Literature DB >> 26973438

A novel method for estimating distributions of body mass index.

Marie Ng1, Patrick Liu2, Blake Thomson3, Christopher J L Murray2.   

Abstract

BACKGROUND: Understanding trends in the distribution of body mass index (BMI) is a critical aspect of monitoring the global overweight and obesity epidemic. Conventional population health metrics often only focus on estimating and reporting the mean BMI and the prevalence of overweight and obesity, which do not fully characterize the distribution of BMI. In this study, we propose a novel method which allows for the estimation of the entire distribution.
METHODS: The proposed method utilizes the optimization algorithm, L-BFGS-B, to derive the distribution of BMI from three commonly available population health statistics: mean BMI, prevalence of overweight, and prevalence of obesity. We conducted a series of simulations to examine the properties, accuracy, and robustness of the method. We then illustrated the practical application of the method by applying it to the 2011-2012 US National Health and Nutrition Examination Survey (NHANES).
RESULTS: Our method performed satisfactorily across various simulation scenarios yielding empirical (estimated) distributions which aligned closely with the true distributions. Application of the method to the NHANES data also showed a high level of consistency between the empirical and true distributions. In situations where there were considerable outliers, the method was less satisfactory at capturing the extreme values. Nevertheless, it remained accurate at estimating the central tendency and quintiles.
CONCLUSION: The proposed method offers a tool that can efficiently estimate the entire distribution of BMI. The ability to track the distributions of BMI will improve our capacity to capture changes in the severity of overweight and obesity and enable us to better monitor the epidemic.

Entities:  

Keywords:  BMI distribution; Beta distribution; L-BFGS-B optimization; Obesity; Overweight

Year:  2016        PMID: 26973438      PMCID: PMC4789291          DOI: 10.1186/s12963-016-0076-2

Source DB:  PubMed          Journal:  Popul Health Metr        ISSN: 1478-7954


Introduction

Overweight and obesity are growing health problems worldwide. In 2013, nearly one third of the world’s population was either overweight or obese [1]. Concern regarding the rising disease burden associated with obesity has become nearly universal, and widespread calls have been made for more consistent and accurate monitoring in all populations [2]. Conventional strategies for monitoring population-level overweight and obesity rely on obtaining point estimates, including mean body mass index (BMI) or prevalence of overweight (BMI ≥ 25) and obesity (BMI ≥ 30) [3, 4]. Mean and prevalence are succinct metrics which provide useful insight into distinct aspects of a population’s distribution of BMI. In addition, these measures are easily interpreted by the general public. However, to rigorously monitor the rapidly evolving obesity epidemic, simply observing measures of mean and prevalence is not adequate. Specifically, as the proportion of overweight and obesity increases, the distribution of BMI will become skewed. This, in turn, affects the ability of mean to accurately reflect the central tendency of the distribution [5-7]. If the goal is simply to obtain a more accurate estimate of central tendency, it may be sufficient to replace mean by median. However, as the epidemic intensifies, there is a growing interest in understanding the shift in the BMI distribution and in tracking changes across subclasses of obesity which include class I (BMI: 30–34.9), class II (BMI: 35–39.9), and class III obesity (BMI ≥ 40) [8]. Furthermore, understanding population distribution of BMI is critical to estimating the associated disease burden. To calculate the population attributable fraction of diseases related to high BMI, for instance, one would need to have an accurate measure of exposure represented by population BMI distribution [9]. Therefore, there is a practical need to look beyond measures of mean and prevalence and to monitor the distribution of BMI as a whole. Monitoring the population distribution of BMI is a challenging task. Existing national surveillance systems do not always include a sample size sufficient for precise approximations of BMI distributions by subpopulation, such as by sex and age [10]. A direct solution would be to increase sample sizes of a survey. However, given the need for regular and timely monitoring, increasing sample sizes will be costly and may not be sustainable in the long run. It would, therefore, be highly desirable to develop a strategy that can effectively use available point estimates from surveys to infer the underlying distribution. In this study, we propose a novel method that utilizes an optimization algorithm to approximate the distribution of BMI using the three commonly available population-level metrics: mean BMI, prevalence of overweight, and prevalence of obesity. The paper is organized as follows: We first provide a brief description of the proposed method. We then describe the simulation experiment used to validate the method and present the results. To illustrate the utility of the method, we apply it to the 2011–2012 US National Health and Nutrition Examination Survey (NHANES) and compare our estimate with the true distribution of BMI. We conclude by discussing the potential extension, limitations, and implications of the method.

Methods

Rationale

The characteristics of a continuous distribution are defined by its probability density function (pdf). Depending on the distribution, the parameters involved in the pdf vary. For instance, a normal distribution has a pdf defined by a measure of central tendency (μ) and a measure of dispersion (σ2) parameters. On the other hand, a beta distribution has a pdf defined by two shape parameters, namely α and β. Although estimates of these parameters are not always immediately available, they can be easily derived from any two pieces of known statistical information. In the case of BMI, three statistics which are commonly available from existing surveys are mean BMI, prevalence of overweight, and prevalence of obesity. They respectively provide information on central tendency and specific quintiles. Based on this information and assumptions about the potential family of distributions, parameters can be obtained analytically. For example, if a normal distribution is assumed, μ can be immediately inferred from the sample mean. σ2 (assuming that sample variance information is not immediately available) can be calculated based on the mean and quintiles using inverse z scores. Suppose prevalence of obesity is 0.025; if BMI is normally distributed, the corresponding z-value would be 1.96. Using the standard z-score calculation formula, , with z = 1.96, X = 30, μ being the sample mean, σ2 can be calculated. Once μ and σ2 are defined, the shape of the distribution is fully realized. The issue with assuming a normal distribution, however, is that as the epidemic shifts, the shape of the BMI distribution will begin to skew. In other words, to accurately capture this shift, the distribution assumed needs to be flexible enough to represent both symmetric and asymmetric patterns. Some of the potential distribution candidates include log normal, and the gamma, beta, and inverse Gaussian distributions. To determine which would best approximate the distribution of actual data, we briefly examined national survey data from the most recent years from six countries with measured height and weight for men and women. The skewness of BMI distributions in these survey data ranged from 0.68 to 1.43, and the kurtosis ranged from 3.94 to 8.96 (see Table 1). While log normal and the gamma distributions offer fit to a variety of unimodal distributions, some of the shapes generated by these two distributions have extreme skewness and kurtosis which are not suitable for the situation at hand. Moreover, for both log normal and the gamma distributions, skewness and kurtosis are defined by a single parameter, which limits their flexibility in capturing distribution of particular shapes. Inverse Gaussian distribution offers reasonable fit to skewed data with varying levels of kurtosis. However, in situations where the data distribution is relatively symmetric, Inverse Gaussian may not be flexible enough to capture them. In contrast, with certain constraints imposed (see next section), the beta distribution offers a variety of symmetric light-tailed and asymmetric heavy-tailed distributions which possess skewness and kurtosis within the observed range. The proposed method capitalizes on the flexibility of the beta distribution to estimate the entire BMI distribution based on information about the mean and quintiles. Further detail is provided in subsequent sections.
Table 1

Skewness and kurtosis of BMI distributions from six countries

ISO3SurveyYearSexSkewnessKurtosis
UGADHS2011Male0.824.87
UGADHS2011Female1.378.96
INDDHS2005Male1.267.17
INDDHS2005Female1.437.29
SAUSaudi Arabia HIS2013Male0.774.22
SAUSaudi Arabia HIS2013Female0.683.94
DOMDHS2013Male1.105.72
DOMDHS2013Female0.904.37
GBRHealth Survey for England2011Male0.945.56
GBRHealth Survey for England2011Female1.024.47
USANHANES2011Male1.135.59
USANHANES2011Female1.275.84
Skewness and kurtosis of BMI distributions from six countries

Estimation of BMI distribution

To estimate the distribution of BMI, we assume that: BMI = C1u + C2 C1 > 0, C2 ≥ 10 where C1 is a positive scaling constant and C2 is a shifting constant. Note that a constraint of greater than or equal to 10 was imposed on C2. Because the lower limit of a population BMI distribution rarely falls below 10, imposing this constraint enhances the accuracy of the optimization results. u is a random variable following the beta distribution with values ranging from zero to one. u ∼ Beta (α, β), α > 1, β > 1 where α and β are the shape parameters. When α > 1, β > 1, and α = β, the beta distribution is unimodal and symmetric. When α > 1, β > 1, and α < β , the distribution is unimodal and positively skewed. In contrast with other distributions such as log normal and gamma, a beta distribution is relatively light-tailed and provides more stable estimation at the tails of the distribution. Estimates of α, β, C1, and C2 are obtained by minimizing the following function: where D refers to the Euclidean distance, which is the shortest distance between two points, in this case two vectors s and t. s is a vector consisting of the observed mean BMI () and prevalence of overweight and obesity (); t is a vector consisting of the predicted mean BMI () and prevalence () for a given set of α, β, C1, and C2. The large-scale bound-constrained optimization algorithm (L-BFGS-B) was used for the optimization [11]. Other optimization algorithms, including conjugate gradient, Nelder-Mead, and Broyden-Fletcher-Foldfarb-Shannon algorithms were considered. However, L-BFGS-B was chosen as it provided a much more efficient optimization process and more stable results.

Simulation

A series of simulations were carried out to examine the performance of the method. Data were simulated from three distributions representing different levels of skewness and kurtosis similar to those observed in the survey data. The first set of data were simulated from a normal distribution. The second and third sets of data were simulated from a log normal and a gamma distribution, respectively. The normal distribution represents a symmetric light-tailed distribution; the log normal distribution represents a slightly skewed and light-tailed distribution; the gamma distribution represents a skewed and heavy-tailed distribution. The intention for simulating from log normal and the gamma distribution is to test the robustness of the method in handling extreme scenarios. If the method performs well under these extreme circumstances, it offers confidence for general use. For consistency, we centered and scaled all three distributions to ensure that they had a mean of 24 and a standard deviation of four. Table 2 summarizes the characteristics of the distributions. Graphical displays of each distribution are shown in Fig. 1.
Table 2

Descriptive statistics of the distributions considered for simulation

NormalLog normalaGammaa
Parametersμ = 24 (mean)σ = 4 (standard deviation)Log(μ) = 0 (log mean)Log(σ) = 0.1 (log standard deviation)κ = 1 (shape)θ = 2 (scale)
Mean24
Standard deviation4
Skewness0.0070.311.95
Kurtosis2.953.128.47

aData generated from log normal and the gamma distributions were scaled to have mean of 24 and standard deviation of four

Fig. 1

Distributions used for simulation. The normal distribution (left) represents a symmetric light-tailed distribution; the log normal distribution (center) represents a slightly skewed and light-tailed distribution; the gamma distribution (right) represents a skewed and heavy-tailed distribution

Descriptive statistics of the distributions considered for simulation aData generated from log normal and the gamma distributions were scaled to have mean of 24 and standard deviation of four Distributions used for simulation. The normal distribution (left) represents a symmetric light-tailed distribution; the log normal distribution (center) represents a slightly skewed and light-tailed distribution; the gamma distribution (right) represents a skewed and heavy-tailed distribution A random sample of 500 observations were drawn from each of the three distributions. The sample mean and prevalence of overweight and obesity were calculated. Based on these three statistics, we applied the proposed method to approximate the distribution of BMI. The process was repeated 1000 times for each of the distributions. To determine how well the empirical distribution estimated from the method approximates the true distribution, we evaluated the biases and mean squared errors in four key statistics: mean, standard deviation, the prevalence of overweight, and the prevalence of obesity. Specifically, for mean, the bias is calculated by the difference between the expected mean BMI derived from the empirical distribution across the 1000 simulations and the true mean of 24: For standard deviation and prevalence of overweight and obesity, the biases are calculated in a similar manner, as follows: where S, , and are the standard deviation, prevalence of overweight, and prevalence of obesity estimated respectively from the empirical distribution for a simulated data set. On the other hand, mean squared errors are calculated as follows: In addition to calculating bias and mean squared errors, the Kolmogrov-Smirnov test was performed to examine how well the predicted distributions matched the actual distributions of the sample. We computed the proportion of the time in which the test falsely rejected the null hypothesis that the empirical and true distribution are equal with α = 0.05.

Applied example

Further validation was performed using data from the 2011–2012 NHANES. Specifically, based on mean and prevalence information by age and sex, we estimated the distributions of BMI for males and females for each 10-year age group from 20 to 70+ years old. The empirical distributions were compared against the distribution of actual data using the Kolmogrov-Smirnov test. All analyses were conducted in R 3.0.1.

Results and discussion

Overall, the proposed methods performed well across all scenarios (see Table 3). The biases in the key distribution parameters were minimal. Specifically, the estimated means were consistently similar to the true mean of 24, with biases ranging from −0.036 to −0.006. The biases in standard deviation estimates were slightly larger, ranging from −0.121 to −0.026. The prevalence of overweight and obesity derived from the empirical distribution was equal to the true values (bias of zero).
Table 3

Biases and mean squared errors (in parentheses) in estimated parameters, and Kolmogrov-Smirnov test results

NormalLog normalGamma
Bias(MSE) \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$ \overline{X} $$\end{document}X¯ −0.006−0.010−0.036
(0.058)(0.062)(0.068)
SD −0.121−0.070−0.026
(0.035)(0.035)(0.146)
\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$ {\widehat{p}}_{\ge 25} $$\end{document}p^25 0.0010.0010.016
(0.001)(0)(0.001)
\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$ {\widehat{p}}_{\ge 30} $$\end{document}p^30 0−0.0020.003
(0)(0)(0)
Kolmogrov-Smirnov test false rejection rate2.5 %2.3 %24.9 %
Biases and mean squared errors (in parentheses) in estimated parameters, and Kolmogrov-Smirnov test results Despite the consistency in the point estimates, the Kolmogrov-Smirnov test indicated that, in some cases, certain aspects of the true distribution were not captured by the empirical distribution. When the true BMI distribution was normal or log normal, the method performed reasonably well. Only 2.5 % and 2.3 % of the 1000 empirical distributions, respectively, exhibited a statistically significant deviation from the true distribution. These rates are considered to be desirable given the α-level of 5 % [12]. However, as the distribution becomes more skewed and heavy-tailed, the discrepancy between the empirical distribution and the true distribution increases. When the true BMI distribution was gamma, approximately 24.9 % of the 1000 empirical distributions exhibited a statistically significant deviation from the true distribution. Further investigation was carried out to identify potential causes of the discrepancy. Figure 2 shows a QQ-plot illustrating the quintile at which discrepancies existed between the empirical and true distributions, with the true distribution being the gamma distribution. As the plot suggests, the discrepancies were mainly restricted to the right tail where the method failed to precisely capture the extreme values. In other words, the presence of outliers and the sparse data at extreme ends pose challenges to the accuracy of the method. Nevertheless, it is worth emphasizing that both the log normal and the gamma distributions represent a relatively high level of kurtosis, meaning that these distributions tend to have heavy tails with extreme values. Moreover, considering the fact that the underlying distribution assumed by the method is distinct from the simulated distributions, the method’s capability in approximating the central tendency and quintiles of these alternative distributions is considered robust.
Fig. 2

An example of a QQ-plot indicating the discrepancy between the empirical and true (the gamma) distributions. Deviation from the 45° line represents a lack of alignment between the two distributions. Major discrepancies existed at the right tail where the method failed to precisely capture the extreme values

An example of a QQ-plot indicating the discrepancy between the empirical and true (the gamma) distributions. Deviation from the 45° line represents a lack of alignment between the two distributions. Major discrepancies existed at the right tail where the method failed to precisely capture the extreme values We applied the proposed method to data from the 2011–2012 NHANES. Using only the mean BMI, prevalence of overweight, and prevalence of obesity for each sex and 10-year age group (from ages 20-70+), we approximated the distributions for each of these subgroups and compared them against the distributions of the actual data. Figure 3 shows the differences between the empirical and the true data distributions. As indicated by the overlapping lines in the density plots, the empirical distributions were reasonably accurate at approximating the distributions of actual data. The QQ-plots similarly suggest that our method accurately approximated the distribution of true data with minor deviations at the tail of the distributions for some age groups, such as males ages 40–49 and 50–59. The Kolmogrov-Smirnov test results (Table 4) indicated that there is no statistically significant difference between the empirical and true distributions.
Fig. 3

Comparison between the empirical distributions and the true data distribution and corresponding QQ-plots. Overlapping lines in the density plots indicate the empirical distributions were reasonably accurate at approximating the distributions of actual data. The QQ-plots similarly suggests minor deviations at the tail of the distributions for some age groups

Table 4

Kolmogrov-Smirnov Test results (p-values) comparing the empirical distribution to the NHANES data distribution

Kolmogrov-Smirnov test statistics and p-values
Age groupMaleFemale
20-290.0430.069
p = 0.755 p = 0.218
30-390.0640.066
p = 0.314 p = 0.280
40-490.0460.056
p = 0.772 p = 0.490
50-590.0480.081
p = 0.721 p = 0.099
60-690.0680.043
p = 0.475 p = 0.833
70+0.0360.063
p = 0.958 p = 0.381
Comparison between the empirical distributions and the true data distribution and corresponding QQ-plots. Overlapping lines in the density plots indicate the empirical distributions were reasonably accurate at approximating the distributions of actual data. The QQ-plots similarly suggests minor deviations at the tail of the distributions for some age groups Kolmogrov-Smirnov Test results (p-values) comparing the empirical distribution to the NHANES data distribution

Conclusions

In this study, we proposed a novel method to approximate the entire distribution of BMI using three commonly available statistics, namely mean BMI and prevalence of overweight and obesity. We assessed the method using a series of simulations, and the results indicated that the method performed well in approximating distributions with a wide range of skewness and kurtosis. We illustrated the application of the method using data from NHANES, which similarly demonstrated the accuracy of the approach. A major appeal of the proposed method lies in its use of readily available health statistics. Distributions of BMI can be approximated without the need to collect a large amount of data. Moreover, past BMI distributions can be retrospectively constructed using historical information on mean BMI and prevalence of overweight and obesity. In addition, the current method is robust and can adequately estimate distributions which do not conform with the underlying distribution (beta distribution) assumed by the method. As part of the Global Burden of Disease Study 2013, we applied the proposed method to historical data to reconstruct the BMI distributions by age and sex for 192 countries from 1980 to 2013. Without utilizing the new approach, obtaining precise BMI distributions would have been impossible as in many countries historical individual-level BMI data were unavailable [13]. One of the limitations of this method, however, is the reduction in accuracy when the true distribution contains outliers. Specifically, our method may be inadequate at capturing outliers at the tails of a distribution. This limitation may be due to the assumption of the beta distribution in our approximation strategy. Although the beta distribution offers the flexibility to model a wide variety of distributional shapes, it is relatively weak at handling extreme kurtosis. Alternative distributions such as log normal and the gamma offer better capability at capturing long, heavy-tailed distributions. Nevertheless, the lack of finite upper bounds for these distributions posed challenges in the optimization process, which led to instability in estimation. Despite this limitation, results from our simulations showed that the prevalence of overweight and obesity estimated from the empirical distributions are unbiased. This implies that, although the method may be limited in identifying the precise BMI value of outliers, it is able to offer an accurate approximation of the proportion of extreme values. Additionally, it is worth emphasizing that the design of the method is very flexible. For this simulation, three values were utilized in the optimization function. Additional statistics, such as prevalence of underweight and prevalence of different obesity classes, could be easily incorporated to the method and improve the accuracy of the distribution approximation. In summary, the algorithm proposed in this paper serves as an efficient method to approximate BMI distributions. In fact, this algorithm can be applied to estimating the distribution of other continuous risk factors such as blood pressure and glucose level and facilitate more accurate assessment of associated disease burden. While the method performed well in various situations, some aspects can be improved. Future studies can explore non-parametric density approximation techniques to expand the flexibility of the method.
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Francisco A García-Guerra; Evariste Gasana; Johanna M Geleijnse; Bradford D Gessner; Pete Gething; Katherine B Gibney; Richard F Gillum; Ibrahim A M Ginawi; Maurice Giroud; Giorgia Giussani; Shifalika Goenka; Ketevan Goginashvili; Hector Gomez Dantes; Philimon Gona; Teresita Gonzalez de Cosio; Dinorah González-Castell; Carolyn C Gotay; Atsushi Goto; Hebe N Gouda; Richard L Guerrant; Harish C Gugnani; Francis Guillemin; David Gunnell; Rahul Gupta; Rajeev Gupta; Reyna A Gutiérrez; Nima Hafezi-Nejad; Holly Hagan; Maria Hagstromer; Yara A Halasa; Randah R Hamadeh; Mouhanad Hammami; Graeme J Hankey; Yuantao Hao; Hilda L Harb; Tilahun Nigatu Haregu; Josep Maria Haro; Rasmus Havmoeller; Simon I Hay; Mohammad T Hedayati; Ileana B Heredia-Pi; Lucia Hernandez; Kyle R Heuton; Pouria Heydarpour; Martha Hijar; Hans W Hoek; Howard J Hoffman; John C Hornberger; H Dean Hosgood; Damian G Hoy; Mohamed Hsairi; Guoqing Hu; Howard Hu; Cheng Huang; John J Huang; Bryan J Hubbell; Laetitia Huiart; Abdullatif Husseini; Marissa L Iannarone; Kim M Iburg; Bulat T Idrisov; Nayu Ikeda; Kaire Innos; Manami Inoue; Farhad Islami; Samaya Ismayilova; Kathryn H Jacobsen; Henrica A Jansen; Deborah L Jarvis; Simerjot K Jassal; Alejandra Jauregui; Sudha Jayaraman; Panniyammakal Jeemon; Paul N Jensen; Vivekanand Jha; Fan Jiang; Guohong Jiang; Ying Jiang; Jost B Jonas; Knud Juel; Haidong Kan; Sidibe S Kany Roseline; Nadim E Karam; André Karch; Corine K Karema; Ganesan Karthikeyan; Anil Kaul; Norito Kawakami; Dhruv S Kazi; Andrew H Kemp; Andre P Kengne; Andre Keren; Yousef S Khader; Shams Eldin Ali Hassan Khalifa; Ejaz A Khan; Young-Ho Khang; Shahab Khatibzadeh; Irma Khonelidze; Christian Kieling; Daniel Kim; Sungroul Kim; Yunjin Kim; Ruth W Kimokoti; Yohannes Kinfu; Jonas M Kinge; Brett M Kissela; Miia Kivipelto; Luke D Knibbs; Ann Kristin Knudsen; Yoshihiro Kokubo; M Rifat Kose; Soewarta Kosen; Alexander Kraemer; Michael Kravchenko; Sanjay Krishnaswami; Hans Kromhout; Tiffany Ku; Barthelemy Kuate Defo; Burcu Kucuk Bicer; Ernst J Kuipers; Chanda Kulkarni; Veena S Kulkarni; G Anil Kumar; Gene F Kwan; Taavi Lai; Arjun Lakshmana Balaji; Ratilal Lalloo; Tea Lallukka; Hilton Lam; Qing Lan; Van C Lansingh; Heidi J Larson; Anders Larsson; Dennis O Laryea; Pablo M Lavados; Alicia E Lawrynowicz; Janet L Leasher; Jong-Tae Lee; James Leigh; Ricky Leung; Miriam Levi; Yichong Li; Yongmei Li; Juan Liang; Xiaofeng Liang; Stephen S Lim; M Patrice Lindsay; Steven E Lipshultz; Shiwei Liu; Yang Liu; Belinda K Lloyd; Giancarlo Logroscino; Stephanie J London; Nancy Lopez; Joannie Lortet-Tieulent; Paulo A Lotufo; Rafael Lozano; Raimundas Lunevicius; Jixiang Ma; Stefan Ma; Vasco M P Machado; Michael F MacIntyre; Carlos Magis-Rodriguez; Abbas A Mahdi; Marek Majdan; Reza Malekzadeh; Srikanth Mangalam; Christopher C Mapoma; Marape Marape; Wagner Marcenes; David J Margolis; Christopher Margono; Guy B Marks; Randall V Martin; Melvin B Marzan; Mohammad T Mashal; Felix Masiye; Amanda J Mason-Jones; Kunihiro Matsushita; Richard Matzopoulos; Bongani M Mayosi; Tasara T Mazorodze; Abigail C McKay; Martin McKee; Abigail McLain; Peter A Meaney; Catalina Medina; Man Mohan Mehndiratta; Fabiola Mejia-Rodriguez; Wubegzier Mekonnen; Yohannes A Melaku; Michele Meltzer; Ziad A Memish; Walter Mendoza; George A Mensah; Atte Meretoja; Francis Apolinary Mhimbira; Renata Micha; Ted R Miller; Edward J Mills; Awoke Misganaw; Santosh Mishra; Norlinah Mohamed Ibrahim; Karzan A Mohammad; Ali H Mokdad; Glen L Mola; Lorenzo Monasta; Julio C Montañez Hernandez; Marcella Montico; Ami R Moore; Lidia Morawska; Rintaro Mori; Joanna Moschandreas; Wilkister N Moturi; Dariush Mozaffarian; Ulrich O Mueller; Mitsuru Mukaigawara; Erin C Mullany; Kinnari S Murthy; Mohsen Naghavi; Ziad Nahas; Aliya Naheed; Kovin S Naidoo; Luigi Naldi; Devina Nand; Vinay Nangia; K M Venkat Narayan; Denis Nash; Bruce Neal; Chakib Nejjari; Sudan P Neupane; Charles R Newton; Frida N Ngalesoni; Jean de Dieu Ngirabega; Grant Nguyen; Nhung T Nguyen; Mark J Nieuwenhuijsen; Muhammad I Nisar; José R Nogueira; Joan M Nolla; Sandra Nolte; Ole F Norheim; Rosana E Norman; Bo Norrving; Luke Nyakarahuka; In-Hwan Oh; Takayoshi Ohkubo; Bolajoko O Olusanya; Saad B Omer; John Nelson Opio; Ricardo Orozco; Rodolfo S Pagcatipunan; Amanda W Pain; Jeyaraj D Pandian; Carlo Irwin A Panelo; Christina Papachristou; Eun-Kee Park; Charles D Parry; Angel J Paternina Caicedo; Scott B Patten; Vinod K Paul; Boris I Pavlin; Neil Pearce; Lilia S Pedraza; Andrea Pedroza; Ljiljana Pejin Stokic; Ayfer Pekericli; David M Pereira; Rogelio Perez-Padilla; Fernando Perez-Ruiz; Norberto Perico; Samuel A L Perry; Aslam Pervaiz; Konrad Pesudovs; Carrie B Peterson; Max Petzold; Michael R Phillips; Hwee Pin Phua; Dietrich Plass; Dan Poenaru; Guilherme V Polanczyk; Suzanne Polinder; Constance D Pond; C Arden Pope; Daniel Pope; Svetlana Popova; Farshad Pourmalek; John Powles; Dorairaj Prabhakaran; Noela M Prasad; Dima M Qato; Amado D Quezada; D Alex A Quistberg; Lionel Racapé; Anwar Rafay; Kazem Rahimi; Vafa Rahimi-Movaghar; Sajjad Ur Rahman; Murugesan Raju; Ivo Rakovac; Saleem M Rana; Mayuree Rao; Homie Razavi; K Srinath Reddy; Amany H Refaat; Jürgen Rehm; Giuseppe Remuzzi; Antonio L Ribeiro; Patricia M Riccio; Lee Richardson; Anne Riederer; Margaret Robinson; Anna Roca; Alina Rodriguez; David Rojas-Rueda; Isabelle Romieu; Luca Ronfani; Robin Room; Nobhojit Roy; George M Ruhago; Lesley Rushton; Nsanzimana Sabin; Ralph L Sacco; Sukanta Saha; Ramesh Sahathevan; Mohammad Ali Sahraian; Joshua A Salomon; Deborah Salvo; Uchechukwu K Sampson; Juan R Sanabria; Luz Maria Sanchez; Tania G Sánchez-Pimienta; Lidia Sanchez-Riera; Logan Sandar; Itamar S Santos; Amir Sapkota; Maheswar Satpathy; James E Saunders; Monika Sawhney; Mete I Saylan; Peter Scarborough; Jürgen C Schmidt; Ione J C Schneider; Ben Schöttker; David C Schwebel; James G Scott; Soraya Seedat; Sadaf G Sepanlou; Berrin Serdar; Edson E Servan-Mori; Gavin Shaddick; Saeid Shahraz; Teresa Shamah Levy; Siyi Shangguan; Jun She; Sara Sheikhbahaei; Kenji Shibuya; Hwashin H Shin; Yukito Shinohara; Rahman Shiri; Kawkab Shishani; Ivy Shiue; Inga D Sigfusdottir; Donald H Silberberg; Edgar P Simard; Shireen Sindi; Abhishek Singh; Gitanjali M Singh; Jasvinder A Singh; Vegard Skirbekk; Karen Sliwa; Michael Soljak; Samir Soneji; Kjetil Søreide; Sergey Soshnikov; Luciano A Sposato; Chandrashekhar T Sreeramareddy; Nicolas J C Stapelberg; Vasiliki Stathopoulou; Nadine Steckling; Dan J Stein; Murray B Stein; Natalie Stephens; Heidi Stöckl; Kurt Straif; Konstantinos Stroumpoulis; Lela Sturua; Bruno F Sunguya; Soumya Swaminathan; Mamta Swaroop; Bryan L Sykes; Karen M Tabb; Ken Takahashi; Roberto T Talongwa; Nikhil Tandon; David Tanne; Marcel Tanner; Mohammad Tavakkoli; Braden J Te Ao; Carolina M Teixeira; Martha M Téllez Rojo; Abdullah S Terkawi; José Luis Texcalac-Sangrador; Sarah V Thackway; Blake Thomson; Andrew L Thorne-Lyman; Amanda G Thrift; George D Thurston; Taavi Tillmann; Myriam Tobollik; Marcello Tonelli; Fotis Topouzis; Jeffrey A Towbin; Hideaki Toyoshima; Jefferson Traebert; Bach X Tran; Leonardo Trasande; Matias Trillini; Ulises Trujillo; Zacharie Tsala Dimbuene; Miltiadis Tsilimbaris; Emin Murat Tuzcu; Uche S Uchendu; Kingsley N Ukwaja; Selen B Uzun; Steven van de Vijver; Rita Van Dingenen; Coen H van Gool; Jim van Os; Yuri Y Varakin; Tommi J Vasankari; Ana Maria N Vasconcelos; Monica S Vavilala; Lennert J Veerman; Gustavo Velasquez-Melendez; N Venketasubramanian; Lakshmi Vijayakumar; Salvador Villalpando; Francesco S Violante; Vasiliy Victorovich Vlassov; Stein Emil Vollset; Gregory R Wagner; Stephen G Waller; Mitchell T Wallin; Xia Wan; Haidong Wang; JianLi Wang; Linhong Wang; Wenzhi Wang; Yanping Wang; Tati S Warouw; Charlotte H Watts; Scott Weichenthal; Elisabete Weiderpass; Robert G Weintraub; Andrea Werdecker; K Ryan Wessells; Ronny Westerman; Harvey A Whiteford; James D Wilkinson; Hywel C Williams; Thomas N Williams; Solomon M Woldeyohannes; Charles D A Wolfe; John Q Wong; Anthony D Woolf; Jonathan L Wright; Brittany Wurtz; Gelin Xu; Lijing L Yan; Gonghuan Yang; Yuichiro Yano; Pengpeng Ye; Muluken Yenesew; Gökalp K Yentür; Paul Yip; Naohiro Yonemoto; Seok-Jun Yoon; Mustafa Z Younis; Zourkaleini Younoussi; Chuanhua Yu; Maysaa E Zaki; Yong Zhao; Yingfeng Zheng; Maigeng Zhou; Jun Zhu; Shankuan Zhu; Xiaonong Zou; Joseph R Zunt; Alan D Lopez; Theo Vos; Christopher J Murray
Journal:  Lancet       Date:  2015-09-11       Impact factor: 79.321

8.  Global, regional, and national prevalence of overweight and obesity in children and adults during 1980-2013: a systematic analysis for the Global Burden of Disease Study 2013.

Authors:  Marie Ng; Tom Fleming; Margaret Robinson; Blake Thomson; Nicholas Graetz; Christopher Margono; Erin C Mullany; Stan Biryukov; Cristiana Abbafati; Semaw Ferede Abera; Jerry P Abraham; Niveen M E Abu-Rmeileh; Tom Achoki; Fadia S AlBuhairan; Zewdie A Alemu; Rafael Alfonso; Mohammed K Ali; Raghib Ali; Nelson Alvis Guzman; Walid Ammar; Palwasha Anwari; Amitava Banerjee; Simon Barquera; Sanjay Basu; Derrick A Bennett; Zulfiqar Bhutta; Jed Blore; Norberto Cabral; Ismael Campos Nonato; Jung-Chen Chang; Rajiv Chowdhury; Karen J Courville; Michael H Criqui; David K Cundiff; Kaustubh C Dabhadkar; Lalit Dandona; Adrian Davis; Anand Dayama; Samath D Dharmaratne; Eric L Ding; Adnan M Durrani; Alireza Esteghamati; Farshad Farzadfar; Derek F J Fay; Valery L Feigin; Abraham Flaxman; Mohammad H Forouzanfar; Atsushi Goto; Mark A Green; Rajeev Gupta; Nima Hafezi-Nejad; Graeme J Hankey; Heather C Harewood; Rasmus Havmoeller; Simon Hay; Lucia Hernandez; Abdullatif Husseini; Bulat T Idrisov; Nayu Ikeda; Farhad Islami; Eiman Jahangir; Simerjot K Jassal; Sun Ha Jee; Mona Jeffreys; Jost B Jonas; Edmond K Kabagambe; Shams Eldin Ali Hassan Khalifa; Andre Pascal Kengne; Yousef Saleh Khader; Young-Ho Khang; Daniel Kim; Ruth W Kimokoti; Jonas M Kinge; Yoshihiro Kokubo; Soewarta Kosen; Gene Kwan; Taavi Lai; Mall Leinsalu; Yichong Li; Xiaofeng Liang; Shiwei Liu; Giancarlo Logroscino; Paulo A Lotufo; Yuan Lu; Jixiang Ma; Nana Kwaku Mainoo; George A Mensah; Tony R Merriman; Ali H Mokdad; Joanna Moschandreas; Mohsen Naghavi; Aliya Naheed; Devina Nand; K M Venkat Narayan; Erica Leigh Nelson; Marian L Neuhouser; Muhammad Imran Nisar; Takayoshi Ohkubo; Samuel O Oti; Andrea Pedroza; Dorairaj Prabhakaran; Nobhojit Roy; Uchechukwu Sampson; Hyeyoung Seo; Sadaf G Sepanlou; Kenji Shibuya; Rahman Shiri; Ivy Shiue; Gitanjali M Singh; Jasvinder A Singh; Vegard Skirbekk; Nicolas J C Stapelberg; Lela Sturua; Bryan L Sykes; Martin Tobias; Bach X Tran; Leonardo Trasande; Hideaki Toyoshima; Steven van de Vijver; Tommi J Vasankari; J Lennert Veerman; Gustavo Velasquez-Melendez; Vasiliy Victorovich Vlassov; Stein Emil Vollset; Theo Vos; Claire Wang; XiaoRong Wang; Elisabete Weiderpass; Andrea Werdecker; Jonathan L Wright; Y Claire Yang; Hiroshi Yatsuya; Jihyun Yoon; Seok-Jun Yoon; Yong Zhao; Maigeng Zhou; Shankuan Zhu; Alan D Lopez; Christopher J L Murray; Emmanuela Gakidou
Journal:  Lancet       Date:  2014-05-29       Impact factor: 79.321

9.  Change in the body mass index distribution for women: analysis of surveys from 37 low- and middle-income countries.

Authors:  Fahad Razak; Daniel J Corsi; S V Subramanian
Journal:  PLoS Med       Date:  2013-01-15       Impact factor: 11.069

10.  WHO European Childhood Obesity Surveillance Initiative: body mass index and level of overweight among 6-9-year-old children from school year 2007/2008 to school year 2009/2010.

Authors:  Trudy M A Wijnhoven; Joop M A van Raaij; Angela Spinelli; Gregor Starc; Maria Hassapidou; Igor Spiroski; Harry Rutter; Éva Martos; Ana I Rito; Ragnhild Hovengen; Napoleón Pérez-Farinós; Ausra Petrauskiene; Nazih Eldin; Lien Braeckevelt; Iveta Pudule; Marie Kunešová; João Breda
Journal:  BMC Public Health       Date:  2014-08-07       Impact factor: 3.295

  10 in total
  3 in total

1.  Health Effects of Overweight and Obesity in 195 Countries over 25 Years.

Authors:  Ashkan Afshin; Mohammad H Forouzanfar; Marissa B Reitsma; Patrick Sur; Kara Estep; Alex Lee; Laurie Marczak; Ali H Mokdad; Maziar Moradi-Lakeh; Mohsen Naghavi; Joseph S Salama; Theo Vos; Kalkidan H Abate; Cristiana Abbafati; Muktar B Ahmed; Ziyad Al-Aly; Ala’a Alkerwi; Rajaa Al-Raddadi; Azmeraw T Amare; Alemayehu Amberbir; Adeladza K Amegah; Erfan Amini; Stephen M Amrock; Ranjit M Anjana; Johan Ärnlöv; Hamid Asayesh; Amitava Banerjee; Aleksandra Barac; Estifanos Baye; Derrick A Bennett; Addisu S Beyene; Sibhatu Biadgilign; Stan Biryukov; Espen Bjertness; Dube J Boneya; Ismael Campos-Nonato; Juan J Carrero; Pedro Cecilio; Kelly Cercy; Liliana G Ciobanu; Leslie Cornaby; Solomon A Damtew; Lalit Dandona; Rakhi Dandona; Samath D Dharmaratne; Bruce B Duncan; Babak Eshrati; Alireza Esteghamati; Valery L Feigin; João C Fernandes; Thomas Fürst; Tsegaye T Gebrehiwot; Audra Gold; Philimon N Gona; Atsushi Goto; Tesfa D Habtewold; Kokeb T Hadush; Nima Hafezi-Nejad; Simon I Hay; Masako Horino; Farhad Islami; Ritul Kamal; Amir Kasaeian; Srinivasa V Katikireddi; Andre P Kengne; Chandrasekharan N Kesavachandran; Yousef S Khader; Young-Ho Khang; Jagdish Khubchandani; Daniel Kim; Yun J Kim; Yohannes Kinfu; Soewarta Kosen; Tiffany Ku; Barthelemy Kuate Defo; G Anil Kumar; Heidi J Larson; Mall Leinsalu; Xiaofeng Liang; Stephen S Lim; Patrick Liu; Alan D Lopez; Rafael Lozano; Azeem Majeed; Reza Malekzadeh; Deborah C Malta; Mohsen Mazidi; Colm McAlinden; Stephen T McGarvey; Desalegn T Mengistu; George A Mensah; Gert B M Mensink; Haftay B Mezgebe; Erkin M Mirrakhimov; Ulrich O Mueller; Jean J Noubiap; Carla M Obermeyer; Felix A Ogbo; Mayowa O Owolabi; George C Patton; Farshad Pourmalek; Mostafa Qorbani; Anwar Rafay; Rajesh K Rai; Chhabi L Ranabhat; Nikolas Reinig; Saeid Safiri; Joshua A Salomon; Juan R Sanabria; Itamar S Santos; Benn Sartorius; Monika Sawhney; Josef Schmidhuber; Aletta E Schutte; Maria I Schmidt; Sadaf G Sepanlou; Moretza Shamsizadeh; Sara Sheikhbahaei; Min-Jeong Shin; Rahman Shiri; Ivy Shiue; Hirbo S Roba; Diego A S Silva; Jonathan I Silverberg; Jasvinder A Singh; Saverio Stranges; Soumya Swaminathan; Rafael Tabarés-Seisdedos; Fentaw Tadese; Bemnet A Tedla; Balewgizie S Tegegne; Abdullah S Terkawi; J S Thakur; Marcello Tonelli; Roman Topor-Madry; Stefanos Tyrovolas; Kingsley N Ukwaja; Olalekan A Uthman; Masoud Vaezghasemi; Tommi Vasankari; Vasiliy V Vlassov; Stein E Vollset; Elisabete Weiderpass; Andrea Werdecker; Joshua Wesana; Ronny Westerman; Yuichiro Yano; Naohiro Yonemoto; Gerald Yonga; Zoubida Zaidi; Zerihun M Zenebe; Ben Zipkin; Christopher J L Murray
Journal:  N Engl J Med       Date:  2017-06-12       Impact factor: 91.245

2.  Burden of obesity in the Eastern Mediterranean Region: findings from the Global Burden of Disease 2015 study.

Authors: 
Journal:  Int J Public Health       Date:  2017-08-03       Impact factor: 3.380

3.  Generalized lambda distribution for flexibly testing differences beyond the mean in the distribution of a dependent variable such as body mass index.

Authors:  K Ejima; G Pavela; P Li; D B Allison
Journal:  Int J Obes (Lond)       Date:  2017-10-30       Impact factor: 5.095

  3 in total

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