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. 2021 Aug 5;16(8):e0255575. doi: 10.1371/journal.pone.0255575

Using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso

Kadari Cissé 1,2,*, Délwendé René Séverin Samadoulougou 3, Joel Dofinissery Bognini 4, Tiga David Kangoye 5, Fati Kirakoya-Samadoulougou 1
Editor: Samuel Seidu6
PMCID: PMC8341491  PMID: 34351987

Abstract

Background

The burden of cardiovascular diseases is rising in the developing world including Sub-Saharan Africa. The rapid rise of cardiovascular disease burden is in part due to undetected and uncontrolled cardiovascular risk factors. The clustering of metabolic syndrome (MetS) components is associated with a high risk of cardiovascular diseases. This complex biochemical disorder is still poorly studied in western Africa. In this study, we aimed to determine the prevalence of metabolic syndrome and its determinants among the adult population in Burkina Faso.

Methods

We performed a secondary analysis of the data from the first national survey on non-communicable diseases risk factors using the World Health Organization (WHO) Stepwise approach. We included 4019 study participants aged 25 to 64 years. The metabolic syndrome prevalence was estimated using six different definitions.

Results

The mean age was 38.6±11.1 years. Women represented 52.4% and three quarters (75%) lived in rural areas. The overall prevalence of metabolic syndrome according to the different definitions was 1.6% (95%CI:1.1–2.2) for the American College of Endocrinology, 1.8% (95%CI: 1.3–2.4) for the WHO, 4.3% (95%CI:3.5–5.2) for the National Cholesterol Education Program Adult Treatment Panel III, 6.2% (95%CI: 5.1–7.6) for the AAH/NHBI, 9.6%(95%CI: 8.1–11.3) for the International Diabetes Federation and 10.9% (95%: 9.2–12.7) for the Joint Interim Statement. The metabolic syndrome components with the highest prevalence were low High density lipoprotein (63.3%), abdominal obesity (22.3%) and hypertension (20.6%). People living in urban areas and those with older age have higher prevalence of metabolic syndrome regardless of the definition used.

Conclusion

Our findings suggest various levels of prevalence of MetS according to the definition used. Identifying the most appropriate criteria for MetS among the adult population is important to early detect and treat this syndrome and its components at the primary health care level to control the rising burden of cardiovascular diseases in the context of ongoing epidemiological transition in the country.

Introduction

Non-communicable diseases (NCDs) included cardiovascular diseases (CVD), are rising worldwide and are considered one of the major health challenges of our century [1]. In developing countries including countries in Sub-Saharan Africa (SSA), NCDs are responsible for 82% (17 million) of the global premature deaths [2]. Among risk factors leading to NCDs, some are preventable such as behavioral and metabolic risk factors [1]. Some of these metabolic risk factors are a part of metabolic syndrome (MetS), which ties together type 2 diabetes mellitus and cardiovascular risk factors including insulin resistance, dyslipidemia, hypertension and abdominal obesity [3, 4].

In the SSA countries, the prevalence of the MetS varies between countries depending on the definition criteria considered [5]. In 2019, a systematic review and meta-analysis of studies conducted in several SSA countries estimated the overall prevalence of MetS in 34,324 healthy participants aged ≥16 years old [6]. According to the different diagnostic criteria, the prevalence varied from 11.1% (95%CI: 5.3–18.9, World Health Organisation (WHO) criteria) to 23.9% (95%CI: 16.5–32.3, Joint Interim Statement (JIS) criteria). The prevalence of MetS was higher in women than in men, and higher in (semi-)urban participants than in rural participants [6]. According to different studies, this prevalence in different adult populations also increased with age [711].

In Burkina Faso, it was estimated that non-communicable diseases accounted for around 33% of all deaths in 2016 [12]. However, very few studies specifically investigated the MetS burden. In a survey carried out in the general population of two districts of the capital city, the prevalence of MetS was estimated at 7% [13]. Other hospital-based studies found a MetS prevalence of 10% (International Diabetes Federation (IDF) criteria) or 12.3% (National Cholesterol Education Program Adult treatment Panel III (NCEP-ATP III) criteria) in HIV patients on antiretroviral therapy [14], 17.5% in patients with high blood pressure [15] and 48.9% in patients with diabetes [16].

A 25% reduction in the overall mortality from cardiovascular diseases, diabetes and others NCDs by 2025 is the first goal to which governments, including that of Burkina Faso, are committed to achieving in the Global Monitoring Framework for NCDs [17]. The importance of MetS in this context lies in its association with increased cardiovascular mortality and all-cause mortality in the general population [18]. It is therefore of utmost importance to get an estimate of its extent in the general population of Burkina Faso where data and research supporting decision-making relative to NCDs prevention/control strategies and impact evaluation are very limited [19]. Thus, the objective of our study was to exploit unique population-based survey data on non-communicable diseases in Burkina Faso, to estimate, for the first time, the national prevalence of the metabolic syndrome using different definitions of MetS and its determinants.

Materials and methods

Study setting

Burkina Faso is a land-locked country in West Africa with an area of 272,967.47 km2. The population was 20,244,080 inhabitants, and people aged over 25 years represented 36% of the population in 2018 according to the estimation of the National Institute of Statistics and Demography [20]. Life expectancy was 56.7 years [21]. Many risk factors contributing to the occurrence of NCDs were reported, and about 33% of all deaths are due to NCDs. Its climate is tropical with a long dry season making it difficult to grow fruits. About 81% of workers were farmers. Administratively, the country is subdivided into 13 regions, 45 provinces, 350 departments, 351 municipalities and 8,228 villages [20].

Data source

a) Study design and population

Our study used data from a cross-sectional survey, the national WHO Steps survey aiming to assess the risk factors for NCDs which was conducted in the 13 regions of Burkina Faso from 26 September to 18 November 2013. Data were collected from a representative sample of people aged 25–64 years old in Burkina Faso. the study was designed to have estimates at the national, regional and place of residence (urban/rural) level. Participants were identified using a three-stage cluster stratified survey sampling. The sampling frame used was taken from the 2006 general population and housing census [22] and updated in 2010 during the Burkina Faso Demographic and Health Survey [23]. This update concerned the enumeration areas (EAs) that correspond to the cluster within the framework of this study. Clusters were organized using region and place of residence. One respondent was identified in each of 4800 selected household [24].

b) Data collection

Data were collected electronically on Personal Digital Assistant (PDA) and consisted of face-to-face interviews after obtaining informed consent from the participant for risk factors linked to NCDs. The data were collected by taking physical and biochemical measurements from the subjects selected to participate in the survey using the WHO STEPS instrument. The survey was conducted in three steps: the first step focused on socio-demographic information, behavioral measures, questions on physical activity, and food hygiene, oral health, screening for cervical cancer and knowledge risk factors for NCDs. Behavioral measures related to the consumption of tobacco and alcohol. The second step measured the following physical parameters: weight, height, waist circumference and blood pressure. At the third step blood sugar and blood cholesterol were measured.

Variables of interest

a) Main outcome or dependent variable

In our study, the dependent variable was a binary variable measure at the individual level that can take two possible values: the presence of metabolic syndrome (1), or absence (0). These criteria were used to define MetS according to the definitions presented in Table 1. These MetS definition were adapted since blood triglyceride level was not collected during the STEP survey in Burkina Faso, due to a lack of adequate sampling equipment. The measurement of MetS components was done following the WHO Stepwise approach [25]. Previous studies using the STEP survey had already reported details of the measurement of two MetS components: hypertension [26] and Fasting blood glucose [27]. The level of blood lipid (total cholesterol and high density lipoprotein cholesterol (HDL) was obtained using a portable device (Cardio-Chek P•A SILVER), which also provided the level of glucose, using a whole blood sample obtained from a finger prick [27, 28]. The waist circumference was measured with a tape measure, applied directly to the skin [28]. The following variables were used to compute MetS according to each definition (see Table 1 for more details):

Table 1. Criteria for metabolic syndrome for each definition.
Criteria WHO (1998–1999) [29, 30] NCEP-ATPIII (2001) [31] IDF (2006 [32]) AACE 2003 [33] NHLB/AHA [34] JIS (2009) [35]
Mandatory criteria • DM (None) • WC≥ 94cm (M)/ 80cm (W)
  • ≥ 2 characteristics (non-diabetic patients):

  • 6.1 ≤ FG< 7.0 mmol/l

  • HDL-c < 1.03 mmol/l (M) / 1.29 mmol/l (W)

  • BP> 130/85 mmHg

(None) (None)
Or Or
• FG≥5.6 • BMI > 30 kg/m2
Conditions Plus≥ 2 other criteria ≥ 3 criteria Plus ≥ 2 other criteria Plus ≥ 1 other criterion ≥ 3 criteria ≥ 3 criteria
Other FG criterion FG≥ 6.1mmol/l FG≥ 5.6 mmol/l Family history of T2DM, FG≥ 5.6 mmol/l FG≥ 5.6 mmol/l
Or known T2DM or treatment or treatment
Other obesity criterion BMI> 30 kg/m2 WC>102cm (M) BMI>25.0 kg/m2; WC>102cm (M) WC≥ 94cm (M)
WC>88cm (W) WC>88cm (W) WC≥ 80cm (W)
Other HDL-c (mmol/l) criterion HDL-c HDL-c HDL-c treatment or HDL-c HDL-c treatment or
<0.9mmol/l(M) <1.03mmol/l (M) <1.03mmol/l (M) <1.03mmol/l (M)
<1.0mmol/l (W) <1.3mmol/l (W) <1.29mmol/l (W) <1.3mmol/l (W) < 1.0 mmol/l (M)
< 1.3 mmol/l (W)
Other BP criterion BP≥ 140/90 mmHg BP≥130/85 mmHg BP≥ 130/85 mmHg or treatment
  • Known HBP or

  • Family history of HBP

BP≥130/85 mmHg BP≥130/85 mmHg
or treatment or treatment
Else criterion
  • Non-Caucasian ethnicity

  • Sedentary lifestyle

  • Age>40 years

AACE: American College of Endocrinology; AHA/NHLBI: American Heart Association and National Heart Lung and Blood Institute; IDF: International Diabetes Federation; JIS: Joint Interim Statement; NCEP-ATPIII: National Cholesterol Education Program Adult Treatment Panel III; WHO: World Health Organization; DM: diabetes mellitus; T2DM: Type 2 Diabetes mellitus; HDL-c: high density lipoprotein; BMI: body mass index; BP: bloodpPressure; WC: waist circumference; FG: fasting glucose; HBP: high blood pressure.

  • Anthropometric factor: weight (Kg), height (m), body mass index (BMI) (18.5≤ BMI <25 = normal, BMI ≥25 = overweight, BMI ≥30 = obesity), and waist circumference, blood pressure

  • Biological factors: total cholesterol, cholesterol HDL, fasting glycemia,

  • Treatment: treatment of diabetes (yes/no), the treatment of hypertension (yes/no) and treatment of dyslipidemia (yes/no).

b) Explanatory variables

Explanatory variables are detailed below:

  • Socio-demographic factors: age (25–34, 35–44, 45–54, and 55–64 years), gender (male/female), education level (no level, primary, secondary or higher), place of residence (urban/rural), region, profession (wage earner, self-employed or jobless),

  • Behavioral factors: smoking (yes/no), use of alcohol (yes/no), number of fruits or vegetables eaten per day, fat intake (yes/no), and number of meals taken out of the household, physical activities: physical activities (high, moderate and low intensity),

Statistical method

We first described the characteristics of the study population through a weighted analysis for complex samples. The MetS weighted prevalence was presented according to definitions and sociodemographic characteristics. Chi-square tests were used to assess association of the independent variables with MetS. We implemented a modified Poisson regression model using a generalised estimating equation to derive prevalence ratios (PR) taking into account the clustering of observations. In our analysis strategy, we implemented an analysis with complete case data. PR with a 95% confidence interval were calculated. Statistical significance was accepted at the 5% level (p <0.05).

Ethics approval and consent to participate

Before collecting data in the field, the survey protocol was approved by the Ministry of Health’s Ethics Committee for Health Research, and the Ministry of Scientific Research and Innovation, and informed consent was required before the participation of any individual selected for the investigation (Deliberation No. 2012-12-092 of 05 December 2012). The confidentiality of the information collected has been mentioned in the informed consent form. Our analysis was also approved by the Ministry of Health’s Ethics Committee for Health Research (Deliberation No. 2020-10-231 of October, 07, 2020).

Results

Sociodemographic profile

A total of 4019 participants have met the inclusion criteria (see Fig 1). The mean age was 38.6±11.1 years and 41.2% were younger than 35 years old. Women represented 52.4% of the study population. Three-quarters (75%) lived in rural areas (see Table 2).

Fig 1. Diagram flow of study participants.

Fig 1

Table 2. Sociodemographic characteristics of the study population.

Sociodemographic characteristics Number Percentage*
Age group, years 4019
25–34 1781 41.2
35–44 1011 27.8
45–54 743 19.4
55–64 484 11.7
Gender 4019
Women 2011 52.4
Men 2008 47.6
Marital status 4014
Single 575 13.2
Married 3439 86.8
Completed level of education 4011
No formal school 3166 79.1
Primary school 596 14.5
Secondary or more 249 6.4
Profession 4014
Wage earner 195 5.1
Self-employed 2875 69.0
Jobless 944 26.0
Residence 4019
Urban 787 25.0
Rural 3232 75.0
Region 4019
Boucle du Mouhoun 419 9.4
Cascades 133 2.7
Centre 311 9.3
Centre-Est 352 7.5
Centre-Nord 377 10.3
Centre-Ouest 352 7.7
Centre-Sud 198 4.4
Est 345 8.4
Haut-Bas 454 12.3
Nord 383 7.7
Plateau-Central 213 7.8
Sahel 289 8.4
Sud-Ouest 193 4.1

*Weighted percentage.

Behavioral and metabolic risk profile

In terms of behavioral risk, 11.3% of the study population were smokers, 4.3% had a history of alcohol abuse, 95.5% had a poor fruit and vegetable intake and 14.0% had low physical activity. The prevalence of obesity was 4.4%. The prevalence of abdominal obesity as defined by JIS was 22.3%. One-fifth (20.6%) had hypertension. Fasting blood glucose levels were high in 5.1% of the study population. High total cholesterol and low HDL have been reported in 2.2% and 63.3% of the study population respectively (see Table 3).

Table 3. Descriptive behavioral and metabolic characteristics of risk factors among the study population.

Risk factors Number Weighted percentage
Behavioral risk factors
Current smoker (n = 4019) 496 11.3
Excessive drinker (n = 4019) 174 4.3
Fruit and vegetable intake 3731
<5 3545 95.5
≥5 186 4.5
Type of fat most commonly used 3912
Vegetable oil 2431 63.1
Butter, lard or fat, margarine 1073 27.0
None or other 408 9.9
Number of meals taken out of the household 3987
<8 3890 97.8
≥8 97 2.3
Physical activity 4019
Intense 2452 60.6
Moderate 1037 25.4
Low 530 14.0
metabolic risk factors
BMI class 4019
Underweight 455 11.9
Normal 2898 70.5
Overweight 510 13.3
Obese 156 4.4
High blood pressure (n = 4019) 808 20.6
Elevated blood glucose (n = 4019) 192 5.1
Hypercholesterolemia (n = 4019) 86 2.2
Low HDL-Cholesterol (n = 4019) 2575 63.3
Abdominal obesity (4019) 812 22.3

Prevalence of metabolic syndrome (MetS)

The prevalence of MetS varied widely depending on the definition used. The highest prevalence was observed by using the JIS definition (10.9%) followed by IDF (9.6%), American Heart Association and National Heart Lung and Blood Institute (AHA/NHLBI (6.2%) and NCEP-ATP III (4.3%). The lowest prevalence was found using American college of Endocrinology (AACE) (1.6%) and the WHO criteria (1.8%) (Tables 4 and 5). The prevalence of MetS was higher among women compared with men in four out of the six definitions used. Based on the WHO and AACE definitions, there was no gender difference in the prevalence of MetS.

Table 4. Prevalence of metabolic syndrome according to each of six definitions by sociodemographic characteristics.

Sociodemographic characteristics WHO NCEP-ATP III IDF
n % [95% CI] n % [95% CI] n % [95% CI]
All participants 68 1.8 [1.3–2.4] 165 4.3 [3.5–5.2] 344 9.6 [8.1–11.3]
Age group, years
25–34 17 1.0 [0.6–1.6] 48 2.9 [2.1–4.0] 101 6.2 [4.9–7.8]
35–44 19 2.0 [1.1–3.4] 40 4.3 [2.9–6.3] 88 9.4 [7.2–12.4]
45–54 17 2.2 [1.2–4.0] 41 5.3 [3.7–7.5] 89 13.9 [10.5–18.1]
55–64 15 3.9 [2.1–7.4] 36 7.5 [5.0–11.1] 66 14.9 [11.3–19.4]
Gender
Women 34 1.8 [1.2–2.7] 124 6.2 [4.9–7.8] 278 14.7 [12.3–17.5]
Men 34 1.9 [1.2–2.9] 41 2.2 [1.5–3.1] 66 4.0 [3.0–5.2]
Marital status
Single 11 2.8 [1.4–5.5] 30 6.3 [4.1–9.5] 59 11.5 [8.4–15.7]
Married 57 1.7 [1.2–2.4] 134 4.0 [3.2–4.9] 283 9.3 [7.8–11.0]
Completed level of education
No formal school 42 1.2 [0.8–1.7] 109 3.3 [2.6–4.2] 251 8.6 [7.2–10.2]
Primary school 13 2.9 [1.5–5.6] 38 7.9 [5.7–10.8] 57 12.6 [9.2–17.1]
Secondary or more 13 7.1 [3.5–13.9] 18 7.6 [4.2–13.3] 35 15.0 [10.3–21.2]
Profession
Wage earner 7 3.4 [1.4–7.7] 13 5.6 [3.1–9.9] 22 11.8 [7.7–17.5]
Self-employed 39 1.5 [1.0–2.3] 93 3.4 [2.6–4.4] 187 7.3 [5.8–9.2]
Jobless 22 2.3 [1.4–3.8] 58 6.3 [4.5–8.8] 132 15.1 [12.2–18.5]
Residence
Urban 29 4.2 [2.7–6.5] 80 9.9 [7.2–13.5] 154 20.7 [15.8–26.6]
Rural 39 1.1 [0.7–1.5] 85 2.4 [1.9–3.0] 190 5.9 [4.9–7.1]

WHO: World Health Organization; NCEP-ATPIII: National Cholesterol Education Program Adult Treatment Panel III; IDF: International Diabetes Federation, CI: Confidence interval; n = number of participants with metabolic syndrome.

Table 5. Prevalence of metabolic syndrome according to each of six definitions by sociodemographic characteristics.

Sociodemographic characteristics AACE AHA/NHLBI JIS
n % [95%CI] n % [95%CI] N % [95%CI]
All participants 60 1.6 [1.1–2.2] 227 6.2 [5.1–7.6] 390 10.9 [9.2–12.7]
Age group, years
25–34 19 0.8 [0.5–1.4] 64 4.0 [3.0–5.3] 116 7.0 [5.6–8.7]
35–44 13 1.6 [0.9–2.8] 60 6.8 [4.8–9.4] 99 10.4 [8.1–13.4]
45–54 15 2.3 [1.3–4.1] 56 7.6 [5.4–10.6] 98 15.4 [11.5–20.4]
55–64 13 3.3 [1.6–5.6] 47 10.6 [7.7–14.6] 77 17.8 [13.7–22.7]
Gender
Women 32 1.7 [1.1–2.4] 168 9.0 [7.2–11.1] 295 15.8 [13.2–18.7]
Men 28 1.5 [0.9–2.4] 59 3.2 [2.3–4.4] 95 5.5 [4.4–6.8]
Marital status
Single 12 1.7 [0.9–3.3] 47 10.5 [7.1–15.3] 70 14.5 [10.8–19.3]
Married 48 1.6 [1.1–2.2] 179 5.6 [4.5–6.8] 318 10.3 [8.7–12.1]
Completed level of education
No formal school 25 0.7 [0.4–1.2] 157 5.1 [4.2–6.3] 282 9.6 [8.0–11.4]
Primary school 11 1.6 [0.9–3.0] 45 10.0 [6.9–14.2] 67 14.7 [11.1–19.1]
Secondary or more 24 11.8 [8.0–17.7] 25 11.4 [7.2–17.6] 40 18.0 [13.0–24.4]
Profession
Wage earner 18 10.0 [6.3–15.6] 14 6.0 [3.3–10.1] 25 12.9 [8.5–19.0]
Self-employed 26 0.9 [.06–1.5] 127 5.0 [3.8–12.5] 216 8.5 [6.9–10.5]
Jobless 16 1.7 [1.0–3.0] 85 9.5 [7.2–12.5] 146 16.5 [13.2–20.5]
Residence
Urban 37 4.4 [3.0–6.7] 104 14.0 [10.4–18.6] 156 21.6 [16.5–27.8]
Rural 23 0.6 [0.4–1.1] 123 3.6 [2.8–4.7] 234 7.3 [6.1–8.7]

ACE: American College of Endocrinology; AHA/NHLBI: American Heart Association and National Heart Lung and Blood Institute; JIS: Joint Interim Statement; CI: confidence interval; n = number of participants with metabolic syndrome.

Determinants of METS

The results of the multivariable analysis are reported in Tables 6 and 7. Among the sociodemographic characteristics listed in Table 2, age and residence were the main determinants of MetS regardless of the definition used. People living in urban areas had a higher risk clustering of MetS components compared with those living in rural areas. The risk of MetS increased with age group, thus participants aged 55 to 64 years had a higher risk compared to those aged 25 to 34 years regardless of the definition used. Gender disparities were reported for four definitions (NCEP-ATP III, IDF, AHA/NHLBI, JIS). For each of these definitions men had a lower risk of MetS compared to women, however, using the WHO and AACE criteria we did not find any difference between men and women regarding MetS risk. We did not find any association between marital status, profession and MetS under any of the definitions. Finally, according to the WHO, NCEP-ATP III, AACE, and AHA/NHLBI definitions, people who did not receive formal education had a lower risk of MetS compared to those who attended school.

Table 6. Determinants of metabolic syndrome according to each of six definitions by sociodemographic characteristics.

Sociodemographic characteristics WHO NCEP-ATP III IDF
aPR [95%CI] aPR [95%CI] aPR [95%CI]
Age group, years P <0.001 P <0.001 P <0.001
25–34 Ref Ref. Ref.
35–44 2.49 [1.24–5.03] 1.70 [1.11–2.61] 1.67 [1.25–2.23]
45–54 3.12 [1.51–6.42] 2.44 [1.65–3.61] 2.44 [1.89–3.16]
55–64 4.12 [1.89–8.99] 3.90 [2.51–6.04] 3.30 [2.44–4.46]
Gender P = 0.75 P <0.001 P <0.001
Women Ref. Ref. Ref.
Men 1.10 [0.61–2.01] 0.35 [0.22–0.53] 0.25 [0.17–0.37]
Marital status P = 0.59 P = 0.66 P = 0.52
Single Ref. Ref. Ref.
Married 1.23 [0.60–2.49] 1.08 [0.76–1.54] 1.10 [0.83–1.45]
Completed level of education P = 0.06 P = 0.012 P = 0.71
No formal school Ref. Ref. Ref.
Primary school 1.75 [0.89–3.47] 1.76 [1.21–2.57] 1.11 [0.82–1.50]
Secondary or more 2.89 [1.15–7.28] 1.38 [0.69–2.73] 1.17 [0.72–1.89]
Profession P = 0.51 P = 0.96 P = 0.89
Wage earner Ref. Ref. Ref.
Self-employed 1.14 [0.40–3.23] 0.93 [0.44–1.98] 1.02 [0.58–1.80]
Jobless 1.62 [0.57–4.67] 0.9 [0.41–1.98] 1.09 [0.60–1.95]
Residence P = 0.043 P <0.001 P <0.001
Urban Ref. Ref. Ref.
Rural 0.52 [0.29–0.95] 0.35 [0.23–0.52] 0.39 [0.29–0.52]

The model was adjusted for all behavioral risk factors in Table 2; WHO: World Health Organization; NCEP-ATPIII: National Cholesterol Education Program Adult Treatment Panel III; IDF: International Diabetes Federation, CI: confidence interval, aPR: adjusted prevalence ratio.

Table 7. Determinants of metabolic syndrome according to each of six definitions by sociodemographic characteristics.

Sociodemographic characteristics AACE AHA/NHLBI JIS
aPR [95% CI] aPR [95% CI] aPR [95% CI]
Age group, years P <0.001 P <0.001 P <0.001
25–34 Ref. Ref. Ref.
35–44 1.38 [0.70–2.71] 1.88 [1.34–2.63] 1.68 [1.31–2.17]
45–54 2.21 [1.15–4.24] 2.38 [1.72–3.27] 2.33 [1.81–2.99]
55–64 4.13 [1.99–8.56] 3.79 [2.62–5.48] 3.30 [2.49–4.36]
Gender P = 0.31 P <0.001 P <0.001
Women Ref. Ref. Ref.
Men 0.74 [0.40–1.34] 0.35 [0.24–0.52] 0.36 [0.27–0.48]
Marital status P = 0.98 P = 0.50 P = 0.96
Single Ref. Ref. Ref.
Married 1.01 [0.52–1.94] 0.90 [0.65–1.24] 1.01 [0.78–1.30]
Completed level of education P = 0.003 P = 0.07 P = 0.28
No formal school Ref. Ref. Ref.
Primary school 2.00 [0.86–4.69] 1.43 [1.03–1.99] 1.20 [0.92–1.57]
Secondary or more 4.06 [1.79–9.25] 1.39 [0.78–2.49] 1.28 [0.82–1.97]
Profession P = 0.10 P = 0.99 P = 0.55
Wage earner Ref. Ref. Ref.
Self-employed 0.45 [0.21–0.94] 1.13 [0.55–2.33] 1.00 [0.59–1.71]
Jobless 0.52 [0.22–1.2] 1.31 [0.63–2.72] 1.14 [0.66–1.97]
Residence P = 0.008 P <0.001 P <0.001
Urban Ref. Ref. Ref.
Rural 0.36 [0.17–0.77] 0.38 [0.26–0.54] 0.46 [0.35–0.61]

The model was adjusted for all behavioral risk factors in Table 2, ACE: American College of Endocrinology; AHA/NHLBI: American Heart Association and National Heart Lung and Blood Institute; JIS: Joint Interim Statement; CI: confidence interval, aPR: adjusted prevalence ratio.

Discussion

To the best of our knowledge, the present study is the first estimation of the burden of MetS and its components in the adult population of Burkina Faso using different definitions of MetS. Our study reported various prevalence of MetS in Burkina Faso, depending on the definition used. Based on the most recent harmonized definition (JIS), we found that 10.9% of the adult population had MetS. We also found that despite the heterogeneity in the definition of MetS, its components were clustered in urban areas and older adults (55 years and more). The differences in the definitions lie mainly in the choice of the thresholds of MetS components [36]. Previous studies reported the great variability of MetS prevalence according to the definitions [37, 38]. Beyond the debate on the appropriate definition of MetS among African populations [39], it is well known that the clustering of MetS significantly increase the risk of many chronic diseases including CVD, diabetes and cancer [38, 40]. The triglyceride level was not considered in the definition of MetS in our study since it was not collected during the STEP survey in Burkina Faso. This might contribute to lower the prevalence of MetS in this study. Nevertheless, the clustering components of MetS doubled the risk of death and tripled the risk of CVD compared to people without the MetS [41]. Because of this, it is important to engage in ongoing efforts (national plan to address NCD and its risk factors including MetS components [42] and the training of physicians specialized in the treatment of metabolic disorders [43]) for early detection and treatment of MetS and its components to reduce CVD.

A previous population-based study in an urban area (Ouagadougou) using the JIS definition of MetS, reported a prevalence of 10.3% in 2012, which is similar to our findings using the same definition [44]. The prevalence of MetS reported in our study is seem to be lower than those reported elsewhere in Africa regardless of definition used. Indeed, a meta-analysis achieved in 2019, found that the pooled prevalence of MetS in the SSA adult population according to different definitions was 11.1% (WHO), 17.1% (NCEP-ATP III), 18.0% (IDF) and 23.9% (JIS) [45]. This meta-analysis also showed that the prevalence of MetS was lower in western Africa compared to southern and eastern Africa. The reasons for this lower prevalence are unclear and thus require further investigations. Yet, adults with any components of MetS and those classified as having MetS have a significantly higher risk of CVD, which justifies the need to identify adults with a clustering of MetS components in routine practice in low and middle-income countries such as Burkina Faso [46]. In these countries, especially in SSA, the rapid rise in morbidity and mortality from CVD has been linked to undetected and uncontrolled vascular risk factors [47].

The components of MetS with the highest prevalence in this study were low HDL, abdominal obesity and hypertension, which is in accordance with those reported in other studies in Africa. Indeed, the main components of MetS among Africans are low HDL, obesity, and hypertension [48]. The predominance of low HDL among the components of MetS among Africans has been documented [48, 49]. Sumner et al [50] have shown that a low HDL level is the most frequent MetS lipid pattern among African populations [50, 51]. The low HDL level among Africans represent a substantial and evolving cardiovascular risk. In this study, the high prevalence of low HDL might be due to high proportion of infection particularly in rural area. The low HDL is known to be associated with infection and systemic inflammatory response [52]. The pattern of dyslipidemia among African populations needs further investigations, which might be addressed by the Human Heredity and Health in Africa (H3Africa) initiative [53]. The high prevalence of dyslipidemia particularly low HDL among African populations means that we need to integrate the effective detection and treatment of dyslipidemia in primary care in Africa countries [49]. Abdominal obesity is the second most prevalent MetS component reported in our study. Abdominal obesity varied across the definition since different thresholds are used to define this component of MetS [54]. For descriptive analysis, we used the most recent thresholds for waist circumference measurement (JIS definition) to define abdominal obesity among the SSA adult population. Abdominal obesity is an important marker of insulin resistance but the relevant cut-off for African adults is still discussed [55, 56]. Due to the importance of MetS in the prevention of CVD, there is a crucial need to set up recommended normal range values of waist and hip circumference in Africans [57]. Hypertension is common among the adult population in SSA, nearly one third (30.8%) have high blood pressure [58] and was the third highest prevalent component of MetS in our study. Elevated fasting blood glucose was the fourth most prevalent component of MetS. The prevalence of MetS decreased by 32% when excluded persons with diabetes [37]. MetS components are still poorly screened in Burkina Faso [44]. The most efficient preventive measures need to be implemented, including lifestyle modifications to address individual and population-wide cardiovascular disease risk in Burkina Faso, since the prevalence of some components of MetS is remarkably high.

The main determinants of MetS in our study were age and residence. We found that the prevalence of MetS was significantly higher in urban areas compared with rural areas regardless of the definition used. Similar findings have been reported in studies conducted in other west African countries including Nigeria [59], Benin [60] and Ghana [61]. Urbanization, associated with nutritional transition, and a sedentary lifestyle, has been linked to an increasing prevalence of MetS in SSA [62]. A higher prevalence of MetS in older age groups have been reported [45, 63]. The ongoing epidemiologic transition (with the aging of the population) contributes to increasing the prevalence of MetS in developing countries like Burkina Faso. In this study, we found out that for four out of six definitions of MetS (NCEP-ATP III, WHO, AACE, AHA/NHLBI), education was significantly associated with increased prevalence of MetS. The association between education level and MetS or diabetes is discussed in the literature. Indeed, Gatimu et al [64] have shown that the education was associated with increased odd of diabetes. Millogo et al [27] have not found this association. Nevertheless, high education level is linked to the increasing adoption of new sedentary lifestyles and changes in dietary intake, which increase the risk of MetS and diabetes [64].

The normal range values of many components of MetS among the African population is still being discussed in the literature, and has motivated calls for a specific definition of MetS among this population [50, 51, 65]. However, it is known that individuals with a reduced number of MetS components have a lower risk of diabetes and cardiovascular diseases [66]. While waiting for the most accurate definition of MetS, substantial efforts are needed to screen and treat the clustering of components of MetS and to reverse the current rising trend of CVD in SSA including Burkina Faso.

Strengths and limitations

The main limitation of this study was the unavailability of data on blood triglycerides, which were not measured during the survey due to the lack of adequate equipment that might underestimate the prevalence of MetS. Definitions of MetS had mainly focused on the western population and systematically included hypertriglyceridemia [45]. However most African people usually have normal triglyceride levels even so, the cardiovascular risk still higher among African population compared to the western population [50]. The data used in this study were collected since 2013, so the situation may have changed. There is a need to update this data to evaluate the temporal change of prevalence of MetS in Burkina Faso. The strengths of this study were the use of different definitions of MetS to provide countrywide prevalence and a robust statistical approach to identify its determinants. This analysis was done in a country that is “starting” an epidemiological transition, which offers an opportunity to control the rising of MetS and NCDs early.

Conclusion

The present study showed various prevalence of MetS in Burkina Faso depending on the definition. At the component level, we found that the prevalence of low HDL, obesity and hypertension were high in the adult population. We also reported that age and residence were the main determinants of MetS. The choose of appropriated definition to early detect and treat MetS in low-income countries such as Burkina Faso are crucial for achieving the sustainable goal of development by controlling the rising burden of CVD.

Acknowledgments

The authors acknowledge Mady Ouédraogo, and Michel Bonkoungou for their contribution to data management. We would like to thank also Dr Sekou Samadoulougou for assisting with study design and statistical analyses.

Abbreviations

ACE

American College of Endocrinology

AHA/NHLBI

American Heart Association and National Heart Lung and Blood Institute

BMI

body mass index

BP

blood pressure

CVD

cardiovascular disease

DM

diabetes mellitus

FG

fasting glucose

HBP

high blood pressure

HDL

high density lipoprotein

IDF

International Diabetes Federation

JIS

Joint Interim Statement

MetS

metabolic syndrome

NCD

noncommunicable disease

NCEP ATP III

National Cholesterol Education Program Adult Treatment Panel III

T2DM

Type 2 diabetes mellitus

WC

waist circumference

WHO

World Health Organization

Data Availability

The dataset of the STEPS survey that was used in this research is available at the Ministry of Health upon request since the data are owned by a third-party organization (ministry of health). The restriction was imposed by the Ministry of Health. Individuals interested can access to the STEPS survey dataset by emailing the ministry of health (Tel: (+226) 25 25 25 25; email: contact@sante.gov.bf) or directly Dr Paulin Somda: k_admos@yahoo.fr (NCDs program coordinator) or Zoma Torez: torezo2000@yahoo.fr (STEP survey data manager)). All survey materials of STEPS survey are available on the WHO website (https://extranet.who.int/ncdsmicrodata/index.php/catalog). The authors confirm that they did not have any special access privileges that others would not have.

Funding Statement

This study is funded by Académie de Recherche et d’Enseignement Supérieur (ARES) of Belgium, in the context of research program for development focused on the cardiovascular diseases in Burkina Faso. The program, which is named CARDIOPREV, is achieved by the Institut de Recherche en Sciences de la Santé (IRSS) in Burkina Faso and the Université Libre de Bruxelles in Belgium. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Carmen Melatti

26 Apr 2021

PONE-D-20-38221

Using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso

PLOS ONE

Dear Dr. Cisse,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

The manuscript has been evaluated by two reviewers, and their comments are available below.

The reviewers have raised a number of concerns that need attention. They request additional information on methodological aspects of the study, and modifications to the Limitations and Discussion sections.

Could you please revise the manuscript to carefully address the concerns raised?

Please submit your revised manuscript by Jun 07 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Carmen Melatti

Staff Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

3. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

4. Your ethics statement should only appear in the Methods section of your manuscript. If your ethics statement is written in any section besides the Methods, please move it to the Methods section and delete it from any other section. Please ensure that your ethics statement is included in your manuscript, as the ethics statement entered into the online submission form will not be published alongside your manuscript.

5. Please include a caption for figure 1.

6. Please include a copy of Table 5b which you refer to in your text on page 14.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This is an important data for Burkina Faso.

Major comments:

The exclusion of TG criteria might contribute to the lower prev of MetS in this study. This should be addressed in the discussion section without extensive speculation on the possible relative unimportance of TG for Africans.

Minor comments:

The higher proportion of low HDL might also be related to the relatively higher infection in rural area. The author should address this in the discussion section.

To improve the clarity and simplicity of the table, the author might want to remove some of the details in the table.

For binomial data, it would be simpler if the author presented only one of the group instead of presenting both groups.

Eg only presenting % of men instead of presenting % of both men and women

only presenting % of subjects with hypetrtension instead of presenting % of subjects with hypertension and % of subjects without hypertension.

Reviewer #2: Thanks for asking me to review this important study on using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso. Studies of this nature are needed to inform policy decisions by funders.

In general, the article is very well written and I congratulate the authors for a job well done.

I however have a few minor observations

1. The data were collected almost 8 years ago. The data is based secondary data from a cross-sectional survey, the national WHO Steps survey 95 aiming to assess the risk factors for NCDs which was conducted in the 13 regions of Burkina Faso 96 from 26 September to 18 November 2013. With temporal changes and increasing western lifestyles, in most SSA countries, 8 years is ample time to not differences. The study is however such an important study for the people of Burkina Faso, that I don’t to recommend a rejection based on the age of the data. Instead, I will recommend an acknowledgement of this limitation, and in the discussion, the authors could mention the need for further a predictive modelling to account of temporal changes, or indeed, update the data if they can get funding.

2. Determinants of metabolic syndrome according to each of six definitions by sociodemographic characteristics: the discussion focused mainly on the characteristics that showed statistical significance. There needs to be some discussions around why, factors such as profession and educational attainment are not associated with metabolic syndrome. This is the finding in other similar studies from ssa. Gatimu et al. https://pubmed.ncbi.nlm.nih.gov/27871259/

3. Minor: Check the spelling on “Levesl” and “peoples”. In fact the 2 sentences need to be phrased better.

a. “The third step was to measure blood sugar levesl and blood cholesterol.

b. “type 2 diabetes [51]. However, in these conditions most African peoples usually have normal”

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Dr Samuel Seidu

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2021 Aug 5;16(8):e0255575. doi: 10.1371/journal.pone.0255575.r002

Author response to Decision Letter 0


5 Jul 2021

PONE-D-20-38221

Using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso

PLOS ONE

Dear Dr. Cisse,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Thank you very much for the opportunity to revise our manuscript.

The manuscript has been evaluated by two reviewers, and their comments are available below.

We thank both reviewers for spending time to read our manuscript.

The reviewers have raised a number of concerns that need attention. They request additional information on methodological aspects of the study, and modifications to the Limitations and Discussion sections.

Could you please revise the manuscript to carefully address the concerns raised?

We have addressed all of comments of academic editor and reviewers. Thank you.

Please submit your revised manuscript by Jun 07 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

• A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

• A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

• An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Carmen Melatti

Staff Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

We have checked the references list. There is no article retracted. Thank you

3. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

Thank you for this remark. We have added the following sentence:

“The dataset of the STEPS survey that was used in this research is available at the Ministry of Health upon request to Bicaba Brice: bicaba_brico@yahoo.fr or Zoma Torez : torezo2000@yahoo.fr ). All survey materials are available on the WHO website (https://extranet.who.int/ncdsmicrodata/index.php/catalog)”.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

The majority of STEPS survey data are available upon request to the NCD Surveillance, Monitoring, and Reporting team (ncdmonitoring@who.int) or on the WHO website (https://extranet.who.int/ncdsmicrodata/index.php/catalog)”. the STEP data of Burkina Faso is not yet available on WHO website; however, it might obtain with ministry of health (bicaba_brico@yahoo.fr).

We will update your Data Availability statement on your behalf to reflect the information you provide.

Thank you

4. Your ethics statement should only appear in the Methods section of your manuscript. If your ethics statement is written in any section besides the Methods, please move it to the Methods section and delete it from any other section. Please ensure that your ethics statement is included in your manuscript, as the ethics statement entered into the online submission form will not be published alongside your manuscript.

Thank you. We have moved the ethics statement to Methods section. (see line 161-167)

5. Please include a caption for figure 1.

Thank you for this remark. We have added a caption of Figure 1 in the manuscript. (see line 176)

6. Please include a copy of Table 5b which you refer to in your text on page 14.

Thank you for this remark. Table 5b was cited in the text however there was a mistake in the table number. we have corrected the number of Table in line 224

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

Thank you

________________________________________

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

Thank you

________________________________________

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

There is no restriction to used the data but it is not available online. To obtain the data, researcher have to email the corresponding author of this manuscript or technicians of health ministry who have conducted the STEP survey ( Bicaba Brice: bicaba_brico@yahoo.fr or Zoma Torez : torezo2000@yahoo.fr ). Thank you.

________________________________________

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Thank you

________________________________________

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This is an important data for Burkina Faso.

Thank you very much.

Major comments:

The exclusion of TG criteria might contribute to the lower prev of MetS in this study. This should be addressed in the discussion section without extensive speculation on the possible relative unimportance of TG for Africans.

We have reformulated the limitation section of the manuscript to delete the extensive speculation (see line 316-318). We addressed in the discussion section the lower prevalence of MetS in our study due to unconsidered TG in the definition of MetS. The part in the discussion section is formulated as follow: “The triglyceride level was not considered in the definition of MetS in our study since it was not collected during the STEP survey in Burkina Faso. This might contribute to the lower prevalence of MetS in this study.” (see line 242-244)

Minor comments:

The higher proportion of low HDL might also be related to the relatively higher infection in rural area. The author should address this in the discussion section.

Thank you for this suggestion. We have added a sentence to discuss the low HDL level. This sentence is “The low HDL level among Africans represent a substantial and evolving cardiovascular risk. In this study, the high prevalence of low HDL might be due to high proportion of infection particularly in rural area. The low HDL is known to be associated with infection and systemic inflammatory response [53].” (see line 268-271)

To improve the clarity and simplicity of the table, the author might want to remove some of the details in the table.

For binomial data, it would be simpler if the author presented only one of the group instead of presenting both groups.

Eg only presenting % of men instead of presenting % of both men and women

only presenting % of subjects with hypertension instead of presenting % of subjects with hypertension and % of subjects without hypertension.

Thank you for this suggestion. We have deleted the line in Table 3 accordingly (see Table 3 in line189).

Reviewer #2: Thanks for asking me to review this important study on using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso. Studies of this nature are needed to inform policy decisions by funders.

In general, the article is very well written and I congratulate the authors for a job well done.

I however have a few minor observations

1. The data were collected almost 8 years ago. The data is based secondary data from a cross-sectional survey, the national WHO Steps survey 95 aiming to assess the risk factors for NCDs which was conducted in the 13 regions of Burkina Faso 96 from 26 September to 18 November 2013. With temporal changes and increasing western lifestyles, in most SSA countries, 8 years is ample time to not differences. The study is however such an important study for the people of Burkina Faso, that I don’t to recommend a rejection based on the age of the data. Instead, I will recommend an acknowledgement of this limitation, and in the discussion, the authors could mention the need for further a predictive modelling to account of temporal changes, or indeed, update the data if they can get funding.

Thank you for this suggestion. We have added a sentence to expression that in the discussion section. “The data used in this study were collected since 2013, so the situation may have changed. There is a need to update this data to evaluate the temporal change of prevalence of MetS in Burkina Faso.” (see line 323-325)

2. Determinants of metabolic syndrome according to each of six definitions by sociodemographic characteristics: the discussion focused mainly on the characteristics that showed statistical significance. There needs to be some discussions around why, factors such as profession and educational attainment are not associated with metabolic syndrome. This is the finding in other similar studies from ssa. Gatimu et al. https://pubmed.ncbi.nlm.nih.gov/27871259/

Thank you for this remark; we have added sentence to address this. See line 297 to 303 “In this study, we found out that for four out of six definitions of MetS (NCEP-ATP III, WHO, AACE, AHA/NHLBI), education was significantly associated with increased prevalence of MetS. The association between education level and MetS or diabetes is discussed in the literature. Indeed, Gatimu et al [64] have shown that the education was associated with increased odd of diabetes. Millogo et al [28] have not found out this association. Nevertheless, high education level is linked to the increasing adoption of new sedentary lifestyles and changes in dietary intake, which increase the risk of MetS and diabetes [64].” (see line 298-305)

3. Minor: Check the spelling on “Levesl” and “peoples”. In fact the 2 sentences need to be phrased better.

a. “The third step was to measure blood sugar levesl and blood cholesterol.

Thank you very much for this remark. we have corrected the spelling error. The sentence was rephrased as follow “At the third step blood sugar and blood cholesterol were measured”. (see line 117-118).

b. “type 2 diabetes [51]. However, in these conditions most African peoples usually have normal”

Thank you very much for this remark. we have corrected the spelling error. The sentence was rephrased as follow “However most African people usually have normal triglyceride levels even so, the cardiovascular risk still higher among African population compared to the western population [51].”. (see line 319-323).

________________________________________

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Dr Samuel Seidu

Thank you.

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

We have corrected the Figure 1 accordingly.

Attachment

Submitted filename: Responses_to_Editor_PLONE_def2.docx

Decision Letter 1

Samuel Seidu

21 Jul 2021

Using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso

PONE-D-20-38221R1

Dear Dr. Cisse,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Samuel Seidu, M.D, FRCP(Edin), FRCGP

Guest Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Samuel Seidu

29 Jul 2021

PONE-D-20-38221R1

Using the first nationwide survey on non-communicable disease risk factors and different definitions to evaluate the prevalence of metabolic syndrome in Burkina Faso

Dear Dr. Cissé:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Samuel Seidu

Guest Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: Responses_to_Editor_PLONE_def2.docx

    Data Availability Statement

    The dataset of the STEPS survey that was used in this research is available at the Ministry of Health upon request since the data are owned by a third-party organization (ministry of health). The restriction was imposed by the Ministry of Health. Individuals interested can access to the STEPS survey dataset by emailing the ministry of health (Tel: (+226) 25 25 25 25; email: contact@sante.gov.bf) or directly Dr Paulin Somda: k_admos@yahoo.fr (NCDs program coordinator) or Zoma Torez: torezo2000@yahoo.fr (STEP survey data manager)). All survey materials of STEPS survey are available on the WHO website (https://extranet.who.int/ncdsmicrodata/index.php/catalog). The authors confirm that they did not have any special access privileges that others would not have.


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