevalence of VDD as 53% (men 20%, women 74%)  compared to the general population, which was 31% (men 22%, women 39%) .
The present study also found that those migrating from areas with sufficient vitamin D all year to a southern Australian environment had a lower CHD risk than those who born in Australia. A study looking at ischemic heart disease, place of birth and, language, utilizing the Australian national hospital morbidity database, found that migrants were at higher risk for cardiovascular diseases . However, the Australian Institute of Health and Welfare has consistently reported that those who born overseas experienced a lower CHD specific mortality rate compared to those who born in Australia [33–35]. Possible reasons for this could be the mandatory health checks imposed pre-migration by the authorities and/or the genetic factors. Although Australian immigration, health checks do not specifically test for CHD , it does include a general health screening. As a result of this healthier individual get the opportunity to settle, and this effect has been termed the “healthy migrant effect” . However if post-migration, this group are at increased risk of VDD and its long-term sequel, further research is needed to discern what are the key factors driving this increased risk of VDD, which may include cultural, socioeconomic and genetic factors.
The prevalence of CHD in Australia has been reported to be 3.0% (males 4.4%, females 2.3%)  and the mean 10-year Framingham cardiovascular risk to be 6.3% . Observational studies have suggested an association exists between vitamin D status and cardiovascular disease outcomes . A meta-analysis in 2012 found a linear inverse association between vitamin D (ranging from 20–60 nmol/L) and cardiovascular disease. They reported a small but significant increase in risk of 1.03 (95% CI 1.00, 1.06) with vitamin D deficiency . While studies suggest an inverse association between vitamin D and vascular and non-vascular mortality, the causality is still unclear . The present study found no association between VDD and cardiovascular risk as estimated by the Framingham risk score (which is derived from a set of long established risk factors; age, sex, plasma cholesterol, blood pressure, diabetes and smoking status). Weak associations between vitamin D and both plasma cholesterol and blood pressure have been suggested by some [40, 41], but certainly not all [42, 43], studies. Whether the influence of VDD on cardiovascular disease risk might be driven via those traditional risk factors or other factors remains unclear.
Strength and limitations
The retrospective data collection method used in the present study was preferred over the prospective data collection to avoid biasing vitamin D testing pattern of the centre. The cohort size was substantially reduced for examination of cardiovascular risk due to lack of availability of risk factor data for some patients. Cholesterol testing within 3 months of vitamin D testing date was used for analyses. As subcutaneous vitamin D synthesis depends on the solar ultraviolet B radiation, there were, as expected, marked seasonal differences . As this study used vitamin D results collected throughout the year, a seasonality adjustment was undertaken. While body mass index (BMI) is an important determinant for both vitamin D status  and CHD  it was not available for a sufficient proportion of the cohort to be used in the analyses undertaken in this study.
Post-migration duration in Australia is an important variable which was not available for this cohort. According to Young , the “healthy migrant effect” diminishes incrementally with the number of years stay post-migration. The absence of this data is a limitation in the current analysis. In addition, migrants were categorised in pre-migration zones by country of origin. As some larger countries may belong to more than one zone, this could lead to a misclassification. Other limitations include lack of information available for use of full-cover clothing, and that those attending medical centres may be different from the general population. Details related to the laboratory methodology for vitamin D testing was also unavailable to the audit and is acknowledged as a limitation. The lack of association between VDD and Framingham risk seen in the present study should be interpreted with caution, given the limited sample size. However the study represents a contemporary picture of vitamin D testing patterns and cardiovascular risk in a public health clinic servicing a large migrant population.
The community based medical centre demonstrated adherence to a high risk strategy for vitamin D testing, with higher priority given to migrants, middle aged adults and females. An increasing risk of VDD in those who migrated from lower latitudes (closer to the equator) was observed. However migrants had lower CHD risk compared to those who born in Australia. This audit suggests that pre-migration zone may be an important factor relating to the future risk of CHD (the lower the latitude of origin the lower the future CHD risk), and may be due to a low smoking rate seen among migrants. Zone of origin should be considered in the development of vitamin D testing guidelines. We found no evidence of an association between VDD and CHD risk in this cohort, but given the multifactorial risk and long latency of cardiovascular disease, longitudinal studies may be required to examine this further.
Recommendations and policy implications
The current study has identified the high prevalence of vitamin D deficiency in migrant populations classified according to their pre-migration zones, and its association with some of the cardiovascular risk factors. In light of the significant burden of vitamin D deficiency, sun exposure, vitamin D testing and supplementation guidelines should consider disadvantaged groups including migrants and their zone of origin.
Holick MF: The vitamin D deficiency pandemic: a forgotten hormone important for health. Public Health Rev. 2010, 32 (1): 267-283.
Bischoff-Ferrari HA, Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B: Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr. 2006, 84 (1): 18-28.
Malabanan A, Veronikis IE, Holick MF: Redefining vitamin D insufficiency. Lancet. 1998, 351 (9105): 805-806.
DeLuca HF: Overview of general physiologic features and functions of vitamin D. Am J Clin Nutr. 2004, 80: 1689S-1696S.
Daly RM, Gagnon C, Lu ZX, Magliano DJ, Dunstan DW, Sikaris KA, Zimmet PZ, Ebeling PR, Shaw JE: Prevalence of vitamin D deficiency and its determinants in Australian adults aged 25 years and older: a national, population-based study. Clin Endocrinol (Oxf). 2012, 77 (1): 26-35. 10.1111/j.1365-2265.2011.04320.x.
Boyages S, Bilinski K: Seasonal reduction in vitamin D level persists into spring in NSW Australia: implications for monitoring and replacement therapy. Clin Endocrinol (Oxf). 2012, 77: 515-523. 10.1111/j.1365-2265.2012.04398.x.
McGillivray G, Skull SA, Davie G, Kofoed SE, Frydenberg A, Rice J, Cooke R, Carapetis JR: High prevalence of asymptomatic vitamin D and iron deficiency in East African immigrant children and adolescents living in a temperate climate. Arch Dis Child. 2007, 92 (12): 1088-1093. 10.1136/adc.2006.112813.
Australian Bereau of Statistics: Migration, Australia 2010-11. 2012, Canberra: Australian Bereau of Statistics
Renzaho AMN, Nowson C, Kaur A, Halliday JA, Fong D, De Silva J: Prevalence of vitamin D insufficiency and risk factors for type 2 diabetes and cardiovascular disease among African migrant and refugee adults in Melbourne. Asia Pac J Clin Nutr. 2011, 20 (3): 397-403.
Saleh A, Amanatidis S, Samman S: The effect of migration on dietary intake, type 2 diabetes and obesity: the Ghanaian Health and Nutrition Analysis in Sydney, Australia (GHANAISA). Ecol Food Nutr. 2002, 41: 255-270. 10.1080/0367-020291909778.
van der Meer IM, Middelkoop BJ, Boeke AJ, Lips P: Prevalence of vitamin D deficiency among Turkish, Moroccan, Indian and sub-Sahara African populations in Europe and their countries of origin: an overview. Osteoporos Int. 2011, 22 (4): 1009-1021. 10.1007/s00198-010-1279-1.
Arabi A, Rassi E, Fuleihan E: Hypovitaminosis D in developing countries-prevalence, risk factors and outcomes. Nat Rev Endocrinol. 2010, 6: 550-561. 10.1038/nrendo.2010.146.
Wang L, Song Y, Manson JE, Pilz S, Marz W, Michaelsson K, Lundqvist A, Jassal SK, Barrett-Connor E, Zhang C, Eaton CB, May HT, Anderson JL, Sesso HD: Circulating 25-hydroxy vitamin D and risk of cardiovascular disease: a meta-analysis of prospective studies. Circulation. 2012, 5: 819-829.
Song Y, Wang L, Pittas AG, Del Gobbo LC, Zhang C, Manson JE, Hu FB: Blood 25-hydroxy vitamin D levels and incident type 2 diabetes: a meta-analysis of prospective studies. Diabetes Care. 2013, 36 (5): 1422-1428. 10.2337/dc12-0962.
Wang TJ, Pencina MJ, Booth SL, Jacques PF, Ingelsson E, Lanier K, Benjamin EJ, Agostino RBD, Wolf M, Vasan RS: Vitamin D deficiency and risk of cardiovascular disease. Circulation. 2008, 117: 503-511. 10.1161/CIRCULATIONAHA.107.706127.
Expert Panel on Detection E, and Treatment of High Blood Cholesterol in Adults: Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA. 2001, 285 (19)): 2489-2497.
D’Agostino RB, Vasan RS, Pencina MJ, Wolf PA, Cobain M, Massaro JM, Kannel WB: General cardiovascular risk profile for use in primary care: the Framingham Heart Study. Circulation. 2008, 117 (6): 743-753. 10.1161/CIRCULATIONAHA.107.699579.
National Vascular Disease Prevention Alliance: Guidelines for the Assessment of Absolute Cardiovascular Disease Risk. 2009, National Vascular Disease Prevention Alliance: Canberra
Zomer E, Owen A, Magliano D, Liew D, Reid C: Validation of two Framingham cardiovascular risk prediction algorithms in an Australian population: the ‘old’ versus the ‘new’ Framingham equation. Eur J Cardiovasc Prev Rehabil. 2011, 18 (1): 115-120.
Dassanayake J, Dharmage SC, Gurrin L, Sundararajan V, Payne WR: Are immigrants at risk of heart disease in Australia ? A systematic review. Aust Health Rev. 2009, 33 (3): 479-491. 10.1071/AH090479.
Tomson J, Emberson J, Hill M, Gordon A, Armitage J, Shipley M, Collins R, Clarke R: Vitamin D and risk of dealth from vascular and non-vascular causes in the Whitehall study and meta-analysis of 12000 deaths. Eur Heart J. 2013, 34: 1365-1374. 10.1093/eurheartj/ehs426.
Bilinski K, Boyages S: Evidence of overtesting for vitamin D in Australia: an analysis of 4.5 years of Medicare Benefits Schedule (MBS) data. BMJ Open. 2013, 3: e002955-
Vitamin D Position Statement – Reviewed October 2013 - Working Group of the Australian and New Zealand Bone and Mineral Society. 2014, http://www.osteoporosis.org.au/sites/default/files/files/Vit%20D%20Position%20Statement%2010%202013%20V2.pdf,
Bilinski KL, Boyages SC: The rising cost of vitamin D testing in Australia: time to establish guidelines for testing. Med J Aust. 2012, 197 (2): 90-
Working group of the Australian and New Zealand Bone and Mineral Society ESoAaOA: Vitamin D and adult bone health in Australia and New Zeland: a postion statement. Med J Aust. 2005, 182: 281-285.
Appropriate Vitamin D Testing. 2014, Downloaded from http://www.nps.org.au/__data/assets/pdf_file/0016/112237/MBS_sample_feedback_letter.pdf on 20/05/2014
Binkley N, Novotny R, Krueger D, Kawahara T, Daida YG, Lensmeyer G, Hollis BW, Drezner MK: Low vitamin D status despite abundant sun exposure. J Clin Endocrinol Metab. 2007, 92 (6): 2130-2135. 10.1210/jc.2006-2250.
Benson J, Skull S: Hiding from the sun - vitamin D deficiency in refugees. Aust Fam Physician. 2007, 36 (5): 355-357.
Skull SA, Ngeow JYY, Biggs BA, Street A, Ebeling PR: Vitamin D deficiency is common and unrecognized among recently arrived adult immigrants from The Horn of Africa. Internal Med. 2003, 33: 47-51. 10.1046/j.1445-5994.2003.00344.x.
Renzaho A: Ischaemic heart diseases and Australian immigrants: the influence of birthplace and language skills on treatment and use of health services. Health Inf Manage J. 2007, 36 (2): 26-36.
Singh M, de Looper M: Australian Health Inequalities: Birthplace. 2002, Canberra: Australian Institute of Health and Welfare
Australian Institute of Health and Welfare 2010: Australia’s Health Series no.12. Cat. no. AUS 122. Australia’s Health 2010. 2010, Canberra
Australian Institute of Health and Welfare 2012: Australia’s Health Series no. 13. Cat. no. AUS 156. Australia’s Health 2012. 2012, Canberra
Fact Sheet 22 - The Health Requirement, National Communications Branch, Department of Immigration and Border Protection, Canberra. 2014, [https://www.immi.gov.au/media/fact-sheets/22health.htm]
Australian Institute of Health and Welfare: Australia’s Health 2010. 2010, Canberra: Australian Institute of Health and Welfare
Australian Institute of Health and Welfare: Cardiovascular Disease Australian Facts 2011. 2011, Canberra: Australian Institute of Health and Welfare
Bennion AS, Luthy KE, Freeborn DS, Beckstrand RL: Effect of serum vitamin D levels on Cardiovascular mortality and Cardiovascular disease risk. J Evid-Based Complement Altern Med. 2012, 17: 206-211. 10.1177/2156587212453050.
Forrest KY, Stuhldreher WL: Prevalence and correlates of vitamin D deficiency in US adults. Nutr Res. 2011, 31: 48-54. 10.1016/j.nutres.2010.12.001.
Forman JP, Scott JB, Ng K, Drake BF, Suarez EG, Hayden DL, Bennett GG, Chandler PD, Hollis BW, Emmons KM, Giovannucci EL, Fuchs CS, Chan AT: Effect of vitamin D supplementation on blood pressure in blacks. Hypertension. 2013, 61: 779-785. 10.1161/HYPERTENSIONAHA.111.00659.
Ponda MP, Huang X, Odeh MA, Breslow JL, Kaufman HW: Vitamin D may not improve lipid levels: A serial clinical laborotory data study. Circulation. 2012, 126: 270-277. 10.1161/CIRCULATIONAHA.111.077875.
Witham MD, Nadir MA, Struthers AD: Effect of vitamin D on blood pressure: a systematic review and meta-analysis. J Hypertens. 2009, 27: 1948-1964. 10.1097/HJH.0b013e32832f075b.
Holick MF: Vitamin D Deficiency. NEJM. 2007, 357: 266-281. 10.1056/NEJMra070553.
Saneei P, Salehi-Abargouei A, Esmaillzadeh A: Serum 25-hydroxy vitamin D levels in relation to body mass index: a systematic review and meta-analysis. Obes Rev. 2013, 14: 393-404. 10.1111/obr.12016.
The Global Burden of Metabolic Risk Factors for Chronic Diseases Collaboration (BMI Mediated Effects): Metabolic mediators of the effects of body-mass index, overweight, and obesity on coronary heart disease and stroke: a pooled analysis of 97 prospective cohorts with 1·8 million participants. Lancet. 2014, 383 (9921): 970-983.
Young C: Mortality, the Ultimate Indicator of Survival: The Differential Experience between Birthplace Groups. Immigrants in Australia: A Health Profile. 1992, Canberra: AGPS
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/14/157/prepub
The authors wish to acknowledge Dr. Marion Bailes for her valuable comments and the practice manager and her staff at Doutta Galla Community Health Service for their support. A/Prof Andre Renzaho is supported by an ARC Future Fellowship (FT110100345).
The authors declare that they have no competing interests.
TR collected the data, analysed and prepared the first draft of the manuscript, CR conceived the study design, reviewed the manuscript and serves as guarantor for the contents of this paper, AO reviewed the analysis and the manuscript, DF supervised the data collection and reviewed the manuscript, UG collected the data, AR coordinated the data collection and reviewed the manuscript. All authors approved the final version.
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Ruwanpathirana, T., Reid, C.M., Owen, A.J. et al. Assessment of vitamin D and its association with cardiovascular disease risk factors in an adult migrant population: an audit of patient records at a Community Health Centre in Kensington, Melbourne, Australia. BMC Cardiovasc Disord 14, 157 (2014) doi:10.1186/1471-2261-14-157
- Vitamin D deficiency
- Cardiovascular diseases
- Framingham 10 year risk score