Skip to content

Advertisement

BMC Obesity

Research article
Open Access
Open Peer Review

This article has Open Peer Review reports available.

How does Open Peer Review work?

Comparative associations between anthropometric and bioelectric impedance analysis derived adiposity measures with blood pressure and hypertension in India: a cross-sectional analysis

  • Kevin Y. Taing1, 2Email author,
  • Michael E. Farkouh3, 4,
  • Rahim Moineddin5, 6,
  • Jack V. Tu6, 7, 8 and
  • Prabhat Jha1, 2
BMC ObesityBMC series – open, inclusive and trusted20174:37

https://doi.org/10.1186/s40608-017-0173-1

©  The Author(s). 2017

Received: 8 September 2016

Accepted: 10 November 2017

Published: 1 December 2017

Open Peer Review reports

Abstract

Background

The utility of bioelectrical impedance analysis (BIA) derived adiposity measures as compared to anthropometric measures for the assessment of adiposity-related health risk is not clear. We aimed to clarify the relationships of BIA and anthropometric derived adipose measures with blood pressure and hypertension, and to compare the discriminative ability of the respective measures for hypertension.

Methods

We used baseline data collected between 2015 and 2016 from the Indian Study on Health of Adults (ISHA), an ongoing population based cohort study in India (N = 5990; age 30–69 years). We examined and compared the associations and discriminative ability between anthropometric (body mass index, waist circumference, hip circumference, waist-hip ratio, waist-height ratio) and BIA (whole body and trunk fat percentage) derived adiposity measures with blood pressure components (systolic pressure, diastolic pressure, pulse pressure, mean arterial pressure, mid-blood pressure) and hypertension.

Results

Regardless of whether the adiposity measure was derived from BIA or anthropometry, all were strongly and positively associated with blood pressure and hypertension. For both men and women, the magnitude of association of BIA measures with blood pressure and hypertension were comparable to those of anthropometric measures. Further, the ability of BIA derived adiposity measures to distinguish between those with and without hypertension was similar to the discriminative ability of anthropometric measures.

Conclusions

As compared to simple anthropometric measures, BIA derived estimates of adiposity provide no apparent advantage in the assessment of blood pressure and hypertension. The observed similarities between adiposity measures suggest that simple anthropometrics may be sufficient to assess adiposity and adiposity-related risks.

Keywords

AnthropometryBioelectrical impedance analysisAdiposityBody mass indexWaist circumferenceBlood pressureHypertensionIndia

Background

In India, demographic, socioeconomic and health transitions have contributed to an increasing burden of adiposity-related diseases, such as cardiovascular disease (CVD) [1, 2]. A well-established consequence of excess adiposity is high blood pressure [3–5], which is a major determinant of CVD related morbidity and mortality [6–9]. Indeed, amongst CVD risk factors high blood pressure accounts for the greatest proportion of deaths in India [1]. Epidemiologic studies of the relationship between adiposity and blood pressure commonly use anthropometric indices [body mass index (BMI), waist circumference (WC), hip circumference (HC), waist-hip ratio (WHR), and waist-height ratio (WHtR)] as surrogate measures of adiposity. However, anthropometric measures are limited in their ability to distinguish differences in body composition, and do not provide estimates of body fat [10, 11]. As such, their adequacy to assess adiposity and adiposity-related health risks has been challenged, with inconsistent findings between studies [11–15].

Criterion methods such as magnetic resonance imaging (MRI) and dual-energy X-ray absorptiometry (DXA) are available to assess body composition and determine relative amounts of adipose tissue, but these methods are costly, invasive and time consuming. Moreover, they are not readily available for large scale use in low and middle-income countries (LMIC), such as India. In comparison, bioelectrical impedance analysis (BIA) represents a relatively low-cost and simple method to obtain estimates of body fat and identify those at increased health risk [16]. Further, with the advent of new BIA models capable of segmental analysis, assessment of whole body and regional (i.e. trunk) distribution of adipose tissue is feasible [17, 18]. The ability of BIA to distinguish differences in body composition and provide estimates of body fat may be of particular importance for a South Asian population. Compared to other ethnic groups, it has been shown that South Asians have higher amounts of body fat despite having similar or lower anthropometric values [19, 20]. As BIA provides estimates of body fat, it may prove to be more advantageous for the early detection and risk stratification of populations with high adiposity-related health risk than simple anthropometric measures in India. However, despite the potential benefits of BIA, there is a paucity of studies from India and other LMIC investigating its utility in assessing adiposity-related risks such as hypertension [21, 22].

As more sophisticated measures of body fat (i.e. those derived from BIA) become readily available, reliable studies evaluating whether they provide any value over simple anthropometric measures are necessary. We therefore examine and compare the associations of anthropometric and BIA derived adiposity measures with blood pressure and hypertension in a large population-based cohort of men and women from India.

Methods

Study design, setting and participants

We conducted a cross-sectional analysis comparing the associations between anthropometric and BIA derived adiposity measures with blood pressure and hypertension in India. The Indian Study on Health of Adults (ISHA) is an ongoing population-based cohort study of men and women age 30–69 years from the general population of the town of Barshi (Maharashtra, India). We used baseline data collected between 2015 and 2016 for our analyses (N = 5996). Of these participants, 6 were excluded because of pregnancy.

Study data sources

Upon arrival to each village, and prior to the recruitment of participants, survey teams met with the local Sarpanch or authorized personal of the village to seek permission for the study. In addition, group meetings were also conducted before the start of the survey to create awareness of the study for those residing in the village community.

Trained surveyors collected data for the baseline survey in three stages over a 7-day activity cycle: enumeration (days 1–2), household health survey (days 3–4) and a health checkup camp (days 5–7). First, field teams enumerated the households in the village, collecting information on household size and the usual residing members. Second, trained surveyors (a male and a female) visited the households and interviewed eligible members (30–69 years of age) to obtain detailed information on demographic, socioeconomic, and lifestyle characteristics, along with blood pressure measurements and antihypertensive medication use. After completion of the interview participants were invited to attend a health checkup camp, and were given an invitation card detailing the time and place of their health checkup. Each health checkup camp was set up in the village with direct input from the Sarpanch or any other administrative head to ensure ease of access for participants. Lastly, participants attended the health checkup camp where their blood pressure was measured, along with physical and body composition measurements.

Blood pressure measurement

After 5 min of rest, three blood pressure measurements were taken at heart level in a seated position using the Omron BP-742CAN (Kyoto, Japan) digital automatic monitor. Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were calculated as the average of the three readings. We calculated pulse pressure, mean arterial pressure, and mid-blood pressure using previously reported formulas [23]. Hypertension was defined as SBP ≥140 or DBP ≥ 90, or reported use of antihypertensive medication.

Physical measurements

A measuring tape was used to measure height to the nearest 0.1 cm [23]. Weight was measured to the nearest 0.1 kg using the Tanita MC780MA body composition analyzer (Tokyo, Japan), without footwear and with subtraction of 0.5 kg for clothing weight. WC and HC were both measured to the nearest 0.1 cm using a measuring tape. For WC, measurements were taken at the level of the umbilicus with arms folded across the chest. For HC, measurements were taken at the point yielding the maximum circumference over the buttocks.

Adiposity measures

The anthropometric measures of adiposity were BMI, WC, HC, WHR, and WHtR. BMI was calculated as weight in kilograms divided by the square of height in meters. WHR was calculated as WC in centimeters divided by HC in centimeters, and WHtR as WC in centimeters divided by height in centimeters. The BIA derived measures of adiposity were whole body fat percentage and trunk fat percentage, as estimated with proprietary algorithms by the Tanita body composition analyzer.

Statistical analysis

We performed all analyses separately for men and women. We calculated Pearson’s partial correlation coefficients for the intercorrelations of the different adiposity measures (BMI, WC, HC, WHR, WHtR, whole body fat percentage, trunk fat percentage) and blood pressure components (SBP, DBP, pulse pressure, mean arterial pressure, mid-blood pressure), adjusted for age. In order to compare the associations between anthropometric and BIA derived adiposity measures with blood pressure and hypertension, we evaluated the relationships using several methods. First, we used multiple linear regression models to quantify the associations between adiposity measures with blood pressure components. Second, we used Poisson regression models to examine the relationships between adiposity measures and hypertension. We estimated the means of each blood pressure component, and calculated the prevalence ratios (PR) for hypertension per sex-specific standard deviation (SD) change in an adiposity measure. We used two models for these analyses. In the first model, adjustments were made for age and level of education (illiterate, primary school, middle school, secondary school, college). In the second model, further adjustments were made variously for either an anthropometric or BIA derived measure of general (BMI, whole body fat percentage) or central (WC, trunk fat percentage) adiposity. 198 individuals (3% of total) who reported current use of antihypertensive medication were excluded from the continuous blood pressure analyses.

Lastly, we used receiver operating characteristic (ROC) curves and the area under the curve (AUC), estimated by logistic regression models with adjustments for age and education, to compare the discriminative ability of each adiposity measure for hypertension. The AUC is a measure of the overall discriminative ability of each adiposity measure for hypertension, with values falling between 0.5 and 1.0, representing no discriminative and perfect discriminative ability, respectively. The AUC for all measures of adiposity were compared using a nonparametric approach for the comparison of multiple AUC from ROC curves [24].

In addition to age and education adjustments, further adjustment for tobacco use (non-user, less than daily user, daily user) and alcohol consumption (non-drinker, current drinker) did not substantially affect any of the estimates (results not presented). We performed all statistical analyses using SAS version 9.3 (SAS Institute, Cary, NC, USA), and provide estimates with their respective 95% confidence intervals (CI).

Results

The means (SD) of anthropometric and BIA derived adiposity measures, blood pressure components, and hypertension prevalence are presented in Table 1. The average age for men and women were 47 (12) and 45 (11) years, respectively, with the overall mean being 46 (11) years in our study. On average, SBP and pulse pressure were higher among men than women, whereas women had slightly higher DBP than men. The average mean arterial pressure, mid-blood pressure, and hypertension prevalence were similar between both sexes. In general, mean BMI and HC were slightly lower for men than women. Likewise, mean fat percentages (whole body and trunk) were also lower for men than women. By contrast, average WC, WHR and WHtR were greater for men than women.
Table 1

Distribution of adiposity measures and blood pressure (N = 5990)

 

Male

Female

 

No. 2764

No. 3226

Age

47.1 (11.7)

45.2 (11.1)

Anthropometric Measures

 Height (cm)

163.4 (6.3)

150.0 (5.7)

 Weight (kg)

60.0 (11.4)

51.0 (10.0)

 Body Mass Index (kg/m2)

22.4 (3.7)

22.7 (4.1)

 Waist Circumference (cm)

82.5 (11.1)

73.5 (10.1)

 Hip Circumference (cm)

90.0 (7.2)

92.1 (8.5)

 Waist-Hip Ratio

0.91 (0.075)

0.80 (0.064)

 Waist-Height Ratio

0.50 (0.067)

0.49 (0.068)

Bioelectrical Impedance Measures

 Whole Body Fat (%)

20.0 (6.4)

32.0 (7.4)

 Trunk Fat (%)

20.6 (7.8)

31.0 (9.2)

Blood Pressure Components (mmHg)

 Systolic Blood Pressure

129.0 (16.5)

127.8 (18.4)

 Diastolic Blood Pressure

83.0 (9.6)

83.6 (9.6)

 Pulse Pressure

46.0 (10.8)

44.2 (12.7)

 Mean Arterial Pressure

98.3 (11.3)

98.3 (11.8)

 Mid-Blood Pressure

106.0 (12.4)

105.7 (13.3)

 Hypertension (%)a

803 (29.1)

984 (30.5)

Values presented as mean (SD), unless indicated. aNo. (%) hypertensive

Overall, the sex-specific correlation coefficients of adiposity measures with blood pressure components were comparable, except for pulse pressure, whereby the correlations were relatively weaker (Table 2). The intercorrelations between anthropometric measures were high, apart from those with WHR, which were relatively lower. Similarly, BIA derived measures of adiposity were also strongly correlated with each other. When considering the pairwise correlation coefficients between anthropometric and BIA derived adiposity measures, BMI had the strongest correlation with body fat and trunk fat percentage for both men and women, whereas WHR had the weakest.
Table 2

Pearson partial correlation coefficients adjusted for age (N = 5792)

 

BMI

WC

HC

WHR

WHtR

Whole Body Fat

Trunk Fat

SBP

DBP

PP

MAP

MBP

BMI

Male:

0.90

0.85

0.64

0.90

0.82

0.82

0.29

0.28

0.18

0.30

0.30

Female:

0.88

0.90

0.47

0.88

0.90

0.93

0.24

0.32

0.09

0.30

0.29

WC

 

Male:

0.83

0.83

0.96

0.80

0.80

0.27

0.29

0.15

0.29

0.29

 

Female:

0.84

0.76

0.96

0.82

0.85

0.24

0.32

0.09

0.30

0.28

HC

  

Male:

0.39

0.76

0.73

0.74

0.24

0.24

0.15

0.25

0.25

  

Female:

0.28

0.77

0.83

0.86

0.21

0.29

0.07

0.27

0.25

WHR

   

Male:

0.84

0.60

0.60

0.21

0.24

0.10

0.24

0.23

   

Female:

0.76

0.46

0.48

0.17

0.21

0.07

0.20

0.19

WHtR

    

Male:

0.79

0.80

0.27

0.28

0.15

0.29

0.29

    

Female:

0.83

0.85

0.25

0.32

0.10

0.31

0.29

Whole Body Fat

     

Male:

0.97

0.30

0.32

0.17

0.33

0.32

     

Female:

0.97

0.23

0.31

0.07

0.29

0.27

Trunk Fat

      

Male:

0.30

0.32

0.15

0.33

0.32

      

Female:

0.23

0.32

0.08

0.30

0.28

SBP

       

Male:

0.79

0.81

0.93

0.97

       

Female:

0.77

0.84

0.93

0.97

DBP

        

Male:

0.28

0.96

0.91

        

Female:

0.30

0.95

0.90

PP

         

Male:

0.55

0.64

         

Female:

0.59

0.68

MAP

          

Male:

0.99

          

Female:

0.99

Correlations exclude those on antihypertensive medication. All correlations significant at p < 0.0001. BMI body mass index, WC waist circumference, HC hip circumference, WHR waist-hip ratio, WHtR waist-height ratio, SBP systolic blood pressure, DBP diastolic blood pressure, PP pulse pressure, MAP mean arterial pressure, MBP mid-blood pressure

Adiposity measures and blood pressure

The differences in mean blood pressure components [mmHg per SD (95% CI)] for each anthropometric and BIA derived adiposity measure are presented in Table 3. Irrespective of whether the measures of adiposity were calculated from anthropometry or BIA, all measures were strongly and positively associated with most blood pressure components for both men and women. The strongest associations were between adiposity measures and SBP, whereas the weakest relationships were observed with pulse pressure.
Table 3

Mean differences in blood pressure for adiposity measures (N = 5792)

 

mmHg per SD (95% CI)

Measurement (SD)

SBP

DBP

PP

MAP

MBP

Male

 Model 1

  Body Mass Index (3.73 kg/m2)

4.56

(3.98, 5.14)

2.71

(2.36, 3.07)

1.85

(1.46, 2.23)

3.33

(2.93, 3.74)

3.64

(3.20, 4.08)

  Waist Circumference (11.13 cm)

4.17

(3.59, 4.76)

2.71

(2.36, 3.06)

1.46

(1.08, 1.85)

3.20

(2.79, 3.60)

3.44

(3.00, 3.88)

  Hip Circumference (7.20 cm)

3.76

(3.18, 4.35)

2.27

(1.91, 2.62)

1.50

(1.11, 1.88)

2.77

(2.36, 3.17)

3.02

(2.57, 3.46)

  Waist-Hip Ratio (0.075)

3.23

(2.64, 3.82)

2.25

(1.89, 2.61)

0.98

(0.59, 1.37)

2.58

(2.16, 2.99)

2.74

(2.29, 3.19)

  Waist-Height Ratio (0.067)

4.21

(3.63, 4.80)

2.69

(2.34, 3.05)

1.52

(1.14, 1.91)

3.20

(2.79, 3.60)

3.45

(3.01, 3.89)

  Whole Body Fat (6.44%)

4.69

(4.11, 5.27)

3.02

(2.67, 3.36)

1.68

(1.29, 2.06)

3.57

(3.18, 3.97)

3.85

(3.42, 4.29)

  Trunk Fat (7.82%)

4.62

(4.04, 5.20)

3.07

(2.72, 3.42)

1.55

(1.17, 1.94)

3.59

(3.19, 3.99)

3.85

(3.41, 4.28)

 Model 2

  Body Mass Index (3.73 kg/m2)a

2.13

(1.12, 3.13)

0.71

(0.10, 1.32)

1.42

(0.75, 2.08)

1.18

(0.49, 1.88)

1.42

(0.66, 2.18)

  Whole Body Fat (6.44%)b

2.96

(1.96, 3.96)

2.44

(1.83, 3.04)

0.52

(−0.14, 1.19)

2.61

(1.92, 3.30)

2.70

(1.95, 3.46)

  Waist Circumference (11.13 cm)c

1.33

(0.37, 2.30)

0.71

(0.13, 1.29)

0.62

(−0.02, 1.26)

0.92

(0.25, 1.59)

1.02

(0.29, 1.75)

  Trunk Fat (7.82%)d

3.55

(2.59, 4.52)

2.50

(1.92, 3.08)

1.05

(0.41, 1.70)

2.85

(2.18, 3.52)

3.03

(2.29, 3.76)

Female

 Model 1

  Body Mass Index (4.06 kg/m2)

4.00

(3.43, 4.57)

3.02

(2.70, 3.33)

0.98

(0.59, 1.38)

3.35

(2.97, 3.72)

3.51

(3.09, 3.93)

  Waist Circumference (10.09 cm)

4.00

(3.43, 4.58)

3.07

(2.75, 3.39)

0.94

(0.54, 1.33)

3.38

(3.00, 3.76)

3.53

(3.11, 3.96)

  Hip Circumference (8.51 cm)

3.47

(2.90, 4.04)

2.76

(2.44, 3.08)

0.71

(0.32, 1.10)

3.00

(2.62, 3.37)

3.11

(2.69, 3.54)

  Waist-Hip Ratio (0.064)

2.86

(2.27, 3.46)

2.06

(1.72, 2.39)

0.81

(0.40, 1.21)

2.33

(1.93, 2.72)

2.46

(2.02, 2.90)

  Waist-Height Ratio (0.068)

4.26

(3.68, 4.84)

3.12

(2.80, 3.44)

1.14

(0.74, 1.53)

3.50

(3.12, 3.88)

3.69

(3.27, 4.11)

  Whole Body Fat (7.38%)

3.73

(3.17, 4.30)

2.94

(2.63, 3.26)

0.79

(0.40, 1.18)

3.21

(2.83, 3.58)

3.34

(2.92, 3.76)

  Trunk Fat (9.23%)

3.86

(3.29, 4.42)

3.04

(2.73, 3.35)

0.82

(0.43, 1.21)

3.31

(2.94, 3.69)

3.45

(3.03, 3.86)

 Model 2

  Body Mass Index (4.06 kg/m2)a

3.31

(2.00, 4.61)

1.89

(1.16, 2.61)

1.42

(0.52, 2.32)

2.36

(1.50, 3.22)

2.60

(1.64, 3.55)

  Whole Body Fat (7.38%)b

0.77

(−0.53, 2.07)

1.25

(0.53, 1.98)

−0.48

(−1.38, 0.41)

1.09

(0.23, 1.95)

1.01

(0.06, 1.96)

  Waist Circumference (10.09 cm)c

2.41

(1.32, 3.50)

1.58

(0.98, 2.18)

0.83

(0.09, 1.58)

1.85

(1.14, 2.57)

1.99

(1.20, 2.79)

  Trunk Fat (9.23%)d

1.85

(0.78, 2.91)

1.73

(1.14, 2.32)

0.12

(−0.61, 0.86)

1.77

(1.06, 2.47)

1.79

(1.01, 2.57)

Estimates exclude those on antihypertensive medication. Model 1, estimates from multiple linear regression, adjusted for age and education. Model 2, model 1 plus additional adjustments for awhole body fat percentage, bbody mass index, ctrunk fat percentage, dwaist circumference. SBP systolic blood pressure, DBP diastolic blood pressure, PP pulse pressure, MAP mean arterial pressure, MBP mid-blood pressure, SD standard deviation, CI confidence interval

On average, the associations between anthropometric derived measures and blood pressure were slightly weaker than BIA derived measures among men. For instance, each SD difference in an anthropometric measure was associated with a 3.23 mmHg to 4.56 mmHg change in SBP, whereas changes in SBP for each SD difference in a BIA measure ranged from 4.62 to 4.69 mmHg. In comparison, the relationship of anthropometric measures with SBP were moderately stronger than BIA measures among women, and ranged from 2.86 to 4.26 mmHg, and 3.73 mmHg to 3.86 mmHg for anthropometric and BIA derived measures, respectively. Apart from pulse pressure, which had much weaker associations with all measures of adiposity, similar (albeit somewhat weaker) relationships were observed between each measure and the remaining blood pressure components.

The further adjustment of an anthropometric measure for a BIA measure, and vice versa, diminished the relation between each (general or central) adiposity measure and all blood pressure components regardless of measurement method. Although attenuated, the association between both an anthropometric and BIA derived measure with blood pressure were, for the most part, independent of each other and remained significant (p < 0.05).

Adiposity measures and hypertension

The PRs (95% CI) for hypertension per SD difference in each measure of adiposity are shown for men and women in Figs. 1 and 2, respectively. Overall, the relationships between either an anthropometric or BIA derived adiposity measure and hypertension were similar. The weakest associations were observed between WHR and hypertension for both men and women [PR: 1.31 (1.24, 1.38) and 1.28 (1.22, 1.34), respectively], whereas the strongest associations were for trunk fat percentage [PR: 1.47 (1.40, 1.55) and 1.46 (1.38, 1.53), respectively]. Nevertheless, regardless of whether the measure of adiposity was calculated from anthropometric or BIA derived measures, the relative difference between them for their relationship with hypertension were slight. For instance, the difference between the anthropometric and BIA measure that had the strongest relationship with hypertension was less than 5% for both sexes.
Figure 1
Fig. 1

Prevalence ratios for hypertension per SD of each adiposity measure among men (N = 2764). Model 1, estimates from Poisson regression, adjusted for age and education. Model 2, model 1 plus additional adjustments for awhole body fat percentage, bbody mass index, ctrunk fat percentage, dwaist circumference. PR, prevalence ratio; SD, standard deviation; CI, confidence interval

Figure 2
Fig. 2

Prevalence ratios for hypertension per SD of each adiposity measure among women (N = 3226). Model 1, estimates from Poisson regression, adjusted for age and education. Model 2, model 1 plus additional adjustments for awhole body fat percentage, bbody mass index, ctrunk fat percentage, dwaist circumference. PR, prevalence ratio; SD, standard deviation; CI, confidence interval

The further adjustment of an anthropometric measure for a BIA measure, and vice versa, resulted in an attenuation of their relationships with hypertension. Among men, there appears to be a more marked attenuation of the association of BMI and WC with hypertension after adjusting for body and trunk fat percentage, respectively (Fig. 1, Model 2). Nonetheless, despite being diminished, all adiposity measures remained significantly (p < 0.05) associated with hypertension regardless of whether or not additional adjustments were made for the other measurement method.

Adiposity measures and ROC curves, AUC for hypertension

Summarized in Table 4 are the ROC curves AUC (95% CI) of each adiposity measure for the discrimination of hypertension. For men and women, all adiposity measures regardless of whether an anthropometric or BIA derived measure demonstrated significant discriminative ability for hypertension, with AUCs ranging from 0.68 to 0.76. Except for HC and WHR, the AUC of each anthropometric measure was similar to the AUC of BIA derived measures for both sexes. However, in comparison to whole body and trunk fat percentage, the AUC for HC and WHR were significantly (p < 0.05) less for both sexes. Nevertheless, the relative sex-specific difference for the AUC between either an anthropometric or BIA derived measure of adiposity was negligible, and not statistically significant between the majority of measures irrespective of their derivation method.
Table 4

Area under the receiver operating characteristic curves (N = 5990)

 

Male

Female

 

Area Under Curve (95% CI)

Anthropometric Measures

 Body Mass Index

0.70 (0.68, 0.72)

0.76 (0.74, 0.77)

 Waist Circumference

0.70 (0.68, 0.72)

0.76 (0.74, 0.77)

 Hip Circumference

0.69 (0.66, 0.71)

0.75 (0.73, 0.76)

 Waist-Hip Ratio

0.68 (0.66, 0.70)

0.73 (0.72, 0.75)

 Waist-Height Ratio

0.70 (0.68, 0.72)

0.76 (0.74, 0.78)

Bioelectrical Impedance Measures

 Body Fat Percentage

0.71 (0.68, 0.73)

0.75 (0.74, 0.77)

 Trunk Fat Percentage

0.71 (0.69, 0.73)

0.76 (0.74, 0.77)

 

Difference Between Area Under Curve (95% CI)

Body Fat Percentagea

 Body Mass Index

−0.0046 (−0.0143, 0.0051)

0.0021 (−0.0035, 0.0077)

 Waist Circumference

−0.0067 (−0.0171, 0.0037)

0.0010 (−0.0062, 0.0082)

 Hip Circumference

−0.0194 (−0.0312, −0.0076)

−0.0083 (−0.0150, −0.0016)

 Waist-Hip Ratio

−0.0242 (−0.0383, −0.0101)

−0.0193 (−0.0305, −0.0082)

 Waist-Height Ratio

−0.0088 (−0.0192, 0.0015)

0.0048 (−0.0025, 0.0121)

 Trunk Fat Percentage

0.0026 (−0.0018, 0.0069)

0.0019 (−0.0020, 0.0058)

Trunk Fat Percentageb

 Body Mass Index

−0.0072 (−0.0168, 0.0024)

0.0002 (−0.0039, 0.0043)

 Waist Circumference

−0.0093 (−0.0193, 0.0008)

−0.0009 (−0.0071, 0.0054)

 Hip Circumference

−0.0219 (−0.0337, −0.0102)

−0.0102 (−0.0160, −0.0043)

 Waist-Hip Ratio

−0.0267 (−0.0408, −0.0127)

−0.0212 (−0.0323, −0.0101)

 Waist-Height Ratio

−0.0114 (−0.0215, −0.0013)

0.0029 (−0.0035, 0.0093)

 Body Fat Percentage

−0.0026 (−0.0069, 0.0018)

−0.0019 (−0.0058, 0.0020)

Area under the receiver operating characteristic curves for the discriminative ability of adiposity measures for hypertension, adjusted for age and education. aDifferences between anthropometric measures and whole body fat percentage area under curve, bdifferences between anthropometric measures and trunk fat percentage area under curve

Discussion

In our study of adults from India, the strength of association of anthropometric (BMI, WC) and BIA (whole body and trunk fat percentage) derived adiposity measures with blood pressure and hypertension were similar. Moreover, the discriminative ability of BIA measures for hypertension was comparable to anthropometric measures. Our findings suggest that BIA derived measures of adiposity have no apparent benefit over simple anthropometrics in the assessment of blood pressure and hypertension.

Although there is potential for the utilization of BIA to assess body composition and health risks, there is a paucity of studies from India reporting its use. Further, very limited information is available on the association between BIA derived body fat and health risks related to CVD. One study among 850 men in India indicates that high body fat percentage, as determined by BIA, is associated with hypertension and high coronary artery disease prevalence [22]. Similarly, we found that body fat percentage was positively associated with blood pressure and hypertension. However, to the best of our knowledge, no study has investigated the relative associations of both anthropometric and BIA derived measures of adiposity with blood pressure and hypertension in India. As such, our study is the first to describe these relationships and further studies in India are necessary for comparison purposes. Nevertheless, considered together with studies conducted elsewhere [14, 15], our findings provide additional support for the adequacy of anthropometric measures to assess adiposity-related health risks.

An often cited limitation of BMI and anthropometric measures in general, is their inability to discern differences in body composition [10]. Hence, the use of BIA is an appealing alternative as it is able to provide estimates of separate body tissues. In spite of this advantage, we only observed modest differences between the associations of anthropometric and BIA derived adiposity measures with blood pressure and hypertension. In particular, the relations of BIA measures were slightly stronger than anthropometric measures among men. By contrast, the associations of BIA measures were slightly weaker for women. The weaker relationships for women may be due, in part, to some imprecision in the estimation of adiposity by BIA among women. For instance, it has been suggested that the relative volume of adipose to muscle tissue may affect BIA. Specifically, greater adipose than muscle tissue among women may affect the calculated resistance by BIA, thus having an effect on the estimated body composition [25]. Future studies considering the use of BIA or anthropometric measures to investigate the association between adiposity and CVD should take into consideration these potential sex-related differences in their associations with blood pressure.

The capability of segmental analysis by BIA may be a useful addition to whole body analysis as it is able to provide information on the distribution of body tissues. However, given our findings, no further value of BIA was obtained from the use of segmental analysis for investigating the association of adiposity with blood pressure and hypertension. Both whole body and trunk fat estimates were highly correlated with each other (i.e. correlation coefficient of 0.97), which may explain, to some extent, the similarities in their observed relationships. Indeed, the use of segmental analysis may be limited by its ability to accurately assess different body components as compared to the body as a whole. For example, using DXA as the reference, it has been shown that estimates of segments (arms, legs, and trunk) may be more prone to error than estimation of whole body composition by BIA [17]. Taking this into consideration, and given the comparability between estimated whole body and trunk fat in our study, the use of a whole body BIA device may be sufficient. Further studies in India are required to investigate whether low-cost whole body BIA devices perform equally well as the more expensive segmental devices.

Apart from HC and WHR, we found no significant differences for the discriminative ability between anthropometric and BIA derived measures of adiposity for hypertension. In comparison to BIA estimated whole body and trunk fat, HC and WHR had significantly lower discriminative power for hypertension. This may be due, in part, to the limited ability of HC alone to distinguish those with greater adiposity, and the potential for decreased precision of WHR as a measure of adiposity. For instance, WHR does not differentiate those with either a small WC and HC or a large WC and HC, both would have a similar WHR. The inability to distinguish these differences may diminish the relationship that WHR has with blood pressure and hypertension, and indeed, among all the adiposity measures, the weakest associations were most consistently observed for WHR. Hence, our results suggest that HC and WHR may have lesser value than the other anthropometric measures considered in our study for assessing hypertension risk. Nonetheless, comparable to the similarities found for the strength of association between anthropometric and BIA measures with blood pressure and hypertension, the overall differences in discriminative ability between all measures were slight.

The limitations of our study warrant mention. First, the generalizability of our findings may be limited by the population-based study. Second, due to the cross-sectional analysis, causal inferences cannot be made for the association of adiposity with blood pressure and hypertension. However, the largely causal relationship between adiposity and blood pressure is well-established [3], and the reverse is implausible. Third, although the use of BIA is a more feasible method than DXA or MRI to derive estimates of body composition, the accuracy of estimated body fat may depend partly on the specific algorithm and equation used by a BIA device. Nevertheless, there is evidence from India demonstrating the likely validity of BIA derived measures as compared to DXA [21]. Further, BIA is the most practical and feasible method to obtain quick estimates of body composition in resource-limited settings. Notwithstanding these limitations, to our knowledge, our study is the first to systematically investigate the utility of BIA estimates of adiposity as compared to simple anthropometric measures in India. Additionally, our findings provide further insight and guidance for future studies considering the use of anthropometric or BIA derived measures to examine adiposity-related health risks in India.

Conclusion

We provide additional evidence to support the adequacy of simple anthropometric measures in evaluating adiposity-related risk. Our findings suggest no material differences between BIA and anthropometric measures of adiposity in relation with blood pressure and hypertension. The observed similarities between adiposity measures may have important implications for facilitating research and risk stratification of populations in remote resource-limited settings where more intricate health measures are not feasible. Nevertheless, as more sophisticated body composition methods become readily available, further studies in India and other LMIC are required to identify the best and most suitable measure of adiposity and its associated risks.

Abbreviations

AUC: 

Area under curve

BIA: 

Bioelectrical impedance analysis

BMI: 

Body mass index

CI: 

Confidence interval

CVD: 

Cardiovascular disease

DBP: 

Diastolic blood pressure

DXA: 

Dual-energy X-ray absorptiometry

HC: 

Hip circumference

ISHA: 

Indian study on health of adults

LMIC: 

Low and middle-income countries

MRI: 

Magnetic resonance imaging

PR: 

Prevalence ratio

ROC: 

Receiver operating characteristic

SBP: 

Systolic blood pressure

SD: 

Standard deviation

WC: 

Waist circumference

WHR: 

Waist-hip ratio

WHtR: 

Waist-height ratio

Declarations

Acknowledgements

We would like to thank the ISHA collaborators.

Funding

This study is supported by grants from the University Health Network (to MF), the Institute for Clinical Evaluative Sciences (to JT), and the University of Toronto (to KT, RM and PJ). The funding sources had no role in the study design; data collection, analysis, interpretation; writing of the manuscript; or decision to submit for publication.

Availability of data and materials

The datasets generated during and/or analysed during the current study are not publicly available because of binding agreements with the government of India.

Authors’ contributions

KT conceived and designed the study, conducted the analyses and drafted the manuscript. PJ participated in data acquisition, and supervised the study. Authors KT, MF, RM, JT, and PJ contributed to data interpretation, and reviewed the manuscript critically for important intellectual content. All authors read and approve the final manuscript.

Ethics approval and consent to participate

Ethical approval for the study was obtained from the Institutional Ethics Review Board of the Tata Memorial Centre. All participants provided written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Centre for Global Health Research, St. Michael’s Hospital, Toronto, Canada
(2)
Dalla Lana School of Public Health, University of Toronto, Toronto, Canada
(3)
Peter Munk Cardiac Centre, University Health Network, Toronto, Canada
(4)
The Heart and Stroke Richard Lewar Centre of Excellence in Cardiovascular Research, University of Toronto, Toronto, Canada
(5)
Department of Family and Community Medicine, University of Toronto, Toronto, Canada
(6)
Institute for Clinical Evaluative Sciences, Toronto, Canada
(7)
Schulich Heart Centre, Sunnybrook Health Sciences Centre, Toronto, Canada
(8)
Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Canada

References

  1. Patel V, Chatterji S, Chisholm D, Ebrahim S, Gopalakrishna G, Mathers C, et al. Chronic diseases and injuries in India. Lancet. 2011;377(9763):413–28.View ArticlePubMedGoogle Scholar
  2. Reddy KS, Shah B, Varghese C, Ramadoss A. Responding to the threat of chronic diseases in India. Lancet. 2005;366(9498):1744–9.View ArticleGoogle Scholar
  3. Timpson NJ, Harbord R, Davey Smith G, Zacho J, Tybjaerg-Hansen A, Nordestgaard BG. Does greater adiposity increase blood pressure and hypertension risk?: Mendelian randomization using the FTO/MC4R genotype. Hypertension. 2009;54(1):84–90.View ArticlePubMedGoogle Scholar
  4. Dorresteijn JA, Visseren FL, Spiering W. Mechanisms linking obesity to hypertension. Obes Rev. 2012;13(1):17–26.View ArticlePubMedGoogle Scholar
  5. Whitlock G, Lewington S, Sherliker P, Clarke R, Emberson J, Halsey J, et al. Body-mass index and cause-specific mortality in 900 000 adults: collaborative analyses of 57 prospective studies. Lancet. 2009;373(9669):1083–96.View ArticlePubMedGoogle Scholar
  6. Rapsomaniki E, Timmis A, George J, Pujades-Rodriguez M, Shah AD, Denaxas S, et al. Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1.25 million people. Lancet. 2014;383(9932):1899–911.View ArticlePubMedPubMed CentralGoogle Scholar
  7. Lewington S, Clarke R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002;360(9349):1903–13.View ArticlePubMedGoogle Scholar
  8. Sauvaget C, Ramadas K, Thomas G, Thara S, Sankaranarayanan R. Prognosis criteria of casual systolic and diastolic blood pressure values in a prospective study in India. J Epidemiol Community Health. 2010;64(4):366–72.View ArticlePubMedGoogle Scholar
  9. Pednekar MS, Gupta R, Gupta PC. Association of blood pressure and cardiovascular mortality in India: Mumbai cohort study. Am J Hypertens. 2009;22(10):1076–84.View ArticlePubMedGoogle Scholar
  10. Snijder MB, van Dam RM, Visser M, Seidell JC. What aspects of body fat are particularly hazardous and how do we measure them? Int J Epidemiol. 2006;35(1):83–92.View ArticlePubMedGoogle Scholar
  11. Prentice AM, Jebb SA. Beyond body mass index. Obes Rev. 2001;2(3):141–7.View ArticlePubMedGoogle Scholar
  12. Kobayashi J, Murano S, Kawamura I, Nakamura F, Murase Y, Kawashiri MA, et al. The relationship of percent body fat by bioelectrical impedance analysis with blood pressure, and glucose and lipid parameters. J Atheroscler Thromb. 2006;13(5):221–6.View ArticlePubMedGoogle Scholar
  13. Nagaya T, Yoshida H, Takahashi H, Matsuda Y, Kawai M. Body mass index (weight/height2) or percentage body fat by bioelectrical impedance analysis: which variable better reflects serum lipid profile? Int J Obes Relat Metab Disord. 1999;23(7):771–4.View ArticlePubMedGoogle Scholar
  14. Lee K, Song YM, Sung J. Which obesity indicators are better predictors of metabolic risk?: healthy twin study. Obesity (Silver Spring). 2008;16(4):834–40.View ArticleGoogle Scholar
  15. Menke A, Muntner P, Wildman RP, Reynolds K, He J. Measures of adiposity and cardiovascular disease risk factors. Obesity (Silver Spring). 2007;15(3):785–95.View ArticleGoogle Scholar
  16. Ricciardi R, Talbot LA. Use of bioelectrical impedance analysis in the evaluation, treatment, and prevention of overweight and obesity. J Am Acad Nurse Pract. 2007;19(5):235–41.View ArticlePubMedGoogle Scholar
  17. Bracco D, Thiebaud D, Chiolero RL, Landry M, Burckhardt P, Schutz Y. Segmental body composition assessed by bioelectrical impedance analysis and DEXA in humans. J Appl Physiol (1985). 1996;81(6):2580–7.Google Scholar
  18. Shafer KJ, Siders WA, Johnson LK, Lukaski HC. Validity of segmental multiple-frequency bioelectrical impedance analysis to estimate body composition of adults across a range of body mass indexes. Nutrition. 2009;25(1):25–32.View ArticlePubMedGoogle Scholar
  19. Misra A, Khurana L. Obesity-related non-communicable diseases: south Asians vs white Caucasians. Int J Obes. 2011;35(2):167–87.View ArticleGoogle Scholar
  20. Lear SA, Humphries KH, Kohli S, Chockalingam A, Frohlich JJ, Birmingham CL. Visceral adipose tissue accumulation differs according to ethnic background: results of the multicultural community health assessment trial (M-CHAT). Am J Clin Nutr. 2007;86(2):353–9.PubMedGoogle Scholar
  21. Vasudev S, Mohan A, Mohan D, Farooq S, Raj D, Mohan V. Validation of body fat measurement by skinfolds and two bioelectric impedance methods with DEXA-the Chennai urban rural epidemiology study [CURES-3]. J Assoc Physicians India. 2004;52:877–81.PubMedGoogle Scholar
  22. Singh RB, Niaz MA, Beegom R, Wander GS, Thakur AS, Rissam HS. Body fat percent by bioelectrical impedance analysis and risk of coronary artery disease among urban men with low rates of obesity: the Indian paradox. J Am Coll Nutr. 1999;18(3):268–73.View ArticlePubMedGoogle Scholar
  23. Taing KY, Farkouh ME, Moineddin R, JV T, Jha P. Age and sex-specific associations of anthropometric measures of adiposity with blood pressure and hypertension in India: a cross-sectional study. BMC Cardiovasc Disord. 2016;16(1):247.View ArticlePubMedPubMed CentralGoogle Scholar
  24. DeLong ER, DeLong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics. 1988;44(3):837–45.View ArticlePubMedGoogle Scholar
  25. Baumgartner RN, Ross R, Heymsfield SB. Does adipose tissue influence bioelectric impedance in obese men and women? J Appl Physiol (1985). 1998;84(1):257–62.Google Scholar

Copyright

© The Author(s). 2017

Advertisement

BMC Obesity

ISSN: 2052-9538

Contact us