Abstract
Purpose of Review
To review recent evidence on childhood hypertension across Africa, identifying knowledge gaps, challenges and priorities, and highlight clinical perspectives in managing primary hypertension.
Recent Findings
Only 15 of the 54 African countries reported on absolute blood pressure (BP) measures, elevated BP, pre- and/or hypertension. The reported hypertension prevalence ranged between 0.0 and 38.9%, while elevated BP and/or pre-hypertnesion ranged from 2.7 to 50.5%. Childhood BP nomograms are lacking across Africa and the rates of hypertension were based on guidelines developed in countries with the lowest to no number of children from African ancestry. The recent studies across Africa also showed little to no detail when reporting BP specific methodology. No recent data informing the use or effectiveness of antihypertensive agents in children and adolesents are available.
Summary
Childhood hypertension is on the rise, while data from Africa remains vastly under-represented. Collaborative research, resources, and policies need to be strengthened in addressing the growing public health concern of childhood onset hypertension on this continent.
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Introduction
Paediatric hypertension—defined by age, sex and height-specific systolic and/or diastolic blood pressure (BP) nomograms—has its roots in early childhood and adolescence [1] as reported in several longitudinal cohorts [2–5]. Hypertension is a public health concern, particularly in Africa where the prevalence is steadily increasing among children and adolescents [6]. With a shift towards elevated BP during childhood as a key driver of adult hypertension, the importance of early elevated BP detection, prevention, and intervention strategies is critical [7].
Hypertension can be stratified by its aetiology into:
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1.
Primary or essential hypertension that remains a condition of multifactorial origin as a result of behavioural, environmental or genetic causes or the interaction of both.
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2.
Secondary hypertension that has multiple aetiologies, including renal, vascular, and endocrine causes.
Although secondary hypertension is more common in children than in adults, primary hypertension in the paediatric population is on the rise [6]. Children and adolescents with primary hypertension present with a typical clinical phenotype similar to the abnormalities observed in hypertensive adults. Behavioural, environmental, biological and/or atypical genetic factors mediate the tendency to develop hypertension [8, 9]. While studies have shown a behaviour-environment association with childhood BP, there remains a lack of large-scale genome-wide association studies specific to the African region, and more so, in children and adolescents. The few genetic studies in children and adolescents reported consistent findings for multiple single nucleotide polymorphisms (as a genetic risk score) to associate with BP levels in children [3, 10] and to predict hypertension in adulthood [11]. Although these landmark studies were limited to the Young Finns Study [12], the Avon Longitudinal Study of Parents and Children [13], and the Western Australian Pregnancy Cohort [14], they do provide important information going forward for new studies to determine similarities or differences in genetic variants in other parts of the world. However, in Africa, 50% of African countries are low-income, and 18 African countries are among the world’s poorest [15]. Consequently, the prevalence and concomitant research of childhood hypertension in Africa is limited as many countries are not monitoring and reporting BP in children given other more pressing demands.
Reliable estimates of childhood hypertension serve as the basis for prevention, treatment, intervention and evidence-based health resource allocation and policy making. However, in Africa, childhood hypertension has rarely been synthesised. Therefore, aside from reporting the recent prevalence of childhood hypertension across Africa, this review will also discuss the impact of risk factors and/or interventions associated with childhood BP; current challenges and priorities; and the clinical perspectives surrounding childhood hypertension across the continent.
Childhood Hypertension in Africa
The Prevalence of Childhood Hypertension in Africa
Of recent (2018–2022) studies that included a broad range of randomised control trials (RCTs), interventions, cohort, case, longitudinal and cross-sectional studies, only 66 studies (Table 1) from 15 countries across Africa reported on BP in African children and adolescent cohorts, either absolute BP measures, elevated BP, pre- and/or hypertension. Considering that Africa is the second largest and second most populous continent, after Asia, childhood hypertension in this setting is underreported (Fig. 1). Majority of the studies were those conducted in the Southern most part of Africa (37.9%), with South Africa contributing to 23 of the 25 studies reported in this region. Although not all studies reported a hypertension prevalence, we found that from the 53 studies that did, the reported childhood hypertension prevalence on the African continent between the years 2018 to 2022 ranged extensively from 0.0% in an Egyptian adolescent study that included n = 77, 12–18-year olds [16] to 38.9% in 2 studies namely a case control study that included n = 72 Egyptian children and adolescents (3–14 years) [17] and that of a RCT on n = 1119 Ugandian adolescents (10–11 years) [18].
Both aforementioned Egyptian [17] and Ugandian [18] studies that reported an alarmingly high prevalence of childhood hypertension in Africa (38.9%) were suggestive that the level of adiposity or body weight in early life may directly influence BP. El-Koofy et al. showed that babies with a low birth weight are at increased risk of high BP in later life due to rapid early weight gain [17]. Lule et al. showed that hypertension was reported in 70.0% of children with obesity determined via Centre for Disease Control (CDC) anthropometric z-scores [18]. These results are therefore suggestive that the rates of hypertension in childhood are increasing with adverse lifestyle behaviours (i.e. childhood obesity) [19].
Northern Africa, specifically Egypt, reported the lowest and highest prevalence of elevated BP or pre-hypertension across Africa, ranging from 2.7% in an intervention study of n = 224 adolescents (12–14 years) [20] to 50.5% in a cross-sectional study of n = 200 adolescents (12–18 years) [21]. The intervention study by Elseifi et al. suggested that the students who were pre-hypertensive for systolic and diastolic BP showed infrequent intake of breakfast per week [20], while the cross-sectional study by Hassan et al., showed that girls with overweight/obesity presented with significantly higher prevalence of hypertension (66.7% vs. 40.8%), diabetes (46.7% vs. 31.2%) and low levels of high-density lipoprotein (64% vs. 59.2%) than normal-weight girls [21]. The largest study was a cross-sectional study that was carried out by Muyumba et al. (2018), that included n = 7523 children and adolescents (aged 3 to 17 years) in Lubumbashi, Democratic Republic of Congo [22••]. This was the first study of its kind to determine threshold percentiles (50, 90 and 95%) for BP specific to age and height for this unique population demographic [22••].
The only systematic review and meta-analysis between 2018 and 2022 pertaining to childhood hypertension in Africa, was conducted by a group of researchers from South Africa that shed light on childhood hypertension across the continent [23••]. Crouch et al. reported that the prevalence of childhood hypertension in Northern and Eastern Africa, accounted for more than 9.5% in these regions [23••]. Significant differences in the hypertension prevalence was also reported with the Southern and Western African regions trailing close behind (Northern (15.2%), Eastern (9.5%), Southern (7.9%), Western (6.0%), and Central (1.6%)) [23••]. The hypertension prevalence in Africa did not significantly differ when looking at population demographics such as age, sex or areas of urbanicity [23••], and can partially be explained by the lack of geographical data from 18 of the 41 studies. Discrepancies in rural–urban differences are well reported in the African context [24, 25••], but the rise in obesity may supersede the urban-rural divide. Although environmental variations of BP seem difficult to justify, a low socioeconomic status, as seen across many African countries, and the incidence of obesity are among the two most probable contributing factors [26, 27••].
Blood Pressure Measurement Techniques and Devices Currently in Use Across Africa
BP measurements at a population level can generate important trends to use as an indicator of population health as a whole. Consequently, global guidelines for proper BP measurement have existed for several years. Despite this, a study conducted by Hassan et al., reported a 0.0% childhood hypertension prevalence in Northern Africa but only recorded BP manually and a single measurement [16]. El-Koofy et al., did not disclose or describe any particular BP methods [17] while Lule et al., reported a 38.9% childhood hypertension prevalence after BP was measured on an automated osciillometric device on 3 separate occasions [18] as suggested by known international guidelines. In several research studies, BP measurement methods and thresholds used are not always properly reported, which can impact on results derived from these studies. We found that from the studies we reported in Table 1, the type of BP measurement device, the number of measurements and/or rest intervals between measurements were generally poorly reported. For instance, 18.2% (12/66) of the reported studies did not disclose or describe detailed BP methodology altogether and a further 31.8% (21/66) had missing information regarding either the type of BP measurement device, the number of measurements and/or the resting interval between meaurements. Significant differences have been reported between the type of BP measurement device used (i.e. manual versus automated oscillometric), the number of measurements taken (i.e. single versus multiple/single versus repeated measurement) and the paediatric clinical practice guideline used to stratify participants into their BP statuses. We noted that the majority of studies in the Northern African region still prefer to acquire BP manually. The prevalence of adverse BP across Africa, must be interpreted with caution firstly considering the lack of countries reporting (Fig. 1; Table 1) and secondly considering the array of BP methodology still currently in use across the continent.
Recent Advances in Childhood Hypertension
Various modifiable risk factors have been linked to higher BP levels and other forms of cardiovascular disease risk in children in Africa (Table 2). These factors have been reported in children and adolescents between the ages of 1–19 years, with the majority of the studies done in Western and Southern African regions. Among the BP associated risk factors, the majority of the findings showed an adverse association between overweight/obesity and pre-hypertension and/or hypertension [27••, 28••, 29–40]. The prevalence of overweight/obesity ranged from 2.2 to 33.0% with the highest prevalence being reported in South Africa. The largest study was a national cross-sectional study done by Amponsem-Boateng et al., and included n = 3165 students aged between 12 and 22 years [38]. This study aimed to screen for hypertension, risks and knowledge/awareness in second-cycle schools in Ghana. The risk factors for early hypertension that were identified included body mass index (BMI), waist circumference and body weight with a high statistical significance between BMI and pre-hypertension as well as hypertension [38]. In these Ghanaian students, 19.9% were hypertensive and 26.1% were pre-hypertensive which may indicate a likely high prevalence of hypertension in the future adult population [38]. It is noteworthy to mention that the majority of the studies in Africa investigating overweight/obesity in children were cross-sectional in design and that different classifications for overweight/obesity were used throughout (i.e. International Obesity Task Force, World Health Organisation (WHO) and CDC).
Linking closely with overweight/obesity is the prevalence of physical inactivity [38, 41–45], with alarmingly high levels being reported in a South African study by Joubert et al. [41]. In this study, n = 109 children aged 8–13 years were included and 39.0% of these children self-reported being physically inactive [41]. Hypertensive children in this study were also more likely to be overweight/obese, but only if they did not meet physical activity recommendations [41]. In a cluster-RCT with n = 853 children aged 8–13 years in eight primary schools in Port Elizabeth, South Africa, cardiorespiratory fitness, sport participation, BMI, and BP were assessed at baseline and after a physical activity intervention [43]. The authors showed that high cardiorespiratory fitness and high sport participation were negatively associated with overweight/obesity, while high sport participation was also associated with lower risk for hypertension [43]. The Ampe (a Ghananian house-hold recreational game that includes a combination of physical workout and social bonding) exercise programme implemented in Ghana for instance, proved effective as a paediatric obesity household intervention that provided the impetus for active lifestyles to reduce BP [45]. Longitudinally, those who participated in the physical activity intervention were less likely to become overweight/obese. These findings highlight the relationship between physical activity and body weight.
With regard to diet [20, 38, 39, 46–48], data from the studies included in this review suggest that sodium intake is a factor of concern. In the Ghanian national cross-sectional study done by Amponsem-Boateng et al., it was shown that adding extra salt to a meal increases the odds of developing hypertension by 36.0% and by 16.0% for pre-hypertension [38]. In a Nigerian study including n = 488 children aged between 10–19 years, the majority consumed far higher levels of sodium and/or far lower levels of potassium than what is recommended with about 39.0% of adolescents with hypertension adding table salt to their already prepared foods [46]. These findings are concerning as the intake of sodium may be set to increase as the African continent undergoes considerable urbanisation.
Early life exposure to unhealthy environmental factors and maternal risk factors [49–53] are linked to an increased risk for elevated BP in children in various African settings. These factors, discussed in the next few paragraphs include among others, hypertension, hypertensive disorders of pregnancy, hyperglycaemia, smoking, alcohol use, overweight/obesity, physical inactivity, and low socioeconomic status [49–53]. Exposure to adverse maternal factors such as smoking, alcohol consumption, and micronutrient deficiency may have a detrimental effect on cardiovascular system development through DNA methylation [54–56].
De Smidt et al. investigated whether there is a link between maternal smoking (nicotine exposure) and alcohol consumption during pregnancy and carotid intima-media thickness (cIMT) in 5-year-old South African children from a low-income environment [53]. The main finding of the study was that exposure to both alcohol and nicotine, maternal adiposity, and male sex of the offspring were associated with an increase in right cIMT at 5 years of age [53]. In contrast, another study in South African children [54], this time from Soweto, a township of Johannesburg, showed that hyperglycaemia first detected in pregnancy was not associated with BP in offspring aged 3–6 years. Regardless of this observation, the prevalence of elevated BP in these children was alarming (49.7%) and warrants further investigations into contributing factors, particularly in low socioeconomic environments to improve detection and develop appropriate interventions.
Recently, a hospital-based cross-sectional study in the Tigray region of Ethiopia assessed foetal and maternal outcomes and associated factors in mothers with hypertensive disorders during pregnancy [52]. A large proportion of the study population (66%) was from rural areas, with rural residence, together with ante- and intrapartum-onset hypertensive disorders of pregnancy later identified as one of the predictors of perinatal complications [52]. More than half of the newborns from hypertensive mothers had adverse outcomes which included among others, low birth weight (20.7%) [52]. This observation highlights the importance of taking into consideration the impact rural versus urban settings have on maternal and subsequently offspring health outcomes, both short and long term, specifically for cardiovascular disease development.
A cross-sectional study in Cameroon explored associations of birth weight with BP and kidney function as assessed by glomerular filtration rate and proteinuria in n = 80 children (aged 5–10 years) [49]. The study population was stratified according to low birth weight (< 2500 g), normal birth weight (2500–3999 g), and high birth weight (≥ 4000 g). When focusing on BP, 9.5% of the low birth weight children had hypertension, while 4.4% of the normal weight children had elevated BP [49]. In seven children with proteinuria, 19.0% had low birth weight [49]. Overall, there was a trend towards a negative association between birth weight and BP and kidney function, although not statistically significant.
The shift from rural to urban settings and associated lifestyle changes have a large impact on cardiometabolic risk factors, not only in adults, but in children, although recent data from Africa is scant. A large cross-sectional study focused on school and college-based healthy children (aged 6–18 years) in a suburban area west of Algiers, North Africa [50]. The prevalence of hypertension increased with age, 8.7% for 6–10-year-old children and the highest prevalence (15.6%) was recorded for those older than 15 years of age [50]. In addition, for both prehypertension and hypertension the prevalence increased with higher BMI and was the highest in obese children, 26.8% and 32.3%, respectively [50]. Time spent engaging in sedentary behaviour such as watching television, internet and electronic gaming was associated with prehypertension [50]. Other population characteristics associated with either prehypertension, hypertension or both included parental history of hypertension or diabetes and maternal and postnatal factors such as gestational age, early term delivery, lower birth weight and shorter breastfeeding periods. More comprehensive studies are needed to inform preventative strategies to tackle risk factors associated with the rising burden of childhood hypertension in Africa.
Current Challenges and Priorities
Methodological Issues
The detection of hypertension in children and adolescents is highly dependent on the proper measurement of BP in research and clinical practice settings and is affected when methodological aspects are not optimal. While BP is a vital sign and a standard diagnostic tool in clinical practice [57], measurement of BP in children and follow-up is often neglected in clinical practice [57]. When measured, several errors have been reported which seem to have universal characteristics for both children and adults. Some of these errors are related to observer bias or mistakes due to a lack of proper training, the patient’s behaviour or experience during measurements, while some errors are inherent to the device algorithms due to proprietary rights from manufacturers who are unwilling to disclose algorithm coefficients and factors used in their algorithm or transfer function development. While the effects of risk factor exposure in children are less extensively known, other factors such as temperature [58], noise exposure [59], pollutants [60] and/or discomfort related to a lack of privacy during the measurement can contribute to errors in BP measurements [61, 62]. In Africa, the methodological issues related to BP measurement, diagnosis and treatment are undeniably more challenging. These challenges include (among others) the limited access to and affordability of paediatric validated BP devices, accredited calibration centres, the lack of African specific nomograms for childhood and adolescent BP, and the non-existence of proper treatment algorithms for the massive population diversity on the African continent. In this section, the methodological issues will be briefly discussed under four main categories namely the patient (“The Patient”), the observer (“The Observer”), BP devices (“The Device”), as well as the protocol and guidelines (“The Protocol and Guidelines”).
The Patient
Measuring BP accurately largely depends on the cooperation of the patient and their understanding of the conditions under which the measurements should be taken. Barriers specific to the patient can include language, age, body size, mood, culture, and illness or circumstances in which BP is measured. In Africa, over 2000 languages are spoken. Furthermore, the rural population comprise more than half of Africa [63], which poses several barriers in terms of education and communication. Basic BP measurement instructions (i.e. back supported and feet flat on the ground without talking) provided by health care professionals are difficult to understand by a large proportion of individuals and may be even more challenging in the childhood population, when local or indigenous languages are mostly learned. The language barrier is accompanied by age, since younger children (e.g. under 5 years) find it more challenging to follow such instructions. These younger age groups are also less likely to keep still for prolonged periods while BP is measured and are often restless with their feet, especially when the feet are not properly supported due to the use of an adult sized chair for a child. Larger children or adolescents on the other hand, provide a challenge in terms of BP cuff size. Some manufacturers do not offer a large range in cuff sizes specific to the paediatric population and observers then need to improvise by using adult-sized cuffs, which may contribute to under- or over- estimatation of BP when the cuff is either too big or too small [64]. Children can be unpredictable in how they tolerate BP measurement and their temperament can influence the BP readings when a child is moody and does not enjoy the experience of the measurements, even more so for ambulatory BP monitoring (ABPM) [65]. Due to several geopolitical issues in many African countries, there also exist cultural conflict when the observer and patient do not share compatible cultural beliefs or tolerability for certain ethnic groups [66]. This is a reality on the African continent and ethnic discord has contributed to many challenges in the clinical spheres of treatment and healing due to the spillover of political favouritism in African countries [67]. Therefore, in some cultures in Africa it works best to measure BP in a group of children and not in isolation, to reduce the risk of fear and stigma when participating in research studies, although this is not what clinical guidelines from developed countries propose. Lastly, in certain disease conditions when it is not possible to measure a child’s BP in the optimal sitting position, there are several challenges due to divergent criteria available in the literature and the lack of clinical practice guidelines in Africa for detecting primary hypertension in children and adolescents.
The Observer
The nurse, medical specialist, clinician, or researcher is referred to as the observer taking the BP measurement. Similar barriers, as for patients, are evident in the clinical setting whereby nurses or clinicians have to measure BP. However, apart from language differences, managing a very young child (position, cuff size, cuff position and arm selection, removing thick or tight fitting clothing, etc.), and device preference (manual sphygmomanometer, auscultatory or automated (oscillometry) may lead to several observer specific barriers that lead to errors in BP measurements. While proper training for BP measurement can not be more emphasised, deviations from protocols are a given in most busy hospitals or clinical settings whereby nurses or doctors do not have enough time to perform proper BP measurements, or in some cases not at all [68]. The real-life environment for medical staff is a challenge by itself in terms of multitasking, time management, the availability of equipment, and the location of practice (e.g. crowded and noisy clinics with limited space but large patient influx in the public sector compared to more controlled environments in the private sector) [69, 70]. An international survey indicated that Africa has the greatest workforce burden for the number of paediatricians per 100,000 children and adolescents under 18 years with a reported median ratio of 0.8 (IQR: 0.4–2.6) [71]. As a result of such rushed environments and circumstances, the standard protocol for accurate BP measurement is overlooked and often no rest period is given to patients before the first BP measurement is taken, while in most cases no further measurements are performed and clinical decisions are based on one non-standardised BP value. In addition, talking remains one of the greatest human errors in BP measurement. When a patient talks while the cuff inflates and deflates, BP is directly affected. Similarly, when nurses, doctors or other medical specialists have discussions during the BP measurement, BP errors are unavoidable.
The Device
The validation of BP devices is one of the persistent global methodological challenges in the hypertension sphere [60]. Several BP devices have been validated for clinical use, while no BP device has been validated in Africa or specifically in any African population group. Validating BP devices in Africa is a priority area since there is a lack of data available that illustrates whether BPs are under- or overestimated by BP devices validated elsewhere. The propriatry nature of automated BP device algorithms, limits the ability to distinctively identify the factors that influence BP readings for a specific manufacturer’s device model(s). It is therefore unknown whether such algorithms account for biological and ethnic differentiation between population groups from various parts of the world [72]. With the majority of validation studies being outdated due to the recent updates of the international validation protocols, such studies were also in violation of the validation protocols as a result of incomplete reporting of essential information [73]. In addition to devices being validated, the regular calibration of BP devices seems neglected. Calibration of aneroid devices is essential for accurate BP measurement, while electronic devices need to be serviced annually by accredited centres to assure BP accuracy over time [70]. In addition to aneroid, automated or semi-automatic oscillerometric devices for clinic use, there are also device related concerns in Africa specific to 24 h ABPM, home BP monitoring and cuffless or wearable technology. While use of ABPM is optimal for clinical practice and in special conditions in paediatrics due to its benefits (i.e. good reproductibility, detection of white-coat and masked hypertension [74], demonstration of BP variability and dipping patterns [75]), access and affordibility are two of the main limitations to use in African and other developing countries. Ambulatory BP monitoring is used in Africa especially in private hospitals and clinical research settings, however, there remains a major risk of device loss and damages of such devices. Home BP monitoring is slightly more challenging due to limited time for proper patient training on the use of the device, the availability of home BP monitors in clincal practice or cost to patients to purchase a validated BP device for home use. Connectivity is another challenge when BP readings need to be sent to a central patient registry for BP telemonitoring, especially in deep-rural areas with limited mobile network infrastructure or high cost for mobile data or wireless connectivity. Although wearable technology is expanding globally, and access is available in African countries, such devices are not currently of much clinical use due to poor reliability and/or accuracy, and lack of validated wearable or cuffless devices [76]. Another critical device-related criteria for accurate BP measurement is the cuff size and placement [77]. In paediatrics, upper arm circumferences are ranging vastly from extremely thin to adult size. Unfortunately, not all BP manufacturers provide a sufficient variety of cuff sizes. Using the wrong cuff size can provide massive errors in BP measurements. Independent of the type of device, the cuff size and placement remain one of the biggest pitfalls in BP measurement accuracy.
The Protocol and Guidelines
Even among the internationally recognised hypertension guidelines there are various discrepencies contributing to confusion and non-standardised methodology when applied in Africa. Especially in low resource settings where time is limited and the clinician to patient ratio is dramatically skewed, studies reported high numbers of paediatric patients not screened for hypertension in primary care. The main reason is the absence of risk factors for hypertension (especially secondary hypertension), increasing the potential to under-diagnose primary hypertension [68]. A study in South Africa has shown that using the mean of the lowest three of five BP measurements in young (5–9 years old) children [27••], almost 40.0% of the children had abnormal BP based on the 2017 American Academy of Pediatric Clinical Practice Guideline (2017, AAP CPG) [77], albeit at a single office visit. The number of BP measurements that should be performed at a single visit in the clinic differs in the currently available guidelines from other countries. Some guidelines advise on discarding the first measurement and use the mean of the second and third [78], while others support using the mean of two measurements or one measurement and only repeated twice if BP was elevated [77]. As expected, BP will drop with consecutive measurements until tolerance is saturated, however, no consensus exist currently on the number of BP measurements required for clinical use. For hypertension status confirmation, a second and third visit is required. But in reality, due to constraints in the primary health care environment, BP is often measured once to determine BP status or not at all in the case of otherwise healthy children or adolescents. Guidelines recommend to allow a 3–5-min rest before and a 1–2-min interval when performing repeated BP measurements with automated BP devices. A rest period prior to BP measurement is necessary to calm the patient and to ensure that all conditions are met to acquire an accurate BP reading. However, a study reported that negligible differences were observed between 30-s and 60-s intervals and indicated that shorter time intervals are more feasible in clinical practice [79], while guidelines still recommend 1-min intervals. Since the recommendation of automated BP devices [80], due to its limited margin of human error, some task groups and authors have indicated that observer training and re-training is non-essential when making use of automated or semi-automated devices. While human errors in terms of auscultation is absent for oscillometric devices, human error is still involved in the selection of cuff sizes, environmental conditions in which BP is measured, proper patient counselling and positioning, adherence to recommended guidelines in terms of resting periods and time intervals in-between measurements and finally recording BP values correctly to a patient record.
The variety of hypertension guidelines in paediatrics is also a potential pitfall for African countries (and others) that do not have their own nomograms for BP in children and adolescents [81••]. Several childhood BP guidelines are in use to allow for the detection of high-risk children and adolescents. These include, among others, the Report on the Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents (NHBPEP) (2004 Fourth Report) [82], 2017 AAP CPG [77] and the European Society of Hypertension (2016 ESH) [78]. These age, sex and body height specific BP guidelines originate from high-income countries (HICs). Several population-based studies in several parts of Asia, Europe, Northern Africa and the United States of America (USA), have prospectively examined the usefulness of these HICs childhood clinical practice guidelines in identifying high-risk children and adolescents [83, 84]. Certainly, adult hypertension guidelines are frequently applied in LMIC settings illustrating that a HIC BP guidelines can perform in a LMIC adult population. A recent mixed cross-section longitudinal study conducted in South Africa highlighted that when the three most applied international childhood clinical practice guidelines (2004 Fourth report; 2016 ESH and 2017 AAP) were used to detect hypertension in an African paediatric cohort, a varied hypertension prevalence was reported [81••]. Consistent with the findings from numerous recent cross-sectional studies conducted worldwide [84–86], the 2017 AAP CPG identified a greater hypertension prevalence and a decrease in the number of children and adolescents with pre-hypertension showing a concomitant upward trend in the prevalence of hypertension [81••, 83, 87]. The most prominent reason for the observed disparities is the notable differences seen in the BP charts or nomograms. The 2017 AAP CPG guideline excludes obese or overweight children and adolescents. In an era where childhood obesity is a growing concern, in conjunction with the fact that body composition (i.e. obesity) is a significant cause for the development of primary hypertension, a population that includes obese or overweight youth will render an heightened overall hypertension prevalence. Another prominent reason for the varied prevalence may be due to the linear growth of the population as nomograms are body height specific. When comparing the various paediatric BP guidelines, the 2017 AAP CPG for example shows a much broader BP range for shorter individuals, while the gaps tends to decrease for taller individuals [77]. Results from the study by Craig et al. (2022), showed that the African paediatric cohort was on average shorter than that expected according to age- and sex-matched growth charts listed by the WHO [81••, 88]. Another recent study carried out on n = 32 248 Zimbabwean children also reported that the African paediatric cohort were shorter and weighed less in comparison to WHO growth charts [89]. Therefore, African youth of a shorter stature may have a lower threshold for elevated BP due to being shifted into a low height percentile. As a result, applying the simple adoption of childhood BP nomograms from a HIC may not be best suited for LMICs with diverse population characteristics. These guidelines may therefore introduce unpredicted bias in evaluating childhood BP resulting in a significant over or under-estimation of the BP status. The need to explore country or region-specific BP guidelines has therefore gained momentum considering the increasing childhood hypertension burden in Africa alone.
Clinical Perspectives—Current Challenges and Priorities
Despite the availability of international BP nomograms [77, 78, 90–92] and proposed paediatric hypertension guidelines [77, 78, 93–95], the applicability thereof in Africa remain uncertain. Available nomograms for childhood BP are from countries with the lowest to no number of citizens from African ancestry compared to Africa. These countries include the USA [77], China [93], Japan [95] and Western European countries [78], while other countries such as Canada [94] and India [96] have their own proposed criteria for detecting hypertension in children and adolescents. While these are all essential documents and useful to paediatricians, paediatric specialists and epidemiologists, there remains much work to be done to define BP nomograms in Africa and to determine the usefulness of international paediatric hypertension guidelines in the African region. Notwithstanding the support for efforts to sensitise the need for region-specific normative data, expert groups from all parts of the world should aim to forge globalised guidelines for the detection and management of primary hypertension in paediatrics.
Another concern is that there are no recent data informing the use of antihypertensive agents in children and adolesents in Africa. Additionally, there are no appropriate data to assess the long-term effectiveness of treatment of high BP in children or adolescents with pharmacological interventions that may have the ability to reduced BP and adverse health outcomes in later life. An Africa-centered collaborative effort to intensify peadiatric hypertensive studies is urgently needed to address this knowledge gap on the African continent.
Conclusion
Despite several efforts to understand childhood onset of hypertension in Africa, remaining challenges include limited access to healthcare, inadequate resources for screening and diagnosis, and poor awareness among caregivers and healthcare professionals regarding the importance of early detection and management. Overall, the studies addressing childhood hypertension have emphasised that research, resources, and policies need to be upscaled to address this burgeoning public health concern.
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Open access funding provided by North-West University. AC is supported by the Department of Science and Innovation (DSI)—National Research Foundation (NRF) Centre of Excellence in Human Development at the University of Witwatersrand, Johannesburg. RK is supported by the South African Research Chairs Initiative (SARChI) of the DSI and the NRF of South Africa (Unique Identification Number: 86895). Any opinion, findings and conclusions or recommendations expressed in this material are those of the authors, and therefore, the DSI or NRF does not accept any liability in this regard. None of the funding bodies contributed to the conceptualisation, data collection or writing of this paper.
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Craig, A., Breet, Y., Gafane-Matemane, L.F. et al. Detecting and Managing Childhood Onset Hypertension in Africa: A Call to Action. Curr Hypertens Rep 25, 211–230 (2023). https://doi.org/10.1007/s11906-023-01247-3
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DOI: https://doi.org/10.1007/s11906-023-01247-3