Abstract
Background
Low birth weight (LBW) continues to be the primary cause of infant morbidity and mortality.
Objective
This study was undertaken to identify the predictors of LBW in Nigeria.
Design
The data for this study was extracted from the 2013 Nigeria Demographic and Health Survey conducted by the National Population Commission. Several questionnaires were used in the survey, some covering questions on pregnancy characteristics. The inclusion criteria include mothers who gave birth to a child 5 years before the interview and aged 15–49 years who were either permanent residents or visitors present in the household on the night before the survey conducted. The birth weight of the infants was recorded from written records from the hospital cards or the mothers’ recall.
Results
The prevalence of LBW in this study was 7.3%. Multiple logistic regression analysis showed an adjusted significant odds ratio for mothers from North West region (aOR 10.67; 95% CI [5.83–19.5]), twin pregnancy (aOR 5.11; 95% CI [3.11–8.39]), primiparous mother (aOR 2.08; 95% CI [1.15–3.77]), maternal weight of less than 70 kg (aOR 1.92; 95% CI [1.32–2.78]), and manual paternal employment (aOR 1.91; 95% CI [1.08–3.37]).
Conclusions
The risk factors for LBW identified in this study are modifiable. In order to reduce this menace in Nigeria, holistic approaches such as health education, maternal nutrition, improvement in socio-economic indices, and increasing the quality and quantity of the antenatal care services are of paramount importance.
Keywords: low birth weight, Nigeria, risk factors, maternal and child health
Introduction
Birth weight is one of the significant predictors of child mental development, future physical growth, and survival. It is one of the important risk factors for child morbidity and mortality (1–4). According to the World Health Organization (WHO), low birth weight (LBW) is defined as an infant birth weight of less than 2,500 g (5). This group of children is considered to have higher risk of neonatal, post-neonatal death, and morbidity (6). Infant with LBW is associated with early and late morbid conditions such as impaired cognitive function (7), psychological disorders (8), and coronary heart disease (9). The factors for LBW are yet to be completely understood even though abundant research has been conducted to ascertain the underlying factors. Although LBW is considered as a multifactorial disease, most of the risk factors are preventable before pregnancy.
There is significant difference in the incidence of LBW between developed and developing countries and between various regions in a country. In developed countries, the occurrence is 7%, while in developing countries it is 15% (10). Globally, recent estimates suggest that there were 18 million of LBW babies born every year (11). In sub-Saharan Africa, the prevalence of LBW varies according to the regions. The prevalence of LBW in Ethiopia was 28.3% (12) while there were 199 LBW infants per 1,000 live births in Zimbabwe (13). In Nigeria, LBW affects about 5–6 million children every year (14). The incidence was 12.1% in Jos (15), 11.4% in Ogun (16), and 16.9% in Maiduguri (17). A number of factors need to be investigated in order to lessen the prevalence of LBW in Nigeria.
There are numerous maternal and fetal factors contributing to the LBW incident (18). LBW is strongly associated with maternal factors such as younger and older age, low socio-economic status, residence in the rural area, and illiteracy (11, 19–22). Mothers aged under 17 and over 35 years are at risk of delivering LBW babies (23). Mothers in deprived socio-economic conditions frequently have LBW infants (12). There is ample evidence to show that maternal factors and risk behaviors during antenatal period play significant roles in the birth weight of babies (24, 25). Pregnant mothers with unhealthy lifestyles that include activities such as smoking were found to be at high risk of delivering LBW babies (26). A previous study also had showed that drugs taken during pregnancy, such as malaria prophylaxis, were associated with the incidence of LBW (17). Other risk factors linked with LBW include maternal height (27), body mass index (BMI) (28), weight (29), parity (26), birth interval (30), multiple gestation, the experience of any physical violence (12), and the lack of skilled antenatal care (31). Paternal factors such as level of education (11), age (30), and employment (31) were also significantly linked to the incidence of LBW.
Antenatal care (ANC) visits are important for maternal and fetus health. ANC refers to pregnancy-related healthcare services provided by skilled health personnel during pregnancy that monitor the well-being of both the mother and the unborn child. It is essential to the purposes of obtaining the best possible outcome and preventing any complications (32). The frequency of ANC visits and parity are significantly associated with birth outcomes such as birth weight (17, 33). Pregnant mothers who attended less than four ANC visits double their risk of delivering LBW babies compared to those visiting four or more times (34, 35). Also, studies found that the prevalence of LBW was high, up to 57% (36) and 61.8% (37), among mothers who did not receive any ANC. Due to the irregularity of ANC visits, pregnant mothers do not comply with the advice or medications recommended by healthcare providers and subsequently will increase the incidence of LBW (38). The quality of each ANC visit also should be emphasized in order to have an effective coverage of care.
LBW is one of the most important public health concerns worldwide and is still the leading cause of prenatal and neonatal deaths. Despite intense research conducted on LBW globally, the factors affecting LBW in Nigeria have not been adequately investigated. Identifying the predictors of LBW and addressing the best prevention strategies will help to avert early the childhood morbidity and mortality resulting from LBW. Therefore, this study was aimed at 1) determining the prevalence of LBW infants in Nigeria, 2) describing the socio-demographic and pregnancy characteristics of mothers who gave birth to LBW babies, and 3) exploring the predictors of LBW in Nigeria using the 2013 Nigeria Demographic and Health Survey (2013 NDHS).
Methods
This manuscript had been developed by utilizing the 2013 NDHS data obtained from the Ministry of Health, Nigeria. NDHS was a cross-sectional survey with a stratified three-stage cluster design. It is the fifth in the series of national surveys implemented by the National Population Commission (NPC). This nationally representative survey covered all 36 states and the Federal Capital Territory in Nigeria. This survey was intended to provide the latest estimates on population and health in Nigeria. The list of enumerated areas prepared for the 2006 Population Census of the Federal Republic of Nigeria was used as to frame the samples. The selection of samples was based on stratified three-stage cluster design which consists of 372 clusters in urban areas and 532 clusters in rural areas, giving a total of 904 clusters. A total of 40,320 households were selected. The inclusion criteria for this study were mothers, aged 15–49 years, who gave birth to a child 5 years before the interview and were either permanent residents or current visitors in the household on the night before the survey conducted. Data collection was carried out between February and May 2013.
A structured questionnaire was used for interviewing the mothers. The questionnaire captured information about the pregnancies such as maternal age, birth interval, parity, time of registration, and frequency of ANC visits from mothers. Socio-demographic details of the mothers such as highest educational attainment, wealth index, localities, and literacy levels were also obtained. Infant characteristics such as sex and mode of delivery were recorded. The questionnaire was translated into different Nigerian languages: Hausa, Igbo, and Yoruba. All questionnaires were pretested among 120 households in November 2012. The questionnaires were modified according to the country's requirement with the advice from health experts.
Prior to the commencement of the study, a complete listing of households was obtained and a mapping exercise was conducted for each cluster from December 2012 until January 2013. Training on how to use the Global Positioning System (GPS) receivers to locate the coordinates of sample households was conducted for the enumerators. All participants were briefed on the objectives, procedures, expected outcomes, benefits, and risk associated with this study. An informed consent was obtained from the mothers prior to the interview. Ethical clearance to conduct NDHS was approved by the National Health Research Ethics Committee of Nigeria, Federal Ministry of Health, Abuja, Nigeria. NDHS data are public access data and were made available to us upon request.
Birth weights of the infants were recorded based on the written records of the hospital cards or mothers’ recall. Birth weights less than 2,500 g were classified as LBW (5). Independent variables studied in this survey were selected based on previous literature reviews on LBW (32, 39–41). Age was recorded as continuous variable and then recoded into categories. Education was recorded as 1) no education, 2) primary, and 3) secondary or higher education. Occupation was categorized as 1) unemployed and 2) employed. Household wealth index was divided into quintiles according to the wealth score, 1) poorest, 2) poor, 3) average, 4) rich, and 5) richest. However, due to similarities between some quintiles, the wealth index has been re-categorized into 1) poor, 2) middle, and 3) rich (42). The heights and weights of the mothers were also measured. Measurements were done using lightweight SECA scales (with digital screens). The measuring boards used in this study were designed by Shorr Productions for use in the survey settings. Maternal height less than 1.45 m (32) and weight 70 kg (40) were chosen as cut off for this study.
Birth order was recorded as continuous variable and then recoded as 1) first and 2) second or more. Information on the number of children ever born or parity was obtained. The period of time between two successive live births or birth interval was recorded. Place of birth was dichotomized into 1) delivery at health facility and 2) delivery at home. The frequency of ANC visits was grouped into 1) less than 4 visit and 2) ≥4 visits. The proportion of pregnant mothers who received four or more ANC visits has been used as a benchmark for adequate ANC (43). In addition, pregnant mothers were asked about the timing of their first ANC visit and were classified as 1) early ANC registration (within the first trimester) and 2) late ANC registration (after the first trimester). The percentage of pregnant mothers who took malaria prophylaxis and intestinal parasite drugs during pregnancy was recorded. According to Kayode et al. (39), pregnancies were classified as 1) wanted then, 2) wanted no more, and 3) wanted later. Mothers also were asked whether they had ever experienced physical violence during pregnancy.
The Statistical Package for the Social Sciences (SPSS) version 20 with a complex samples procedure was used for the analysis. Frequency and percentages with 95% confidence interval were used to describe the characteristics of the LBW babies. The chi-square analysis procedure in the complex samples add-on module in SPSS was used to test the associations between socio-demographic and pregnancy characteristics with birth weight of the babies. P-value < 0.05 indicates significant association. The multivariate logistic regression procedure was used to determine the predictors of LBW babies in Nigeria. Significant predictors were identified based on 95% CI. All variables were tested in a simple model using logistic regression to obtain the unadjusted logistic regression. All factors for LBW were included in the model. The variables were entered using manual stepwise method. All significant variables reaching p<0.05 were retained in the model.
Results
There were 5,189 babies who were weighed after delivery during the 5 years preceding the survey. The proportion of LBW in this study was 7.3%. Among LBW babies, 39.5% were from written records from the hospital cards.
The results for the socio-demographic characteristics of mothers who delivered LBW babies are presented in Table 1. LBW is significantly higher among children whose mothers were aged 15–24 years (11.5%) and mothers without formal education (14.9%). About 10% of the unemployed and non-married mothers gave birth to LBW babies. The birth weights of infants varied by geopolitical zone. The North West region had the highest proportion of LBW, a significant 27.2% of the population. Among different ethnic groups, Hausa mothers had a significantly higher proportion of LBW compared to other ethnic groups. The proportion of LBW was significantly higher among mothers with poor wealth indices (16.7%) and was also more common in the rural areas (9.7%). There was also significant association between paternal educational level and LBW.
Table 1.
Factors | Total baby weighed n (%) | Low birth weight% (95% CI) | p* |
---|---|---|---|
Maternal age (years) | |||
15–24 | 761 (14.5) | 11.5 (8.9, 14.8) | 0.014b |
25–34 | 3,067 (60.2) | 7.8 (6.7, 9.0) | |
35–49 | 1,361 (25.3) | 7.2 (5.6, 9.1) | |
Maternal education | |||
No education | 290 (5.6) | 14.9 (10.8, 20.2) | 0.002b |
Primary | 799 (14.9) | 8.0 (5.9, 10.8) | |
Secondary or higher | 4,100 (79.5) | 7.7 (6.7, 8.8) | |
Maternal employment | |||
Unemployed | 1,112 (21.2) | 10.0 (7.9, 12.5) | 0.056 |
Employed | 4,077 (78.8) | 7.7 (6.7, 8.8) | |
Paternal age (years) | |||
16–35 | 1,825 (37.7) | 8.2 (6.8, 10.0) | 0.852 |
36–55 | 2,900 (59.3) | 8.0 (6.8, 9.3) | |
More than 55 | 170 (3.1) | 8.0 (7.1, 9.1) | |
Paternal education | |||
No education | 193 (3.7) | 14.4 (9.3, 21.5) | 0.015b |
Primary | 858 (16.7) | 6.8 (5.1, 9.1) | |
Secondary or higher | 3,988 (79.6) | 8.1 (7.0, 9.2) | |
Paternal employment | |||
Others | 1,814 (35.5) | 7.1 (5.8, 8.7) | 0.484 |
Manual | 1,668 (34.5) | 8.7 (7.1, 10.7) | |
Agricultural | 524 (8.3) | 8.6 (6.0, 12.1) | |
Sales | 1,034 (21.7) | 8.5 (6.6, 10.8) | |
Marital status | |||
Married | 4,698 (90.8) | 7.9 (7.0, 9.0) | 0.112 |
Non-married | 491 (9.2) | 10.5 (7.6, 14.4) | |
Wealth index | |||
Poor | 290 (5.1) | 16.7 (12.0, 23.0) | <0.001c |
Middle | 2,190 (39.7) | 8.8 (7.4, 10.5) | |
Rich | 2,709 (55.2) | 6.9 (5.8, 8.2) | |
Religiona | |||
Catholic and other Christian | 3,872 (75.1) | 8.3 (7.2, 9.5) | 0.673 |
Islam | 1,288 (24.9) | 7.9 (6.4, 9.7) | |
Ethnicity | |||
Others | 1,796 (32.7) | 12.5 (10.6, 14.6) | <0.001c |
Igbo | 1,613 (33.3) | 6.0 (4.7, 7.7) | |
Hausa | 307 (5.5) | 15.4 (11.2, 21.0) | |
Yoruba | 1,473 (28.5) | 4.3 (3.2, 5.8) | |
Residence type | |||
Urban | 3,616 (73.1) | 7.6 (6.6, 8.8) | 0.048b |
Rural | 1,573 (26.9) | 9.7 (8.0, 11.7) | |
Geopolitical zone | |||
North Central | 771 (10.2) | 7.5 (5.5, 10.1) | <0.001c |
North East | 374 (5.8) | 13.0 (9.6, 17.4) | |
North West | 308 (9.4) | 27.2 (21.8, 33.3) | |
South East | 1,299 (25.2) | 4.7 (3.5, 6.3) | |
South South | 850 (15.3) | 11.5 (9.1, 14.4) | |
South West | 1,587 (34.1) | 3.4 (2.5, 4.6) |
The p-value is based on chi-square test.
Percentages are calculated based on less than 5,189 infants
p<0.05
p<0.001.
Results for the pregnancy characteristics of mothers who gave birth to LBW babies are shown in Table 2. The number of previous pregnancies, maternal weight and height, frequency of ANC visit, maternal BMI, and the experience of physical violence during pregnancy were significantly associated with LBW. Among the LBW, there was a greater proportion of multiparous and maternal weight less than 70 kg. More than 80% of the mothers with LBW were multiparous and had weight less than 70 kg. More than half of the LBW, representing 61.7%, were babies born to mothers with normal BMI. Single pregnancy, maternal height ≥1.45 m, ≥4 ANC visits and no experience of any physical violence during pregnancy were associated with a significantly higher proportion of LBW.
Table 2.
Factors | Total baby weighed n (%) | Low birth weight% (95% CI) | p* |
---|---|---|---|
Birth order | |||
First child | 1,427 (27.7) | 28.0 (22.9, 33.8) | 0.889 |
Second or more child | 3,762 (72.3) | 72.0 (66.2, 77.1) | |
Birth interval (months)a | |||
< 18 | 278 (7.5) | 7.9 (4.7, 12.8) | 0.536 |
18–36 | 2,005 (53.1) | 49.2 (42.0, 56.5) | |
> 36 | 1,458 (39.3) | 42.9 (36.0, 50.2) | |
Place of birtha | |||
Home delivery | 369 (7.3) | 8.9 (6.3, 12.5) | 0.242 |
Health facility delivery | 4,807 (92.7) | 91.1 (87.5, 93.7) | |
Parity | |||
Primiparous | 877 (17.0) | 19.5 (15.1, 24.9) | 0.252 |
Multiparous | 4,312 (83.0) | 80.5 (75.1, 84.9) | |
Mode of birtha | |||
Vaginal birth | 4,772 (92.8) | 91.8 (87.9, 94.5) | 0.486 |
Caesarean birth | 369 (7.2) | 8.2 (5.5, 12.1) | |
Number of pregnancy | |||
Single | 4,986 (96.0) | 89.6 (85.8, 92.4) | <0.001c |
Twin | 203 (4.0) | 10.4 (7.6, 14.2) | |
Sex of infant | |||
Male | 2,629 (49.9) | 47.6 (41.6, 53.6) | 0.436 |
Female | 2,560 (50.1) | 52.4 (46.4, 58.4) | |
Maternal height (m)a | |||
Less than 1.45 m | 26 (0.5) | 1.5 (0.5, 4.3) | 0.012b |
1.45 m and above | 5,126 (99.5) | 98.5 (95.7, 99.5) | |
Maternal weight (kg)a | <0.001c | ||
Less than 70 kg | 3,498 (67.3) | 80.2 (75.0, 84.6) | |
70 kg and above | 1,664 (32.7) | 19.8 (15.4, 25.0) | |
Maternal BMIa | |||
Underweight | 171 (3.2) | 3.2 (1.7, 6.1) | <0.001c |
Normal weight | 2,542 (49.5) | 61.7 (55.7, 67.3) | |
Overweight | 1,572 (30.8) | 24.0 (19.4, 29.4) | |
Obese | 852 (16.5) | 11.1 (7.8, 15.4) | |
Maternal smoking statusa | |||
Non-smoker | 5,140 (99.6) | 99.9 (99.5, 100.0) | 0.069 |
Smoker | 28 (0.4) | 0.1 (0.0, 0.5) | |
Frequency of ANC visita | |||
Less than 4 visits | 353 (6.8) | 12.6 (9.2, 16.9) | <0.001c |
≥ 4 visits | 4,579 (93.2) | 87.4 (83.1, 90.8) | |
Timing of ANC visita | |||
Early ANC registration | 1,661 (33.1) | 28.6 (23.4, 34.5) | 0.109 |
Late ANC registration | 3,441 (66.9) | 71.4 (65.5, 76.6) | |
Index pregnancy wanteda | |||
Wanted then | 4,584 (88.3) | 87.4 (83.1, 90.7) | 0.145 |
Wanted later | 455 (8.8) | 11.1 (8.0, 15.2) | |
Wanted no more | 140 (2.8) | 1.5 (0.6, 3.8) | |
Use of malaria prophylaxis during pregnancya | |||
No | 1,078 (29.4) | 28.7 (22.6, 35.7) | 0.847 |
Yes | 2,645 (70.6) | 71.3 (64.3, 77.4) | |
Drugs for intestinal parasite during pregnancya | |||
No | 2,963 (79.2) | 75.7 (69.2, 81.2) | 0.216 |
Yes | 797 (20.8) | 24.3 (18.8, 30.8) | |
Experience any type of violence during pregnancya | |||
No | 2,995 (93.2) | 88.2 (81.4, 92.7) | 0.015b |
Yes | 172 (6.8) | 11.8 (7.3, 18.6) |
The p-value is based on chi-square test
Percentages are calculated based on less than 5,189 infants
p<0.05
p<0.001.
The determinants of each variable were presented in Table 3. The determinants for LBW in Nigeria were paternal employment, geopolitical zone, parity, number of pregnancies, and maternal weight. Mothers from North West region were 10.67 times more likely to deliver LBW (aOR 10.67; 95% CI [5.83–19.5]). Primiparous mothers were 2.08 times more likely to deliver a LBW baby (aOR 2.08; 95% CI [1.15–3.77]). Twin pregnancy (aOR 5.11; 95% CI [3.11–8.39]), maternal weight of less than 70 kg (aOR 1.92; 95% CI [1.32–2.78]), and manual paternal employment (aOR 1.91; 95% CI [1.08–3.37]) were more likely to be associated with LBW.
Table 3.
Univariable logistic regression | Multivariable logistic regression | |
---|---|---|
Factors | Odds ratio (95% CI) | |
Paternal employment | ||
Agricultural | 1.00 | 1.00 |
Others | 0.81 (0.53, 1.26) | 1.27 (0.69, 2.33) |
Manual | 1.02 (0.66, 1.58) | 1.91 (1.08, 3.37) |
Sales | 0.98 (0.62, 1.57) | 1.63 (0.88, 3.04) |
Geopolitical zone | ||
South West | 1.00 | 1.00 |
North Central | 2.28 (1.45, 3.60) | 2.45 (1.46, 4.13) |
North East | 4.23 (2.65, 6.75) | 4.93 (2.66, 9.15) |
North West | 10.56 (6.87, 16.22) | 10.67 (5.83, 19.50) |
South East | 1.39 (0.89, 2.16) | 1.09 (0.55, 2.15) |
South South | 3.65 (2.42, 5.51) | 1.95 (1.07, 3.55) |
Parity | ||
Multiparous | 1.00 | 1.00 |
Primiparous | 1.21 (0.87, 1.67) | 2.08 (1.15, 3.77) |
Number of pregnancy | ||
Single | 1.00 | 1.00 |
Twin | 3.31 (2.22, 4.94) | 5.11 (3.11, 8.39) |
Maternal weight (kg) | ||
70 kg and above | 1.00 | 1.00 |
Less than 70 kg | 2.08 (1.53, 2.83) | 1.92 (1.32, 2.78) |
Discussion
Information on infants’ birth weight and size at birth is essential to avert the complications resulting from LBW. In the present study, 5,189 birth weights of children were measured in the 5 years preceding the survey. This is not surprising because majority of the births did not take place in the health facility, and children are less likely to be weighed at birth in a non-institutional setting. The prevalence of LBW in this study was 7.3%, which is lower than the global prevalence in developed countries (17%) (44). The prevalence of LBW in India is higher than the current prevalence in Nigeria. Studies from two medical colleges and one civil hospital in India found that the prevalence of LBW was 26.8% (45). This is expected as the study was conducted among pregnant mothers in tertiary care, where many high-risk pregnant mothers are referred. In addition, significant predictors of LBW were identified. Paternal employment, geopolitical zone, parity, number of earlier pregnancies, and maternal weight were significant predictors of LBW in Nigeria.
This study has shown that maternal age and education, paternal education, wealth index, ethnicity, type of residence, and geopolitical zone were significantly associated with the birth weights of the infants. The association of birth weight with locality, wealth index, and maternal education observed in this study has also been reported by Jayant et al. (32). Lower wealth index, maternal education, and mothers who reside in rural areas were significantly associated with a higher percentage of infants with LBW. Many studies have shown that low levels of educational attainment were predictors of adverse birth outcomes, such as preterm birth and LBW (46–48). It is noted that higher level of education could improve the socio-economic status of the family and subsequently the odds for delivering LBW infants could be reduced. Education will guide the pregnant mothers to make decisions about their reproductive health and improve their interactions with the healthcare system (49).
The proportion of LBW children in the rural areas was higher than that of the urban areas in this study. It could be due to the fact that rural women are more susceptible to poor diet, infections during pregnancy, and inadequate ANC facilities (32). The proportion of LBW was higher among younger mothers compared to other age groups. Our findings were similar to those of the study conducted in India (29). Pregnancy at a young age is detrimental to the health of both mother and the unborn child. Among teenage mothers, the physical development of the girl is still not complete (50). Indeed, most of the younger mothers were unprepared, unaware or inexperienced (51).
With regards to pregnancy characteristics, our study found that number of earlier pregnancies, maternal height, weight and BMI, the experience any type of violence during pregnancy, and the frequency of ANC visits were significantly associated with the birth weights of the infants. The majority of the LBW infants were born to mothers who were late for their ANC registration. Inadequate ANC increases the risk of delivering LBW infants (45). Access to high-quality ANC should be highlighted since it not only enhances maternal health, but also creates opportunities for counseling and risk detection. Risk factors for LBW should be identified during ANC visits. Through this initiative, numerous opportunities exist during pregnancy to minimize the risk of LBW. This study had also identified that maternal weight was significantly associated with LBW in Nigeria. There is ample evidence to show that maternal weight is related to LBW (29, 38).
Logistic regression analysis was computed to determine the predictors of LBW in Nigeria. Among the factors tested, five risk factors were identified as significant for LBW. The risk factors were geopolitical zone, primiparous women, twin pregnancy, maternal weight less than 70 kg, and paternal employment. The most important risk factor associated with LBW in Nigeria was pregnant mothers living in the North West region. This might result from the facts that the presence of skilled attendants at births is particularly low and the number of teenage pregnancy is high in this region (52). Mothers with weight less than 70 kg were two times at risk for delivering LBW babies. It has been proven that maternal stature is one of the significant risk factors for LBW (29), underscoring the need to improve the nutritional status of women, especially during adolescence, in order to ensure that they have ideal weights. Hence, the risk factors for LBW could be reduced. This study also showed that primiparous women had two times the usual risk of delivering a LBW baby. Documented evidence has observed that being a primiparous woman is one of the risk factors for LBW (53, 54). Indeed, most of the primiparous women were young, with the subsequent increased risk of having a LBW baby. Pregnant mothers with twin pregnancies were more prone to having LBW babies. Twin pregnancy has been well-recognized as a risk factor for LBW (55), possibly because all the aspects related to fetal growth are shared between two fetuses (41).
Pregnant women exposed to tobacco products were at high risk of delivering LBW babies (45). However, in the present study, smoking status was not found to be a significant risk factor for LBW. The number of smoking pregnant mothers in this study was very low. Information on birth weight or size at birth is important for the design and implementation of programs aimed at reducing neonatal and infant mortality. Our study suggests that there are still a number of factors for LBW not studied in this survey that should be assessed in the future. Factors like poor maternal nutritional status during the antenatal period (12), history of abortion (32), pregnancy-induced hypertension (56), gestational age (38), and anemia (36) should be investigated in the future.
LBW is an indicator of infant's survival, growth, and psychosocial development (57). In the light of this sequela, the early detection of at-risk pregnancies, together with intensive ANC is crucial.
The result of the current study had provided valuable information on the significant risk factors associated with LBW infants, based on the recent national survey in Nigeria. The findings from this study will provide insight for public health professionals and policy makers to implement strategies or intervention programs to reduce the prevalence of LBW in the future. Our study has some limitations. Recall bias is possible during data collection. Birth weights of the infants were obtained from written records from the hospital cards or mothers’ recall. Moreover, a low number of LBW babies were recorded in health facilities, because most births do not take place in these facilities, which may have resulted in an underestimation of the prevalence of LBW in this study.
Conclusions
Paternal employment, geopolitical zone, parity, number of pregnancies, and maternal weight were the significant factors for LBW in Nigeria. Even though LBW is influenced by a multiplicity of factors, the incidence of LBW could be reversed if maternal risk factors are detected earlier and appropriate prevention strategies are delivered to the high-risk group. From a public health perspective, it is an advantage that most of these factors can be modified.
Improvement in the ANC services in Nigeria is needed. Multi-faceted approaches could deliver better services to the pregnant mothers in Nigeria. Such approaches would include health education, maternal nutrition, improvement in socio-economic indices, and more and better-quality ANC services.
Acknowledgements
We value the collaboration with Usmanu Danfodiyo University, Sokoto, Nigeria in coming up with this manuscript. Obtaining the data and development of this manuscript were supported by the University of Malaya Research Grant UMRG – Africa-Asia Development University Network (RP026-2012C).
Authors' contributions
MD and NA did the analysis. NA drafted the paper. MD, NA, OMO and NAA involved in the critical revision of the paper. All authors read and approved the final version of the manuscript.
Conflicts of interest and funding
The authors declare that there is no conflict of interest arising from this study.
References
- 1.Moss W, Darmstadt GL, Marsh DR, Black RE, Santosham M. Research priorities for the reduction of prenatal and neonatal morbidity and mortality in developing country communities. J Perinatol. 2002;22:484–95. doi: 10.1038/sj.jp.7210743. [DOI] [PubMed] [Google Scholar]
- 2.Lawn JE, Cousens S, Zupan J. 4 million neonatal deaths: When? Where? Why? Lancet. 2005;365:891–990. doi: 10.1016/S0140-6736(05)71048-5. [DOI] [PubMed] [Google Scholar]
- 3.Uthman OA. Effect of low birth weight on infant mortality: analysis using Weibull Hazard Model. Int J Epidemiol. 2008;6:8. [Google Scholar]
- 4.Daynia EB, Tobias FC, Peter AC. Determinants of survival in very low birth weight neonates in a public sector hospital in Johannesburg. BMC Pediatr. 2010;10:10–30. doi: 10.1186/1471-2431-10-30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.World Health Organization. Low birthweight newborns (percentage) Geneva, Switzerland: World Health Organization; Available from: http://www.who.int/whosis/indicators/compendium/2008/2bwn/en/index.html [cited 23 February 2015] [Google Scholar]
- 6.Gupta RK. Care of low birth weight neonates. JK Sci. 2008;10:158–9. [Google Scholar]
- 7.Richards M, Hardy R, Kuh D, Wadsworth ME. Birth weight and cognitive function in the British birth 1946 cohort: longitudinal population based study. BMJ. 2001;322:199–203. doi: 10.1136/bmj.322.7280.199. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Olsen P, Vainionpaa L, Paakko E, Korkman M, Pyhtinen J, Järvelin MR. Psychological findings in preterm children related to neurologic status and magnetic resonance imaging. Pediatrics. 1998;102:329–36. doi: 10.1542/peds.102.2.329. [DOI] [PubMed] [Google Scholar]
- 9.Eriksson JG, Forsen T, Tuomilehto J, Winter PD, Osmond C, Barker DJ. Catch-up growth in childhood and death from coronary heart disease: longitudinal study. BMJ. 1999;318:427–31. doi: 10.1136/bmj.318.7181.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Ramakrishnan U. Nutrition and low birth weight: from research to practice. Am J Clin Nutr. 2004;79:17–21. doi: 10.1093/ajcn/79.1.17. [DOI] [PubMed] [Google Scholar]
- 11.Badshah S, Mason L, Mckelvie K, Payne R, Lisboa PJ. Risk factors for low birthweight in the public-hospitals at Peshawar, NWFP-Pakistan. BMC Public Health. 2008;8:197. doi: 10.1186/1471-2458-8-197. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Assefa N, Berhane Y, Worku A. Wealth status, mid upper arm circumference (MUAC) and antenatal care (ANC) are determinants for low birth weight in Kersa, Ethiopia. PLoS One. 2012;7:e39957. doi: 10.1371/journal.pone.0039957. doi: http://dx.doi.org/10.1371/journal.pone.0039957. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Feresu SA, Harlow SD, Welch K, Gillespie BW. Incidence of and sociodemographic risk factors for stillbirth, preterm birth and low birth weight among Zimbabwean women. Paediatr Perinat Epidemiol. 2004;18:154–63. doi: 10.1111/j.1365-3016.2003.00539.x. [DOI] [PubMed] [Google Scholar]
- 14.Olu Dunant S. The birth weight of Nigerian babies. J Trop Pediatr. 2005;41:140–1. [Google Scholar]
- 15.Yilgwan CS, Abok II, Yinnang WD, Vajime BA. Prevalence and risk factors of low birth weight in Jos. Jos J Med. 2009;4:12–15. [Google Scholar]
- 16.Olowonyo T, Oshin S, Obasanjo-Bello I. Some factors associated with low birthweight in Ogun State, Nigeria. Niger Med Pract. 2006;49:154–7. [Google Scholar]
- 17.Takai IU, Bukar M, Audu BM. A prospective study of maternal risk factors for low birth weight babies in Maiduguri, North-Eastern Nigeria. Niger J Basic Clin Sci. 2014;11:89–98. [Google Scholar]
- 18.Singh G, Chouhan R, Sidhu K. Maternal factors for low birth weight babies. Med J Armed Forces India. 2009;65:10–12. doi: 10.1016/S0377-1237(09)80045-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Vahdaninia M, Tavafian SS, Montazeri A. Correlates of low birth weight in term pregnancies: a retrospective study from Iran. BMC Pregnancy Childbirth. 2008;8:12. doi: 10.1186/1471-2393-8-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Dubois L, Girard M. Determinants of birthweight inequalities: population-based study. Pediatr Int. 2006;48:470–8. doi: 10.1111/j.1442-200X.2006.02256.x. [DOI] [PubMed] [Google Scholar]
- 21. Leal M, Gama C, Cunha CB. Consequences of sociodemographic inequalities on birth weight. Parental Childbirth Care. 2006;40:466–73. doi: 10.1590/s0034-89102006000300015. [DOI] [PubMed] [Google Scholar]
- 22.Sarkar NN. The impact of intimate partner violence on women's reproductive health and pregnancy outcome. Inform Health Care Obstetr Gynecol. 2008;28:266–71. doi: 10.1080/01443610802042415. [DOI] [PubMed] [Google Scholar]
- 23.Rassmussen KM. Is there a causal relationship between iron deficiency anemia and weight at birth, length of gestation and perinatal mortality? J Nutr. 2001;13(Suppl):590S–603S. doi: 10.1093/jn/131.2.590S. [DOI] [PubMed] [Google Scholar]
- 24.Ganesh S, Harsha HN, Jayaram S, Kotian MS. Determinants of low birth weight: a case control study in a district hospital in Karnataka. Indian J Pediatr. 2010;77:87–8. doi: 10.1007/s12098-009-0269-9. [DOI] [PubMed] [Google Scholar]
- 25.Kapil U. Multiple micronutrient supplements will not reduce incidence of low birth weight. Indian J Community Med. 2009;34:85–6. doi: 10.4103/0970-0218.51221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Gao W, Paterson J, Carter S, Percival T. Risk factors for preterm and small-for-gestational-age babies: a cohort from the Pacific Islands Families Study. J Paediatr Child Health. 2006;42:785–92. doi: 10.1111/j.1440-1754.2006.00978.x. [DOI] [PubMed] [Google Scholar]
- 27.Awoleke JO. Maternal risk factors for low birth weight babies in Lagos, Nigeria. Arch Gynecol Obstet. 2012;285:1–6. doi: 10.1007/s00404-011-1885-y. [DOI] [PubMed] [Google Scholar]
- 28.Heaman M, Kingston D, Chalmers B, Sauve R, Lee L, Young D. Risk factors for preterm birth and small-for-gestational-age births among Canadian women. Paediatr Perinat Epidemiol. 2013;27:54–61. doi: 10.1111/ppe.12016. [DOI] [PubMed] [Google Scholar]
- 29.Chabra P, Sharma AK, Grover UL, Agarwal OP. Prevalence of LBW and its determinants in an urban resettlement area of Delhi. Asia Pac J Public Health. 2004;16:95–8. doi: 10.1177/101053950401600203. [DOI] [PubMed] [Google Scholar]
- 30.Sebayang SK, Dibley MJ, Kelly PJ, Shankar AV, Shankar AH. Determinants of low birthweight, small-for-gestational-age and preterm birth in Lombok, Indonesia: analyses of the birthweight cohort of the SUMMIT trial. Trop Med Int Health. 2012;17:938–50. doi: 10.1111/j.1365-3156.2012.03039.x. [DOI] [PubMed] [Google Scholar]
- 31.Nobile CG, Raffaele G, Altomare C, Pavia M. Influence of maternal and social factors as predictors of low birth weight in Italy. BMC Public Health. 2007;7:192. doi: 10.1186/1471-2458-7-192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Jayant D, Phalke DB, Bangal VB, Peeyuusha D, Sushen B. Maternal risk factors for low birth weight neonates: a hospital based case-control study in rural area of Western Maharashtra, India. Natl J Community Med. 2011;2:394–8. [Google Scholar]
- 33.Mbuagbaw LC, Gofin R. A new measurement for optimal antenatal care: determinants and outcomes in Cameroon. Matern Child Health J. 2011;15:1427–34. doi: 10.1007/s10995-010-0707-3. [DOI] [PubMed] [Google Scholar]
- 34.Mohanty C, Prasad R, Srikanth Reddy A, Ghosh JK, Singh TB, Das BK. Maternal anthropometry as predictors of low birth weight. J Trop Pediatr. 2005;52:24–9. doi: 10.1093/tropej/fmi059. [DOI] [PubMed] [Google Scholar]
- 35.Janjua ZN, Delzell E, Larson RR. In: Determinants of low birth weight in Urban Pakistan. Public Health Nutrition, editor. Birmingham AL: UAB.EDU; 2008. [DOI] [PubMed] [Google Scholar]
- 36.Joshi HS, Subba SH, Dabral SB, Diwedi S, Kumar D, Singh S. Risk factors associated with low birth weight in newborns. Indian J Community Med. 2005;30:142–4. [Google Scholar]
- 37.Idris MZ, Gupta A, Mohan U, Srivastava AK, Das V. Maternal health and LBW among institutional deliveries. Indian J Community Med. 2000;25:156–60. [Google Scholar]
- 38.Agarwal K, Agarwal A, Agarwal VK, Agarwal P, Chaudhary V. Prevalence and determinants of “low birth weight” among institutional deliveries. Ann Nigerian Med. 2011;5:48–52. [Google Scholar]
- 39.Kayode GA, Amoakoh-Coleman M, Agyepong IA, Ansah E, Grobbee DE, Klipstein-Grobusch K. Contextual risk factors for low birth weight: a multilevel analysis. PLoS One. 2014;9:e109333. doi: 10.1371/journal.pone.0109333. doi: http://dx.doi.org/10.1371/journal.pone.0109333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Viengsakhone L, Yoshida Y, Harun-Or-Rashid M, Sakamoto J. Factors affecting low birth weight at four central hospitals in Vientiane, Lao PDR. Nagoya J Med Sci. 2010;72:51–8. [PMC free article] [PubMed] [Google Scholar]
- 41.Negandhi PH, Negandhi HN, Zodpey S, Ughade SN, Biranjan JR. Risk factors for low birth weight in an Indian urban setting: a nested case control study. Asia Pac J Public Health. 2014;26:461–9. doi: 10.1177/1010539511431486. [DOI] [PubMed] [Google Scholar]
- 42.Agho KE, Dibley MJ, Odiase JI, Ogbonmwan SM. Determinants of exclusive breastfeeding in Nigeria. BMC Pregnancy Childbirth. 2011;11:2. doi: 10.1186/1471-2393-11-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.World Health Organization (WHO) Keeping promises, measuring results. Geneva: WHO; 2011. Commission on Information and Accountability for Women's and Children's Health. [Google Scholar]
- 44.Goldenberg RL. Low birth weight in United States. Am J Clin Nutr. 2007;13(Suppl):5845–5. doi: 10.1093/ajcn/85.2.584S. [DOI] [PubMed] [Google Scholar]
- 45.Mumbare SS, Maindarkar G, Darade R, Yenge S, Tolani MK, Patole K. Maternal risk factors associated with term low birth weight neonates: a matched-pair case control study. Indian Pediatrics. 2012;49:25–8. doi: 10.1007/s13312-012-0010-z. [DOI] [PubMed] [Google Scholar]
- 46.Auger N, Roncarolo F, Harper S. Increasing educational inequality in preterm birth in Québec, Canada, 1981–2006. J Epidemiol Community Health. 2010;65:1091–6. doi: 10.1136/jech.2009.102350. [DOI] [PubMed] [Google Scholar]
- 47.Correia S, Barros H. Small-for-gestational age Portuguese babies: the effect of childhood social environment, growth and adult socioeconomic conditions. Prev Med. 2015;70:102–7. doi: 10.1016/j.ypmed.2014.11.027. [DOI] [PubMed] [Google Scholar]
- 48.Pillas D, Marmot M, Naicker K, Goldblatt P, Morrison J, Pikhart H. Social inequalities in early childhood health and development: a European-wide systematic review. Paediatr Res. 2014;76:418–24. doi: 10.1038/pr.2014.122. [DOI] [PubMed] [Google Scholar]
- 49.World Health Organization Regional Office for Europe. Review of the social determinants and health divide in the WHO European region: final report; UCL Institute of Health Equity; 2013. Available from: http://www.euro.who.int/__data/assets/pdf_file/0004/251878/Review-of-socialdeterminants-and-the-health-divide-in-the-WHOEuropean-Region-FINAL-REPORT.pdf [cited 15 April 2015] [Google Scholar]
- 50.Joshi SM, Pai NP. Effect of the maternal bio-social determinants on the birth weight in a slum area of Greater Mumbai. Indian J Community Med. 2000;25:121. [Google Scholar]
- 51.Anand K, Garg BS. A study of factors affecting LBW. Indian J Community Med. 2000;25:57–61. [Google Scholar]
- 52.Maternal Health in Nigeria Statistical Overview. Global One. 2015. Version 30 June 2011. Available from: http://www.globalone2015.org/wp-content/uploads/2011/11 [cited 26 June 2012]
- 53.Acharya D, Nagraj K, Nair NS, Bhat HV. Maternal determinants of intrauterine growth retardation: a case control study in Udupi District, Karnataka. Indian J Community Med. 2004;29:181–3. [Google Scholar]
- 54.Salam A, Abdul S. Birth weight co-relate to mother's age and parity: one year urban hospital study-Karnataka. J Obstet Gynaecol India. 1996;46:447–54. [Google Scholar]
- 55.Deswal BS, Singh JV, Kumar D. A study of risk factors for low birth weight. Indian J Community Med. 1999;24:127–31. [Google Scholar]
- 56.Rahman LA, Hairi NN, Salleh N. Association between pregnancy induced hypertension and low birth weight: a population based case-control study. Asia Pac J Public Health. 2008;20:152–8. doi: 10.1177/1010539507311553. [DOI] [PubMed] [Google Scholar]
- 57.Bale JR, Stoll BJ, Lucas AO, editors. Improving birth outcomes: meeting the challenge in the developing world. Washington, DC: The National Academic Press; 2003. [PubMed] [Google Scholar]