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Journal of Obesity
Volume 2013 (2013), Article ID 968754, 6 pages
Preliminary Blood Pressure Screening in a Representative Sample of Extremely Obese Kuwaiti Adolescents
1Department of Physiology, Arabian Gulf University (AGU), Road 2904, Building 293, 329 Manama, Bahrain
2CMMS, Arabian Gulf University (AGU), Road 2904, Building 293, 329 Manama, Bahrain
Received 21 July 2013; Revised 19 September 2013; Accepted 2 October 2013
Academic Editor: Yuichiro Yano
Copyright © 2013 Rima Abdul Razzak et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
A relationship between blood pressure (BP) and obesity has been found in young adults, but no data are available for adolescents in Kuwait. 257 adolescent (11–19 years) participants were categorized into two groups according to their BMI; 48 nonobese (21 males: 43.7% and 27 females: 56.3%) with mean age of years and 209 obese (128 males: 61.25% and 81 females: 38.75%) with mean age of years. The mean BMI was kg/m2 for the nonobese group and kg/m3 for the obese group. Most BP measures based on a single screening were significantly higher in the obese group. The prevalence of elevated BP was significantly higher in the obese subjects (nonobese: 13%; obese: 63%; ). In the obese group, there was a significant positive correlation between total sample BMI and all BP measures except the pulse pressure. There was a similar rate of elevated blood pressure between males and females (64% versus 60%; ). For both isolated systolic elevated BP and isolated diastolic elevated BP, the prevalences were comparable between the males (systolic: 42%; diastolic: 5%) and females (systolic: 34%; diastolic: 14%). Only systolic BP was positively correlated with BMI in obese adolescent males (Spearman ; ), with a significant correlation between BMI with diastolic (Spearman ; ) and mean BP (Spearman ; ) in females.
Clinical studies have already confirmed a strong relationship between obesity and hypertension  with visceral obesity seeming to represent the most important risk factor for hypertension and cardiovascular disease . Although the exact mechanism of how obesity is a cause of hypertension is unknown, many theories have been suggested such as activation of the renin-angiotensin-aldosterone system, oxidative stress, sympathetic overdrive, chronic vascular inflammation and endothelial dysfunction, which leads to structural changes such as thickening of the intima and media of the vessel wall [3, 4]. Obesity is an increasing worldwide health problem phenomenon especially in adolescents, and it is one of the main factors, in addition to family history, contributing to the increase in the prevalence and rate of diagnosis of hypertension in children and adolescents , with primary hypertension being very common in adolescents . The consequence of adolescent obesity was reported in a study which showed that BMI greater than the 75th percentile in adolescence usually lead to an increased risk of death from cardiovascular disease  in adulthood.
Many studies have emphasized the increasing obesity among adolescents in Kuwait. A study carried out in 2005 on adolescent Kuwaiti girls showed that they rank the highest in obesity compared with the same sex and age group in Egypt and Lebanon . More recently Musaiger et al.  showed that in comparison to other Arabic states, Kuwaiti adolescents showed the highest prevalence of obesity for both males (34.8%) and females (20.6%). This extends to Kuwaiti adolescents being among the highest in obesity prevalence not only in the Gulf countries but in the world reaching up to 40–46% [10, 11]. This was attributed to the rapid socio-economic growth in Kuwait and Arabian Gulf states in general, with the availability and consumption of fast food increasing by adolescent individuals.
In Kuwait, the prevalence of hypertension in young and middle aged Kuwaiti citizens of a minimum age of 21 years  was determined, with the study emphasizing the influence of body mass index on blood pressure and a major lack of previous knowledge or awareness of hypertension in hypertensive individuals. Surprisingly, in spite of the high prevalence of obesity in Kuwaiti adolescents, data on the prevalence of elevated blood pressure or hypertension in obese Kuwaiti adolescents does not exist. Accordingly, the purpose of this study was (1) to preliminarily estimate the prevalence of elevated BP in a representative small sample of extremely obese Kuwaiti adolescents and (2) to investigate the relationship between BP and body mass index (BMI) based on a single screening. As there is inconsistent or regular blood pressure monitoring in children and adolescents during visits to health centers in Kuwait, the importance of this study is to emphasize the significance of early detection of hypertension and intervention in adolescents with hypertension in Kuwait.
2. Materials and Methods
This study took place in Kuwait, a member of the Arabian Gulf states. Data for this study was collected between July and September, 2012. 257 participants of different adolescent ages (11–19 years) were selected on a volunteer-basis from Kuwait University, Capacity Academy courses, Kuwait Science Club (KSC), the Scientific Center, Saad Club, AL-Habara Club, Health Center and Shaab Leisure Park. The selection of subjects was based on examiners’ subjective estimation of obesity by sight, and to avoid embarrassment to the obese volunteers, some non-obese subjects were also asked to volunteer. Information about the participants’ age, gender, family history, smoking, alcohol, diet habits, exercise, cardiovascular disease and previous history of hypertension was also taken.
Before blood pressure (BP) measurement, the participants were asked about their intake of any stimulants. The weight and height of the participants were measured in a standing position (bare feet) using a precision electronic scale (HD-313 Digital Weight Scale, Tanita) and a stadiometer (Seca 222, Seca) respectively. The weight was measured in kilograms (kg) and the height in centimeters (cm). After measuring the weight and height the body mass index (BMI) was calculated as weight divided by height squared (kg/m2). BMI has been recommended as the most acceptable, valid and reproducible measure of body fat in children and adolescents which is both valid and reproducible . In normal children, BMI increases slightly with age, thus BMI percentiles, which are age specific, are used to define risk categories [14, 15], and BMI criteria of the International Obesity task Force (IOTF) were used to define obesity. The IOTF classification system provides extended BMI cut-points by age and sex for overweight, obesity, and severe obesity among children aged 2–18 years . Subjects with a BMI >30 kg/m2 were categorized as obese or severely obese according to the extended BMI cut-points. In this study, they would only be referred to as obese subjects. As the main aim of this study was to estimate the prevalence of elevated BP in a representative small sample of extremely obese Kuwaiti adolescents, the sample size of non-obese subjects in this study was much smaller (; 27 females: 56.3% and 21 males: 43.7%) than the obese sample (; 81 females: 38.75% and 128 males: 61.25%). The subjects in the severely obese group were divided into three adolescence stages, but this was not carried out for the non-obese group due to the small sample size.
An oscillometric fully-automated wrist device (BP W100, Microlife, Switzerland) was used to measure BP; the device had a blood pressure measurement range of 30–280 mm Hg and a statistic accuracy within ±3 mm Hg. As designated on the device, it was clinically validated according to the European Society of Hypertension (ESH) and the British Hypertension Society (BSH) protocols that require that automated device be compared with blood pressures measured by trained observers using a mercury sphygmomanometer and stethoscope. The width of the cuff was adjusted to the wrist circumference, and BP was measured in a comfortable sitting position two times on the right wrist with the arm supported and the cuff at the level of the heart, with 1 minute interval between the measurements. The average systolic and diastolic pressures were used to define BP. Percentiles of systolic and diastolic BP was generated using the World Health Organization (WHO) reference tables for Blood Pressure Levels by Age and Height Percentile. BP was diagnosed according to the official guidelines issued by the American Heart Association. Even though the new guidelines recommend multiple BP measurements at different sessions to define persistent hypertension and pre-hypertension, BP was measured two times in only one session in the present study. Accordingly, we adopted Din-Dzietham et al.  definition of high (elevated) blood pressure instead of hypertension however the same cutoff points of classification were used (Table 1). Elevated or high BP was considered for systolic and/or diastolic pressures >95th percentile for age.
Data was analyzed using the GraphPad InStat3 software. Descriptive statistics were presented as means, standard deviations (SDs) and percentages. The Kolmogorov and Smirnov test was used to assess the normality of the data. Comparison of means was carried out by the appropriate statistical test: two-sample Student’s tests were performed for between group comparisons of continuous variables with a normal distribution, and the Mann-Whitney test on variables with non-normal distributions. Spearman’s rho was used for testing statistical dependence between two variables. For treatment of frequencies, the Fischer’s Exact test was used. For all tests, the significance level was fixed at 0.05.
The mean age was years for the non-obese subjects and years for the obese subjects. The BMI values in the non-obese group followed a Gaussian distribution. In the obese group, the BMI values of the whole sample and some of the different age groups did not follow a normal distribution. Accordingly the mean was reported but the median was used for statistical comparison.
The mean BMI for the non-obese group was kg/m2, with no difference between sexes (male: mean BMI = kg/m2; female: mean BMI = kg/m2, ). Comparison as in Table 2 between the obese and non-obese subjects shows very significantly larger values of BMI in the obese sample.
Table 3 also illustrates the mean BMI values for each sex at different stages of adolescence. Clearly, the mean BMI value is greater than 30 kg/m2 for both sexes and coincides with cut-off values for severe obesity according to ITFO. There was no significant difference at any adolescent stage when comparing with the Mann-Whitney Test the median values for males and females (Median: males: 33.90, females, 33.00; ).
BP values in Tables 2 and 3 represent measurement of a single screening. Comparison in blood pressure parameters between the non-obese and obese group shows that the systolic BP and MAP in the obese subjects were very significantly larger than the non-obese group, with the diastolic BP marginally showing a difference (Table 2).
Table 3 values focus on BP measures from the obese subjects at three adolescent stages. It is obvious that there was a progressive increase in blood pressure measures with adolescence age, and values of all BP measures were highest for the age group of 17−19 years in both sexes. For systolic BP, the range in obese males was 102–179.5 mm Hg, and in obese females was 102–158 mm Hg, with the mean being significantly greater in males than females by almost 7 mmHg (, ) in the middle adolescent stage and 8.5 mm Hg (, ) in late adolescent stages. For diastolic BP, the range in males was 59–138 mm Hg, and in females was 50–129 mm Hg. Even though there was no statistical significance, it is worth pointing out that it was only in the late adolescent stage the diastolic pressure in males was about 6 mm Hg higher than in females.
As for the frequency of subjects with high BP in each group, Tables 2 and 3 show that 133 (63%) obese subjects had elevated BP on this initial screening according to the classification of the American Heart Association; there were only 6 subjects with elevated BP n the non-obese sample, representing a significantly less percentage than in the obese group (13% versus 63%; Fisher’s Exact test, ).
In the obese group, males as compared to females, had a non-significantly higher rate of elevated BP on first screening (64% versus 60%; Fisher’s Exact test, ) however the spread along adolescence years was different in both sexes (Table 3). In males the percentage of subjects with elevated BP increased with increasing adolescence stage, and an opposite pattern was evident in the females. In males there was an increase of 9% prevalence between early adolescence and middle adolescence, and there was a 12% increase between middle adolescence and late adolescence. In females, there was a decrease of 8% prevalence between early adolescence and middle adolescence and 6% between middle adolescence and late adolescence.
In the 133 obese subjects with elevated BP, the type of elevated BP which was contributing to the elevated BP was evaluated by frequency plot (Figure 1). The figure shows that more than half (70/133; 53%) of the obese subjects had both elevated systolic and diastolic BP. Males contributed more to the high isolated systolic BP (35/83; 42%) than females (17/50; 34%) but non-significantly (Fisher’s Exact test, ), while the opposite was true for females who non-significantly contributed more to the high isolated diastolic BP (7/50; 14%) compared to males (4/83; 5%) (Fisher’s Exact test, ).
Spearman correlation analyses between body mass index (BMI) and different measures of BP show that BMI of the total obese sample was significantly and positively correlated with systolic, diastolic and very significantly with the mean arterial pressure (MAP), but with no association with the pulse pressure (Table 4). Analysis further shows that in males, it was only the systolic BP that was significantly related to BMI, while in females both the diastolic BP and MAP were significantly correlated to BMI.
4. Discussion and Conclusion
The current study emphasizes many major findings relating obesity and hypertension in adolescents in Kuwait. Due to inconsistencies in working definitions of severe obesity, we adopted the newly published IOTF cut-points of obesity and extreme obesity, because they are now recommended for international use . Accordingly, all our obese adolescent subjects are considered obese to extremely obese, since the minimum BMI was 30 kg/m2 for both sexes and the range was up to 56.4 kg/m2.
In the obese sample, it is clear that the BP values were increasing with age, with minimal difference between the early stages of adolescence in the mean systolic BP in females, but occurring at later stages. The significant difference in systolic BP between males and females in mid and late adolescence stages confirm the fact that sexual dimorphism in arterial blood pressure appears in adolescence. This dimorphism persists throughout adulthood  up to 60 years of age, with average systolic and diastolic pressures in men being higher than aged-matched females by 6-7 and 3–5 mm Hg respectively . This may be attributed to the blood pressure lowering effect of estradiol in women and in our study to the possibility that menstrual regularity and sex hormone levels are still not well established in early adolescence.
It is also evident from the results that there was a high rate of elevated BP in the obese adolescent group. The association of the presence of obesity with much higher rates of hypertension has been previously established in other countries. In the report by McNiece et al.  on high school students, the prevalence of hypertension and pre-hypertension combined was more than 30% in obese adolescent boys and 23–30% in obese adolescent girls depending on ethnicity. Another study by Sorof et al.  reported a hypertension prevalence of 10.7% in multi-ethnic adolescents with BMI ≥95th percentile after 3 screenings. In our subjects, systolic, diastolic and mean BP was strongly associated with the BMI in the total obese sample. Systolic BP, diastolic BP and mean BP all increased with BMI. The high rate of isolated systolic high BP (39%), as well as elevated systolic along with elevated diastolic blood pressure (53%) in the obese adolescents in this study is alarming. In adults, isolated systolic hypertension was found to pose a strong and independent risk of cardiovascular mortality , with isolated systolic hypertension being more associated than isolated diastolic hypertension with risk of coronary heart disease, stroke and end-stage renal disease . A relatively recent systematic review and meta-regression analysis study that examined the tracking of blood pressure (BP) from childhood to adulthood has confirmed that childhood BP is associated with BP in later life .
There are a number of shortcomings in our study. Initially, the size of the non-obese sample was small and may not be an appropriate representation of the non-obese Kuwaiti adolescent population. However, the main aim of this paper was to focus on obese subjects and to estimate the prevalence of elevated BP in this representative group. An additional limitation is the high prevalence of elevated BP in the obese sample, and this could be attributed to methodological factors. An important factor is our measurement of BP on one single occasion. The new guidelines recommend multiple BP measurements at different sessions to define persistent hypertension and prehypertension . This is because it was previously shown that the number of subjects showing elevated BP values at the first measurement was double or more the number of subjects having BP measurement on two or three different visits . In Sorof’s study on school-aged children, the prevalence of elevated blood pressure after first, second and third screenings was 19.4%, 9.5% and 4.5% respectively. Following this rational, this implies that if additional screening measurements had been performed on subsequent occasions in the current study, it is almost certain that the overall prevalence of elevated BP would have continued to decrease probably to 30% on the second screening. Nevertheless, elevated single BP measurements should not be undermined, because 68% of adolescent boys and 43% of adolescent girls diagnosed with prehypertension and hypertension combined, on the basis of a single BP measurement, had prehypertension or hypertension 2 years later .
Another methodological factor for the high incidence of elevated BP could be the use of the automated oscillometric wrist BP monitor instead of the upper arm monitor. There has been much debate in recent years over the clinical accuracy of wrist BP monitors. A recent study led by Doshi et al.  have shown that even when a validated wrist device was used for BP measurement in a standardized protocol, there were significant differences for systolic BP and diastolic BP measured at the arm and wrist. In their study on obese patients, they found higher wrist values, with the majority of patients having systolic BP or diastolic BP absolute differences of ≥5 mm Hg between the two methods, and approximately one third having a difference of ≥10 mm Hg in systolic BP and diastolic BP.
In conclusion, the low degree of awareness among Kuwaitis of the risks of adolescent obesity has to be rectified in the light of the risk of the rapid socioeconomic growth in Kuwait. Actions such as increasing awareness programs in schools in Kuwait as well as continuous monitoring of blood pressure in children and adolescents during health center visits have to be emphasized and implemented further in Kuwait.
- J. E. Hall, “The kidney, hypertension, and obesity,” Hypertension, vol. 41, no. 3, pp. 625–633, 2003.
- A. M. Sironi, A. Gastaldelli, A. Mari et al., “Visceral fat in hypertension: influence on insulin resistance and β-cell function,” Hypertension, vol. 44, no. 2, pp. 127–133, 2004.
- J. A. N. Dorresteijn, F. L. J. Visseren, and W. Spiering, “Mechanisms linking obesity to hypertension,” Obesity Reviews, vol. 13, no. 1, pp. 17–26, 2012.
- K. Rahmouni, M. L. G. Correia, W. G. Haynes, and A. L. Mark, “Obesity-associated hypertension: new insights into mechanisms,” Hypertension, vol. 45, no. 1, pp. 9–14, 2005.
- J. M. Sorof, D. Lai, J. Turner, T. Poffenbarger, and R. J. Portman, “Overweight, ethnicity, and the prevalence of hypertension in school-aged children,” Pediatrics, vol. 113, no. 3, pp. 475–482, 2004.
- G. B. Luma and R. T. Spiotta, “Hypertension in children and adolescents,” The American Family Physician, vol. 73, no. 9, pp. 1558–1568, 2006.
- W. Kiess, A. Galler, A. Reich et al., “Clinical aspects of obesity in childhood and adolescence,” Obesity Reviews, vol. 2, no. 1, pp. 29–36, 2001.
- R. T. Jackson, M. Rashed, N. Al-Hamad, N. Hwalla, and M. Al-Somaie, “Comparison of BMI-for-age in adolescent girls in 3 countries of the Eastern Mediterranean Region,” Eastern Mediterranean Health Journal, vol. 13, no. 2, pp. 430–440, 2007.
- A. O. Musaiger, M. Al-Mannai, R. Tayyem et al., “Prevalence of overweight and obesity among adolescents in seven Arab countries: a cross-cultural study,” Journal of Obesity, vol. 2012, Article ID 981390, 5 pages, 2012.
- S. W. Ng, S. Zaghloul, H. I. Ali, G. Harrison, and B. M. Popkin, “The prevalence and trends of overweight, obesity and nutrition-related non-communicable diseases in the Arabian Gulf States,” Obesity Reviews, vol. 12, no. 1, pp. 1–13, 2011.
- M. M. Abdul-Rasoul, “Obesity in children and adolescents in Gulf countries: facts and solutions,” Advances En Diabetologia, vol. 28, no. 3, pp. 64–69, 2012.
- F. Al-Jarky, N. Al-Awadhi, H. Al-Fadli, A. S. Tawfic, A. R. Al-Sebai, and M. Al Mousawi, “Prevalence of hypertension in young and middle aged Kuwaiti citizens in primary health care,” Kuwait Medical Journal, vol. 37, no. 2, pp. 116–119, 2005.
- M. C. Bellizzi and W. H. Dietz, “Workshop on childhood obesity: summary of the discussion,” The American Journal of Clinical Nutrition, vol. 70, no. 1, 1999.
- A. Pietrobelli, M. S. Faith, D. B. Allison, D. Gallagher, G. Chiumello, and S. B. Heymsfield, “Body mass index as a measure of adiposity among children and adolescents: a validation study,” Journal of Pediatrics, vol. 132, no. 2, pp. 204–210, 1998.
- R. M. Malina and P. T. Katzmarzyk, “Validity of the body mass index as an indicator of the risk and presence of overweight in adolescents,” The American Journal of Clinical Nutrition, vol. 70, no. 1, pp. 131S–136S, 1999.
- T. J. Cole and T. Lobstein, “Extended International (IOTF) body mass index cut-offs for thinness, overweight and obesity,” Pediatric Obesity, vol. 7, pp. 284–294, 2012.
- R. Din-Dzietham, Y. Liu, M.-V. Bielo, and F. Shamsa, “High blood pressure trends in children and adolescents in national surveys, 1963 to 2002,” Circulation, vol. 116, no. 13, pp. 1488–1496, 2007.
- A. Himmelmann, A. Svensson, and L. Hansson, “Influence of sex on blood pressure and left ventricular mass in adolescents: the hypertension in pregnancy offspring study,” Journal of Human Hypertension, vol. 8, no. 7, pp. 485–490, 1994.
- V. L. Burt, P. Whelton, E. J. Roccella et al., “Prevalence of hypertension in the US adult population: results from the third National Health and Nutrition Examination Survey, 1988–1991,” Hypertension, vol. 25, no. 3, pp. 305–313, 1995.
- K. L. McNiece, T. S. Poffenbarger, J. L. Turner, K. D. Franco, J. M. Sorof, and R. J. Portman, “Prevalence of hypertension and pre-hypertension among adolescents,” Journal of Pediatrics, vol. 150, no. 6, pp. 640–644, 2007.
- H. M. Perry Jr., J. P. Miller, J. D. Baty, S. E. Carmody, and M. P. Sambhi, “Pretreatment blood pressure as a predictor of 21-year mortality,” The American Journal of Hypertension, vol. 13, no. 6, pp. 724–733, 2000.
- J. He and P. K. Whelton, “Elevated systolic blood pressure as a risk factor for cardiovascular and renal disease,” Journal of Hypertension, vol. 17, supplement, no. 2, pp. S7–S13, 1999.
- X. Chen and Y. Wang, “Tracking of blood pressure from childhood to adulthood: a systematic review and meta-regression analysis,” Circulation, vol. 117, no. 25, pp. 3171–3180, 2008.
- National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents, “The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents,” Pediatrics, vol. 114, no. 2 supplement, pp. S555–S576, 2004.
- B. Falkner, S. S. Gidding, R. Portman, and B. Rosner, “Blood pressure variability and classification of prehypertension and hypertension in adolescence,” Pediatrics, vol. 122, no. 2, pp. 238–242, 2008.
- H. Doshi, A. B. Weder, R. L. Bard, and R. D. Brook, “Does “hidden undercuffing“ occur among obese patients? Effect of arm sizes and other predictors of the difference between wrist and upper arm blood pressures,” Journal of Clinical Hypertension, vol. 12, no. 2, pp. 82–88, 2010.