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Prevalence of metabolic syndrome and components in rural, semi-urban and urban areas in the littoral region in Cameroon: impact of physical activity



Living areas in developing countries impact seriously lifestyle by modifying energy consumption and energy expenditure. Thus, urbanization is associated with less practice of physical activity (PA), a leading cause of metabolic syndrome (MetS) which prevalence vary in African countries. The present study aimed to assess the effect of PA on MetS according to urbanization level in the littoral region, Cameroon.


A cross-sectional study was conducted in three geographical settings (urban, semi-urban, and rural) in the littoral region in Cameroon. A total of 879 participants were included (urban: 372, semi-urban: 195 and rural: 312). MetS was defined according to the International Federation of Diabetes 2009. The level of PA was assessed using the Global Physical Activity questionnaire.


Low level of PA was (P < 0.0001) reported in urban (54.5%), semi-urban (28.7%) and rural (16.9%) and high level in rural area (77.9%). The prevalence of MetS was higher in urban areas (37.2%), then rural (36.8%) and finally semi-urban (25.9%). Hyperglycemia (p = 0.0110), low HDL-c (p < 0.0001) and high triglyceridemia (p = 0.0068) were most prevalent in urban residents. Participants with low level of PA were at risk of MetS (OR: 1.751, 95% CI 1.335–2.731, p = 0.001), hyperglycemia (OR: 1.909, 95% CI 1.335–2.731, p = 0.0004) abdominal obesity(OR: 2.007, 95% CI 1.389–2.900, p = 0.0002), low HDL-c (OR: 1.539, 95% CI 1.088–2.179, p = 0.014) and those with moderate level of PA were protected against high blood pressure(OR: 0.452, 95% CI 0.298–0.686, p = 0.0002) and compared to those with high level of PA. Urban dwellers were at the risk of MetS compared to rural residents (OR: 1.708, 95% CI. 1.277–2.285, p = 0.003) and protected against high blood pressure (OR:0.314, 95% CI 0.212–0.466, p < 0.0001), abdominal obesity (OR: 0.570, 95% CI 0.409–0.794, p = 0.0009), and low HDL-c (OR: 0.725, 95% CI 0.534–0.983, p = 0.038) compared to rural residents.


MetS was more prevalent in urban dwellers and was associated with a low level of PA.


According to the world health organization (WHO), there is an increase in urbanization. The world’s population living in urban areas is 54%, and that proportion is expected to reach 66% in 2050. Projections show that urbanization combined with the overall growth of the world’s population could add another 2.5 billion people to urban populations by 2050, with close to 90% of the increase concentrated in Asia and Africa [1]. Most of the expected urban growth will take place in developing countries in Asia and Africa [1].

Living areas in African countries are commonly associated with an increased prevalence of non-communicable diseases and cardiovascular risk factors with high incidence in urban region [2]. Urbanization has a profound impact on the physical environment leading to air pollution, urban heat islands, and other effects, which are known to have an impact on metabolic health [3]. Living area is also associated with changes in nutrition comportments such as increased consumption of energy-rich foods and an increase in physical inactivity which is the leading cause of non-communicable diseases such as obesity, hypertension, and diabetes which are most prevalent in urban areas [4]. Metabolic syndrome (MetS) is defined as a cluster of abnormalities including abdominal obesity, hyperglycemia, hypertension, and dyslipidemia present in the same individual [5, 6].

The prevalence of MetS has reached epidemic proportions worldwide and varies between populations, race, gender, socio-economic status [7], and geographical settings [8]. MetS is a reality in Africa, the prevalence of the MetS varie between different populations in Africa [9], and it prevalence ranges from 0 to 50% or even higher depending on the population, areas (rural and urban) and the used criteria [10].

Sub-Saharan African countries which are the least urbanized in the world are facing one of the fastest rates of urbanization in the world, perceptible through rapid demographic and epidemiologic transitions [11]. MetS is also associated with physical inactivity [12] which is recognized as a global pandemic, responsible for more than 5 million deaths per year.

Physical inactivity is one of the primary targets to reduce non-communicable diseases [13,14,15]. In 2018, WHO updated the global recommendations on physical activity for the health of 2010, based on the latest available science, including sedentary behavior, in the urgent need to achieve a global reduction of 15% of physical inactivity in order to promote health in 2030 [16]. Physical activity (PA) contributes to preventing and managing non-communicable diseases and cluster components of MetS, and it lack is a major cause of chronic diseases [17, 18]. Decreased levels of PA are negatively correlated with health, the environment, economic development, community well-being, and quality of life. Insufficiently active people have a 20–30% increased risk of death compared to sufficiently active people [18]. WHO reported an important decrease in the practice of PA and a proportion of adults aged 18 and over was more concerned in 2016 [16, 18]. This decrease in PA is related to the level of urbanization, in high-income countries, 26% of men and 35% of women were insufficiently physically active compared to 12% of men and 24% of women in low-income countries [18]. Low or decreasing PA levels often correspond with a high or rising gross national product [18]. PA and its impacts on non-communicable diseases are related to socio-economic grounds and the living areas [19]. The association between PA, geographical settings, and MetS is worrying in developing countries. Hence, the present study aimed to determine prevalence of MetS according to living areas and the impact of PA in the littoral region in Cameroon.


Study design and study population

This was a cross-sectional and prospective study conducted in the littoral region of Cameroon. The littoral region is one of the ten administrative regions of Cameroon. The littoral region is an important economic region in which the economic capital is found. The study was conducted in the urban, semi-urban, and rural areas of the region.

Geographical settings were defined according to the BUCREP criteria [20]. The urban area is characterized by a high population density, mainly composed of civil servants, businessmen, and students, with important infrastructures, and a high level of urbanization. In a rural area, there is no agglomeration of population, the populations for the most part draw their income from agriculture, fishing and breeding. The semi-urban zone is located halfway between urban and rural areas [20].


The study ran from April to August 2021. Participants were randomly recruited and were of both genders aged 18 years and more residing in the study areas during the study period. Pregnant and lactating women, persons with cardiometabolic diseases, those on medication, and with physical disabilities were not included in our study. The study minimum sample was calculated using the Lorentz formulas with a prevalence of 8.4% of obesity reported by Tachang et al. [21] and the minimum was 120 participants. A total of 879 participants were recruited, and thus constituted, urban: 372, semi-urban: 195 and rural: 312 participants.

Ethics approval

The study was approved by the Institutional Ethics Committee for Human Health Research of the University of Douala (No CE-UDO/07/2020/T), and by the regional delegation of the Ministry of Public Health. The study was conducted in accordance with the guidelines of the Helsinki Declaration of 1975, as revised in 2008. Also, research authorizations granted to hospital administration staff were obtained. Written informed consents were obtained from all. Data were collected anonymously and were confidential.

Socio-demographic and behavioral informations

A questionnaire developed from the World Health Organization (WHO) STEPS manual for surveillance of risk factors of NCDs and adapted to the study context was used to collect socio-demographic information (age, level of education, marital status, medication diagnostic cardiometabolic disease, etc.) information on habits related to healthy living, alcohol intake and smoking (answering by “yes” or “no” to the question) in particular; and information about the medical history of study participants. The Alcohol Use Disorders Identification Test (AUDIT) was used to assess the participant’s alcohol consumption.



Weight and body composition were measured using a bioelectric impedance meter Terraillon Wellness Coach (USA). Height was measured using a measuring tape. The body mass index (BMI) was calculated to assess the degree of obesity of each participant according to the Quetelet formula as the weight (Kg) divided by the square of the height (m2). The participants were classified according to their BMI as follows: normal weight (BMI < 25), overweight (BMI ≥ 25–29.9,) and obese (BMI > 30 kg/m2). Waist circumference (WC) was measured with an inelastic tape between the lower edge of the costal arch and the iliac bone’s upper crest in a standing position with an accuracy of 0.5 cm [22] and waist-to-height ratio (WHtR) was calculated as WC divided by the height.

Blood pressure and heart rate

Systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate (HR) were taken using an electronic blood pressure monitor (JERISON, China) placed on the subject’s left arm in a sitting position. The first measurement was taken after a 10 min rest in a sitting position and was followed by another measurement after 5 min intervals, the average of the two measurements was used to assess the presence or absence of high blood pressure.

Physical activity

Levels of PA were determined based on the Global Physical Activity Questionnaire (GPAQ) analysis guide developed by WHO [23]. This questionnaire comprises 16 questions grouped to capture PA undertaken in different behavioral domains; these are work, transport, and leisure or recreation time during a typical week. GPAQ collects information on the practice of physical activities (frequency, duration, and intensity of activities) and on sedentary behavior. The questionnaire takes into account activities at work, during transport, and leisure activities. The results were scored and participants were classified as having low, moderate and high levels of PA.


For each fasting subject (12–14 h of fasting), blood glucose was measured between 8 and 10 am using a MyStar Extra glucometer (SANOFI, China). Blood samples were taken from the ulnar vein, and a volume of 10 ml was collected and conserved in EDTA tubes by venepuncture in the hand of each participant. The sera were obtained by blood centrifugation at 4000 rpm for 20 min in a Techmel & Techmel (USA) centrifuge and then placed in cryotubes, and aliquots were frozen at -20 °C for further biochemical analyses.

The levels of total cholesterol (TC), HDL-C, and triglycerides (TG) were determined using a UVmini 1240 spectrophotometer (SHIMADZU) according to the Biorex kit material (respectively, Cholesterol CHO-Rev 01 of 1271/2008, Triglycerides BXC0271 and HDL CHO-Rev 01 of 1271/2008) [24, 25]. Low-density lipoprotein (LDL) was calculated using the Friedewald et al. [26] formula if the triglycerides are less than 400 mg/dl (4.6 mmol/l). LDL-c was calculated by subtracting HDL-c and VLDL from total cholesterol. The serum standards used for calibration were provided by the manufacturer.

The insulin resistance was assessed by calculating the Homeostatic Model Assessment Insulin resistance (HOMA-IR) using the following

$${\text{HOMA}} - {\text{ IR }} = \frac{{\left[ {{\text{C}} - {\text{peptide}}} \right]{ } \times {\text{fasting glucose}}}}{22.5}$$

The C-peptide blood concentration was determined by ELISA (enzyme-linked immunosorbent assay) using the Mercodia C-peptide Ultrasensitive ELISA test (Mercodia AB Sylveniusgatan 8A SE-754 50 Uppsala, Sweden). The special Mercodia C-peptide ELISA kit is calibrated using the International Reference Reagent for C-peptide, IRR C-peptide 84/510 [27]. The HOMA-IR was evaluated in 600 individuals, 200 per area which were submitted to dosage of C-peptide.

Metabolic syndrome criteria

Harmonized definition of MetS by the International Diabetes Federation of 2009 [6] was used whose:

  • central obesity that was defined by a waist circumference ≥ 94 cm in men and ≥ 80 cm in women,

  • High fasting glucose level ≥ 100 mg/dL (5.6 mmol/L);

  • hypertriglyceridemia-serum triglyceride level ≥ 150 mg/dL (1.7 mmol/L);

  • Low HDL cholesterol-serum; HDL cholesterol < 40 mg/dL (1.0 mmol/L) in men and < 50 mg/dL (1.3 mmol/L) in females);

  • High blood pressure [systolic blood pressure (SBP) ≥ 130 mmHg and/or diastolic blood pressure (DBP) ≥ 85 mmHg.

Participants with 3 or more of the 5 MetS components were considered to have MetS.

Statistical analysis

Statistical analysis was performed with the Statistical Package for Social Sciences (SPSS) software, Version 21.0 (SPSS, Inc. Chicago, U.S.A. IBM Corp.). Results of sociodemographic, behavioral information, ponderal status, MetS and its components and level of PA were expressed as proportions (%) for quantitative variables and means ± standard deviation (SD), the distribution pattern of variables was checked. The Chi-2 test was performed to compare unpaired proportions and Student’s t test on unpaired series was performed to compare quantitative variables between urban, semi-urban and rural areas. Stepwise multivariate analysis was performed to examine the association between the level of PA, MetS and its cluster components, also between geographical settings, MetS and its components. The significance was set with a p-value < 0.05.


The distribution of participants by living area varied significantly with respect to sociodemographic information (Table 1). More than 50% of males were living in rural areas, while most of the females (51.1%) were living in urban areas (p < 0.0001). A large majority of participants living in urban area were under 35 years and those over 35 years old were in the rural area (p < 0.0001). More than half (70.9%) of participants having completed primary studies were living in a rural area, while 55.2% of those having completed secondary studies were living in urban areas (Table 1). Also, participants smoking and drinking alcohol were more in a rural area (51.4%, p = 0.006 and 39.5%, p = 0.0002, respectively) It should be noted that 77.9% of those having a high level of physical activity (PA) were living in rural areas (p < 0.0001). In contrast, 51.3% and 54.5% of those having either moderate or low levels of PA were living in urban areas. A low level of PA was significantly reported in females compared to males in urban (87.4%, p < 0.001), semi-urban (70.1%, p < 0.01) and rural (64.3%, p < 0.01).

Table 1 Sociodemographic characterization of the participants

Anthropometric, physiological and lipid profile data by living areas are depicted in Table 2. Participants from the urban area had the lowest mean weight values compared to their counterparts from semi-urban areas and rural areas. Likely, the same patterns were observed for WC (p < 0.0001) and WhtR (p < 0.0001). Body water was significantly higher in participants from rural areas while those from semi-urban areas had the highest values of body fat and bone mass. SBP DBP and HR also varied significantly between areas, with, for instance, highest HR values in urban areas compared to those from semi-urban and rural settings. Regarding lipid profile, glycemia and triglyceridemia were both higher in individuals from rural areas, while TC, HDL and LDL were highest in those from the urban settings, and the differences were all statistically significant (Table 2).

Table 2 Anthropometric, physiological and lipidemia profile of participants

Overall MetS was diagnosed in 57.7% of the participants and was more prevalent in female (p < 0.0001) in the overall population and each geographic setting (urban, semi-urban, and rural). The prevalence of MetS components varied geographically significantly (p < 0.05) with highest values found in participants from urban areas (37.2%) and rural (36.8%). Then, HFBG (p = 0.0110), low HDL-c (p < 0.0001) and high triglyceridemia (p = 0.0068) were most prevalent in participants from urban settings (Fig. 1). In contrast, HBP (p < 0.0001) and abdominal obesity (p = 0.0002) were most found among individuals from rural settings.

Fig. 1
figure 1

MetS and components according to living areas. HBP: high blood pressure, HFBG: High levels of fasting blood glucose, Hypo HDL-c: Low levels of blood HDL-c, MetS: Metabolic syndrome, Data are expressed as percentage, * < 0.05; ** < 0.01; *** < 0.001 as determined by Chi2test

According to gender, the more prominent MetS components were HFBG, HBP, Abdominal obesity and Low HDL-c. Therefore, it has been noticed that HBP was more prevalent in male in overall population (52%, p < 0.0001) and superior in female in urban (87.8%, p < 0.01) and semi-urban (51.7%, p < 0.05). Abdominal obesity and low HDL-c were high in female in a study population (81.7%, p < 0.0001 and 73.4%, p < 0.0001, respectively) in each study site, in urban (85.6%, p < 0.01; 89.8%, p < 0.001 respectively), semi-urban (51.7%, p < 0.05; 72.5%. p < 0.001, respectively) and rural areas (75.0%, p < 0.001; 57.1%, p < 0.001, respectively). HFBG was high in female compared to male in semi-urban region (63.7%, p < 0.05) (Fig. 2).

Fig. 2
figure 2

MetS and components according to gender in every living areas. HBP: high blood pressure, HFBG: High levels of fasting blood glucose, Hypo HDL-c: Low levels of blood HDL-c, MetS: Metabolic syndrome, Data are expressed as percentage, * < 0.05; ** < 0.01; *** < 0.001 as determined by Chi2test a MetS and components according to gender in urban region, b MetS and components according to gender in semi-urban region, c MetS and components according to gender in rural region

An inverted relation between MetS burden and level of PA was noted. This syndrome was more prevalent (p < 0.0001) in participants with a low level of PA (44.36%) compared to their counterparts with PA classified as moderate (31.68%) and high (23.96%). Curiously, we did not consistently find this pattern upon stratification by living areas. This pattern was noticed in urban areas only where the prevalence of MetS was 58.5% in participants having low, compared to those with moderate and high PA levels. In rural areas, MetS prevalence was significantly (p = 0.01) highest in individuals with a high level of PA, while no statistically significant difference was found in semi-urban settings (Fig. 3).

Fig. 3
figure 3

Prevalence of MetS according to level of physical activities and living areas MetS(+): Metabolic syndrome present

Multivariate analysis show that compared to participants with high level of PA those with low level were significantly at risk of MetS (OR: 1.751, 95% CI 1.335–2.731, p = 0.001) HFBG (OR: 1.909, 95% CI 1.335–2.731, p = 0.0004) abdominal obesity(OR: 2.007, 95% CI 1.389–2.900, p = 0.0002), low HDL-c (OR: 1.539, 95% CI 1.088–2.179, p = 0.014) and those with moderate level of PA were protected against HBP(OR: 0.452, 95% CI 0.298–0.686, p = 0.0002) and compared to those with high level of PA. According to geographical setting urban dwellers had 1.708 great risk of MetS compared to rural residents and were also at risk of HFBG (OR:1.611, 95% CI 1.170–2.219, p = 0.003) and protected against HBP (OR:0.314, 95% CI 0.212–0.466, p < 0.0001), Abdominal obesity (OR:0.570, 95% CI 0.409–0.794, p = 0.0009), and Low HDL-c (OR:0.725, 95% CI 0.534–0.983, p = 0.038) compared to rural residents. However, semi-urban participants were at risk of Low HDL-c (OR: 2.371, 95% CI 1.573–3.573, p < 0.0001) compared to rural site. In addition, participants from urban areas compared to those from rural areas had a 70% reduction in the risk of high triglyceridemia (OR: 0.300, 95% CI 0.135–0.664, p = 0.003) (Table 3).

Table 3 Association between level of PA, geographical setting, MetS and its components


The present study aimed to determine the impact of PA on the occurrence of MetS in living areas. According to the criteria defined by the IDF consensus in 2009, the prevalence of MetS shows high prevalence in urban participants, followed by rural areas and semi-urban areas.

Other studies highlighted that MetS is emerging alarmingly in urban populations in low-income countries. These results are in accordance with those reported by others researchers who found high prevalence of MetS in urban dwellers compared to rural. In a study conducted in Benin by Ntandou et al.[29] on MetS and its components between urban, semi-urban and rural dwellers using the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATP III) criteria noticed high prevalence in urban (11%) followed by semi-urban (6.4%) and rural population (4.1%). In Cameroon, a study focused on PA and the MetS among adults in the rural and urban regions by Assah et al. [30] using the NCEP-ATP III criteria reported high prevalence of MetS in urban dwellers (17.7%) compared to rural (3.5%). Even, Ntentie et al. [30] in a cross-sectional study also in Cameroon between urban, less urbanized, and rural areas reported a low prevalence of MetS in a rural area (7%) and high in less urbanized (17.4%) and urbanized areas (12.7%). Thanikachalam et al. [3] also assessed the impact of built environmental changes on the prevalence of MetS in a rapidly urbanizing population in South India and reported a high prevalence of MetS in urban (44.6%) and semi-urban communities (35.2%) compared to rural (31.8%).

The prevalence of MetS in the present study and some of its prominent cluster components were high in women. This result is in accordance with those of other researchers who established that MetS is more prevalent in women [30,31,32,33]. In a recent systematic review and meta-analysis on the prevalence of MetS in sub-Saharan Africa, Faijer-Westerink et al. [34] highlighted that the prevalence of MetS was highest in urban areas precisely in women. Even Ntandou et al. [28] in Benin found high levels of MetS, abdominal obesity, and low HDL-c in women than in men.

Moreover, our results don’t corroborate some of those reported by Ayina et al. [35] in a study in one administrative subdivision of our study region where they studied the urban–rural difference of MetS components. They reported high levels of total cholesterol, high triglyceridemia, waist circumference, and hyperglycemia in urban dwellers [35]. But according to the gender, some of their results were different from ours where they noticed high prevalence of total cholesterol, waist circumference, and low levels of HDL-c in urban men urban dwellers compared to females [35].

However, it has been observed the persistence of MetS central obesity and HFBG in the rural environment despite high and moderate level PA noticed (Fig. 1 & Table 1) and rural participants were at risk of HBP, abdominal obesity, and low HDL-c and protected against HFBG (Table 3). According to Popkin [36], this positive obesity gradient noticed in females in each study site can be ascribed to the westernization a nutrition transition process that is ongoing in developing countries. This result will be related to age and toxicological behaviors. More than half of the participants of the rural site (58.5%) were over 35 years old and were smoking (51.4%) and consuming alcohol (39.5%) than those living in urban and semi-urban sites (Table 1). Also, nearly half (47.6%) of the rural population was obese (Table 1).

It is well known that age [37], alcohol [38] and smoking cigarettes [39] constitute important risk factors for MetS. Thus, the regular practice of PA can’t be a real means of primary prevention of MetS. On the physiological aspect, cigarette smoking stimulates the sympathetic nervous system with increase glycogen and lipid catabolism [40] and also increases blood cortisol and growth hormone [39]. Tobacco smoking also elevates plasma cortisol concentration and aggravated insulin resistance can cause localization of visceral fat mass and increase abdominal obesity. This is in accordance with a study of Fezeu et al. [41] who noticed in Cameroon that urbanization is characterized by an increase in body mass index in the rural area and obesity which is considered as a major factor of the MetS [42]. Also, one of the first changes appears in cities before reaching less urbanized areas and exposing the people to obesity and other nutrition-related chronic diseases [36].

We observed a positive relationship between low PA and MetS in the overall study population and in urban and semi-urban. Also, low PA was associated with HFBG, abdominal obesity, and low HDL-c (Table 3). In the present study participants living in rural areas were more active with high (77.9%) and moderate (25.2%) prevalence of PA compared to those in urban and semi-urban (Table 1). Other studies have highlighted those rural dwellers were more active with high level PA [29, 43, 44]. Assah et al. [29] in a study on the urban–rural difference in energy expenditure, PA, and MetS; noticed that a low level of PA was strongly independently associated with a high prevalence of MetS in Cameroonians urban dwellers compared to rural residents.

Other studies reported a high level of PA in rural dwellers compared to the urban and low prevalence of MetS and some of its components [30, 45, 46]. Even, Ntentie et al. [30] have established that low level of PA was strongly associated with the occurrence of MetS. Moreover, rural–urban difference in PA with high level of rural residents has been linked to non-communicable diseases. This difference reflects the differences prevalence of in non-communicable diseases between rural–urban populations in Africa with high prevalence in the urban population [47,48,49]. However, it should be highlight that the level of PA in urbanized environments is inherent to socio-economic conditions, in particular the built environment where it has been shown its impact throughout the life. In a recent study conducted in South Africa Wayas et al. [50] found that perceived walkability among adolescents from low-income neighborhoods was worse than that from high-income neighborhoods, although the association with PA and ‘BMI is not clear.

Herein, many studies showed the evidence that PA practiced at a moderate and high level is a powerful tool for the primary prevention of metabolic disease and that it exerts its protective effects by improving the metabolic phenotype of non-skeletal muscle tissues, including the liver, vasculature, adipose tissue and pancreas [51]. In a physiologic way, PA exerts a positive effect by reducing components of MetS. There is evidence that high level of PA and MetS parameters has an inverse association, and persons with high level of PA have lower risks of developing MetS. Low levels of PA are associated with increased adiposity and decreased blood pressure, LDL-c, and higher HDL cholesterol [52]. PA improves lipid profile by increasing HDL concentration and decreasing LDL and triglyceride concentrations [53]. Previously several studies have determined the association between the level of PA and the prevalence of Mets [54,55,56]. The mechanism of high PA on MetS might be related to an important reduction of the level of inflammation. PA practiced at moderate and high levels is associated with a better profile of inflammatory factors and adipocytokines that lower MetS. Also, another possible physiological justification is the stimulation of the secretion of pro-inflammatory cytokines by a high level of PA. Regular practice of PA also improves body composition, dyslipidemia, and endothelial function also increases anti-inflammatory cytokines, decreases body fat, and decreases adhesion molecules expression [57,58,59].


This study highlights the effect of living areas on the Mets, with a high prevalence of MetS in urban areas. This high prevalence of Mets and some of its components in urban areas are linked to a significant decrease in the practice of PA at high intensities by the inhabitants of these geographical settings. This emphasizes the use of PA as a non-pharmacological intervention for the primary prevention of MetS and its components in developing countries. Thus, the regular practice of PA in urban areas becomes an unavoidable necessity to fight against non-communicable diseases associated with urbanization. However, the practice of PA should be associated with the observation of hygienic behaviors, without smoking and alcoholism.

Availability of data and materials

Data can be shared upon contact with the correspondence author.



Physical activity


Systolic blood pressure


Diastolic blood pressure


Waist circumference


Body mass index


Waist to hip ratio


Total cholesterol


High-density lipoprotein cholesterol



MET équivalent:

Metabolic equivalent


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Special thanks to the departmental officials of the Ministry of Public Health for the administrative facilities, and also thanks to the administrative authorities for the sensitization of the populations of rural areas to participate in the study. Also Acknowledge Hospital administrative staff and paramedical staff for their complete availability for taking laboratory parameters, for the free treatment of people diagnosed suffering from MetS.


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Authors and Affiliations



NCB, NBE and YJM collected data, interpreted the results and drafted the manuscript; JMN, CNAA conceived the study, collected data, performed the data analysis, interpreted the results and drafted the manuscript; ECBL performed data analysis; WRG, JGBNB, CD, JG, NB, A. drafted the manuscript; ANPB, AT supervised the study and draft the manuscript; SHM and BB supervised the study; LSEN provided advice and guidance in all aspects of the work.

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Correspondence to Clarisse Noel Ayina Ayina.

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The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Ethics Committee for Human Health Research of the University of Douala (No CE-UDO/07/2020/T).

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Bilog, N.C., Mekoulou Ndongo, J., Bika Lele, E.C. et al. Prevalence of metabolic syndrome and components in rural, semi-urban and urban areas in the littoral region in Cameroon: impact of physical activity. J Health Popul Nutr 42, 95 (2023).

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