Concordance between self-reported pre-pregnancy body mass index (BMI) and BMI measured at the first prenatal study contact
© The Author(s). 2016
Received: 25 January 2016
Accepted: 16 July 2016
Published: 26 July 2016
The 2009 Institute of Medicine (IOM) gestational weight recommendations are tailored to women’s pre-pregnancy body mass index (BMI). Limited evidence exists on methods for estimating women’s pre-pregnancy BMI, particularly for women living in low and middle income countries. Using data from collected among Peruvian pregnant women, we compared the concordance between self-reported pre-pregnancy BMI with BMI measured at the earliest prenatal study visit.
Data were from the Pregnancy Outcomes Maternal and Infant Study (PrOMIS), a cohort of pregnant women at the Instituto Nacional Materno Perinatal (INMP) in Lima, Peru. 2605 women aged 18 to 49 years (mean ± SD gestational age = 10.9 ± 3.3 weeks) were included in the study. Self-reported pre-pregnancy weight and height and measured weight and height were collected at the first prenatal study contact. We assessed the concordance between measured and self-reported BMI; and, the agreement among indicators of nutritional status obtained using measured and self-reported BMI.
On average, weight measured at the first prenatal study visit was 0.27 kg higher than self-reported pre-pregnancy weight (p < 0.05); and, measured height was 0.02 m lower than self-reported pre-pregnancy height (p < 0.001). Correspondingly, measured BMI was 0.71 kg/m2 higher than self-reported BMI (p < 0.001). Scatter and Bland-Altman plots indicated strong concordance between measured and self-reported BMI. The proportion of women in the normal BMI category tended to be higher when using self-reported BMI (59.6 %) than when using measured BMI (50.4 %). Conversely, the proportion of women in the overweight or obese BMI categories tended to be lower when using self-reported BMI (38.2 %) than when using measured BMI (47.7 %).
Self-reported pre-pregnancy BMI was strongly correlated with BMI measured at the first prenatal study contact. The findings potentially suggest that, in this context, there is minimal change between pre-pregnancy BMI and BMI measured at the first prenatal study contact; or, that women in this study just recalled their most recent measured anthropometrics (including values obtained during the index pregnancy but before enrollment in the PrOMIS study).
KeywordsSelf-reported pre-pregnancy weight, height and BMI Weight, height, and BMI measured early during pregnancy Concordance Peru South America Low- and middle–income country
While there is no global consensus on gestational weight gain (GWG) recommendations, many countries base their GWG guidelines or policies on women’s pre-pregnancy nutritional status . For instance, the 1990 and the 2009 Institute of Medicine (IOM) GWG recommendations in the US are based on women’s pre-pregnancy body mass index (BMI: calculated as weight in kg divided by the square of height in meters) category [2, 3]. To highlight, women entering pregnancy with normal BMI (i.e. 18.5–24.9 kg/m2 according to the World Health Organization classifications) are recommended to gain, on average, 0.5 kg per week during the second and third trimesters. There is evidence, for example, that approximately 40–60 % of US women gain weight in excess of the 2009 IOM recommendations while 15–20 % gain less than what is recommended [4–6]. Gaining weight within IOM recommendations of each BMI category prevents adverse maternal and neonatal outcomes associated with excessive or inadequate GWG. For pregnant women, excessive GWG has been associated with several adverse health outcomes including pre-eclampsia, caesarian delivery, gestational diabetes, and postpartum weight retention [7–12]. For neonates, excessive weight gain during pregnancy is associated with being born large for gestational age, low 5 min Apgar scores, seizures, and childhood obesity [4, 13, 14]. Inadequate GWG, on the other hand, has been linked to small for gestational age neonates and preterm birth [4, 10, 15].
To comply with IOM or other nationally approved GWG recommendations, it is recommended to use pre-pregnancy BMI obtained from weight and height measured at the most recent pre-conception visit . If available, measured pre-pregnancy anthropometrics (weight and height) would enable midwives and obstetricians diagnose women’s pre-pregnancy nutritional status (BMI). Measured maternal pre-pregnancy BMI, however, is difficult to obtain as a majority of pregnancies are not planned; and, even among women with planned pregnancies, the majority do not seek pre-conceptional care. In the US, for example, it has been reported that 50 % of all pregnancies are not planned . In low and middle income countries (LMICs), such as Peru, the proportions of women with unplanned pregnancies or who do not seek pre-conceptional care are unknown; and, could be more prevalent than the reported values for high income settings. As such, in most contexts, measured pre-pregnancy anthropometrics are rarely available for most women entering pregnancy. In their absence, clinicians and researchers can rely on self-reported pre-pregnancy anthropometrics or anthropometrics measured at the earliest prenatal contact to obtain a reliable estimate of pre-pregnancy BMI and to facilitate counseling on GWG [17, 18]. Indeed, use of self-reported weight and height for estimation of pre-pregnancy BMI [19, 20] or in other contexts [21, 22] is a common feature in nutritional assessment. Studies conducted mainly in high income countries have demonstrated the extent to which self-reported pre-pregnancy BMI compares to its proxies including imputed values of pre-pregnancy BMI  or BMI measured early during pregnancy [19, 20]. Limited data exist on the level of agreement between self-reported pre-pregnancy BMI and BMI measured at the earliest prenatal contact among women living in LMICs.
Therefore, using data collected among Peruvian pregnant women, we studied the concordance between BMI obtained from self-reported pre-pregnancy weight and height and BMI from measured at the earliest prenatal study contact (mean ± SD gestational age: 10.9 ± 3.3 weeks).
Data presented in this study were analyzed from the Pregnancy Outcomes, Maternal and Infant Study (PROMIS) cohort, an ongoing prospective study of pregnant women enrolled in prenatal clinics at the Instituto Nacional Materno Perinatal (INMP) in Lima, Peru. The INMP is the main referral hospital for maternal and perinatal care in Peru. Methodological details of the PrOMIS study cohort have been previously published [23, 24]. Briefly, women were eligible for inclusion in this study if they initiated prenatal care prior to 18 weeks of gestation. Between February 2012 and March 2014, 3162 women who had their first prenatal care visit at INMP met the 18 weeks of gestation eligibility criteria. Women were excluded from the study if they were younger than 18 years, did not speak Spanish or were more than 18 weeks of gestation.
Trained personnel used structured questionnaires to interview study participants in a private setting. Sociodemographic and lifestyle information, medical and reproductive history were collected. Participants’ age was categorized as follows: 18–19, 20–29, 30–34, 35 year or older. Other socio-demographic variables included: ethnicity (Mestizo vs. other); marital status (married or living with a partner vs. other); educational attainment (6 years or lower, 7–12 years, and greater than 12 years); employment status during pregnancy (employed vs. not employed); parity (nulliparous vs. multiparous); smoking status before this pregnancy (smoked vs. never smoked); and, smoking status in the index pregnancy (smoking vs. not smoking).
During interviews, participants were asked to report their pre-pregnancy body weight and height. At the first prenatal study visit, and after interviews were completed, trained research nurses measured participants’ anthropometrics (weight and height) as per standard anthropometric procedures . Briefly, body weight (in kg to the nearest 0.1 kg) was measured using a reliable digital weighing scale (Soehnle Solar Fir , Leifheit AG, Leifheitstrabe 1, 56377, Nassau/Germany) while participants were wearing light clothing and no shoes. Body height (in cm to the nearest 0.1 cm) was measured using portable Shorr-type wall mounted height board with a measuring slide and a heel plate. The position of the head was standardized by asking participants to stand straight without shoes and with the heels together. Height and weight were measured twice without delay between measurements and a third measurement was taken when the first two measurements differed by ≥0.5 kg or ≥1.0 cm.
Frequency distributions (counts and percentages) and measures of central tendency (mean, median, standard deviations) of sociodemographic and lifestyle characteristics of participants were examined first. Self-reported pre-pregnancy BMI and BMI from weight and height measured at the first prenatal study contact were calculated as weight (in kilograms) divided by height (in meters) squared. BMI was categorized based on the WHO guidelines in four categories (underweight: <18.5 kg/m2, normal: 18.5–24.9 kg/m2, overweight: 25.0–29.9 kg/m2, and obese >30 kg/m2). Histograms, normal quantile plots, skewness and kurtosis normality tests were used to assess the distributional properties of self-reported and measured height, weight and BMI. Measures of height, weight and BMI were considered to approximate a normal distribution if absolute values of skewness we less than one (<1) . As perfect normal distributions are expected to have kurtosis values of three (3) , we took kurtosis values between 3 and 5 to approximate normality. We used paired t tests to assess statistically significant differences between measured and self-reported values. Concordance between measured and self-reported prevalence of underweight, normal, overweight and obese nutritional categories was assessed using Cohen’s weighted kappa statistic . In addition, we used Scatter and Bland-Altman plots  to examine individual concordance between self-reported pre-pregnancy and measured BMI during the interview. The Y-axis of the Bland-Altman plots was based on differences between self-reported BMI and measured BMI. The X-axis was the mean of self-reported pre-pregnancy BMI and mean of measured BMI. Limits of agreement were calculated as the mean difference (MD) ± 1.96*standard deviations (SD). All analyses were performed using STATA software (version 14, StataCorp, College Station, TX, USA). The level of statistical significance was set at p < 0.05 and all tests were two sided.
Socio-demographic and lifestyle characteristics of participants in the PrOMIS cohort
Mean ± SDa or n (%)b
Gestational age at recruitment
10.9 ± 3.3 weeks
28.0 ± 6.2 years
129 (5.0 %)
1488 (57.1 %)
544 (20.9 %)
444 (17.0 %)
Mestizo (Mixed race ancestry)
1980 (76.1 %)
621 (23.9 %)
Married or living with partner
2095 (80.7 %)
500 (19.3 %)
1316 (50.7 %)
1282 (49.4 %)
Education level (years of education)
101 (3.9 %)
1394 (53.7 %)
1103 (42.4 %)
1200 (46.1 %)
1404 (53.9 %)
This pregnancy was planned
1097 (42.3 %)
1498 (57.7 %)
Smoked before this pregnancy
543 (20.9 %)
2055 (79.0 %)
Currently smoking in this pregnancy
101 (3.9 %)
2495 (96.1 %)
Mean difference comparisons between measured and self-reported anthropometrics for pregnant women in the PrOMIS cohort (N = 2605)
Mean difference (SD)
59.21 ± 10.05
58.94 ± 9.89
−0.27 ± 4.54*
1.53 ± 0.05
1.55 ± 0.06
+0.02 ± 0.03**
25.35 ± 3.97
24.65 ± 3.87
−0.71 ± 2.17**
Statistical agreement between measured and self-reported BMI (kg/m2) (N = 2605)
20 (41.7 %)
32 (2.4 %)
0 (0.0 %)
1 (0.3 %)
Overall observed agreement =74.5 %; Weighted kappa statistic = 0.73
27 (56.3 %)
1,175 (89.9 %)
343 (36.0 %)
10 (3.4 %)
1 (2.0 %)
99 (7.6 %)
553 (58.0 %)
101 (34.0 %)
0 (0.0 %)
1 (0.1 %)
57 (6.0 %)
185 (62.3 %
48 (100 %)
1307 (100 %)
953 (100 %)
297 (100 %)
Results from the present study indicate a high level of concordance between self-reported pre-pregnancy BMI and BMI measured at the first prenatal study contact (mean gestational age = 10.9 ± 3.3 weeks). Self-reported weight was significantly lower than measured weight; and, self-reported height was significantly higher than measured height. This resulted in significantly higher measured BMI than pre-pregnancy BMI obtained from self-report.
The observed mean difference between self-reported pre-pregnancy weight and measured weight (0.27 kg) was smaller when compared to similar values reported in studies among women living in high-income countries. For instance, among US women, Shin et al. using data from the National Health and Nutrition Examination Survey found that self-reported pre-pregnancy weight was 2.3 kg lower compared with weight measured in the first trimester of pregnancy . Similarly Holland and colleagues in their study of pregnant women receiving prenatal care at obstetric clinics in Massachusetts reported that self-reported pre-pregnancy weight was 1.8 kg lighter than weight measured at the first prenatal visit (mean gestational age =9.7 ± 2.1 weeks) . The observation of a small mean difference between self-reported pre-pregnancy and measured weight in the present study potentially suggests that women in this study were more truthful when recalling their most recent measured weight. It is possible that women recalled weight measured in the index pregnancy, in their homes or at the INMP clinic or at other clinics, but before enrollment into the present study. Women in this study may have weighed themselves in their homes and in the index pregnancy but prior to when we enrolled them. It is, however, unlikely that women in our study had reported to the INMP or other clinics in the index pregnancy at gestational ages that were earlier than the 10.9 ± 3.3 weeks of gestation (the gestational age at which women were enrolled into the present study). The observed differences between the self-reported pre-pregnancy and measured weights, therefore, may be due to other reasons. These include, for example, that women in this study experienced minimal weight gain following conception to the time of their first prenatal study visit and weight measurement. Physiological conditions of pregnancy such as nausea, vomiting and hyperemesis gravidarum might have acted separately or jointly to minimize weight gained prior to recruitment into the PrOMIS study cohort. There might also have been small inconsistencies in the recalled and actual measurements such as differences in the scales used, clothing, time of day and voiding status. As such women’s recalled pre-pregnancy weight was very close or similar to values measured at the first contact due to a combination of factors.
A large mean difference between self-reported and measured height (2 cm) was observed in this study. Limited studies have documented differences between self-reported and measured height among pregnant women living in higher income countries or LMICs. For example, Paez et al. studied 30 pregnant women participating in an intervention to prevent postpartum diabetes and reported a 0.56 cm higher? difference in self-reported and measured height during pregnancy . Studies involving non-pregnant women have also reported relatively lower mean differences between self-reported and measured height e.g. 0.70 cm among a healthy overweight working women in the Netherlands  or 0.30 cm among female general practice patients in Australia. It is possible that the large difference between measured and self-reported height observed this study is largely due to social desirability bias i.e. women preferring to mention that they are taller than they are actually are or due to other unknown factors that need to be examined in future studies e.g. through formative studies.
We did not have measured pre-pregnancy weight and height; and, this study does not fully address the question of how reliable or valid pre-pregnancy BMI is compared to measured pre-pregnancy BMI. Behavioral and economic reasons hinder access to pre-conceptional care upon which pre-pregnancy BMI can be measured . We observed small differences between self-reported pre-pregnancy BMI and BMI obtained at the first prenatal visit in this study; and, assuming minimal weight gain during the early pregnancy period, it is reasonable to recommend use of self-reported pre-pregnancy BMI or BMI obtained from values measured early during pregnancy as proxies for measured pre-pregnancy BMI. Using either or both of these BMI proxies would be particularly helpful for providing appropriate weight gain counseling during the perinatal period.
Our study has several strengths. This study used a large sample size and is the first study to examine differences in self-reported pre-pregnancy BMI and BMI obtained early during pregnancy among women living in a non-high income country. However, there are some limitations to our findings. Most women in this study (95.1 %) had seven or more years of education. Our results may not be generalizable in LMICs contexts where education levels among pregnant women in antenatal care may be lower. Also, were not able to establish true reliability and validity of self-reported pre-pregnancy BMI as we did not have measured pre-pregnancy weight or height. Lastly, a substantial proportion of pregnant women in this study (17.6 %) did not provide any self-reported pre-pregnancy weight or height possibly indicating that they did not know these measures. Investigators planning to use self-reported pre-pregnancy weight or height among Peruvian pregnant women or women living in other similar contexts need to be aware that a substantial proportion of their study participants may not know such measures. Inability to recall pre-pregnancy anthropometrics probably lends further support to using weight and height measured early during the pregnancy to calculate early pregnancy BMI as a proxy for pre-pregnancy nutritional status.
The BMI obtained using self-reported pre-pregnancy weight and height strongly correlated with BMI obtained using anthropometrics measured at the first prenatal study contact. This potentially suggests that, in this context, there is minimal change between pre-pregnancy weight and similar anthropometrics measured early during pregnancy; or, that women in this study just recalled their most recently measured height and weight (including values obtained during the index pregnancy but before the first prenatal study visit). In this or similar contexts, we recommend use of weight and height measured early during pregnancy; and, then calculating the early pregnancy BMI as a proxy for pre-pregnancy BMI.
The authors wish to thank the dedicated staff of Asociacion Civil Proyectos en Salud (PROESA), Peru and Instituto Nacional Materno Perinatal, Peru (INMP), for their expert technical assistance with this research.
This research was supported by an award from the National Institutes of Health (NIH; R01-HD-059835). The NIH had no direct role in the design, implementation and reporting of results from this study.
Availability of data
This study is part of an ongoing cohort study and, thus, data for this project will not be shared.
MAW conceived, designed and obtained funding for the study. BKN, BG and MAW analyzed the data and drafted the manuscript. All authors, BKN, SES, BG, and MAW, interpreted the data, critically revised the draft for important intellectual content, and subsequently read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by Institutional Review Boards (IRBs) of the Instituto Nacional Materno Perinatal (INMP) and the Human Research Administration Office at the Harvard T.H. Chan School of Public Health. All study participants provided written informed consent prior to being interviewed.
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.
- Scott C, Andersen CT, Valdez N, Mardones F, Nohr EA, Poston L, et al. No global consensus: a cross-sectional survey of maternal weight policies. BMC Pregnancy Childbirth. 2014;14:167.View ArticlePubMedPubMed CentralGoogle Scholar
- IOM. Nutrition during pregnancy: weight gain, nutrient supplements. Washington, DC: National Academies Press; 1990.Google Scholar
- IOM. Nutrition during pregnancy: reexamining the guidelines. Washington, DC: National Academy Press. 2009.Google Scholar
- Stotland NE, Cheng YW, Hopkins LM, Caughey AB. Gestational weight gain and adverse neonatal outcome among term infants. Obstet Gynecol. 2006;108:635–43.View ArticlePubMedGoogle Scholar
- Gould Rothberg BE, Magriples U, Kershaw TS, Rising SS, Ickovics JR. Gestational weight gain and subsequent postpartum weight loss among young, low-income, ethnic minority women. Am J Obstet Gynecol. 2011;204:52.e1–11.View ArticleGoogle Scholar
- Moore Simas TA, Doyle Curiale DK, Hardy J, Jackson S, Zhang Y, Liao X. Efforts needed to provide Institute of Medicine-recommended guidelines for gestational weight gain. Obstet Gynecol. 2010;115:777–83.View ArticlePubMedGoogle Scholar
- Kiel DW, Dodson EA, Artal R, Boehmer TK, Leet TL. Gestational weight gain and pregnancy outcomes in obese women: how much is enough? Obstet Gynecol. 2007;110:752–8.View ArticlePubMedGoogle Scholar
- Gunderson EP, Abrams B, Selvin S. The relative importance of gestational gain and maternal characteristics associated with the risk of becoming overweight after pregnancy. Int J Obes Relat Metab Disord. 2000;24:1660–8.View ArticlePubMedGoogle Scholar
- Siega-Riz AM, Viswanathan M, Moos M-K, Deierlein A, Mumford S, Knaack J, et al. A systematic review of outcomes of maternal weight gain according to the Institute of Medicine recommendations: birthweight, fetal growth, and postpartum weight retention. Am J Obstet Gynecol. 2009;201:339.e1–14.View ArticleGoogle Scholar
- DeVader SR, Neeley HL, Myles TD, Leet TL. Evaluation of gestational weight gain guidelines for women with normal prepregnancy body mass index. Obstet Gynecol. 2007;110:745–51.View ArticlePubMedGoogle Scholar
- Kabiru W, Raynor BD. Obstetric outcomes associated with increase in BMI category during pregnancy. Am J Obstet Gynecol. 2004;191:928–32.View ArticlePubMedGoogle Scholar
- Stotland NE, Hopkins LM, Caughey AB. Gestational weight gain, macrosomia, and risk of cesarean birth in nondiabetic nulliparas. Obstet Gynecol. 2004;104:671–7.View ArticlePubMedGoogle Scholar
- Wrotniak BH, Shults J, Butts S, Stettler N. Gestational weight gain and risk of overweight in the offspring at age 7 y in a multicenter, multiethnic cohort study. Am J Clin Nutr. 2008;87:1818–24.PubMedGoogle Scholar
- Oken E, Taveras EM, Kleinman KP, Rich-Edwards JW, Gillman MW. Gestational weight gain and child adiposity at age 3 years. Am J Obstet Gynecol. 2007;196:322.e1–8.View ArticleGoogle Scholar
- Vesco KK, Sharma AJ, Dietz PM, Rizzo JH, Callaghan WM, England L, et al. Newborn size among obese women with weight gain outside the 2009 Institute of Medicine recommendation. Obstet Gynecol. 2011;117:812–8.View ArticlePubMedGoogle Scholar
- Finer LB, Henshaw SK. Disparities in rates of unintended pregnancy in the United States, 1994 and 2001. Perspect Sex Reprod Health. 2006;38:90–6.View ArticlePubMedGoogle Scholar
- Amorim AA, Linne Y, Kac G, Laurenco MP. Assessment of weight changes during and after pregnancy: practical approaches. Matern Child Nutr. 2008;4:1–13.View ArticlePubMedGoogle Scholar
- Harris HE, Ellison GT. Practical approaches for estimating prepregnant body weight. J Nurse Midwifery. 1998;43:97–101.View ArticlePubMedGoogle Scholar
- Shin D, Chung H, Weatherspoon L, Song WO. Validity of prepregnancy weight status estimated from self-reported height and weight. Matern Child Health J. 2013;18:1667–74.View ArticleGoogle Scholar
- Holland E, Moore Simas TA, Doyle Curiale DK, Liao X, Waring ME. Self-reported pre-pregnancy weight versus weight measured at first prenatal visit: effects on categorization of pre-pregnancy body mass index. Matern Child Health J. 2013;17:1872–8.View ArticlePubMedGoogle Scholar
- Paez KA, Griffey SJ, Thompson J, Gillman MW. Validation of self-reported weights and heights in the avoiding diabetes after pregnancy trial (ADAPT). BMC Med Res Methodol. 2014;14:1–8.View ArticleGoogle Scholar
- Dekkers JC, van Wier MF, Hendriksen IJ, Twisk JW, van Mechelen W. Accuracy of self-reported body weight, height and waist circumference in a Dutch overweight working population. BMC Med Res Methodol. 2008;8:69.View ArticlePubMedPubMed CentralGoogle Scholar
- Barrios YV, Gelaye B, Zhong Q, Nicolaidis C, Rondon MB, Garcia PJ, et al. Association of childhood physical and sexual abuse with intimate partner violence, poor general health and depressive symptoms among pregnant women. PLoS One. 2015;10:e0116609.View ArticlePubMedPubMed CentralGoogle Scholar
- Gelaye B, Kajeepeta S, Zhong Q-Y, Borba CPC, Rondon MB, Sanchez SE, et al. Childhood abuse is associated with stress-related sleep disturbance and poor sleep quality in pregnancy. Sleep Med. 2015;16:1274–80.View ArticlePubMedPubMed CentralGoogle Scholar
- Cogill B. Anthropometric indicators measurement guide, 2003. Washington, DC: Food and Nutrition Technical Assistance Project; 2003.Google Scholar
- Bulmer MG. Principles of Statistics. New York, NY,: Dover Publications, Inc.; 1979.Google Scholar
- Cohen J. Weighted kappa: nominal scale agreement provision for scaled disagreement or partial credit. Psychol Bull. 1968;70:213–20.View ArticlePubMedGoogle Scholar
- Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986;1:307–10.View ArticlePubMedGoogle Scholar
- Atrash HK, Johnson K, Adams M, Cordero JF, Howse J. Preconception care for improving perinatal outcomes: the time to act. Matern Child Health J. 2006;10:S3–11.View ArticlePubMedGoogle Scholar