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Sex-and-Gender Differences in Cardiovascular Risk Factors and Their Correlates Among Adults in Freetown, Sierra Leone: A Population-Based Health-Screening Survey

James Baligeh Walter Russell1*, Theresa Ruba Koroma1, Sallieu Samura2, Abdul Jalloh1, Joshua Coker1, Mohamed Smith1, Durodami Radcliff Lisk1

1Department of Internal Medicine, Faculty of Clinical Sciences & Dentistry, College of Medicine & Allied Health Sciences, University of Sierra Leone.

2Department of Mathematics and Statistics, Fourah Bay College, University of Sierra Leone.

*Corresponding author: James Baligeh Walter Russell, Professor of Internal Medicine and Cardiologist, Deputy Vice Chancellor – College of Medicine & Allied Health Sciences, University of Sierra Leone

Received: 11 December 2025; Accepted: 19 December 2025; Published: 24 December 2025

Article Information

Citation: James Baligeh Walter Russell, Theresa Ruba Koroma, Sallieu Samura, Abdul Jalloh, Joshua Coker, Mohamed Smith, Durodami Radcliff Lisk. Sex-and- Gender Differences in Cardiovascular Risk Factors and Their Correlates Among Adults in Freetown, Sierra Leone: A Population-Based Health-Screening Survey. Archives of Internal Medicine Research. 8 (2025): 372-382.

DOI: 10.26502/aimr.0231

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Abstract

Background:

Sex-and-gender differences are crucial modifiers of cardiovascular health, yet most guidelines in sub-Saharan Africa are not sex-and-gender specific. The aim of the study was to examine the relationship between sex-and-gender differences and the prevalence of traditional cardiovascular risk factors and their correlates in a populationbased cross-sectional study in Sierra Leone.

Methods:

A stratified multistage random sampling technique was employed to recruit 2394 adults aged 20 years and older from October 2021 to October 2023 in Western Area Urban, Sierra Leone. Data collection comprised three components: clinical assessments, self-reported health behaviours, and biochemical measurements, all based on the WHO stepwise approach.

Results:

No significant age differences were observed between genders (females 42.06 ± 12 years vs. males 41.76 ± 12.6 years, p = 0.550). Males showed higher prevalence of hypertension (37.4% vs. 33.4%, p = 0.068), diabetes (9.2% vs. 7.4%, p = 0.101), overweight (34.2% vs. 32.3%, p = 0.323), and obesity (10.2% vs. 9.9%, p = 0.818). Conversely, females had significantly higher Body Mass Index (BMI) [25.0 ± 5.0 vs. 24.6 ± 4.4, p = 0.029], waist circumference (WC) [93.6 ± 4.5 vs. 80.0 ± 5.0, p < 0.001], triglyceride levels [1.7 ± 0.35 vs. 1.6 ± 0.32, p =0.013], total cholesterol [5.1 ± 0.77 vs. 4.9 ± 0.66, p < 0.001], and low HDL-C [1.28 ± 0.29 vs. 1.3 ± 0.24, p = 0.016]. Females also had higher odds of dyslipidaemia [OR=1.339; 95% CI: (1.101-1.629), p=0.003] and alcohol consumption [OR=1.229; 95% CI: (1.026 - 1.472), p=0.025]. Women faced 1.8 times greater odds [AOR=1.849; 95% CI: (0.713 - 1.010), p=0.030] of hypertension, 1.4 times higher odds [AOR=1.441; 95% CI: (1.176 - 1.765), p <0.001] of dyslipidaemia, and 1.2 times greater odds [AOR=1.225; 95% CI: (1.0123 - 1.481), p=0.037] of alcohol use compared to men. In women, BMI, WC, and blood sugar levels showed stronger correlations than in men.

Conclusion:

This study highlights the higher prevalence of cardiovascular risk factors in women in Sierra Leone, indicating the importance of implementing targeted health policies and interventions to reduce these disparities.

Keywords

Sex-and-gender differences; cardiovascular risk factors; Sierra Leone

Sex-and-gender differences articles; cardiovascular risk factors articles; Sierra Leone articles

Article Details

Introduction

Over the past decades, cardiovascular research has mainly focused on men, leading to an underappreciation of sex and gender differences in cardiovascular risk factors. [1,2,3]. Recently, enormous efforts by researchers and Women’s Health Initiatives have enhanced our understanding of both sex and gender disparities in cardiovascular disease (CVD) and improved recognition of heart disease in women [4,5,6]. Although it is often assumed that women have a lower incidence of cardiovascular risk compared to men, clinical evidence increasingly indicates that women experience higher mortality rates and worse prognostic outcomes after acute cardiovascular events [3].

The prevention, management and overall health outcomes in cardiovascular medicines are closely linked to the roles played by sex and gender [3,7,8,9]. Despite these, crucial roles, sex and gender are variable factors that significantly impact clinical practice, public health and research in cardiovascular medicine. While several studies from developing countries have reported sex and gender differences in cardiovascular risk factors, there is a notable lack of fata on these differences in Africa, particularly in sub-Saharan Africa (SSA) [9,10,11,12].

Sex is a biological variable dictated by genetics, while gender is a complex social construct shaped by customs, religions, traditions, societal beliefs, and individual behaviour within a historical and social context [13]. The differences in cardiovascular risk factors related to sex and gender arise from the interplay of biological and behavioral factors [11,14]. Biological elements, like variations in sex hormones and chromosomes, may safeguard females from hypertension until menopause, after which gender differences in hypertension tend to diminish [15].

Behavioral factors such as body mass index (BMI), smoking, alcohol intake, unhealthy eating habits, and low physical activity levels also influence these differences. However, the relationship between biological and behavioral risk factors is quite complex [9,16]. Smoking, which is more prevalent among men, has more serious consequences for women due to gender differences in nicotine processing, although these differences have decreased in recent decades [17]. Female smokers face about a 25% higher risk of developing ischemic heart disease or stroke compared to male smokers [18,19]. While women generally follow healthier diets, they are often less physically active than men [20].

Addressing disparities in sex and gender necessitates a clear understanding of their differences. It is important to acknowledge that, while connected, these two concepts are not identical. Despite the rising impact of cardiovascular disease in sub-Saharan Africa (SSA), the links between sex, gender, and CVD are still not well understood.

Research from West Africa, especially Sierra Leone, is scarce. No existing studies from Sierra Leone have explored this topic. This study aimed to examine sex and gender differences in the prevalence of cardiovascular risk factors and their related factors among adults in Freetown, Sierra Leone, based on identifiable risks from the Ecobank (Sierra Leone) study database. Our results will offer crucial insights to inform future research, as well as prevention and treatment strategies for non-communicable diseases (NCDs).

METHODS

Ethical approval and registration

Ethical approval was granted by the Sierra Leone Ethics and Scientific Review Committee. The study was registered at https://www.researchregistry.com/browse-the-registry#home/ with the ID researchregistry8201. Case records were assigned serial-coded numbers to ensure anonymity, and all data were managed confidentially. This study adhered to the STROBE guidelines for reporting observational studies in epidemiology.

Study design, setting and cohort group

A cross-sectional, population-based study was carried out from October 2021 to October 2023 among adults in West Area Urban, Freetown, Sierra Leone. Funded by Ecobank Sierra Leone Limited, this programme focused on screening and raising awareness about NCDS. Freetown, the capital of Sierra Leone, has a diverse population of approximately 1.5 million residents [21]. It was chosen as the study site because it is the country's main commercial hub, with a demographic composition that includes all ethnic groups, and where Krio and English are the primary languages spoken.

Sample size, recruitment, and selection

A stratified multistage random sampling approach was used, selecting all official electoral constituencies and dividing them into subzones based on the 2015 census data [21].. Pregnant or lactating women, individuals with mental illness or dementia, and those unwilling to give consent were excluded from the study. The sample size was determined using the Leslie Kish formula, considering the estimated 22% prevalence of hypertension in Sierra Leone, with 5% precision and a 95% confidence interval [22, 23]. To account for potential bias, non-response, and data unavailability, the sample was oversampled by 20%. With a design effect of eight sub-zonal communities, the final estimated sample size was 2531.

Selected participants from sub-zonal communities were invited to National Victoria Park in Freetown for an “Awareness and Screening Campaign for Non-Communicable Diseases.” Trained medical students, doctors, and nurses carried out the campaign. Participants who completed the screening questionnaires and measurements were subsequently referred to an accredited laboratory for blood sample collection.

Data Collection and Measurements

Demographic and Behavioural Characteristic Data

Data were collected using the WHO stepwise approach, consisting of three categories: clinical assessments (such as blood pressure and anthropometric measurements), self-reported health behaviours (like smoking and alcohol consumption), and biochemical measurements (including lipid profiles and blood glucose). Data confidentiality was preserved by assigning serial coded numbers.

Physical activity was evaluated and classified as "Low," "Moderate," or "Vigorous" using the WHO physical activity questionnaire [24]. Alcohol intake was measured weekly, calculated by multiplying the number of beer bottles consumed each week by 5% (the alcohol content) and 300 mL (the volume of a typical beer bottle), then dividing by 1000 [25]. In Sierra Leone, a standard beer bottle contains 300 mL of liquid with 5% alcohol. Participants were identified as smokers if they had smoked more than 100 cigarettes in their lifetime or were still smoking during the interview [26]. Those who had quit smoking at least 28 days prior to the interview were classified as ex-smokers. During data collection, translators were present to assist participants who did not understand English.

Anthropometric measurements and biochemical analyses

Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured on the right arm of seated participants using an OMRON M3 electronic monitor after a 5-minute rest. Two consecutive measurements were taken, and the average recorded. Hypertension was defined as an average SBP of 140 mm Hg or higher, DBP of 90 mm Hg or greater, or current antihypertensive medication use [27].

Participants' weight, height, and waist circumference were measured while wearing light clothing and barefoot. Weight was recorded to the nearest 0.1 kg, and height to 0.01 m. Body mass index (BMI) was calculated and classified as underweight (BMI < 18.5), normal weight (18.5-24.9), overweight (25.0-29.9), or obese (≥ 30). [28]. Waist circumference (WC) was measured at the midpoint between the last rib and the iliac crest. Abdominal obesity was defined as WC exceeding 88 cm for women and 102 cm for men. [29]

Clinical biochemistry measurements

Blood samples were obtained from participants' median cubital veins between 8:00 and 10:00 AM after an 8 to 10-hour fast. The samples were processed within 4 hours using the Beckman Coulter: AU480 Chemistry System to measure glucose, total cholesterol, triglycerides, HDL-C, and LDL-C.

Diabetes mellitus was characterised by a fasting blood glucose (FBG) of 7.0 mmol/L or higher, HbA1c of at least 6.5%, or the use of insulin or oral hypoglycaemic drugs. Pre-diabetes was indicated by an FPG between 6.1 mmol/L (110 mg/dL) and 6.9 mmol/L (124.9 mg/dL). . Dyslipidaemia was identified when triglycerides (TG) reached 1.70 mmol/L (150 mg/dL) or more, total cholesterol (TC) was 6.22 mmol/L (240 mg/dL) or above, LDL cholesterol was 3.3 mmol/L (130 mg/dL) or higher, HDL cholesterol was below 1.04 mmol/L (40 mg/dL), or if lipid-lowering medications were used..

Participants' blood samples were collected from the median cubital vein between 8:00 and 10:00 AM after an overnight fast of 8 to 10 hours. These samples were processed within 4 hours of collection according to manufacturers' protocols, using the Beckman Coulter AU480 Chemistry System. Measurements included glucose, total cholesterol, triglycerides, HDL-C, and LDL-C. Diabetes mellitus was defined as a fasting blood glucose (FBG) level of 7.0 mmol/L or higher, HbA1c ≥ 6.5%, or the use of insulin or oral hypoglycaemic agents. Pre-diabetes was identified with FPG between 6.1 mmol/l (110 mg/ dL) and 6.9 mmol/l (124.9 mg/dL) [30]. Dyslipidaemia was characterised by triglycerides≥ 1.70 mmol/L (150 mg/dL), total cholesterol≥ 6.22 mmol/L (240 mg/dL), LDL-C≥ 3.3 mmol/l (130 mg/dL), HDL-C <1.04 mmol/L (40 mg/dL), or the use of lipid-lowering medications, indicating abnormal lipid levels [31]..

Statistical Analysis

Data analysis was conducted using IBM SPSS Statistics version 2.6 and STATA version 17. We examined baseline characteristics, cardiometabolic risk factors, and target organ damage by sex and geographic zones. Categorical variables were shown as counts and percentages, with differences evaluated via the Pearson chi-square (χ²) test. Continuous variables were reported as means ± standard deviations (SD) and compared through one-way analysis of variance (ANOVA). When relevant, median values and interquartile ranges (IQR) were also provided. To explore associations between demographic factors and cardiovascular risk, multivariable logistic regression analysis was performed. A p-value of ≤ 0.05 (two-sided) was deemed statistically significant.

Results

Of the 2,531 eligible individuals, 2,394 participated, yielding a response rate of 94.6%. Fifty-four participants missed the "Ecobank - Cardiovascular Health Screening Campaign" at National Victoria Park, and 76 could not complete the screenings. Distribution was evenly spread among the eight sub-zonal communities, with no significant variation in population distribution (p = 0.950).

Socio-demographic and behavioural profile of the study sample

The socio-demographic characteristics of the participants are summarized in Table 1. The average age was 41.9 ± 12.3 years (20 -75years), with no significant age difference between genders (females: 42.06 ± 12 years; males: 41.76 ± 12.6 years, p = 0.550).

Table 1: Gender differences in socio-demographic characteristics of participants.

Characteristics

Total n(%)

Female n(%)

Male n(%)

P-value(χ2)

Basic characteristics

No.

2394

1250

1144

 

Age, by group

20-29

447(18.7)

255(57.0)

192(43.0)

<0.001(28.9)

30-39

703(29.4)

383(54.5)

320(45.5)

40-49

684(28.6)

359(52.5)

325(47.5)

50-59

356(14,9)

141(39.6)

215(60.4)

>60

204(8.5)

112(54.9)

92(45.1)

INCOME (Currency = Leone)

0-500

920(38.4)

504(54.8)

416(45.2)

0.052(7.715)

500-1000

666(27.8)

319(47.9)

347(52.1)

1100-2000

490(20.5)

256(52.2)

234(46.2)

>2000

318(13.3)

171(53.8)

147(46.2)

Education level

None

618(25.8)

318(51.5)

300(48.5)

0.095(6.361)

Primary

479(20.0)

273(57.0)

206(43.0)

Secondary

835(34.9)

432(51.7)

403(48.3)

Tertiary

462(19.3)

227(49.1)

235(50.9)

Marital status

single

955(39.9)

504(52.8)

451(47.2)

0.699(1.428)

Married

737(30.8)

372(50.5)

365(49.5)

Separated/Divorce

586(24.5)

310(52.9)

276(47.1)

Widow

115(4.8)

63(54.8)

52(45.2)

Occupation

Employed

500(20.9)

302(60.4)

198(39.6)

<0.001(27.6)

Self-employed

531(22.2)

241(45.4)

290(54.6)

Unemployed

930(38.8)

466(50.1)

464(49.9)

Retired

167(7.0)

96(57.5)

71(42.5)

Student

264(11.0)

145(54.9)

119(45.1)

BLOOD PRESSURE (mmHg)

Normal

1061(44.3)

510(48.1)

551(51.9)

0.002(15.15)

Pre-hypertension

489(20.4)

278(56.9)

211(43.1)

Hypertension stage 1

644(26.9)

360(55.9)

284(44.1)

Hypertension stage 2

200(8.4)

102(51.0)

98(49.0)

FRUITS/VEGETABLE

<3 serving

2182(91.1)

1143(52.4)

1039(47.6)

0.592(0.28)

>3 serving

212(8.9)

107(50.5)

105(49.5)

Alcohol

Never

1486(62.1)

783(52.7)

703(47.3)

0.014(8.14)

Current

652(27.2)

316(48.5)

336(51.5)

Previous

256(10.7)

151(59.0)

105(41.0)

Alcohol intake

Daily

345(14.4)

151(43.8)

194(56.2)

0.046(6.14)

Weekly

285(11.9)

150(52.6)

135(47.4)

Monthly

134(5.6)

57(42.5)

77(57.5)

Smoking

Never

2073(86.6)

1088(52.5)

985(47.5)

0.797(0.45)

Current

198(8.3)

100(50.5)

98(49.5)

Ex-smoker

123(5.1)

62(50.4)

61(49.6)

Daily physical activity

Low

895(37.4)

481(53.7)

414(46.3)

0.002(12.38)

Moderate

939(39.2)

515(54.8)

424(45.2)

Vigorous

511(21.3)

233(45.6)

278(54.4)

Measures of adiposity

BMI  (kg/m2)

Underweight

38(1.6)

21(55.3)

17(44.7)

0.066(7.2)

Normal

1502(62.7)

794(52.9)

708(47.1)

Overweight

612(25.6)

329(53.8)

283(46.2)

Obese

240(10.0)

106(44.2)

134(55.8)

Waist circumference (94cm men, 80cm women)

Normal

1882(78.6)

870(46.2)

1012(53.8)

0.003(8.569)

Abnormal

512(21.4)

274(53.5)

238(46.5)

WHtR risk

Normal (≤0.5)

1050(43.9)

36(3.4)

1014(96.6)

<0.001(1786.73)

Increased risk (0.51- 0.59)

1276(53.3)

1146(89.8)

130(10.2)

High risk (>0.6)

68(2.8)

68(100)

0(0.0)

WHR (0.90 men, 0.85 women)

Low

763(31.9)

753(98.7)

10(1.3)

0.210(3.12)

Moderate

273(11.4)

271(99.3)

2(0.7)

High

207(8.6)

207(100)

0(0.0)

Laboratory

Lipids

Total Cholesterol (TC) (≥6.2mmol/l)

Normal

2163(90.4)

1171(54.1)

992(45.9)

<0.001(32.25)

High

231(9.6)

79(34.2)

152(65.8)

LDL-C  (≥3.3mmol/l)

Normal

2077(86.8)

1083(52.1)

994(47.9)

0.858(0.03)

High

317(13.2)

167(52.7)

150(47.3)

HDL-C (≤1.04mmol/l)

Normal

2129(88.9)

1142(53.6)

987(46.4)

<0.00115.68)

High

317(13.2)

108(40.8)

157(59.2)

TRIGLYCERIDE  (≥1.7mmol/l)

Normal

1862(77.8)

1011(54.3)

851(45.7)

<0.001(14.58)

High

530(22.1)

238(44.9)

292(55.1)

DIABETES (mmol/l)

Normal (>6mmol/l)

2084(87.1)

1080(51.8)

1004(48.2)

0.234(2.9)

Pre-diabetes (6.0 - 6.9mmol/l)

103(4.3)

51(49.5)

52(50.5)

Diabetes (>7.0mmol/l)

199(8.3)

115(57.8)

84(42.2)

                       

The results showed that a notable portion of participants (38.4%) had low-income levels, earning between 0 and 500 Leones. No significant difference was observed in this income group between women (54.8%) and men (41.6%) (p = 0.052). While more women completed primary and secondary education, a higher percentage of men graduated from tertiary institutions. However, the differences in educational achievement between genders were not statistically significant (p = 0.095).

Most participants (38.8%) were unemployed. Among them, 45.4% of men and 54.6% of women were self-employed (p < 0.001). Women were more likely to consume alcohol (p = 0.014), whereas men had a higher average daily alcohol intake (p = 0.046).

Women engaged in significantly less daily physical activity than men (p = 0.002). The overall fruit consumption was low at 8.9%, with no difference between genders (p = 0.592). Smoking rates were similar for both genders (p = 0.797).

Gender Differences in Risk Factors for Cardiovascular Diseases

Table 2 presents the prevalence of cardiovascular risk factors, indicating higher rates among males for hypertension (37.4% vs. 33.4%, p = 0.068), diabetes (9.2% vs. 7.4%, p = 0.101), overweight (34.2% vs. 32.3%, p = 0.323), and obesity (10.2% vs. 9.9%, p = 0.818). Conversely, females exhibited significantly higher BMI (25.0 ± 5.0 vs. 24.6 ± 4.4, p = 0.029), waist circumference (93.6 ± 4.5 vs. 80.0 ± 5.0, p < 0.001), triglycerides (1.7 ± 0.35 vs. 1.6 ± 0.32, p = 0.013), total cholesterol (5.1 ± 0.77 vs. 4.9 ± 0.66, p < 0.001), and lower HDL-C (1.28 ± 0.29 vs. 1.3 ± 0.24, p = 0.016).

Table 2: Gender differences in cardiovascular risk factors in mean.

Characteristics

Total (2394)

Female (1144)

Male (1250)

p-value

N±SD

Mean ± SD

Mean ± SD

Age

41.9±12.3

42.06±12.0

41.76±12.6

0.55

Weight

74.3±14.9

74.8±15.6

73.8±14.2

0.78

Height

1.7±0.05

1.7±0.05

1.7±0.05

0.302

BMI

24.8±4.7

25.0±5.0

24.6±4.4

0.029

WC

87.1±8.3

93.6±4.5

80.0±5.0

< 0.001

SBP

127.8±23.3

127.5±23.4

128.1±23.2

0.516

DBP

85.7±11.3

85.4±11.6

86.0±11.0

0.188

Triglyceride

1.65±0,34

1.7±0.35

1.6±0.32

0.013

Total Cholesterol

5.0±0.72

5.1±0.77

4.9±0.66

< 0.001

Low HDL-C

1.3±0.27

1.28±0.29

1.3±0.24

0.016

LDL-C

3.0±0.66

2.98±0.66

3.0±0.65

0.315

FBS

5.1±1.6

5.0±1.61

5.2±1.66

0.08

HBA1C

5.2±1.03

5.2±0.96

5.2±1.09

0.964

Table 3 presents the distribution of cardiovascular risk factors by gender. Hypertension was found in 35.3% of participants, while diabetes mellitus affected 8.3%. Additionally, a substantial proportion of individuals were overweight (33.2%), obese (10%), consumed alcohol (37.9%), had abnormal waist circumference (21.4%), and engaged in insufficient physical activity (37.4%). Importantly, women showed significantly higher rates than men in elevated waist circumference, total cholesterol, triglyceride levels, and low physical activity.

Table 3: Prevalence of cardiovascular risk factors according to sex.

Characteristics

Total n(%)

Female n(%)

Male n(%)

p-value

Overweight

796(33.2)

369(32.3)

427(34.2)

0.323

Obese

240(10.0)

113(9.9)

127(10.2)

0.818

Abnormal waist circumference

512(21.4)

274(24.0)

238(19.0)

0.003

Hypertension

844(35.3)

382(33.4)

462(37.4)

0.068

Alcohol intake

908(37.9)

 467(37.4)

441(38.5)

0.025

Hx of smoking

195(8.3)

 103(9.2)

 92(7.5)

0.139

Diabetes

199(8.3)

84(7.4)

115(9.2)

0.101

High Cholesterol

231(9.6)

152(13.3)

79(6.3)

<0.001

High LDL-C

317(13.2)

150(13.1)

167(13.4)

0.858

High Triglyceride

530(22.2)

292(25.5)

238(19.1)

<0.001

Low daily physical activity

895(37.4)

481(40.1)

414(39.0)

0.002

Logistic regression analyses (Table 4) indicated that females have higher odds of dyslipidemia [OR = 1.339; 95% CI: (1.101-1.629), p = 0.003] and alcohol consumption [OR = 1.229; 95% CI: (1.026-1.472), p = 0.025]. Adjusted odds ratios (AOR) demonstrated that women are 1.8 times more likely to have hypertension [AOR = 1.849; 95% CI: (0.713-1.010), p = 0.030], 1.4 times more likely to have dyslipidemia [AOR = 1.441; 95% CI: (1.176-1.765), p < 0.001], and 1.2 times more likely to consume alcohol [AOR = 1.225; 95% CI: (1.0123-1.481), p = 0.037] than men. Among women, BMI, waist circumference, and elevated blood sugar levels showed stronger associations.

Table 4: Univariate and Multivariate logistic regression of gender and cardiovascular risk factors.

Variables

Univariate OR

Multivariate OR

COR 95% CI

p-value

AOR 95%CI

p-value

Overweight

No

Ref.

Ref.

Yes

0.918(0.774 - 1.088)

0.323

1.018(0.831 - 1.246 )

0.079

Obese

No

Ref.

Ref.

Yes

0.968(0.741 - 1.266) 

0.818

0.941(0.686 - 1.290)

0.526

Smoking

Never

Ref.

Ref

Yes

1.248(0.930 - 1.673) 

0.802

 1.269(0.940 - 1.712)

0.158

Hypertension

No

Ref.

Ref

Yes

0.855(0.723 - 1.012) 

0.068

1.849(0.713 - 1.010)

0.03

Dyslipidemia

No

Ref.

Ref.

Yes

1.339(1.101 - 1.629) 

0.003

1.441(1.176 - 1.765)

<0.001

Diabetes Mellitus

No

Ref.

Ref.

Yes

0.782(0.583 - 1.049) 

0.101

 0.826(0.611 - 1.117)

0.135

ALCOHOL

No

Ref.

Ref.

Yes

1.229(1.026 - 1.472)

0.025

1.225(1.0123 - 1.481)

0.037

Physical activity

No

Ref.

Ref.

Yes

1.090(0.927 - 1.289)

0.31

1.090(0.919 - 1.293)

0.323

Fruits/Vegetable intake

<3 servings

Ref.

Ref.

>3 servings

1.079(0.814 - 1.431)

0.595

1.063(0.795 - 1.421)

0.682

fortune-biomass-feedstock

Figure 1: Correlates of cardiovascular risk factors.

Discussion

Sex and gender disparities in cardiovascular risk factors are increasingly recognized as significant issues not only in developed countries but also in low- and middle-income countries (LMICs), where the burden of cardiovascular disease (CVD) is growing. Despite greater awareness of cardiovascular health, there is limited scientific research from sub-Saharan Africa (SSA) on this topic, especially in Sierra Leone, where recent health screening campaigns have collected substantial data. This study is a pioneering report on sex and gender differences in the prevalence of cardiovascular risk factors among adults in West Africa, offering key insights into the nature of these disparities. The observed differences in CVD risk factors in Sierra Leone highlight complex interactions between biological, socio-cultural, and structural factors. 

Our results show a high rate of risk factors for cardiovascular disease in Sierra Leone: hypertension (35.3%), diabetes mellitus (8.3%), overweight (33.2%), obesity (10.0%), abdominal obesity (21.4%), dyslipidaemia (21.4%), low physical activity (37.4%), smoking (8.3%), and alcohol consumption (37.9%). We observed significant gender differences, especially in BMI, abdominal obesity, and lipid profiles. The high prevalence of excess weight among women aligns with findings from Cameroon, Kenya, and Tanzania (12, 32-34). This trend likely reflects socio-cultural factors such as gender-specific work roles, sedentary lifestyles, and cultural attitudes toward weight, where femininity is often linked to a heavier body.

In contrast, studies from Mexico and China have shown higher obesity rates in men compared to women, emphasising cultural differences in gender-specific health outcomes. [37, 38]. The high prevalence of hypertension among men in our study aligns with findings from Njelekela et al. and Sandberg et al. [12, 12,15]. However, differences exist with Dev et al. ’s results, likely due to variations in study design, participant demographics, and lifestyle factors. Since two-thirds of our cohort were under 50, the protective role of estrogen against hypertension in women before menopause may explain why hypertension is less common, despite higher obesity rates. [39]..

Despite notable increases in BMI, waist circumference, and WHtR among women, our study observed a lower incidence of hypertension in this group, aligning with results from Tanzanian research. [12]. This raises questions about the link between obesity and hypertension, implying that women might need a higher level of adiposity to experience significant blood pressure increases. This is worrisome because rising obesity rates in younger women are linked to greater cardiovascular risk. [42].

Further notable gender-related differences were seen in lipid profiles, with women showing higher total cholesterol and triglycerides but lower HDL levels. [43, 44]. These differences could be due to greater adiposity in women, which is known to affect lipid metabolism.

The prevalence of type 2 diabetes mellitus in Sierra Leone has been increasing, with rates of 2.4% in 1997, 3.5% in 2009, 6.2% in 2017, and 5.5% in 2020. Our study reports the highest prevalence to date at 8.3%, with a notably higher prevalence in females (9.2%) than in males (7.5%). This is the first study in Sierra Leone to include HbA1c measurements in diabetes screening. Combining HbA1c with fasting blood sugar (FBS) may have contributed to the higher prevalence observed among urban adults. Researchers express concern that relying solely on fasting blood sugar, commonly used in population surveys, might miss many undiagnosed cases, especially in early stages. The higher prevalence among females aligns with a meta-analysis of sub-Saharan Africa, which found women in Southern African countries are more affected than men, whereas in Eastern, Central, and Western Africa, women have lower prevalence than men. Additionally, increased overweight and obesity rates among females contribute to this higher prevalence.

In Africa, smoking rates are rising [43]. Although the overall smoking prevalence in this study is low, a notably higher percentage of women smokers (9.2%) compared to men (7.5%) was observed, with a women-to-men ratio of approximately 0.8 [43,49]. Our findings align with data from Nauru, Denmark, and Sweden [50]. Despite variations in smoking prevalence across Africa, the gender difference observed in our study is a significant risk factor for cardiovascular diseases, highlighting the need for more comprehensive national policies on prevention and cessation programs in Sierra Leone.

Our study revealed a high rate of physical inactivity among participants, especially among females who are significantly more inactive than males. This finding supports existing research indicating that women in Africa often face socio-cultural barriers that restrict their outdoor activities, contributing to greater inactivity. Such sedentary behaviour increases the risk of cardiovascular issues and other negative health effects. [31, 51]

Logistic regression indicated that women have higher odds of dyslipidemia and alcohol use than men. The multivariate analysis further showed increased adjusted odds for hypertension, dyslipidemia, and alcohol consumption among women. Moreover, a strong link was found between body mass index (BMI), waist circumference (WC), and elevated blood sugar levels in women. These gender-related findings align with other research, despite differences in socio-cultural settings.

This study highlights the burden of cardiovascular risk factors (CVRF) among adults in Sierra Leone, with a particular focus on the increased vulnerability of women. It counters the misconception that women are less susceptible to cardiovascular diseases and has important policy implications for health promotion and lifestyle interventions targeting female-specific risk factors.

The study has multiple strengths, such as a large sample size representative of the general population, rigorous laboratory measures like HbA1c, and data collection by trained clinicians using a validated WHO Stepwise tool. Additionally, it adhered to the 'STROBE' reporting guidelines.

However, there are limitations, such as the inability to establish causality because of its cross-sectional design and limited generalizability since it only examined urban adults. Despite these limitations, the study provides valuable insights into gender-specific cardiovascular risk factors in urban Africa.

In conclusion, the differences in cardiovascular disease by sex and gender are especially significant in Africa. The study shows increasing cardiovascular risks in Sierra Leone, notably among women, possibly due to genetic and environmental influences. Adopting gender-responsive health approaches can enhance prevention and decrease the disease burden. Future research should incorporate gender-specific factors into risk assessments. Long-term studies could reveal how these factors change over time and the effects of interventions.

Acknowledgments

The ECOBANK (SL) Study group: Dr Jattu Rahman-Sesay, Dr. Tejan Mansaray, Dr. Jajuah, Dr. Mac-Jajuah, Dr. Mohamed Samura, Dr Abdul Karim Bah, Dr Evelyn Hawa Kamara, Dr Chernor Abubakarr Barrie, Paul Thoronka, Dr. Osman Kanneh, Dr. Alieu Kanu, Dr. Vidal Dupigny, Dr. Scholastica Nduisi, Dr. Omar Bah.

We express gratitude to all nurses from the Ministry of Health and Sanitation for serving as data collectors in ensuring that this study was successful. A big thank you to: Zainab Kargbo, Fatmata Koroma, Abigail Pratt, Claudia Campbell, Angel Jones, Lovetta Davies, Fatmata Bangura, Albert Rogers, Abibatu Jones, Sylvia Kanyako and Gillian Jones. We are also grateful for the technical laboratory assistance provided by the Ecomed Advance Medical Laboratory and the staff of Prime Care Medical Clinic who supported in the cardiac screening of the participants. We wish to thank all the participants enrolled in this study.

Financial disclosures

This research was funded by Ecobank Sierra Leone Limited. J.B.W. Russell served as a consultant for this study and earned consulting fees from Ecobank (S.L). The views expressed are solely those of the authors. The funders had no role in study design, data collection, analysis, interpretation, or writing. The corresponding author had full access to all data and made the final decision to publish.

Conflict of Interest

The authors declare no conflict of interest.

Informed Consent

The informed consent, which was cleared by the IRB was given to every recruited participant.

Author’s Contributions

JBW Russell conceptualized and designed the overall study, and contributed to formal analysis and the original draft writing. Abdul Jalloh also conceptualised and designed the study. TR Koroma handled data curation, formal analysis, and contributed to the writing of the original draft. SK Samura was responsible for data curation and conducted formal statistical analysis. J.M. Coker and D.R. Lisk reviewed and edited the manuscript. M Smith managed the project administration and participant recruitment. All authors critically reviewed the manuscript, contributed important intellectual content, and approved the final draft.

Data Availability

Any inquiries regarding the supporting data availability of this study should be directed to the corresponding author.

No writing assistance was utilized in the production of this manuscript.

References

  1. Melloni, J.S. Berger, T.Y. Wang et al. Representation of women in randomized clinical trials of cardiovascular disease prevention Circ. Cardiovasc. Qual. Outcomes, 3 (2010): pp. 135-142
  2. E. Manson, J. Hsia, K.C. Johnson et al.Estrogen plus progestin and the risk of coronary heart disease N. Engl. J. Med., 349 (2003): pp. 523-534
  3. Mosca, Lori, Elizabeth Barrett-Connor, et al. "Sex/gender differences in cardiovascular disease prevention: what a difference a decade makes." Circulation 19 (2011): 2145-2154.
  4. Chester RC, Kling JM, Manson JE. What the Women’s Health Initiative has taught us about menopausal hormone therapy. Clin Cardiol. 2018;41:247-252.
  5. N. Hamulyak, A.J. Brockmeier, J.D. Killas, et al. Women’s health in The BMJ: a data science history. BMJ Open, 10 (2020).
  6. Mauvais-Jarvis F, Bairey Merz N, Barnes PJ, et al. Sex and gender: modifiers of health, disease, and medicine. Lancet 396 (2020): 565-582.
  7. Spence JD, Pilote L. Importance of sex and gender in atherosclerosis and cardiovascular disease. Atherosclerosis 241 (2015): 208-210.
  8. McGregor AJ, Chin EL, Rojek MK, et al. Sex and gender health education summit: advancing curricula through a multidisciplinary lens. J Womens Health 28 (2019): 1728-1736.
  9. Regensteiner JG, Libby AM, Huxley R, et al. Integrating sex and gender considerations in research: educating the scientific workforce. Lancet Diabetes Endocrinol 7 (2019): 248-250.
  10. Connelly PJ, Jandeleit-Dahm KAM, Delles C. Sex and gender aspects in vascular pathophysiology. Clin Sci (Lond) 134 (2020): 2203-2207.
  11. Pelletier R, Khan NA, Cox J, et al. Sex versus gender-related characteristics. J Am Coll Cardiol 67 (2016): 127-135.
  12. Marina A Njelekela, Rose Mpembeni, Alfa Muhihi et al. Gender-related differences in the prevalence of cardiovascular disease risk factors and their correlates in urban Tanzania. Comparative Study BMC Cardiovasc Disord 9 (2009): 30.
  13. Clayton JA, Gaugh MD. Sex as a biological variable in cardiovascular diseases: JACC focus seminar1/7. J Am Coll Cardiol 79 (2022): 1388-1397.
  14. Westerman S, Wenger NK. Women and heart disease, the underrecognized burden: sex differences, biases, and unmet clinical and research challenges. Clin Sci 130 (2016): 551-563.
  15. Sandberg K, Ji H. Sex differences in primary hypertension. Biology of Sex Differences 3 (2012): 1-21.
  16. National Institutes of Health, RFA-OD-19-029: The Intersection of Sex and Gender Influences on Health and Disease (R01 Clinical Trial Optional). 2019. https://grants.nih.gov/grants/guide/rfafiles/
  17. RR Huxley, M Woodward. Cigarette smoking as a risk factor for coronary heart disease in women compared with men: a systematic review and meta-analysis of prospective cohort studies. Lancet, 378 (2011): pp. 1297-1305
  18. Halimi J-M, Giraudeau B, Cacès E, et al. The risk of hypertension in men: direct and indirect effects of chronic smoking. J Hypertens 20 (2002): 187-193.
  19. SA Peters, RR Huxley, M Woodward. Smoking as a risk factor for stroke in women compared with men: a systematic review and meta-analysis of 81 cohorts, including 3,980,359 individuals and 42,401 strokes. Stroke, 44 (2013): pp. 2821-2828
  20. MH Forouzanfar, A Afshin, LT Alexander, et al. Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet, 388 (2016): pp. 1659-1724
  21. von Elm E, Altman DG, Egger M, et al; STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. J Clin Epidemiol 61 (2008): 344-349.
  22. Statistics Sierra Leone. 2015 population and housing census, 2015. Available: https://www. statistics. sl/ images/ StatisticsSL/ Documents/ final- results_- 2015_ population_ and_ housing_ census. Pdf. 2015.
  23. Kish L. Survey sampling. IX + 643 S., 31 Abb., 56 Tab., Preis 83 S. New York, London: John Wiley & Sons, Inc, (1965).
  24. Geraedts TJM, Boateng D, Lindenbergh KC, et al. Evaluating the cascade of care for hypertension in Sierra Leone. Trop Med Int Health 26 (2021): 1470-80.
  25. What is moderate-intensity and Vigorous-intensity physical activity? Available: https://www. who. int/ dietphysicalactivity/ physical_activity_ intensity/ en/ [Accessed 16th August 2019]. 2019
  26. Alcohol units. Available: https://www. nhs. uk/ live- well/ alcoholsupport/ calculating- alcohol- units/ [Accessed 14 Dec 2018]. 2018.
  27. St Claire S, Fayokun R, Commar A, et al. The World Health Organization's World No Tobacco Day 2020 Campaign Exposes Tobacco and Related Industry Tactics to Manipulate Children and Young People and Hook a New Generation of Users. J Adolesc Health 67 (2020): 334-337.
  28. Hernandez-Vila E. A review of the JNC 8 Blood Pressure Guideline. Tex Heart Inst J 42 (2015): 226-228.
  29. Body mass index. BMI, 2018. Available: http://www. euro. who int/ en/ health- topics/ disease- prevention/ nutrition/ a- healthy- lifestyle/body- mass- index- bmi [Accessed 19 Dec 2018]. 2018.
  30. Okosun IS, Choi S, Dent MM, et al. Abdominal obesity defined as a larger than expected waist girth is associated with racial/ethnic differences in risk of hypertension. J Hum Hypertens 15 (2001): 307-312.
  31. Diagnosis and classification of diabetes mellitus. Diabetes Care 34 (2011): S62-69.
  32. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). Jama 285 (2001): 2486-2497.
  33. Sobngwi E, Mbanya J, Unwin N, et al: Physical activity and its relationship with obesity, hypertension and diabetes in urban and rural Cameroon. Int J Obes Relat Metab Disord 26 (2001): 1009-1016.
  34. Christensen DL, Eis J, Hansen AW, et al.: Obesity and regional fat distribution in Kenyan populations: impact of ethnicity and urbanization. Ann Hum Biol 35 (2008): 232-249.
  35. Njelekela M, Negishi H, Nara Y, et al.: Cardiovascular risk factors in Tanzania: a revisit. Acta Trop 79 (2001): 231-239.
  36. Siervo M, Grey P, Nyan OA, et al: A pilot study on body image, attractiveness and body size in Gambians living in an urban community. Eat Weight Disord 11 (2006): 100-109.
  37. Walker AR, Adam F, Walker BF: World pandemic of obesity: the situation in Southern African populations. Public Health 115 (2001): 368-372.
  38. Meaney, E., A. Lara-Esqueda, G.M. Ceballos-Reyes et al. Cardiovascular risk factors in the urban Mexican population: The FRIMEX study. Public Health, 121 (2007): 378-384.
  39. Wu, D.M., L. Pai, N.F. Chu, P.K. et al., 2011. Prevalence and clustering of cardiovascular risk factors among healthy adults in a Chinese population: The MJ health screening center study in Taiwan. Int. J. Obesity, 25 (2011): 1189-1195.
  40. Dev R, Favour-Ofili D, Raparelli V, et al. Sex and Gender Influence on Cardiovascular Health in Sub Saharan Africa: Findings from Ghana, Gambia, Mali, Guinea, and Botswana. Global Heart 17 (2022): 63.
  41. Unwin NC: Rural and urban differences in diabetes prevalence in Tanzania: the role of obesity, physical inactivity and urban living. Trans R Soc Trop Med Hyg 94 (2000): 637-644.
  42. Vorster HH: The emergence of cardiovascular disease during urbanization of Africans. Public Health Nutr 5 (2002): 239-243
  43. Kotsis V, Stabouli S, Papakatsika S, et al. Mechanisms of obesity-induced hypertension. Hypertension Research 33 (2010): 386-393.
  44. Keates AK, Mocumbi AO, Ntsekhe M, et al. Cardiovascular disease in Africa: epidemiological profile and challenges. Nature Reviews Cardiology 14 (2017): 273-293.
  45. Ikem I, Sumpio BE. Cardiovascular disease: the new epidemic in sub-Saharan Africa. Vascular 19 (2011): 301-307.
  46. Ceesay MM, Morgan MW, Kamanda MO, et al. Prevalence of diabetes in rural and urban populations in southern Sierra Leone: a preliminary survey. Trop Med Int Health 2 (1997): 272-277.
  47. Sundufu AJ, Bockarie CN, Jacobsen KH. The prevalence of type 2 diabetes in urban Bo, Sierra Leone, and in the 16 countries of the West Africa region. Diabetes Metab Res Rev 33 (2017).
  48. Odland ML, Bockarie T, Wurie H, et al. Prevalence and access to care for cardiovascular risk factors in older people in Sierra Leone: a cross-sectional survey. BMJ Open 10 (2020)
  49. Hilawe EH, Yatsuya H, Kawaguchi L, et al. Differences by sex in the prevalence of diabetes mellitus, impaired fasting glycaemia and impaired glucose tolerance in sub-Saharan Africa: a systematic review and meta-analysis. Bull World Health Organ 91 (2013): 671-682D.
  50. Hitchman SC, Fong GT. Gender empowerment and female-to-male smoking prevalence ratios. Bull World Health Organ 89 (2011): 195-202.
  51. St Claire S, Fayokun R, Commar A, et al. The World Health Organization's World No Tobacco Day 2020 Campaign Exposes Tobacco and Related Industry Tactics to Manipulate Children and Young People and Hook a New Generation of Users. J Adolesc Health 67 (2020): 334-337.
  52. BeLue R, Okoror TA, Iwelunmor J, et al. An overview of cardiovascular risk factor burden in sub-Saharan African countries: a socio-cultural perspective. Globalization and Health 5 (2009): 1-12.

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