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Lipid profile and dyslipidemia among school-age children in urban Ghana



Dyslipidemia during childhood has been associated with higher risk of atherosclerosis later in life. Information on the lipid profile of Ghanaian children is scarce. The aim of this study was to assess the lipid profiles of school children between the ages of 9–15 years, living in urban Ghana.


A total of 802 randomly selected school-age children participated in the Ghana School Survey implemented in Kumasi and Accra, Ghana. A structured questionnaire was used to collect information on child and maternal socio-demographic characteristics (including age, education, and occupation), 7-day food frequency, home and school activity, as well as measurement of weight and standing height. Weight, height, and age data were converted into BMI-for-age indices to determine weight status. Finger-prick fasting blood samples were taken from the school-age children. Total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL-C) and low-density lipoprotein (LDL-C) cholesterol levels were determined using the CardioChek® PA Test System. Reference lipid levels based on the US National Cholesterol Education Program 2001 guidelines were used to determine the proportion of children with dyslipidemia.


The mean TC, LDL-C, HDL-C, and TG levels were 149.0 ± 57.0 mg/dl, 80.1 ± 38.6 mg/dl, 53.5 ± 19.4 mg/dl, and 71.4 ± 54.7 mg/dl, respectively. Mean TC/HDL-C ratio was 3.0 ± 1.0. The proportion of children with abnormal values were 12.1% for TC, 4.5% for TG, 28.4% for HDL-C, 9.2% for LDL-C, and 6.6% for TC/HDL-C ratio. The levels of dyslipidemia (HDL, LDL, and TC/HDL-C ratio) were higher among overweight/obese compared to normal-weight children. More frequent fruit consumption was also linked with lower LDL-C (p = 0.020) while watching television (TV) in the mornings was linked with both higher TC (p = 0.011) and TG (p = 0.006).


Majority of urban-dwelling Ghanaian school children had normal lipid profiles. However, the higher levels of dyslipidemia observed among overweight and obese children suggest the need for population level physical activity and dietary interventions among children to reduce risk of cardiovascular diseases in adult life.

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Cardiovascular diseases (CVD), formerly believed to be common only among affluent societies are now becoming leading causes of death in developing countries such as Ghana. The Ghana Health Service estimates that CVDs were the leading cause of institutional deaths in 2008, accounting for 14.5% of all reported deaths [1]. A study at the Korle-Bu Teaching Hospital indicated that CVDs constituted more than one-fifth of all causes of death from 2006 to 2010 [2]. Dyslipidemia, particularly in terms of cholesterol and triglyceride levels, has been identified as an important risk factor of CVD. Abnormalities in lipoprotein metabolism represent about 50% of the population-attributable risk of developing CVDs [3]. Consequently, both cardiovascular risk assessment and CVD management are based on the blood levels of these lipids, particularly, low-density lipoprotein cholesterol (LDL-C) [4,5,6].

Available evidence indicates that atherosclerosis, the process that subsequently leads to CVD, starts in childhood and progresses gradually into adulthood. The Bogalusa Heart Study and the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research, both conducted in the United States of America, showed that high concentrations of low density lipoprotein cholesterol (LDL-C) and low levels of high density lipoprotein cholesterol (HDL-C) in children and youth were associated with higher risk of atherosclerosis later in life [7, 8]. As such, it is important that efforts to reduce CVD should start during childhood.

Little is known about the lipid profile of children and adolescents in Ghana. One study that was conducted in the Ga-East Municipality showed a low level of hypercholesterolemia (2.8%) among overweight and obese school children [9]. However, the study did not provide data on the levels of LDL-C and HDL-C as well as the ratio of total cholesterol (TC) to HDL-C, which is considered as a more sensitive and specific index of cardiovascular risk [10]. Evidence of dyslipidemia among children is needed to inform the development of strategies as well as resources needed to address CVDs. The objective of this study was, therefore, to determine the prevalence of dyslipidemia among school-going children in urban Ghana. Evidence from the study will be useful for understanding blood lipid situation among school children in Ghana, as a first step to designing appropriate public health response.


Study participants

This study was part of the Ghana School Survey that was designed to assess the prevalence and determinants of overweight and obesity among school-aged children in urban Ghana (Aryeetey et al. 2017 [11]). The study population included 802 school children between the ages of 9–15 years who were recruited between December 2009 and February 2012 from 121 schools located in Accra and Kumasi, the two largest cities in Ghana. To obtain the sub-sample that was used in the present study, each overweight or obese child who was recruited was matched with a child of normal Body Mass Index (BMI) of the same age and sex. To be eligible to participate in the study, children must be between the ages of 9–15 years. The study was approved by the Ethical Review Boards of McGill University, Canada (A09-B21-09A) and Noguchi Memorial Institute for Medical Research, University of Ghana, Legon (004/09–10). Permissions were obtained from the Ghana Education Service and Heads of all participating schools before data collection. Written informed consent was obtained from all participating children and their parents at recruitment into the study. Only children who expressed their willingness to participate and obtained signed parental consent were included.

Data collection

A wide variety of data were collected in the study as reported elsewhere [11]. Data included in the current analysis were socio-demographic characteristics of the school children as well as caregivers/parents dietary behavior, physical activity, anthropometric measurements and biomarkers of blood lipids. Briefly, a structured questionnaire was used to collect information on caregiver and child age as well as caregiver education, occupation, and household living situation, including ownership of a list of home assets. A food-frequency questionnaire was used to describe the 7-day frequency of consumption of a list of at least 60 foods and beverages. Physical activity was assessed with structured questions on participation in sports, household chores and routine transportation to and from school. Body weight and height of children were measured at the respective school premises. Participants were required to remove all heavy clothing and accessories such as shoes or sandals, belts, watch, and sweaters, and their pockets were emptied prior to being measured. Body weight was measured to the nearest 0.1 kg using the Tanita Digital Scale (model BWB-800, Tanita Corporation, USA). Height measurements were taken to the nearest 0.1 cm using the Shorr Board (Shorr Productions, Olney, MD). All measurements were done and recorded in duplicate. Weight and height measurements were converted to body mass index-for-age Z-scores (BMIZ) using the World Health Organization’s AnthroPlus 2009. Overweight/obesity was defined as BMIZ > 1.0 [12].

For children identified for the lipid profile assessment, parents were informed the day before sample collection that their children had been selected for the lipid profile determination. They were requested to ensure that children did not eat any food before coming to school the following day. They were also to ensure that the child ate supper latest by 7 pm the day before the blood draw. On the day of the lipid profile determination, the children were to report to school early, by 8 am. After the tests had been completed, the children were provided with breakfast by the project (comprising of bread, and 200 ml of malted cocoa beverage).

On the day of the lipid determination, each participating child was asked whether he/she had eaten breakfast or any food or drink that morning. If the child had eaten breakfast that morning, they were not included and therefore no finger prick blood was taken. Finger prick blood samples were collected only on children who had not eaten any breakfast that morning and were in 8–12 h overnight fast. The procedure for the finger prick blood collection was explained to the child and asked if they consented to the procedure. It the child indicated they did not want to continue, he or she was excluded. Upon consent, the tip of the index finger was first cleaned with alcohol-soaked cotton ball before taking the finger-prick blood. A drop of the whole blood was placed on the lipid strip and inserted in the CardioChek® PA Test System (Indianapolis, U.S.A) following the manufacturer’s guidelines. The lipid profile including total triglycerides (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL-C), and low density lipoprotein cholesterol (LDL-C) were determined using the CardioChek® PA Test System (Indianapolis, U.S.A).

Trained interviewers administered the questionnaire to the school children to collect socio-demographic information about the child and his or her household. All data collection was carried out between December 2009 and February 2012.

Data analyses

Descriptive statistics of continuous variables were presented as means and standard deviation and categorical variables as percentages. The percentage of children with abnormal lipid concentrations was calculated using the reference values described in the US National Cholesterol Education Program 2001 Guidelines [6]. The following values were classified as abnormal lipid concentrations: TC ≥ 200 mg/dl, LDL-C ≥ 130 mg/dl, HDL-C ≤ 40 mg/dl, and TG ≥ 150 mg/dl. The ratio of TC to HDL was calculated for each participant and children with values greater than 4.5 considered to be at borderline or high cardiovascular risk [10, 13]. The Student’s t-test for Independent samples was used to compare the mean lipid concentrations of overweight/obese and normal-weight children. Multilevel mixed-effects linear regression models were fitted to generate unbiased effect estimates and standard error for covariates of blood lipid indicators. All statistical analyses were conducted using SAS (version 9.2, Cary, NC, USA) and Stata (Version 12, StatCorp, TX, USA) and statistical significance was considered at p <  0.05.


Data for 802 children aged 9–15 years were included in the current analyses. Of these, more than 60% were females (Table 1). The mean age of the participating children was 12.2 ± 1.6 years. Generally, there were no differences in demographic characteristics of normal-weight and overweight/obese children; educational level of the mothers of overweight/obese children was higher compared to normal-weight children. Dietary and physical activity behaviors were similar across overweight children and those who are no (Table 2). The only exceptions concerning dietary and activity were frequency of breakfast skipping (p = 0.013), motorized transportation to school (p = 0.002) and participation in sports (p = 0.001).

Table 1 Socio-demographic characteristics of school age children and their caregivers/mothers
Table 2 Dietary and physical activity habits of Ghanaian children 9–15 years

Except for HDL-C, fasting blood lipid concentrations of most of the school children were within the normal ranges of reference values (Table 3). The mean TC, LDL-C, HDL-C, and TG concentrations were 149.0 ± 57.0 mg/dl, 80.1 ± 38.6 mg/dl, 53.5 ± 19.4 mg/dl, and 71.4 ± 54.7 mg/dl, respectively. There were no differences between boys and girls in terms of fasting blood lipid concentrations, except the level of TC among the overweight/obese children (Table 3). Overweight/obese children had significantly higher levels of TG (76.6 ± 60.8 mg/dl v 66.5 ± 47.8 mg/dl, p = 0.009) and LDL-C (85.1 ± 41.7 mg/dl v 75.4 ± 34.9 mg/dl, p = 0.004), and lower HDL-C levels (51.3 ± 19.8 mg/dl v 55.7 ± 18.9 mg/dl, p = 0.0011) compared to normal-weight children. Additionally, overweight/obese children tended to have greater mean TC concentration than those with normal weight, although the difference was not statistically significant (152.8 ± 62.6 mg/dl versus 145.3 ± 50.9 mg/dl, p = 0.0627). Although the mean TC to HDL-C ratio indicated that the school age children were at low cardiovascular risk, overweight/obese children had a significantly higher ratio (3.2 ± 1.0 v 2.8 ± 0.9, p <  0.001) compared to normal weight children.

Table 3 Blood lipid levels of school-going urban Ghanaian children aged 9–15 years, classified by weight status

More than one-quarter of the children (28.4%) had HDL-C levels that were indicative of high or borderline cardiovascular risk (Table 4). Additionally, hypercholesterolemia (indicated by elevated total cholesterol) was indicated in more than 10%. The levels of dyslipidemia were significantly different between overweight/obese and normal-weight children (Table 4), but not between boys and girls.

Table 4 prevalence of dyslipidemia among school-going urban Ghanaian children aged 9–15 years, classified by weight status

In multivariate regression modelling, TC was linked with watching television in the morning prior to going to school (p = 0.011) (Table 5). Overweight status predicted a lower HDL-C concentration (p = 0.001). On the other hand, overweight predicted a higher LDL-C (p = 0.002). LDL-C was also linked with child age (p = 0.010), less frequent consumption of fruit (p = 0.020) and watching television in the morning (p = 0.006).

Table 5 Risk factors linked with blood lipid indicators among school age children in Ghana


This study provides information on the lipid profile of school-going children in urban Ghana. With the exception of HLD-C, the levels of lipids and lipoproteins of the children were mostly within the desirable values. In a majority of school children (71.6%), the concentration of HDL-C was below the level that presents a negative risk factor for CVD (≥ 60 mg/dl) [5]. The observed mean HDL-C concentration was lower than what was reported among 13–19 year old children in Tunisia (58.0 mg/dl), but higher when compared to the HDL-C levels of school children of similar age range in Turkey (49.0–49.8 mg/dl) and Brazil (41.1–48.7 mg/dl) [14,15,16,17]. These geographical differences could be due to various factors including genetics, diet, and physical activity habits of the children. Related to the low HDL-C levels is the observation that the most prevalent type of dyslipidemia was in relation to HDL-C, a finding that is similar to studies conducted in Sri Lanka (23.3%) and Brazil (29.5%) [16, 18]. However, in a study among younger Brazilian children (5–8 years) lower prevalence of impaired HDL-C concentration (17.2%) was reported [19].

The observed low HDL-C levels in our study suggest that school-going children in urban Ghana may be at marginal risk of CVD later in life. In Spain and Japan, high levels HDL-C in children was given as a potential explanation for the relatively low Coronary Heart Disease mortality rates compared to other developed countries [20, 21]. Evidence from large epidemiological studies suggests that each 1 mg/dl increase in HDL-C is associated with a decrease of 2–3% in the risk of coronary artery disease [22]. The protective effect of HDL-C may be due to its role in reverse cholesterol transport and its ability to prevent the oxidation of LDL-C [23].

The level of lipids and lipoproteins in both children and adults can be affected by a number of factors, including diet and physical activity which are modifiable behaviors. Although dyslipidemia can result from genetic disorders such as homozygous familial hypercholesterolemia, it usually results from secondary type which is often related to sub-optimal lifestyles [24]. A study in Brazil that included overweight and obese children reported a positive association between elevated TC (β = 0.36, p = 0.04) and the consumption of full fat dairy products, as well as between elevated TG (β = 0.017, p = 0.04) and the percentage of total energy obtained from saturated fat [17]. Studies also indicate that while high intakes of fats and proteins as percentages of total energy increase TC and LDL-C levels, a higher percentage of carbohydrates than the recommended macronutrient range is associated with low HDL-C levels [25, 26]. In Greece, HDL-C level was inversely associated with a lifestyle of higher consumption of sugar-sweetened beverages, more screen time (e.g. television watching), and shorter sleep duration among 9–13 year old children [27]. Additionally, having more eating events and higher levels of physical activity was inversely associated with TC (β = − 0.064, p = 0.006), LDL-C (β = − 0.065, p = 0.004), and TC to HDL-C ratio (β = − 0.049, p = 0.049) in the multivariate models. Physically active lifestyle has been shown to improve HDL/LDL-C ratio through an increase in lipoprotein lipase activity [28].

The intake of sugar-sweetened drinks among Ghanaian school children is high, with an average consumption of about 314 ml per day recorded among 8–18 year old school children [9]. Additionally, majority of the children (60.9%) in that study engaged in less than 60 min of physical activity daily. Less than one-third of the school children who participated in the Global School-based Student Health Survey engaged in sporting activities at least three times in a week [29]. There is, therefore, need for interventions that will improve lifestyles, particularly dietary and physical activity habits of children and adolescents as part of comprehensive strategy to reducing the risk of CVD later in life.

Our study did not find significant differences in the lipid profiles of boys and girls, with the exception of TC among overweight/obese children. The available literature on the sex differences in the lipid profile of school children provides inconsistent results [30]. Among 5–14 year old Colombian children, a greater proportion of girls had undesirable levels of TC (7.9% v 3.0%, p < 0.05), LDL-C (11.6% v 4.7%, p < 0.05), and TG (6.9% v 5.7%, p < 0.05) compared to their male counterparts [31]. Similar finding was reported by Ghannem et al. among 13–19 year old Tunisian children [15]. On the other hand, one study in Brazil did not observe any differences in the lipid levels of boys and girls [16], similar to our findings. Another study in Brazil reported a sex difference in HDL-C levels only, TC, LDL-C, and TG levels were similar for boys and girls [19].

In the present study, overweight and obese children had significantly undesirable levels of lipids compared to normal weight children. This finding is consistent with reports from other settings. In Tunisia, the BMI of 13–19 year old children correlated with TC (r = 0.13, p < 0.0001) [15]. Manios et al. reported that among Turkish school children, overweight boys had significantly higher level of TC, LDL-C, TC/HDL-C ratio, and TG, and overweight girls had lower HDL-C levels compared to their normal weight counterparts [32]. Similar results have been reported among school children in Greece, Spain, and the United States of America [33,34,35]. These findings indicate the clustering of CVD risk factors among children. Considering that modifiable factors such as diet and physical activity levels are associated with both obesity and lipid profile, lifestyle changing interventions that begin in childhood and adolescence can be helpful in reducing the cardiovascular risks later in life.

A strength of this study is that it provides comprehensive lipid profile of Ghanaian school children who live in urban settings. However, it is limited in that we focused on a narrow set of CVD risk factors. Thus, the study does not provide data on other previously identified risk factors such as fasting glucose, insulin resistance, blood pressure, and smoking habits of the children [36,37,38].


In conclusion, majority of school children living in urban Ghana had desirable lipid profiles. There was, however, a substantial proportion with low levels of HDL-C. Additionally, higher levels of dyslipidemia were observed among overweight/obese children. Possible explanations for this observation are the high consumption of sugar-sweetened beverages and low level of physical activity that have been reported among the study population by earlier studies. Thus, interventions that aim to improve the diet and physical activity levels during childhood and adolescence may be needed to reduce the cardiovascular risk later in life.



Body mass index


body mass index-for-age Z-scores


Cardiovascular diseases


High density lipoprotein cholesterol


Low-density lipoprotein cholesterol


Pathobiological determinants of atherosclerosis in youth


Total cholesterol






  1. 1.

    Ghana Health Service. The health sector in Ghana: fact and figures 2009. Accra. 2010.

  2. 2.

    Sanuade O, Anarfi J, de Graft Aikins A, Koram K: Patterns of cardiovascular disease mortality in Ghana: a 5-year review of autopsy cases at Korle-Bu teaching hospital. Accessed 30 July 2013 from 2013.

    Google Scholar 

  3. 3.

    Yusuf S, Hawken S, Ounpuu S, et al. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004;364:937–52.

    Article  PubMed  Google Scholar 

  4. 4.

    Anderson TJ, Grégoire J, Hegele RA, Couture P, Mancini GBJ, McPherson R, Francis GA, Poirier P, Lau DC, Grover S, et al. 2012 update of the Canadian cardiovascular society guidelines for the diagnosis and treatment of dyslipidemia for the prevention of cardiovascular disease in the adult. Can J Cardiol. 2013;29(2):151–67.

    Article  PubMed  Google Scholar 

  5. 5.

    Jellinger P, Smith D, Mehta A, Ganda O, Handelsman Y, Rodbard H, Shepherd M, Seibel J, Atherosclerosis ATFfMoDaPo. American Association of Clinical Endocrinologists’ guidelines for management of dyslipidemia and prevention of atherosclerosis. Endocr Pract. 2012;18(Suppl 1):1–78.

    Article  PubMed  Google Scholar 

  6. 6.

    NCEP 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):2486–97.

    Article  Google Scholar 

  7. 7.

    Newman W III, Freedman D, Voors A, Gard P, Srinivasan G. Relation of serum lipoprotein levels ans systolic blood pressure to early atherosclerosis. The Bogalusa heart study. N Engl J Med. 1986;314:138–44.

    Article  PubMed  Google Scholar 

  8. 8.

    PDAY Research Group. Relationship of atherosclerosis in young men to serum lipoprotein cholesterol concentrations and smoking. JAMA. 1990;264(23):3018–24.

    Article  Google Scholar 

  9. 9.

    Steiner-Asiedu M, Addo P, Bediako-Amoa B, Fiadjoe F, Anderson A. Lifesyle and nutrition profile of overweight and obese school children in the Ga-east district of Ghana. Asian J Med Sci. 2012;4(3):99–102.

    CAS  Google Scholar 

  10. 10.

    Millan J, Pinto X, Munoz A, Zuniga M, Rubies-Prat J, Pallardo L, Masana L, Mangas A, Hernandez-Mijares A, Gonzalez-Santos P, et al. Lipoprotein ratios: physiological significance and clinical usefulness in cardiovascular prevention. Vasc Health Risk Manag. 2009;5:757–65.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Aryeetey R, Lartey A, Marquis GS, Nti H, Colecraft E, Brown P. Prevalence and predictors of overweight and obesity among school-aged children in urban Ghana. BMC Obes. 2017;4:38.

    Article  PubMed  PubMed Central  Google Scholar 

  12. 12.

    de Onis M, Onyango A, Borghi E, Nishida C, Siekmann J. Development of a WHO growth reference for school-aged children and adolescents. Bull World Health Organ. 2007;85:660–7.

    Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Kocaoglu B, Moschonis G, Dimitriou M, Kolotourou M, Keskin Y, Sur H, Hayran O, Manios Y. Parental educational level and cardiovascular disease risk factors in schoolchildren in large urban areas of Turkey: directions for public health policy. BMC Public Health. 2005;5:13–21.

    Article  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Can M, Piskin E, Guven B, Acikgoz S, Mungan G. Evaluation of serum lipid levels in children. Pediatr Cardiol. 2013;34(3):566–9.

    Article  PubMed  Google Scholar 

  15. 15.

    Ghannem H, Darioli R, Limam K, Harrabi I, Gaha R, Trabelsi L, Fredj A, Bouslama A. Epidemiology of cardiovascular risk factors among schoolchildren in Sousse, Tunisia. J Cardiovasc Risk. 2001;8:87–91.

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Ribas S, da Silva L. Dyslipidemia in schoolchildren from private School in Belem. Arq Bras Cardiol. 2009;92(6):412–7.

    Article  PubMed  Google Scholar 

  17. 17.

    Rinaldi A, de Oliveira E, Moreto F, Gabriel G, Corrente J, Burini R. Dietary intake and blood lipid profile in overweight and obese schoolchildren. BMC Res Notes. 2012;5:598–604.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Wickramasinghe VP, Arambepola C, Bandara P, Abeysekera M, Kuruppu S, Dilshan P, Dissanayake BS. Distribution of obesity-related metabolic markers among 5-15 year old children from an urban area of Sri Lanka. Ann Hum Biol. 2013;40(2):168–74.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Pereira JA, Rondo PHC, Lemos JO, de Oliveira E, Rocha C, Hipolito T. Nutritional status and lipid profile of young children in Brazil. J Trop Pediatr. 2013;59(1):54–8.

    Article  PubMed  Google Scholar 

  20. 20.

    Dwyer T, Iwane H, Dean K, Odagiri Y, Shimomitsu T, Blizzard L, Srinivasan G, Nicklas L, Wattigney W, Riley M, et al. Differrences in HDL cholesterol concentrations in Japanese, American, and Australian children. Circulation. 1997;96(9):2830–6.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Garces C, Gil A, Benavente M, Viturro E, Cano B, de Oya M. Consistently high plasma high-density lipoprotein cholesterol levels in children in Spain, a country with low cardiovascular mortality. Metabolism. 2004;53(8):1045–7.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Gordon D, Probstfield J, Garrison R, et al. High-density lipoprotein cholesterol and cardiovascular disease. Four prospective American studies. Circulation. 1989;79:8–15.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Harper C, Jacobson T. New perspectives on the management of low levels of high-density lipoprotein cholesterol. Arch Intern Med. 1999;159:1049–57.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Pereira P, de Arruda I, Cavalcanti A, Diniz Ada S. Lipid profile of school children from Recife, PE. Arq Bras Cardiol. 2010;95(5):606–13.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Knuiman JT, West CE, Katan MB, Hautvast JGAJ. Total cholesterol and high density lipoprotein cholesterol levels in populations differing in fat and carbohydrate intake. Arteriosclerosis. 1987;7(6):612–9.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Mahley RW, Arslan P, Pekcan G, Pépin GM, Ağaçdiken A, Karaağaoğlu N, Rakıcıoğlu N, Nursal B, Dayanıklı P, Palaoğlu KE, et al. Plasma lipids in Turkish children: impact of puberty, socioeconomic status, and nutrition on plasma cholesterol and HDL. J Lipid Res. 2001;42(12):1996–2006.

    CAS  PubMed  Google Scholar 

  27. 27.

    Moschonis G, Mavrogianni C, Karatzi K, Iatridi V, Chrousos GP, Lionis C, Manios Y. Increased physical activity combined with more eating occasions is beneficial against dyslipidemias in children. The healthy growth study. Eur J Nutr. 2013;52(3):1135–44.

    Article  PubMed  Google Scholar 

  28. 28.

    Santamarina-Fojo S, Dugi K. Structure, function and role of lipoprotein lipase in lipoprotein. Curr Opin Lipidol. 1994;5:117–25.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Centers for Disease Control and Prevention (CDC): Global School-based Student Health Survey: Ghana Senior High 2012 Factsheet. 2012.

    Google Scholar 

  30. 30.

    Haney EM, Huffman LH, Bougatsos C, Freeman M, Fu R, Steiner RD, Helfand M, Nelson HD: U.S. preventive services task force evidence syntheses, formerly systematic evidence reviews. In: Screening for Lipid Disorders in Children and Adolescents. Edn. Rockville (MD): Agency for Healthcare Research and Quality (US); 2007.

  31. 31.

    Villarreal E, Forero Y, Poveda E, Baracaldo C, Lopez E. Cardiovascular risk markers in schoolchildren from five provinces of eastern Colombia. Biomedica. 2008;28:38–9.

    Article  PubMed  Google Scholar 

  32. 32.

    Manios Y, Kolotourou M, Moschonis G, Sur H, Keskin Y, Kocaoglu B, Hayran O. Macronutrient intake, physical activity, serum lipids and increased body weight in primary schoolchildren in Instanbul. Pediatr Int. 2005;47:159–66.

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    DeStefano F, Berg R, Griese G. Determinants of serum lipid and lipoprotein concentrations in children. Epidemiology. 1995;6:446–9.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Garces C, Gutierrez-Guisado J, Benavente M, Cano B, Viturro E, Ortega H, de Oya M. Obesity in Spanish schoolchildren: relationship with lipid profile and insulin resistance. Obes Res. 2005;13(6):959–63.

    Article  PubMed  Google Scholar 

  35. 35.

    Manios Y, Yiannakouris N, Papoutsakis C, Moschonis G, Magnos F, Skenderi K, Zampelas A. Behavioral and physiological indices related to BMI in a cohort of primary schoolchildren in Greece. Am J Hum Biol. 2004;16:639–47.

    Article  PubMed  Google Scholar 

  36. 36.

    Radisauskas R, Kuzmickiene I, Milinaviciene E, Everatt R. Hypertension, serum lipids and cancer risk: a review of epidemiological evidence. Medicina (Kaunas, Lithuania). 2016;52(2):89–98.

    Article  Google Scholar 

  37. 37.

    Tomkin GH, Owens D. Diabetes and dyslipidemia: characterizing lipoprotein metabolism. Diabetes Metab Syndr Obes. 2017;10:333–43.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Lepira FB, M'Buyamba-Kabangu JR, Kayembe KP, Nseka MN. Correlates of serum lipids and lipoproteins in Congolese patients with arterial hypertension. Cardiovasc J S Afr. 2005;16(5):249–55.

    CAS  PubMed  Google Scholar 

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The study team appreciates the cooperation and support of teachers, parents and school children for their patience and time spent in participating in the data collection process. We also appreciate the facilitative role of the school officials as well as research assistants (Mawuli Avedzi, Hussein Mohamed, and Deda Ogum). Seth Adu-Afarwuah and Duah Dwomoh are acknowledged for support with data analyses.


This work was carried out with the aid of a grant from the International Development Research Centre, Ottawa, Canada (#104519–017).

Availability of data and materials

The datasets analysed during the current study are available from the corresponding author on reasonable request. Alternatively, the data may be accessed from ( However, access to the data will be restricted by an embargo requiring contact with the Investigators due to ongoing analyses, until January 2018, when the embargo will be lifted.

Author information




The study was conceived and designed by AL and GSM. The manuscript was drafted by RA and AL with contributions by GSM, and HN. All authors revised and approved the final manuscript.

Corresponding author

Correspondence to Richmond Aryeetey.

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Ethics approval and consent to participate

The study was approved by the Ethical Review Boards of McGill University, Canada (A09-B21-09A), and the Noguchi Memorial Institute for Medical Research, University of Ghana, Legon (004/09–10). Written informed consent was obtained from all parents whose children participated in the study. In addition, each participating child provided signed assent before the questionnaire was administered.

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No identifying information of study participants is included in the manuscript.

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The authors declare that they have no competing interests.

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Lartey, A., Marquis, G.S., Aryeetey, R. et al. Lipid profile and dyslipidemia among school-age children in urban Ghana. BMC Public Health 18, 320 (2018).

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  • Lipid profile
  • Dyslipidemia
  • School
  • Child
  • Cholesterol
  • Ghana