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Untangling weight from height: A generalised body mass index (gBMI) approach to evaluating child and adolescent nutritional status in India
For correspondence: Dr Santu Ghosh, Department of Biostatistics, St Johns Medical College, Bengaluru 560 034, Karnataka, India e-mail: santu.g@stjohns.in
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Received: ,
Accepted: ,
How to cite this article: Majumder R, Kurpad AV, Sachdev HS, Kuriyan R, Thomas T, Ghosh S. Untangling weight from height: A generalised body mass index (gBMI) approach to evaluating child and adolescent nutritional status in India. Indian J Med Res. 2026;163:655-63. doi: 10.25259/IJMR_2555_2025.
Abstract
Background and objectives
Weight-for-height (WHZ) and body mass index (BMI)-for-age (BAZ) are commonly used to assess child overnutrition but have limitations: they conflate skeletal growth with body weight, correlate with height, and inadequately distinguish fat from lean mass, particularly during puberty. This study proposes an India-specific generalised body mass index (gBMI), an age- and sex-specific power-type index adapted from Benn’s concept, to better capture adiposity.
Methods
Exponent parameters for gBMI were estimated using healthy-child data, selected by WHO selection criteria, from the National Family Health Survey (NFHS-3,4,5) and the Comprehensive National Nutrition Survey (CNNS), comprising 12,466 children under 5 years and 6,487 aged 5–19 years. Polynomial regression to model age- and sex-specific variation in the weight–height relationship was used to estimate the exponents of height, and growth curves were generated using generalised additive models for location, scale, and shape (GAMLSS) with location scale and shape (LMS) methods. Validation employed independent data from 457 urban schoolchildren aged 5–16 years in Bengaluru, including fat and lean mass measured by dual-energy X-ray absorptiometry (DXA).
Results
The exponent varied with age (1.3 in infancy, ∼2.9 in pubertal boys, 2.7 in girls, stabilising at ∼2 in late adolescence). Unlike BMI, gBMI residuals showed near-zero correlation with height. gBMI-for-age Z-scores (gBAZ) showed lower wasting in children under 5 years (10.7% vs. 19.2% using WHZ) and higher adolescent overnutrition (8.7% vs. <1% using BAZ). Validation showed stronger association of gBAZ with body fat (r=0.70) than BAZ (r=0.65).
Interpretation and conclusions
The gBMI provides an adaptable, height-independent, and adiposity-sensitive index for assessing malnutrition and obesity in children and adolescents. Its use could refine nutritional surveillance and interventions, with potential wider applicability with longitudinal evaluations.
Keywords
Anthropometry
BMI
gBMI
Obesity
Z-score
Malnutrition among children and adolescents is assessed by comparing anthropometric measurements to established standard growth charts.1 Chronic malnutrition is typically evaluated using height-for-age, while acute malnutrition is measured by adjusted weight-for-age like combination of weight-for-age (WAZ) and weight-for-height (WHZ) or body mass index (BMI)-for-age (BAZ). These indicators are compared against standard distributions using location, scale, and shape parameters, and then transformed into standard normal Z-scores for interpretation.2,3 However, assessing acute malnutrition using this latent dimension is challenging because weight and height relationships change significantly with age, which can bias estimates of its prevalence.4 Using multiple, highly correlated indices like weight-for-age and weight-for-height to assess acute malnutrition in children can be misleading, since these may not accurately reflect the true nutritional status. There is a need to develop a single, unified index to assess malnutrition consistently across young children and adolescents.
Optimal nutritional assessment indexes should also separate skeletal growth (height) from the latent body weight component independent of height, as most weight variation relates to linear growth accompanied by tissue development.5 It has been shown that the correlation between BMI and height is particularly strong in early childhood, becoming more complex during puberty,6 where the initial positive association of weight with height can become confounded due to reduced height gain during this period.7,8 Therefore, developing growth indexes that isolate weight from height would improve the accuracy and age-independence of anthropometric evaluations.
BAZ and WHZ also do not distinguish between fat mass and fat-free mass.5,9-11 This is important, as in early childhood, BAZ scores have been linked to fat-free mass in adulthood.12 Therefore, for being overweight and obesity specifically, the criteria of a good index are that a) it should be highly correlated with measures of relative adiposity, and b) it should be independently distributed from height. Alternative indexes such as waist circumference, waist-to-hip ratio, and power-type indexes like Rohrer’s ponderal index13 and Benn’s index14 have been explored, but their complexity limits their practical application in clinical and public health settings. Benn’s Index extends the traditional BMI by allowing the exponent of height to be estimated rather than fixed, but research has shown that this exponent varies substantially by age, sex, and population.7,15-21 As a result, it is critical to evaluate height exponents in BMI across different ages and sexes within each population to ensure more accurate and unbiased assessments of adiposity.
The BMI or BAZ was initially developed for adults and never intended to assess obesity status in children and adolescents. However, by appropriately altering the power of height in the BMI relationship to make the index truly uncorrelated with height, this might be appropriate for use in specific age groups. Therefore, primary objective of this study is to propose a generalised body mass index (gBMI) adopted from work by Benn in 197114 and validate the same for Indian children and adolescents. In addition, the study has developed a gBMI-for-age reference for assessing acute malnutrition among Indian children and adolescents.
Methods
This observational study based on data from multiple cross-sectional national surveys was undertaken by the department of Biostatistics and Epidemiology, St John’s Research Institute, Bengaluru, India between May 2024 and August 2025. Ethical approval for the study was obtained from the Institutional Ethics Committee of St. John’s Medical College, Bengaluru, India, which is registered with the regulatory authority. Multiple rounds of National Family Health Surveys (NFHS)22-24 and Comprehensive National Nutritional Survey (CNNS)25 data were utilised to develop the gBMI, which was validated against a cross-sectional data set collected from apparently healthy children aged 5–16 years attending urban schools in Bengaluru, Karnataka, India, between December 2011 and October 2013. All assessments were conducted at St. John’s Research Institute and Medical College Hospital with ethical approval by the Institutional Ethics Committee, parental consent, and child assent (for those over 10 years).
Extraction of healthy subset
A subset of healthy children from above mentioned national surveys was selected using selection criteria adopted from WHO Multicentre Growth Reference Study (MGRS)26 to ensure that study participants had optimal growth potential under ideal conditions. The description of detailed selection criteria can be found in Majumder et al 202427 but summary diagram is depicted in Figure 1.28
![Steps of selection of analytical sample [anaemia is defined as per World Health Organization (WHO) criteria28].](/content/175/2026/163/5/img/IJMR-163-5-655-g1.png)
Applying these to NFHS-3, 4, 5, and CNNS identified 13,245 children under five years (1,821; 4,531; 4,918; 1,934, respectively). From CNNS, 3,583 children aged 5–9 years and 3,077 aged 10–19 years were included. About 85% belonged to the top wealth quintile. Anthropometric Z-score distributions were comparable across surveys.29
Derivation of gBMI
A validation dataset included 317 healthy children (143 boys, 174 girls) aged 5–16 years from urban Bengaluru schools (2011–2013). Data collected comprised anthropometry (weight, height measured twice with <1% variability) and body composition (fat and fat-free mass). Body composition was measured using a DXA scanner (Lunar Prodigy advanced whole-body scanner GE Medical Systems, software version 12.30), following standard protocols by a trained technician. The coefficient of variation (CV) for fat mass was 2%. The analysis was conducted on children between 5-16 years. Children with chronic illness and on medications affecting body composition were excluded. The statistical method adopted the concept from Benn 1971.14 Here, it was assumed that, for any given age(t) and sex:
This relation could be linearised by a simple log transformation:
Where, were the standard deviation of and was the Pearson correlation coefficient. Hence, could be estimated by the least squares technique in terms of the regression slope, as follows:
As the log transformation is a one-to-one monotone transformation, this would not alter the relationship between weight and height. The gBMI can then be estimated as:
Note that the choice of this exponent, , will vary across different study populations as well as across age groups. Several studies15-20 have shown that the exponent varies across different ages(t) of children and adolescents as well as for adults.
To account for the variation in the relationship between weight, height, by age and sex, the exponent parameter (αt) was estimated by a polynomial regression model as follows:
where, were q order polynomials of age(t). The order of polynomials was estimated by optimal choice of adjusted R2 with statistically significant regression coefficients. The exponential parameter is age dependent according to the model assumption, which can be expressed as:
Where, and,
can be estimated by least square method from equation (1).
This technique was then applied to estimate age-and sex-specific for Indian children and adolescents, using a healthy subset extracted from multiple national surveys representing the entire country. Prior to analyses of this healthy subset, children below the 5th and above the 95th percentile of the BMI distribution were excluded, to avoid variability due to unobserved factors. Homogeneity in the mean and variance of growth metrics of under 5-year children has been demonstrated elsewhere29 across all the four surveys used here, using a similar extracted healthy subset of children, hence, these data were combined. Considering different permutations and combinations of , we set them at 4, optimising the number of parameters and potential gain in model predictivity by increasing and decreasing the order of polynomial by the adjusted R2. Using these estimated exponent parameters, the gBMI was calculated for the children in the selected healthy sample. Further the correlation between residual of the equation (1) and height was examined by Pearson’s correlation coefficient and scatter diagrams.
Observing the dependency of gBMI on age, a generalised linear model for location, scale and shape (GAMLSS) with box-cox power exponential (BCPE) family was applied to estimate age- and sex-specific distributions of gBMI in terms of L, M and S values. This was performed for every month of age, from 0 to 19 years, separately for boys and girls, like other anthropometric growth standards.27,30 Penalised cubic smoothing splines were used for mean, variance and skewness models which learnt degrees of freedom from the data. Observing that the estimated degrees of freedom for kurtosis () model was close to 2, we restricted . The goodness of fit of the model was examined by Q-Q normal and worm plots. Finally, the Z-score for gBMI-for-age (gBAZ) was calculated for the children of the entire CNNS and NFHS 5 data, by the Box-Cox-Cole-Green transformation.3
The prevalence of thinness and overweight were then estimated across age groups of Indian children and adolescents in the NFHS-5 (for under five) and the CNNS (for 5 to 19-year-old children), using these derived gBAZ references, and then compared against similar estimates from the WHO references of BAZ and WHZ and India specific growth reference.27 Acute malnutrition was defined specifically as thinness and overweight. Thinness was assessed by gBMI for age Z-score below -2 and above 2 for overweight. For existing metrics similar Z-score criteria were used to assess thinness or overweight. To validate the use of gBMI over BMI, the distribution of body fat was compared across different Z-score categories for both the metrics gBMI and BMI; and their associations with body fat mass were evaluated.
The statistical software R version 4.2.1 (R Core Team, 2022, Vienna, Austria) was used for data analysis. The accepted false positive error for all statistical tests was set at 5%.
Results
After excluding the upper and lower 5% of calculated BMI values, the final analytical ‘healthy child’ sample included 12,466 under 5-year children (CNNS: 1,824; NFHS-3: 1,785; NFHS-4: 4,412; NFHS-5: 4,445) and 6,487 children aged 5–19 years (CNNS: 3,583 aged 5–9; 3,077 aged 10–19). The dataset comprised 9,991 boys and 8,962 girls: 1,293 boys and 1,279 girls below one year; 5,269 boys and 4,625 girls aged 1 to below five years; 1,881 boys and 1,626 girls aged 5–9 years; and 3,351 boys and 2,979 girls aged 10–19 years. Detailed age- and gender-specific frequency distributions are provided in Supplementary Figure 1.
The estimated exponent parameter ( for gBMI was calculated separately for each age (in months) for boys and girls using the analytical sample. Age-dependent exponent parameters ( for Indian children aged 0–19 years are presented in Supplementary Table I, and the trend over age is illustrated in Figure 2. The estimated exponents ( ranged from 1.3 to 2.9 for both boys and girls. At early ages (0–59 months), both sexes had similar exponent values, which increased simultaneously from 1.3 to 2.6 up to age 6 years. A rapid increase in the exponent parameters was observed between age 8 to 14 years. In this period, exponent estimates ranged from 2.6 to 2.9. For boys, the highest exponent value (2.9) was recorded at age 11, while girls reached their maximum (2.7) at age 10. After this periods, the exponents ( gradually declined, reaching a value of 2 at age 19 ( Fig. 2). Overall, the exponent values for boys were generally higher than those for girls. Estimated Pearson’s correlation coefficients (with 95% confidence intervals) for the residuals from the height models (m) were calculated for both boys and girls, and their associations are shown in scatter plots ( Fig. 3). The estimated correlations were close to zero for both sexes.

![Association of height with the relative adiposity [i.e., residuals of equation (1)] from the healthy sample of Indian 0-19 yr (A) boys and (B) girls depicted almost null. This confirms that gBMI is free from influence of linear growth of height.](/content/175/2026/163/5/img/IJMR-163-5-655-g10.png)
GAMLSS estimates are presented in Supplementary Table II. Figure 4 displays the gBMI-for-age Z-score (gBAZ) reference centile curves for boys and girls aged 0–19 years. The model demonstrates a satisfactory fit to the data, as indicated by the goodness-of-fit metrics shown in Supplementary Figure 2.
Table summarises the prevalence of acute undernutrition and overnutrition among children and adolescents in different age groups (<5 yr, 5–9 yr, 10–14 yr, and 15–19 yr) using three references: WHO growth standard (WHZ for <5yr and BAZ for >5yr children)31 India-specific growth references (WHZ for <5yr and BAZ for >5yr children),32 and the gBAZ (this analysis, for all children). The NFHS 5 data was used for this evaluation in <5yr children and data from the CNNS was used for >5yr children.
For acute undernutrition, as measured by wasting, the WHO standard consistently produced higher prevalence rates across all age groups compared to both the India specific and gBMI references. Among children under five years, the prevalence of wasting according to the WHO weight-for-height standard was 19.2%, 10.9%, according to India-specific weight-for-height growth reference, and 10.7% by the current gBMI reference. Similarly, in the 10–14-year age group, the prevalence of thinness was 22.9% by the WHO BAZ, markedly higher than the estimates by the India-specific reference (5.7%) and the current gBAZ (3.4%) reference (Table).
| Standard | Prevalence (%, 95% CI) | |||
|---|---|---|---|---|
|
Age <5 yr (Boys: 114378 Girls: 106885) |
Age:5-9 yr (Boys: 20059 Girls: 18296) |
Age:10-14 yr (Boys: 9543 Girls: 8845) |
Age:15-19 yr (Boys: 7690 Girls: 7462) |
|
| Undernutrition | ||||
| Thinness (WHZ<-2 or BAZ<-2 or gBAZ<-2) | ||||
| WHO | 19.2 (18.9, 19.6) | 19.3 (18.6, 20.0) | 22.9 (22.0, 23.8) | 17.0 (16.2, 17.7) |
| India | 10.9 (10.6, 11.2) | 5.3 (4.9, 5.7) | 5.7 (5.2, 6.1) | 3.2 (2.8, 3.5) |
| gBMI | 10.7 (10.4, 10.9) | 5.01 (4.6, 5.4) | 3.4 (3.0, 3.8) | 2.0 (1.7, 2.4) |
| Overweight/obesity | ||||
| Overweight or obese (WHZ>2 or BAZ>2 or gBAZ>2) | ||||
| WHO | 3.4 (3.3, 3.5) | 2.1 (1.9, 2.4) | 1.3 (1.1, 1.5) | 0.05 (0.01, 0.09) |
| India | 4.4 (4.2, 4.6) | 2.8 (2.5, 3.1) | 1.6 (1.4, 1.8) | 0.79 (0.59, 0.98) |
| gBMI | 2.4 (2.3, 2.5) | 2.2 (1.9, 2.8) | 3.9 (3.5, 4.3) | 8.7 (8.1, 9.5) |
BMI, body mass index; WHO, World health organization; WHZ, weight for height Z-score; BAZ, BMI for age Z-score
For overweight (WAZ>2) or obesity (BAZ>2), the WHO standard yielded the lowest prevalence estimates across all age groups. For example, in the 10–14-year age group, the prevalence was 1.3% by WHO standard compared to 1.6% by India-specific growth reference27 and 3.9% by the current gBMI reference. Among adolescents aged 15–19 years, the prevalence by the gBMI reference was significantly higher (8.7%) compared to the WHO BMI standard (0.05%) and the India-specific BMI reference (0.79%) (Table).
Figure 5 shows the association of BAZ and gBAZ with body fat mass (kg) across different Z-score categories within validation data set. The boxplots (Figure 5 for example) demonstrate that, for both indices, FM increased with higher Z-score categories, indicating a positive association. However, in higher Z-score ranges, particularly above 2, the gBAZ showed higher median fat mass values than BAZ, suggesting an improved sensitivity in capturing adiposity. This observation is further supported by the correlation analysis; where gBAZ exhibited a slightly stronger correlation with fat mass (r=0.70) than BAZ (r=0.65). These findings indicate that the gBAZ may serve as a more robust index than the conventional BAZ in reflecting actual fat mass among children and adolescents.


Discussion
The present study addresses critical limitations in conventional weight-for-height measures that are used to assess nutritional status among children and adolescents, with reference to acute undernutrition and obesity. This is consistent with previous findings that BMI, although commonly used for adults, does not differentiate between fat mass and fat free mass. Moreover, the dependence of BMI on height is particularly problematic during childhood growth phases and puberty.1,9,11,12
In response to these challenges, the present analysis has proposed a novel, population-specific metric, the generalised body mass index (gBMI), which adapts the power-type index concept originally described by Benn (1971).14 By estimating an age- and sex-specific exponent parameter that modifies the weight-to-height relationship, the gBMI isolates weight to be independent of height, thus providing an age-appropriate and more accurate indicator of acute undernutrition and obesity. The exponent values were found to vary dynamically with age and sex, reflecting physiological growth changes, particularly during puberty when rapid changes in body composition occur.33,34 This dynamic adjustment overcomes the key limitation of BMI, that is, its fixed exponent of 2, which inadequately captures complex growth patterns in developing children.31
The study’s robust methodology, utilising large, nationally representative datasets from NFHS and CNNS surveys, ensured the generation of reliable and generalisable reference standards for Indian children and adolescents. The careful extraction of healthy children based on WHO criteria minimised confounding factors, increasing the metric’s validity for optimal growth assessment. Furthermore, the validation using an independent cross-sectional dataset from urban Bengaluru, which included direct measures of body fat through DXA, reinforced the index’s practical clinical applicability.
The gBMI exponent ranged from 1.3 in infancy to peaks of 2.9 in pubertal boys and 2.7 in girls, but thereafter stabilising to 2 by late adolescence, highlighting the physiological rationale for an adaptable exponent. Importantly, correlation analyses confirmed that the gBMI residuals were independent of height, affirming the success of the methodological approach in disentangling weight from linear growth. Several studies have reported that the exponent of height in the BMI formula varies, particularly in children under 5 years and during puberty.15-20,32 Recent studies have also estimated age-specific height exponents for allometric indices among children across multiple countries including data from India and have proposed pooled or region-specific estimates.7,21,32 However, none have established a consistent or universal exponent-for-age across different populations using representative, healthy samples of children and adolescents. Therefore, the gBMI formula should be population-specific, or further comprehensive studies are needed to determine a uniform exponent for age applicable across populations.
When comparing prevalence estimates of acute undernutrition and overweight in Indian children, the gBAZ yielded lower estimates of wasting than the WHO WHZ or BAZ standards but aligned more closely with India-specific WHZ or BAZ references.27 Moreover, gBAZ detected a substantially higher prevalence of overnutrition in adolescents compared to the WHO and Indian-specific references,27,30 highlighting its increased sensitivity to adiposity. Despite the validation dataset having a low prevalence of overweight and obese children, the relatively stronger correlation of gBAZ with measured body fat mass compared to conventional BMI-for-age Z-scores underscores the enhanced capability of gBMI to reflect adiposity more accurately, which is crucial for evaluating targeted nutritional interventions. This attribute confirms the theoretical advantage of using a population- and age-specific power index to assess nutritional status rather than relying on fixed power indices like BMI.
However, this study has several limitations. Estimates derived from cross-sectional health datasets across multiple surveys may be subject to bias. The proposed reference for gBMI-for-age should be validated using longitudinal cohort data before it is considered for policy implementation. Additionally, the validation component is limited by the supplementary dataset, which contains insufficient numbers of overweight or obese adolescents to robustly assess the efficacy of gBMI as a measure of excess adiposity compared to BMI.
In conclusion, the findings from this analysis reveal that the gBMI provides a meaningful improvement over existing indices by offering an adaptable, height-independent, and adiposity-correlated measure for assessing acute undernutrition and overweight/obesity in Indian children and adolescents. The use of gBMI can refine nutritional surveillance, enabling better identification of at-risk populations and more effective public health interventions specific to the diverse physiological growth trajectories in this population. Future research should explore the longitudinal predictive validity of gBMI in relation to health outcomes and its applicability in Indian as well as other populations. Incorporating gBMI into clinical and public health practice warrants evaluation for feasibility and impact on malnutrition monitoring and obesity prevention programmes.
Author contributions
RM: Conceptualised the study, statistical analysis, manuscript writing; AVK: manuscript writing; HPS: manuscript writing; RK: validation dataset; TT: Conceptualised the study, statistical analysis, verified the data, manuscript writing; SG: Conceptualised the study, statistical analysis, verified the data, manuscript writing. All authors have read and approved the final printed version of the manuscript.
Financial support and sponsorship
This study was supported by intramural funds of Department of Biostatistics, St John’s Medical College, Bengaluru, India.
Conflicts of Interest
None.
Use of Artificial Intelligence (AI)-Assisted Technology for manuscript preparation
The authors confirm that there was no use of AI-assisted technology for assisting in the writing of the manuscript and no images were manipulated using AI.
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