Journal of Pregnancy
Volume 2018 (2018), Article ID 1982134, 5 pages
https://doi.org/10.1155/2018/1982134

Research Article

Maternal Anthropometric Measurements Do Not Have Effect on Birth Weight of Term, Single, and Live Births in Addis Ababa City, Ethiopia

Chalachew Bekele Shiferaw,¹ Walelegn Worku Yallew,² and Gizachew Tadele Tiruneh³

¹St. Paul Hospital Millennium Medical College, Addis Ababa, Ethiopia
²University of Gondar College of Medicine and Health Sciences, Institute of Public Health, Gondar, Ethiopia
³JSI Research and Training Institute Inc./L10K Project, Addis Ababa, Ethiopia

Correspondence should be addressed to Chalachew Bekele Shiferaw; ch.bekele12@yahoo.com

Received 3 July 2018; Revised 14 October 2018; Accepted 18 November 2018; Published 2 December 2018

Academic Editor: Marco Scioscia

Copyright © 2018 Chalachew Bekele Shiferaw et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Low birth weight is a global public health problem for mortality and morbidity in any age group. The objective of this study is to investigate the effect of maternal anthropometric measurements on birth weight. A cross-sectional study was conducted from Nov 25, 2012, to Feb 25, 2013, in maternity public hospitals in Addis Ababa city, Ethiopia. The effect is investigated using correlation, linear regression, independent sample T-test, one-way ANOVA, and finally multivariate linear regression analysis. A total of 605 women and their newborns took part in this study and prevalence of low birth weight is 8.3%. On adjusted multivariate linear regression analysis, maternal anthropometric measurements did not have an effect on birth weight. Since maternal mid-upper arm circumference ≤ 20 cm and body mass index ≤18.5kg/m² are almost nil in this study, generalization is difficult to general population where undernourished women are common in the rural Ethiopia and similar study is recommended in those areas. Antenatal care visits, gestational age, and female sex of newborn had statistically significant effect in determining the risk of low birth weight. Women who were living with large family members had a heavier newborn than counterparts. This might be due to the fact that pregnant women have better care and social support in Ethiopian context, so advising pregnant women to live with family members should be considered to enhance social support during pregnancy in Ethiopia. Maternal anthropometric measurements have no significant effect in determining birth weight in the city and we recommend similar studies where undernourished women are common.

1. Introduction

Low birth weight (LBW) is a weight at birth less than 2,500 grams irrespective of gestational age. A baby’s low weight at birth is either the result of preterm birth (i.e., before 37 weeks of gestation) or the result of restricted fetal (intrauterine) growth [1]. This condition is a worldwide problem, especially where starchy tubers and cereals form the staple food. Africans’ major nutritional problem is protein-energy malnutrition; as a result of this, there is a higher percentage of women with low weight, height, and mid-upper arm circumference (MUAC) in the region [2].

Globally, more than 20 million (15%) infants are born with LBW and it is concentrated in two regions of the developing world: Asia and Africa. Seventy-two percent of LBW infants in developing countries are born in Asia and 22% in Africa, of which 13% to 15% found in Sub-Saharan Africa with little variation across the region as a whole [1]. In Ethiopia, the incidence of LBW has significant variation across the area of residence, 17% in rural and 9% of the urban area [3]. Studies in other areas of the country like in Gondar referral teaching hospital and rural population of Kersa also reported 17% and 28% prevalence, respectively [4, 5]. A similar study from Sri Lanka showed that 8.7% of 563 births had LBW [6].

The causes of LBW are multifactorial including complication during pregnancy, genetic, environmental, social-cultural, demographic, and nutritional variables [7, 8]. Women who previously had a child, are educated, and had higher wealth were less likely to deliver a low birth weight baby [9, 10]. Newborns of women who gained more than 24 kg during pregnancy were 148.9g heavier at birth compared to infants of women who gained 8–10 kg and the odds ratio of giving birth to an infant greater than 4000 gram was 2.26 [11]. Overweight and obese women had similar risks of LBW like normal-weight mothers (BMI 18.5-25 kg/m²) [12]. The risk of preterm birth appeared significantly higher in overweight and obese women [13]. Wealth status, MUAC, and antenatal care (ANC) were determinants for low birth weight in Kersa, Ethiopia [5]. Prenatal physical activity, depressive symptoms, and social class did not significantly predict offspring weight outcomes [9, 14] whereas in another study depressive and anxiety symptoms were significantly associated with LBW [15].

LBW is closely associated with fetal and neonatal mortality and morbidity, inhibited growth, and cognitive development. It is also a risk factor for chronic diseases later in life like adult-onset diabetes, coronary heart disease, high blood pressure, and intellectual, physical, and sensory disabilities [16].

Anthropometry provides a simple, reliable, and low-cost method of assessing nutritional status by measuring maternal physical structure which can be universally applied at primary care level. Identification of the effect of those anthropometric parameters on birth weight is important in order to determine the level of care and priorities for a referral to centers where reasonable neonatal care is available. As such, the objective of this study is to investigate this to provide evidence-based information that can be used in the future to reduce birth weight-related complications.

2. Methods

A cross-sectional study was conducted, in maternity public hospitals of Addis Ababa city, Ethiopia, and we used simple cluster sampling method. First the study participants were divided into four clusters: Tirunesh Beijing, Yekatit-12, Gahandi Memorial, and Zewditu Maternity Hospitals in the city. Yekatit-12 and Gahandi Memorial Maternity Hospitals were selected randomly and then consecutive sampling technique (including all eligible participants) was employed till the calculated sample was achieved in the three-month data collection. Hospitals average monthly client load was 100 and 175 deliveries/month for Yekatit-12 and Gahandi Memorial Hospitals, respectively. Based on this, samples were proportionally allocated 149 for Yekatit-12 Hospital and 456 for Gahandi Memorial Hospital and we finished data collection within three months.

The sample size of 605 was calculated using Open Epi, Version 2, and single proportion formula n= Z(α/2)2 P(1-P) /d2 assuming a 17.1% proportion of LBW from previous study in Gondar Teaching Hospital, Ethiopia, at a 95% confidence level and 3% margin of error.

The weight of the newborn, maternal height, mid-upper arm circumference (MUAC), and maternal age were exclusively taken during data collection by the study team. Weight gain during pregnancy, gestational age, date of birth, and history of diabetes mellitus during pregnancy were taken from medical record. Some women did not have antenatal care follow-up and some medical records were not filled correctly; in these cases data was taken by interviewing women by trained midwives within 72 hours of birth. Birth weight was taken using baby weight scales after checking the scale with known weight control. Adult MUAC measuring tape was used to measure maternal MUAC. The height of women was measured on barefoot in centimeter using standard height measuring board and recorded to the nearest 1 cm. Gestational age was taken in weeks starting from last menstrual period (LMP). In cases when women did not know their LMP, health provider’s decision on medical records was taken.

The objective of the study was just to see the effect of maternal anthropometrics measurement on birth weight and we tried to see the effect independent of potential factors that affect birth weight. Therefore, maternal diabetes, preterm, postterm, and unknown gestational age were exclusion criteria to reduce potential confounders and stillbirths also were excluded since we could not find outcome variable birth weight for still births.

Data were entered, cleaned, and edited using Epi Info version 3.5.1 and then exported to SPSS version 15 for further analysis. After checking for the fulfillment of the assumptions needed to make inferences about the correlation coefficient, bivariate analysis was done using correlation, independent sample T-test, one-way ANOVA, and simple linear regression. Pearson correlation coefficient (r), unadjusted coefficient B, mean difference, and p-values less than 0.05 were used to fit into the multivariate linear regression model. All independent variables which had the association in bivariate analysis with the p-value of less than 0.05 were included in multiple leaner regression model to determine the independent predictors of birth weight. The variables with p<0.05 in multivariate linear regression analysis were considered as significant predictors of birth weight.

The study was approved by the ethical review board of University of Gondar (UOG), Addis Continental Institute of Public Health (ACIPH) and City Government of Addis Ababa Health Bureau. All eligible study subjects were verbally invited and informed about the expected outcomes, benefits, and risks to take part in this study. They were informed of their right to refuse participating in the research and withdraw at any time they wished to, without losing any of their rights as a client of the hospital.

3. Results

3.1. Maternal Demographics, Antenatal Care, and Prepregnancy Characteristics

Maternal gravidity, gestational age, and anthropometrics characteristics are shown in Table 1. The mean age of respondents was 26 ± 5 years. Regarding marital status, 94% (567) were married and 6% (38) were single. About 14% (81) of the respondents were illiterate, 38% (221) attended formal elementary education (1-8 years), and 48% (281) attended secondary and above. Out of 605 newborn babies, 320 (53%) were males and 281 (47%) were females.

Table 1: Maternal age, gravidity, gestational age, and anthropometric characteristics of women at public hospitals in Addis Ababa city, Ethiopia, Nov 25, 2012 to Feb 25, 2013.

Characteristics
N ()

Age of mother in years (n=601)

    ≤ 20
77 (12.81%)

    21-30
425 (70.70%)

    31 – 40
98(16.30%)

    ≥ 41
01(00.16%)

Religion (n=600)

    Orthodox
431(71.83%)

    Muslim
115(19.16%)

    Protestant
54(09.00%)

Gravidity of women (n=603)

    gravid 1
257(42.62%)

    gravid 2
175(29.02%)

    gravid 3
93(15.42%)

    gravid 4
39(06.47%)

    gravid 5
19(02.65%)

    gravid ≥6
20(3.31.6%)

Gestational age in weeks (n=605)

    37 weeks
26(4.30.5%)

    38 weeks
130(21.49%)

    39 weeks
116(19.17%)

    40 weeks
133(21.98%)

    41 weeks
116(19.17%)

    42 weeks
84(13.88%)

Mean maternal anthropometric parameters
Mean (±SD)

    Maternal height (cm)
156± 06

    Pre-pregnancy weight (gm.)
54835 ± 8861

    Term weight (gm.)
63765±9205

    Pregnancy weight gain (gm.)
9150±5746

    Term BMI (kg/m2)
26±03

    Pre-pregnancy BMI (kg/m2)
22±03

    MUAC (cm)
26±03

3.2. Newly Born Characteristics

From a total of 603 newborns, 320 (53%) were males and 281 (47%) were females. The mean weight of the newborn is 3085gm and the prevalence of low birth weight is 8.3%. Independent samples T-test was done to see the association of newborn sex with birth weight. The analysis showed that the mean difference in birth weight between male and female was 91gm (Male > female).

3.3. Determinants of LBW

3.3.1. Bivariate Analysis

In the first binary linear regression and correlation model maternal variable parameters, gravidity, gestational age, number of ANC, household family size, and maternal age were significantly associated with birth weight (Table 2).

Table 2: Bivariate linear regression analysis between maternal age, anthropometry, family size, number of ANC, gravidity, gestational age, and income with birth weight.

Independent variables
Coefficients

B
Std. error
t
Sig.

MUAC
27.323
6.301
4.337
< 0.001

Height
14.071
3.184
4.419
< 0.001

Pre-pregnancy weight
.013
.002
5.128
< 0.001

Term weight
.014
.002
6.025
<0.001

Pregnancy weight gain
.010
.004
2.452
0.015

Term BMI
28.308
6.354
4.455
< 0.001

Pre-pregnancy BMI
20.290
6.489
3.127
.002

Gravidity of mother
44.494
15.359
2.897
.004

Gestational age in weeks
55.265
13.822
3.998
< 0.001

Number of ANC visits
26.719
7.912
3.377
.001

Household family size women belonged
58.635
14.308
4.098
< 0.001

Maternal age in years
17.909
4.201
4.263
< 0.001

3.3.2. Multivariate Analysis

Adjusted multivariate linear regression analysis is done for independent variables (maternal anthropometric parameters, maternal age, gestational age, gravidity of women, antenatal care visit, household family size, and sex of the newborn) which have significant association on bivariate analysis (Table 3).

Table 3: Multivariate linear regression showing the association between dependent variables and dependent variable.

Model
Unstandardized Coefficients
t
Sig
95% Confidence Interval for B

Independent variables
B
Std. Error
Lower bound
Upper bound

Constant
-2316.99
1933.22
-1.19
.231
-6116.73
1482.74

MUAC of women
-8.95
10.48
-.85
.394
-29.56
11.66

Pre-pregnancy weight
.000
.008
-.06
.950
-.016
.015

Height of women
12.13
11.50
1.05
.292
-10.47
34.73

Term weight of women
.001
.013
.08
.936
-.02
.027

Term BMI of women
39.75
32.28
1.23
.219
-23.69
103.20

Pre-pregnancy BMI of women
-9.85
20.07
-.49
.624
-49.30
29.59

Sex of the newborn
-128.84
44.32
-2.90
.004
-215.95
-41.73

Gravidity of women
-16.92
23.77
-.71
.477
-63.65
29.80

Gestational age in weeks
64.09
15.50
4.13
<0.001
33.62
94.55

Number of ANC visits
22.86
9.20
2.48
.013
4.77
40.94

HH family size
59.07
18.77
3.14
.002
22.18
95.96

Maternal age
9.05
5.60
1.61
.107
-1.96
20.07

4. Discussion

Maternal anthropometric characteristics (height, BMI, MUAC, prepregnancy, and term weight) had no significant effect to determine the risk of low birth weight. In India, short mothers had 2.74- and 9.0-fold greater risk of delivering LBW baby than average and tall mothers, respectively [7]. In Sudanese women also a maternal height of < 156 centimetres had a statistically significant effect on determining the risk of LBW, but BMI had no significant effect [17]. Overweight and obese women had similar risks of LBW like normal-weight mothers [12]. In the rural population of Kersa, Ethiopia MUAC is determinant for low birth weight [5]. The possible reason for this difference might be due to lower undernutrition state of women in this study (BMI≤ 20 kg/m² and MUAC ≤ 20 cm were 0.7% and 1%, respectively) and it might be higher in rural population.

Lower family size of women belonged has a significant risk of LBW. Even though the mechanism of action is not clear, this might be due to the following reasons: First, when women have a higher family size they could have a higher number of previous pregnancies and older age than their counterparts. Being older and multiparous may determine the birth weight; because women who previously have a child were less likely to deliver a low birth weight (LBW) baby [9, 10] and young maternal age showed a significant risk of low birth weight [8], but both maternal age and parity/gravidity have no effect on birth weight in this study. Second, pregnant women who are alone or with some family member might have depression and anxiety symptoms more than pregnant women who are living in large family, because depressive and anxiety symptoms were associated with low birth weight [15]. Third, social support is widely believed to affect health and feeding practice. Biological fathers and parents coresidence with pregnant mothers had been determinant factors for birth weight in rural South Africa women [18].

Low weight at birth is either the result of preterm birth or the result of restricted fetal (intrauterine) growth [1]. This study is conducted in term birth and the gestational age differences significantly affected birth weight in multivariate linear regression. Antenatal care is determinant for low birth weight [5]. This is because women, who attended antennal care, get the education about feeding, treatment for their illness, supplements, and vaccination. Similarly, in this study lower number of antenatal care visits is an independent determinant factor for LBW.

5. Conclusions and Recommendation

Maternal anthropometric measurements have no significant effect in determining birth weight in the city. Since maternal MUAC less than 20 cm and BMI less than 18.5kg/m2 were almost nil in this study, generalization is difficult to sites where undernourished women are common, so we recommended similar study in such areas.

Data Availability

The data used to support the findings of this study are included within the article.

Disclosure

The research did not receive specific funding, but it was performed as part of the education of the corresponding authors, in University of Gondar.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

We acknowledge the kind help and encouragement we received from the Addis Continental Institute of Public Health (ACIPH), University of Gondar (UOG), Addis Ababa City Public Hospitals. Our deepest gratitude goes to the women who participated in this study and to all data collectors and supervisors for their dedicated work.

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