Objective: This study aimed to assess the prevalence of metabolic syndrome among school-aged children in three municipalities of Abidjan, Côte d’Ivoire, and to analyze its anthropometric and biological determinants. Methods: A cross-sectional survey was conducted among 1,251 children aged 5 to 15 years. Among them, 64 children (31 obese and 33 normal-weight) underwent biological testing. Anthropometric measurements (BMI, waist circumference, abdominal circumference), blood pressure, and biochemical parameters (blood glucose, triglycerides, HDL cholesterol) were collected. The diagnosis of metabolic syndrome was based on the NCEP ATP III criteria. Statistical analyses were performed using SPSS 20, employing Student’s t-test, the chi-square test, and Pearson’s correlation coefficients. Results: Obese children had significantly higher values for weight, BMI, waist circumference, and blood pressure compared to the control group (p < 0.05). The prevalence of metabolic syndrome was 25%, with a higher frequency among girls (20.3%) than among boys (4.7%). Abdominal obesity, hypertension, and low HDL cholesterol were the most common abnormalities. A positive correlation was observed between BMI and waist circumference (r = 0.788, p = 0.001), as well as between waist circumference and systolic blood pressure (r = 0.493, p = 0.004). Hyperuricemia was strongly associated with metabolic syndrome, suggesting its potential role as an early biomarker of cardiovascular risk. Conclusion: This study highlights a concerning prevalence of metabolic syndrome among obese children in Ivorian schools, particularly among girls. Abdominal obesity and hyperuricemia appear to be key factors in the development of cardiometabolic complications. These results underscore the urgent need for targeted prevention strategies, including early screening, the promotion of a balanced diet, and physical activity, in order to reduce the future burden of cardiovascular disease in Côte d’Ivoire.
| Published in | Journal of Food and Nutrition Sciences (Volume 14, Issue 5) |
| DOI | 10.11648/j.jfns.20261405.11 |
| Page(s) | 271-280 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Prevalence, Metabolic Syndrome, Children, Obesity
Normal weight n = 33 | Obese n = 31 | P | |
|---|---|---|---|
Age (years) | 9,19 ± 1,85 | 9,79 ± 1,94 | 0,201 |
Weight (kg) | 29,13 ± 6,56 | 45,87 ± 11,85 | 0,012 |
Height (m) | 1,34 ± 0,11 | 1,43 ± 0,11 | 0,081 |
BMI (kg/m2) | 16,37 ± 1,7 | 22,25 ± 3,15 | 0,012 |
Waist Circumference (cm) | 62,55 ± 5,26 | 73,66 ± 7,94 | 0,005 |
Abdominal Circumference (cm) | 60,54 ± 3,88 | 74,27 ± 8,7 | 0.004 |
Systolic Blood Pressure (mm Hg) | 10,83 ± 8,4 | 11,98 ± 8,36 | 0,006 |
Diastolic Blood Pressure (mm Hg) | 6,14 ± 4,2 | 7,62 ± 16,30 | 0,012 |
Blood Glucose (g/L) | 0,72 ± 0,12 | 0,80 ±-0,19 | 0,081 |
Obese girl n = 17 | Obese boy n =14 | P | |
|---|---|---|---|
Age (years) | 10,12 ± 2,39 | 9,33 ± 1,29 | 0,215 |
Weight (kg) | 49,34 ± 11,6 | 41,14 ± 10,89 | 0,008 |
Height (m) | 1,44 ± 0,1 | 1,40 ± 0,11 | 0,051 |
BMI (kg/m2) | 23,44 ± 3 | 20,60 ± 2,76 | 0,004 |
Waist Circumference (cm) | 75,41 ± 7,7 | 71,73 ± 8,31 | 0,361 |
Abdominal Circumference (cm) | 82,35 ± 16,9 | 68,47 ± 14,06 | 0,001 |
Systolic Blood Pressure (mm Hg) | 12,10 ± 7,7 | 11,77 ± 9,73 | 0,038 |
Diastolic Blood Pressure (mm Hg) | 8,23 ± 16,9 | 6,82 ± 14,64 | 0,001 |
Blood Glucose (g/L) | 0,82 ± 0,14 | 0,86 ± 0,23 | 0,565 |
Triglycerides (g/l) | 1,26 ± 0,32 | 1,34 ± 0,88 | 0,061 |
Total Cholesterol (g/L) | 2,11 ± 0,25 | 2,17 ± 0,27 | 0,251 |
HDL cholesterol (g/l) | 0,44 ± 0,1 | 0,47 ± 0,11 | 0,381 |
LDL Cholesterol (g/l) | 1,48 ± 0,33 | 1,55 ± 0,32 | 0,061 |
Uric Acid (mg/L) | 63,45 ± 13,7 | 48,02 ± 15,35 | 0,001 |
Waist circumference | BMI | Systolic blood pressure | Low HDL | Triglyceride | ||
|---|---|---|---|---|---|---|
Waist circumference | r = | 1,00 | 0,788 | 0,493 | -0,156 | 0,230 |
P = | 0,0001 | 0,004 | 0,394 | 0,206 | ||
BMI | r = | 0,788 | 1,00 | 0,705 | -0,307 | 0,321 |
P = | 0,0001 | 0,0001 | 0,088 | 0,074 | ||
Systolic blood pressure | r = | 0,493 | 0,705 | 1,00 | -0,389 | 0,148 |
P = | 0,004 | 0,0001 | 0,028 | 0,419 | ||
Low HDL | r = | -0,156 | -0,307 | -0,389 | 1,00 | -0,168 |
P = | 0,394 | 0,088 | 0,028 | 0,357 | ||
Triglyceride | r = | 0,230 | 0,321 | 0,148 | -0,168 | 1,00 |
P = | 0,206 | 0,74 | 0,419 | 0,357 | ||
Normal (%)% n = 33 | Obese (%)% n = 31 | P | |
|---|---|---|---|
Waist circumference > 90 | 0 | 28,1 (9) | 0,001 |
Waist circumference < 90 | 100 (31) | 71,9 (23) | |
Systolic blood pressure > 95 | 3,1 (1) | 53,1 (17) | 0,001 |
Systolic blood pressure < 95 | 96,9 (30) | 46,9 (14) | |
Diastolic blood pressure > 95 | 6,2 (2) | 53,1 (17) | 0,001 |
Diastolic blood pressure < 95 | 93,7 (29) | 46,9 (14) | |
Blood glucose > 1.10 g/l | 6,2 (2) | 9,4 (3) | 0,291 |
Blood glucose < 1.10 g/l | 93,7 (29) | 90,6 (28) |
UHC | University Hospital Center |
MS | Metabolic Syndrome |
WC | Waist Circumference |
HT | Hypertension |
BMI | Body Mass Index |
DBP | Diastolic Blood Pressure |
SBP | Systolic Blood Pressure |
DC | Developing Country |
| [1] | McMichael A. J., 2000. The urban environment and health in a world of increasing globalization: issues for developing countries. Bulletin of the World Health Organization, 78(9): 1117-1126. |
| [2] | Reardon T., Timmer P. C., Barrett B. C. & Berdegué J., 2003. The rise of supermarkets in Africa, Asia, and Latin America. American Journal of Agricultural Economics. 85(5): 1140-1146. |
| [3] | Omran A. R., 2005. The epidemiologic transition: a theory of the epidemiology of population change. 1971. Milbank Quarterly, 83(4): 731-757. |
| [4] | Drewnowski A., 2000. Nutrition transition and global dietary trends. Nutrition. 16(7): 486-487. |
| [5] | Popkin B. M., 2006. Global nutrition dynamics: the world is shifting rapidly toward a diet linked with noncommunicable diseases. American Journal of Clinical Nutrition, 84: 289-298. |
| [6] | Fernald L. C., Gutierrez J. P., Neufeld L. M., Olaiz G., Bertozzi S. M. & Mietus-Snyder M., 2004. High prevalence of obesity among the poor in Mexico. Jama. 2 (21): 2544-2545. |
| [7] | Albala C., Vio F., Kain J. & Uauy R., 2002. Nutrition transition in Chile: determinants and consequences. Public Health Nutrition. 5 (1A): 123-128. |
| [8] | OMS. 2006. Le defi de l’obesite dans la region europeenne de l’OMS et les strategies de lutte EUR/06/5062700/6 conference ministerielle europeenne de l’OMS. Rapport sur la lutte contre l’obesite. Istanbul, Turquie. 321p |
| [9] | Prentice A. M., 2006. The emerging epidemic of obesity in developing countries. International Journal of Epidemiology, 35(1): 93-99. |
| [10] | De Onis M. & Blossner M., 2000. Prevalence and trends of overweight among preschool children in developing countries. American Journal of Clinical Nutrition. 72(4): 1032-1039. |
| [11] | Daniels S. R., Arnett D. K., Eckel R. H., Gidding S. S., Hayman L. L., Kuma & Nyika S., 2005. Overweight in children and adolescents: pathophysiology, consequences, prevention, and treatment. Circulation. 19, (15): 1999-2012. |
| [12] | Monge R. and Beita O., 2000. Prevalence of coronary heart disease risk factors in costa rican adolescents. J Adolesc Health; 27: 210–7, 1054-139x. |
| [13] | Raitakari O. T., Porkka K. V., Viikari J. S., Ronnemaa T. and Akerblom H. K., 1994. Clustering of risk factors for coronary heart disease in children and adolescents. The cardiovascular risk in young fi nns study. Acta Paediatr; 83: 935–40. |
| [14] | Singh R., Bhansali R. & Siely R., 2007. Prevalence of metabolic syndrome in adolescents from a north Indian population, 86(2): 65-68. |
| [15] | Twisk J. W., Kemper H. C., Van Mechelen W. and Post G. B., 2001. Clustering of risk factors for coronaryheart disease. The longitudinal relationship with lifestyle. Ann Epidemiol; 11: 157–65. |
| [16] | Andersen L. B., Wedderkopp N., Hansen H. S., Cooper A. R., and Froberg K., 2003. Biological cardiovascular risk factors cluster in danish children and adolescents: the european youth heart study. Prev Med; 37: 363–7. |
| [17] | Milligan R. A., Thompson C., Vandongen R., Beilin L. J. and Burke V., 1995. Clustering of cardiovascular risk factors in australian adolescents: association with dietary excesses and defi ciencies. Journal Article Review Review, Tutorial. J Cardiovasc Risk; 2: 515–23, 1350-6277. |
| [18] | Twisk J W, Boreham C, Cran G, Savage JM, Strain J, and Van Mechelen W., 1999. Clustering of biological risk factors for cardiovascular disease and the longitudinal relationship with lifestyle of an adolescent population: the Northern Ireland young hearts project. J Cardiovasc Risk; 6: 355–62. |
| [19] | American Diabetes Association., 2000. Type 2 diabetes in children and adolescents. Diabetes Care, 23: 381-389. |
| [20] | OMS. 1995. Utilisation et interpretation de l’anthropometrie. Rapport d’un comite d’experts OMS Serie de Rapports techniques 854. Genève. OMS: 498 p. |
| [21] | Rolland-Cachera M. F., Deheeger M. & Bellisle F., 2001. Waist circumference values in French boys and girls aged 6 to 16 years. International Journal of Obesity, 25(2): S132. |
| [22] | OMS. 2011 Guideline: Vitamin A supplementation in infants and children 6–59 months of age. Geneva, World Health Organization. Report of a WHO expert committee. Serie de Rapports techniques 854. Genève. OMS: 238 p. |
| [23] | Cook S., Weitzman M. & Auinger P., 2003. Prevalence of a metabolic syndrome phenotype in adolescents: finding from the third national health and nutrition examination survey; 1988 - 1994. Archives of Pediatrics and Adolescent Medicine, 157: 821-827. |
| [24] | De Man S. A., Andre J. L., Bachmann H., Grobbee D. E., Ibsen K. K. & Laaser U. 1991. Blood pressure in childhood: Pooled findings of six European Studies. Journal of Hypertension, 9: 109-114. |
| [25] | Ireton M., 2006. Le capital biologique humain. Une experience Colombienne. Relations entre les variables biometriques, geographiques, socio-economiques et nutritionnelles d’enfants et d’adolescents scolarises d’El Yopal, Casanare, Colombie, 2000-2002. Fundacion Auxologica TEA, Bogota-Colombie. 58-61. |
| [26] | Janssen I., Katzmarzyk P. T., Srinivasan S. R., Chen W., Malina R. M. & Bouchard C., 2005. Combined influence of body mass index and waist circumference on coronary artery disease risk factors among children and adolescents. Pediatrics. 115: 1623-1630. |
| [27] | Hirschler V., Aranda C., Calcagno M., Maccalini G. & Jadzinsky M., 2005. Can waist circumference identify children with the metabolic syndrome? Archives of Pediatrics and Adolescent Medicine. 159: 740-744. |
| [28] | Sorof J. & Daniels S., 2002. Obesity hypertension in children: a problem of epidemic proportions. Hypertension. 40: 441-447. |
| [29] | Ogden C. L., Carroll M. D., Curtin L. R., McDowell M. A., Tabak C. J. & Flegal K. M., 2006. Prevalence of overweight and obesity in the united states, 1999-2004. Journal of the American Medical Association, 295: 1549-1555. |
| [30] | Samuel F. H., Miguel K. K., Lorenzo R. C. & Jose I. S., 2009. Increase in Body Mass Index and Waist Circumference is associated high blood pressure in children and adolescents in Mexico City. Archives of Medical Research, 40: 208-215. |
| [31] | Benmohammed K., Nguyen M. T., Khensal S., Valensi P. & Lezzar A., 2011. Arterial hypertension in overweight and obese adolescent: Role of abdominal diposity. Diabetes and Metabolism. 37: 291-297. |
| [32] | Bougnères P. & Le Stunff C., 2007. Diabète non insulinodependant chez l’enfant et l’adolescent obèse: un problème mal pose. Realites Pediatriques. 13: 119-122. |
| [33] | Druet C., Dabbas M. & Baltaske V., 2006. Insuline resistance and the metabolic syndrome in obese French children. Clinical Endocrinologie, 64: 672-678. |
| [34] | Wiegrand S., Maikowski U. & Blankestein O., 2004. Type 2 diabetes and impaired glucose tolerance in European children and adolescents with obesity: a problem that is no longer restricted to minority groups. European Journal Endocrinology. 15: 199-206. |
| [35] | Atabek M. E., Pirgon O. & Kurtoglu S., 2006. Prevalence of metabolic syndrome in obese Turkish children and adolescents. Diabetes Research and Clinical Practice, 72: 315-321. |
| [36] | Gao B., Zhou J., Ge J., Zhang Y., Chen F. & Lau W. B., 2012. Association of maximum weight with hyperuricemia risk: a retrospective study of 21,414 Chinese people. PloS One; 7: e51186. Diabetes Metabolism. 24: 195-199. |
| [37] | Johnson R. J., Lanaspa M. A. & Gaucher E. A., 2011. Uric acid: A Danger Signal from the RNA World that may have a role in the Epidemic of Obesity, Metabolic Syndrome and CardioRenal Disease: Evolutionary Considerations. Semin Nephrol; 31: 394–399. |
| [38] | Erdogan D., Gullu H., Caliskan M., Yildirim E., Bilgi M. & Ulus T., 2005. Relationship of serum uric acid to measures of endothelial function and atherosclerosis in healthy adults. International Journal of Clinical Practice. 59p. |
| [39] | Lee J-M., Kim H. C., Cho H. M., Oh S. M., Choi D. P. & Suh I., 2012. Association between serum uric acid level and metabolic syndrome. Journal of Preventive Medicine and Public Health, 45: 181–187. |
| [40] | Han G-M., Gonzalez S. & DeVries D., 2014. Combined effect of hyperuricemia and overweight/obesity on the prevalence of hypertension among US adults: result from the National Health and Nutrition Examination Survey. Journal of Human Hypertension, 28: 579–586. |
| [41] | Rathmann W. & Funkhouser E., 1998. Dyer AR, Roseman JM. Relations of hyperuricemia with the various components of the insulin resistance syndrome in young black and white adults: the CARDIA study. Coronary Artery Risk Development in Young Adults. Annals of Epidemiology. 8: 250–261. |
APA Style
Francoise, F. A., Evrard, B. P., Fulgence, A. Y., Francis, B. N., Jeanne, K. A., et al. (2026). Prevalence of Metabolic Syndrome Among Obese Children in Cote d’Ivoire. Journal of Food and Nutrition Sciences, 14(5), 271-280. https://doi.org/10.11648/j.jfns.20261405.11
ACS Style
Francoise, F. A.; Evrard, B. P.; Fulgence, A. Y.; Francis, B. N.; Jeanne, K. A., et al. Prevalence of Metabolic Syndrome Among Obese Children in Cote d’Ivoire. J. Food Nutr. Sci. 2026, 14(5), 271-280. doi: 10.11648/j.jfns.20261405.11
AMA Style
Francoise FA, Evrard BP, Fulgence AY, Francis BN, Jeanne KA, et al. Prevalence of Metabolic Syndrome Among Obese Children in Cote d’Ivoire. J Food Nutr Sci. 2026;14(5):271-280. doi: 10.11648/j.jfns.20261405.11
@article{10.11648/j.jfns.20261405.11,
author = {Fossou Assamala Francoise and Brou Paterne Evrard and Allo Yapo Fulgence and Batai Nemahiouon Francis and Kanga Akoua Jeanne and Doubran Djoman Prisca Joelle and Ahui Bitty Marie Louise},
title = {Prevalence of Metabolic Syndrome Among Obese Children in Cote d’Ivoire},
journal = {Journal of Food and Nutrition Sciences},
volume = {14},
number = {5},
pages = {271-280},
doi = {10.11648/j.jfns.20261405.11},
url = {https://doi.org/10.11648/j.jfns.20261405.11},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jfns.20261405.11},
abstract = {Objective: This study aimed to assess the prevalence of metabolic syndrome among school-aged children in three municipalities of Abidjan, Côte d’Ivoire, and to analyze its anthropometric and biological determinants. Methods: A cross-sectional survey was conducted among 1,251 children aged 5 to 15 years. Among them, 64 children (31 obese and 33 normal-weight) underwent biological testing. Anthropometric measurements (BMI, waist circumference, abdominal circumference), blood pressure, and biochemical parameters (blood glucose, triglycerides, HDL cholesterol) were collected. The diagnosis of metabolic syndrome was based on the NCEP ATP III criteria. Statistical analyses were performed using SPSS 20, employing Student’s t-test, the chi-square test, and Pearson’s correlation coefficients. Results: Obese children had significantly higher values for weight, BMI, waist circumference, and blood pressure compared to the control group (p < 0.05). The prevalence of metabolic syndrome was 25%, with a higher frequency among girls (20.3%) than among boys (4.7%). Abdominal obesity, hypertension, and low HDL cholesterol were the most common abnormalities. A positive correlation was observed between BMI and waist circumference (r = 0.788, p = 0.001), as well as between waist circumference and systolic blood pressure (r = 0.493, p = 0.004). Hyperuricemia was strongly associated with metabolic syndrome, suggesting its potential role as an early biomarker of cardiovascular risk. Conclusion: This study highlights a concerning prevalence of metabolic syndrome among obese children in Ivorian schools, particularly among girls. Abdominal obesity and hyperuricemia appear to be key factors in the development of cardiometabolic complications. These results underscore the urgent need for targeted prevention strategies, including early screening, the promotion of a balanced diet, and physical activity, in order to reduce the future burden of cardiovascular disease in Côte d’Ivoire.},
year = {2026}
}
TY - JOUR T1 - Prevalence of Metabolic Syndrome Among Obese Children in Cote d’Ivoire AU - Fossou Assamala Francoise AU - Brou Paterne Evrard AU - Allo Yapo Fulgence AU - Batai Nemahiouon Francis AU - Kanga Akoua Jeanne AU - Doubran Djoman Prisca Joelle AU - Ahui Bitty Marie Louise Y1 - 2026/09/08 PY - 2026 N1 - https://doi.org/10.11648/j.jfns.20261405.11 DO - 10.11648/j.jfns.20261405.11 T2 - Journal of Food and Nutrition Sciences JF - Journal of Food and Nutrition Sciences JO - Journal of Food and Nutrition Sciences SP - 271 EP - 280 PB - Science Publishing Group SN - 2330-7293 UR - https://doi.org/10.11648/j.jfns.20261405.11 AB - Objective: This study aimed to assess the prevalence of metabolic syndrome among school-aged children in three municipalities of Abidjan, Côte d’Ivoire, and to analyze its anthropometric and biological determinants. Methods: A cross-sectional survey was conducted among 1,251 children aged 5 to 15 years. Among them, 64 children (31 obese and 33 normal-weight) underwent biological testing. Anthropometric measurements (BMI, waist circumference, abdominal circumference), blood pressure, and biochemical parameters (blood glucose, triglycerides, HDL cholesterol) were collected. The diagnosis of metabolic syndrome was based on the NCEP ATP III criteria. Statistical analyses were performed using SPSS 20, employing Student’s t-test, the chi-square test, and Pearson’s correlation coefficients. Results: Obese children had significantly higher values for weight, BMI, waist circumference, and blood pressure compared to the control group (p < 0.05). The prevalence of metabolic syndrome was 25%, with a higher frequency among girls (20.3%) than among boys (4.7%). Abdominal obesity, hypertension, and low HDL cholesterol were the most common abnormalities. A positive correlation was observed between BMI and waist circumference (r = 0.788, p = 0.001), as well as between waist circumference and systolic blood pressure (r = 0.493, p = 0.004). Hyperuricemia was strongly associated with metabolic syndrome, suggesting its potential role as an early biomarker of cardiovascular risk. Conclusion: This study highlights a concerning prevalence of metabolic syndrome among obese children in Ivorian schools, particularly among girls. Abdominal obesity and hyperuricemia appear to be key factors in the development of cardiometabolic complications. These results underscore the urgent need for targeted prevention strategies, including early screening, the promotion of a balanced diet, and physical activity, in order to reduce the future burden of cardiovascular disease in Côte d’Ivoire. VL - 14 IS - 5 ER -