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Erschienen in: BMC Public Health 1/2020

Open Access 01.12.2020 | Research article

The differential effect of maternal dietary patterns on quantiles of Birthweight

verfasst von: Aweke A. Mitku, Temesgen Zewotir, Delia North, Prakash Jeena, Rajen N. Naidoo

Erschienen in: BMC Public Health | Ausgabe 1/2020

Abstract

Background

Maternal dietary habits during pregnancy are considered essential for development and growth of the fetus as well as maternal health. It has an effect on the birthweight of infants. However, little is known about the effect of dietary patterns on birthweight in urban South Africa. This study aimed to investigate differential effect of dietary patterns of pregnant women on quantiles of birthweight.

Methods

Data for the study were obtained from a Mother and Child in the Environment birth cohort study in Durban South Africa. Quantile regression was used to investigate the effect of maternal dietary patterns on quantiles of birthweight. Data collection was conducted during the period of 2013 to 2017 in Durban South Africa. Using factor analysis, eight dietary groups were identified from 687 pregnant women in the cohort. Quantile regression analysis was employed to identify the differential effects of the seven dietary groups and demographic factors on the birthweight.

Results

The quantile regression estimates at the 50th quantile and the ordinary regression estimates painted the same picture about the conditional mean effect of covariates on the birthweight. But unlike the quantile regression the ordinary regression fails to give insights about the covariates effect disparities at the low and/or upper birthweight quantiles. All the dietary groups show a significant differential effect at different birthweight quantiles. For instance, increased frequency of protein rich foods intake was associated with reduction in birthweight at lower and upper quantiles; increased frequency of junk foods intake has a slight increase in birthweight at the lower quantiles but significantly higher increase at the 95th quantile (p < 0.001); increase in consuming vegetable rich foods, reduced birthweight at 95th quantile (p < 0.001). The results further showed that employment (p = 0.006) and family size (p = 0.002) had differential effects across different birthweight quantiles.

Conclusions

Both maternal undernutrition and overnutrition of protein rich foods, junk foods, snack and energy foods and vegetable rich foods have shown a substantial varying effects on those infants with birthweights in the lower and upper birthweight quantiles.
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Abkürzungen
FFQ
Food Frequency Questionnaires
MACE
Mother and Child in the Environment
MCD
Minimum Covariance Determinant

Background

Adequate nutrition is vital during pregnancy, both for improved maternal and child health. Women are at risk of having an inadequate nutritional status during pregnancy due to the high nutritional demands during pregnancy. Inadequate maternal nutrition during pregnancy is related to adverse birth outcomes, poor infant survival, respiratory disease in early childhood and then, later in life, cardiovascular diseases and obesity [16]. For women living in developing countries, poor quality and quantity of food are major factors for the increased risk of malnutrition during pregnancy [7]. Birthweight has been related to both short and long-term health outcomes and thus, is commonly used as proxy, for studying infant development [8].
Dietary pattern analysis has become a useful tool in epidemiological studies that pursue to better represent a holistic account of the diet [9, 10] and explore the relationship between dietary exposures and health outcomes [11]. It allows the formulation of food-based dietary recommendations [12]. However, individual diets are usually composed of variety of different food items which contain a multitude of nutrients and phytochemicals that function both synergistically and interactively [9]. Dietary patterns characterized by high intakes of vegetables, fruit and dairy products were associated with higher birthweight. Dietary patterns related to low birthweight were often characterized by high loadings of processed and high-fat meat, fats and oils, and sugar rich products in high-income countries [13].
Previous studies showed nutritional status of mothers [1416] and socio-demographic [16] factors had an association with birthweight. Both very high and very low birthweights are associated with detrimental outcomes. Therefore, modelling risk factors associated with solely lower or upper birthweights using techniques such as linear regression is not necessarily appropriate. Thus, the aim of this study is to assess the effect of maternal dietary pattern on the birthweight quintiles by adjusting the effect of socio-demographic factors.
Most of the statistical techniques used in previous studies for estimating the effect of continuous responses were either with conditional means [17] or through dichotomization, a common practice in epidemiological research. Despite the clinical usefulness contained in the dichotomized outcome, this practice of only considering two outcomes leads to a loss of power and information, due to the choice of the cut-off point of these dichotomous variable [1820]. Using quantile regression instead of the common methods linear or logistic regression models led to new insights in the data sets [2124]. In health sciences, quantile regression has become popular in relation to studies of body mass index [2326]. Accordingly, we adopt quantile regression to model quantiles of birthweight on the nutritional status of mothers [1416].

Methods

Data

The Mother and Child in the Environment (MACE) birth cohort study was conducted in Durban, South Africa. The study had enrolled a cohort of 996 pregnant women at three hospitals in the south (Wentworth Hospital, Prince Mshiyeni Hospital and King Edward VIII Hospital) and at three hospitals in the north (Addington and Mahathma Gandhi, and King George V Hospitals) from March 2013 up to May 2017. The field workers determined if the pregnant women met the inclusion criteria and all pregnant women that did, were invited and recruited into the study. The inclusion criteria were gestational age less than 20 weeks, resident for the full duration of the pregnancy in the geographical area within which the clinic and monitoring station was located, and for the follow-up period of 5–6 years in the cohort. Women with multiple pregnancies as well as 309 miscarriages, loss to follow up and termination of pregnancy were excluded. This study is a retrospective analysis on the remainder 687 enrolled subjects who were followed up during their pregnancy, through to labour and delivery.
Socio-demographic information was taken from enrolment dataset which is conducted with face-to-face interviews by trained enumerators. The enrolment questionnaire also consists variables about antenatal history, place of birth and residential history. For the identification of maternal dietary patterns, a food frequency questionnaire (FFQ), which listed 75 items was administered in the third trimester of their pregnancy. The questionnaire collected information on the 75 food items common to maternal dietary situations during pregnancy. The FFQ specifically designed to reflect South African food consumption habits assessed the use of foods or food groups and the consumption frequency (number of times per day, week or month) as common serving sizes. The selected frequency category for each food item in the FFQ was standardized to times per day. The detailed content of the FFQ and data processing have been described elsewhere [15] and validated [27, 28]. Data was captured at the time of interview using a mobile telephone system, automatically uploading data onto the study database using wireless technology. In South Africa, iron and foliate supplements are standard and all mothers have got these supplements.
To reduce the 75 dietary food items from the FFQ into a set of manageable latent characteristics, with minimal loss of information, exploratory factor analysis of promax orthogonal rotation was performed. The absolute magnitude of the rotated factor loadings greater than 0.30 was used as a threshold value for a variable to belong to a latent group. A scree plot, along with the percentage of variance explained by each factor, resulted eight latent dietary factors for further analyses. Collectively these factors explained 88.33% of the variability within the sample. The summary result with the factor loadings and naming of the latent factors is given in Table 1.
Table 1
Factor loadings of different food items in the eight latent dietary factors identified using factor analysis with Promax rotation
Dietary patterns
Food items
Factor loadings coefficient*
Cumulative variance explained (%)
“Snack and energy foods”
Energy bars
0.87486
46.41%
Energy drinks
0.85251
Ice cream
0.76687
Chocolate
0.74735
Drinking yoghurt
0.70387
Milk drinks
0.70378
Milkshake
0.66289
Fruit salad
0.63208
Cheese sauce
0.62704
Cheese
0.56129
Chicken with skin
0.47309
Chips
0.46882
Cold meat
0.46529
Red meat
0.43206
Flame grilled fast food chicken
0.42456
Hot dogs
0.40035
Sausages
0.39612
Fizzy soft drinks
0.38538
Fruit juice
0.35977
Hamburgers
0.31074
Pizza
0.30266
Rusks
0.30247
Cooking oil
−0.33744
“Fast foods and spreads”
Dripping
0.76641
11.12%
Salad dressing low fat
0.76498
Fat Holsum
0.74403
Schnitzels
0.70762
Skimmed
0.6791
Chocolate spread
0.60188
Bunny chow
0.58556
Venison
0.55576
Fizzy diet soft drinks
0.51667
Fish steamed
0.50548
Whole wheat
0.49309
Dried fruit
0.47822
Red meat fat removed
0.47779
Cookies
0.45296
Fried fast food chicken
0.4281
Pasta
0.42541
Organ meat
0.40937
Nuts and peanuts
0.36348
Pizza
0.34863
Pies and sausage rolls
0.34244
Vetkoek
0.33541
Rusks
0.32428
Hot dogs
0.31508
Butter
0.3194
Fizzy soft drinks
−0.31292
“Junk foods”
Butter
0.62300
10.45%
Sweets
0.60625
Muffins
0.59219
Chips
0.56772
Mixed salad
0.56106
Fruit juice
0.5389
Fresh fruit
0.53471
Fizzy soft drinks
0.42281
Vetkoek
0.39649
Coffee creamer
0.38703
Cooking oil
0.38482
Hamburgers
0.36097
Cooked vegetables
0.35781
Cereals Rice Crispies
0.31854
Soft margarine
−0.77394
“Protein rich foods”
Fried fish
0.67237
6.35%
Fish tinned
0.54825
Fried fish in fat
0.52289
Eggs cooked or poached
0.46767
White brown bread
0.43925
Potato chips
0.4079
Chicken with skin
0.40252
Chicken without skin
−0.34525
Red meat fat removed
−0.40646
“Starch foods”
Potato
0.66418
4.56%
Breakfast cereals
0.52251
Potato with fat
0.47055
Legumes
0.45527
Full cream
0.40847
Cooked vegetables
0.36178
Cheese sauce
0.35377
Pasta
0.32992
Jam
0.32221
“Nuts and rice foods”
Peanut butter
0.55276
3.63%
Nuts and peanuts
0.39124
Rice mealie rice
0.34955
“Vegetable rich foods”
Vegetables
0.61485
3.13%
Organ meat
0.40243
Butter
−0.34338
“Alcoholic drinks”
Shooters
0.80795
2.67%
Cocktails
0.79207
*Factor loadings ≥3.0 or ≤ −3.0. Food groups are sorted by size of loading coefficients

Statistical analysis

We explored the data on quantiles of birthweight and observed that extreme birthweight outcomes occur over several maternal strata; including marital status, educational level, employment status and annual income, as well as infant strata, specifically gender. The quantile regression model provides the effects of maternal diet across the distribution of birthweight taking into consideration outliers. In other words, the quantile e regression is particularly useful with data that are heterogeneous in that the tails and the central location of the conditional distributions vary differently with the covariates [22]. The effect of covariates on quantiles of the response distribution are pertinent. The covariates considered in this study were the eight latent dietary factors and socio-demographic factors. Quantile regression for a set of covariates, X, on the (τ ×100)th quantiles of y is given by
$$ {\boldsymbol{Q}}_{\boldsymbol{\tau}}\;\left(\boldsymbol{y}/\boldsymbol{X}\right)={\boldsymbol{X}}^{\boldsymbol{t}}\;\boldsymbol{\beta}\;\left(\boldsymbol{\tau} \right)+\boldsymbol{\varepsilon} $$
where 0 < τ < 1 and ε = (ε1, …, εn)t is a vector of independent errors. The parameter estimates, β(τ) have the same interpretation as those of any other linear model, i.e. each βj(τ) coefficient can be interpreted as the marginal change in the (τ ×100)th quantile, due to the marginal change in corresponding jth covariate [22, 29, 30]. The quantile regression coefficients are computed by minimizing the asymmetric weighted sum of absolute errors through linear programing methods:
$$ \underset{\boldsymbol{\beta}}{\mathbf{\min}}\left[\sum \limits_{\boldsymbol{i}:{\boldsymbol{\beta}}_{\boldsymbol{i}}\mathbf{\ge}{\boldsymbol{x}}^{\prime}\boldsymbol{\beta}}\boldsymbol{\tau} \left|{\boldsymbol{\beta}}_{\boldsymbol{i}}-{\boldsymbol{x}}_{\boldsymbol{i}}^{\prime }{\boldsymbol{\beta}}^{\boldsymbol{\tau}}\right|+\sum \limits_{\boldsymbol{i}:{\boldsymbol{\beta}}_{\boldsymbol{i}}\mathbf{\le}{\boldsymbol{x}}^{\prime}\boldsymbol{\beta}}\left(\mathbf{1}-\boldsymbol{\tau} \right)\left|{\boldsymbol{\beta}}_{\boldsymbol{i}}-{\boldsymbol{x}}_{\boldsymbol{i}}^{\prime }{\boldsymbol{\beta}}^{\boldsymbol{\tau}}\right|\right] $$
The model was built by fitting all the main effects followed by sequential assessment of whether any interaction terms need to be incorporated in to the model. Consequently, only two two-way interaction term of employment status with marital status and maternal education improved the main effect quantile regression model fit. Outliers can adversely influence the fit of the model thereby invalidating the appropriate statistical inferences [31]. However, quantile regression is fairly robust to outliers as their influence functions are bounded in the Y-space [22]. Existence of single case outlier diagnostic can be checked based on the standardized median absolute deviation of residuals [32]. The robust and multivariate location and scale diagnostics computed using the minimum covariance determinant (MCD) method were applied to expose all the single case high leverage points and outliers [33]. We used the standardized residuals and Quantile-Quantile plots for checking the goodness of fit of the model. All the statistical analyses were performed using SAS, version 9.4.

Results

The overall mean birthweight of the 687 children in the birth cohort was 3107.0 g (g) with a median of 3140.0 g. The data included 357 male and 328 female infants, with 80.6% of mothers being single and 79.5% with high school education. Majority of the women in the cohort were unemployed (81.5%), have no personal income (47.9%) and 48.8% of them were nulliparous. The 95th quantile of birthweight was higher in infants born to women who were married, primary or less education or were primaparous. Male offspring, older maternal age, lower education were observed to have lower birthweight at 5th quantile. The quantiles of birthweight by socio-demographic characteristics are summarized in Table 2.
Table 2
Descriptive statistics and quantiles of birthweight by socio-demographic characteristics of women in MACE birth cohort
Variable
N (%)
P5
P10
P25(Q1)
Median
P75(Q3)
P90
P95
Marital status
 Married
93 (13.6)
2084
2400
2900
3300
3560
3990
4031
 Living together
39 (5.7)
2080
2400
2800
3112
3430
3800
3970
 Single
554 (80.8)
2090
2400
2840
3115
3400
3720
3980
Maternal age
 Teenage (less than 25 yrs)
116 (16.9)
2070
2331
2740
3060
3300
3560
3640
 Prime of fertility (25–29 yrs)
416 (60.6)
2100
2440
2876
3160
3430
3800
4000
 Adult age (30 years and above)
155 (22.6)
2031
2340
2800
3170
3400
3800
4000
Maternal education
 Primary or less
16 (2.3)
1570
1800
2775
3210
3495
3870
4260
 Secondary school
546 (79.5)
2083
2400
2815
3105
3400
3710
3920
 College or university
125 (18.2)
2096
2410
2960
3210
3480
3970
4120
Employment
 Employed
127 (18.5)
2080
2360
2820
3100
3480
3850
4010
 Unemployed
560 (81.5)
2090
2400
2860
3140
3400
3730
4000
Maternal annual income
 No personal income
329 (47.9)
2090
2400
2885
3160
3400
3800
4000
 Less than R30000
276 (40.2)
2090
2400
2800
3100
3400
3700
3980
 R30000 and above
82 (11.9)
2083
2530
2840
3150
3480
3800
3970
Parity
 Nulliparous
334 (48.8)
2080
2360
2790
3100
3340
3630
3850
 Primaparous
220 (32.1)
2079
2060
2870
3230
3500
3895
4045.5
 Multiparous
131 (19.1)
2280
2500
2900
3150
3410
3800
3990
Infant Gender
 Male
359 (52.3)
2084
2370
2860
3170
3450
3900
4060
 Female
328 (47.7)
2090
2410
2830
3125
3370
3600
3810
Table 3 shows the results from estimation of the final quantile regression model and ordinary least squares regression. Before we make any inference from the model results we examine its goodness of fit. All the goodness of fit assessment results in Fig. 1 showed that the final model fits the data adequately.
Table 3
Quantile regression parameter estimates and 95% confidence intervals of dietary latent factors for the 5th, 10th, 25th, 50th, 75th, 90th, and 95th quantiles of birthweight, adjusted for demographic and socio-economic characteristics
Quantiles
5th
10th
25th
50th
75th
90th
95th
OLS
 
(95% CI)
(95% CI)
(95% CI)
(95% CI)
(95% CI)
(95% CI)
(95% CI)
(95% CI)
Intercept
2741.8** (2570.2, 2913.4)
3060.9** (2612.9, 3508.8)
3067.5 (2785.1, 3349.9)
3190.4** (3019.4, 3361.4)
3514.7** (3313.5, 3715.8)
4095.5** (3871.7, 4319.3)
4756.6** (4592.7, 4920.5)
3395.1**(3173.6, 3616.7)
Snack and energy protein foods factor
4.6 (38.8, 47.9)
96.3 (−16.8, 209.5)
22.6 (−48.8, 93.9)
−0.4 (−43.6, 42.7)
2.5 (−48.3, 53.3)
52.6 (−3.9, 109.1)
65.8** (24.4, 107.2)
17 (−38.7, 73.2)
Fast foods and spreads factor
2.2 (−37.0, 41.4)
−50.9 (− 153.4, 51.4)
−2.0 (−66.5, 62.6)
− 15.2 (− 54.3, 23.9)
36.6 (−9.4, 82.6)
−11.4 (−62.5, 37.8)
−26.9 (−64.4, 10.5)
−11.5 (−62.1, 39.2)
Junk foods factor
27.6 (−18.6, 73.8)
21.8 (− 99.2, 141.8)
32.6 (− 43.4, 108.6)
34.0 (− 12.0, 80.1)
25.4 (− 28.7, 79.5)
−5.8 (− 66.0, 54.4)
81.5** (37.4, 125.6)
41.8 (− 17.8, 101.4)
Protein rich foods factor
− 62.2** (− 102.8, − 21.5)
−76.7 (− 182.9, 29.4)
−71.0 (− 137.9, − 4.1)
−16.3 (− 56.8, 24.2)
14.0 (− 33.6, 61.7)
3.4 (− 49.6, 56.5)
− 64.9** (−103.8, − 26.1)
−20.3 (−72.8, 32.2)
Starch foods factor
42.5* (5.4, 79.5)
15.5 (−81.2112.2)
−29.5 (− 90.5, 31.5)
10.2 (− 26.7, 47.2)
25.3 (− 18.1, 68.7)
39.9 (− 8.4, 88.3)
−8.2 (− 43.6, 27.2)
10.7 (− 37.2, 58.5)
Nuts and rice foods factor
46.7* (6.6, 86.8)
94.2 (− 10.5, 194.9)
37.0 (− 29.0, 103.0)
47.2* (7.2, 87.1)
41.1 (−5.8, 88.1)
14.6 (− 37.7, 66.9)
76.4** (38.4, 114.9)
42.1 (−9.7, 93.8)
Vegetable rich foods factor
119.5** (74.4, 164.6)
77.2 (− 40.5, 194.9)
38.0 (− 36.3, 112.2)
14.4 (− 30.5, 59.4)
5.7 (− 47.2, 58.5)
1.9 (− 56.9, 60.8)
−75.7** (− 118.8, − 32.7)
5.6 (− 52.6, 63.8)
Alcoholic drinks factor
−46.6 (− 194.8, 101.6)
−140.9 (− 527.9, 245.9)
− 288.2 (− 532.2, − 44.3)
−84.8 (− 232.6, 62.9)
− 149.9 (− 323.6, 23.8)
− 426.6 (− 619.9, − 233.3)
− 558.1* (− 699.6, − 416.6)
− 195.9* (− 387.3, −4.6)
Marital status (REF=Single)
 Married
−82.7 (189.1, 23.8)
286.4 (−143.4, 716.2)
37.5 (−137.7, 212.7)
−207.6** (101.5, 313.7)
194.5** (69.7, 319.3)
174.0* (35.2, 32.8)
36.3 (−65.4, 137.9)
115.7 (− 21.8, 253.0)
 Living together
283.0** (118.4, 447.7)
84..5 (− 193.3, 362.4)
54.3 (− 216.7, 325.3)
− 71.8(− 235.9, 92.3)
−16.4 (− 209.4, 176.6)
−185.2 (− 399.9, 29.6)
−309.4** (− 466.7, − 152.2)
−13.3 (− 225.8, 199.3)
Maternal age (REF=Prime of fertility)
 Teenage
−1.4 (−95.0, 92.2)
14.2 (− 230.2, 258.5)
− 41.9 (− 195.9, 112.2)
−27.0 (− 120.3, 66.3)
−51.7 (− 161.4, 58.0)
−153.4* (− 275.5, − 31.3)
− 201.2** (− 290.6, − 111.8)
− 40.2 (− 161.0, 80.7)
 Adult age(30 years and above)
− 167.5** (− 255.4, − 79.5)
213.2 (− 442.7, 16.3)
−106.9 (− 251.6, 37.9)
−53.8 (− 141.4, 33.9)
−121.1* (− 224.1, − 17.9)
− 167.3** (− 282.0, − 52.6)
− 221.8** (− 305.8, − 137.8)
−116.7* (− 230.2, − 3.1)
Maternal education (REF = College or University)
 Primary or less
− 435.8* (− 673.3, − 198.2)
− 666.2* (− 1286.3, − 46.1)
− 437.1* (− 828.1, − 46.1)
−53.7 (− 290.4, 183.1)
−6.9 (− 285.4, 271.5)
−242.8 (− 552.7, 67.0)
−105.4 (− 332.2, 121.4)
− 250.9 (− 557.5, 55.8)
 High school
− 90.6 (− 185.9, 4.7)
−281.2* (− 529.8, − 32.6)
−112.5 (− 269.3, 44.2)
−51.1 (− 146.0, 43.8)
−58.8 (170.4, 52.9)
−160.2* (− 284.4, − 35.9)
− 215.5** (− 306.5, − 124.6)
−135.9* (− 258.9, − 12.9)
Employment (REF=Unemployed)
 Employed
−188.4 (− 387.9, 11.3)
− 569.5* (− 1090.5, − 48.4)
−95.7 (− 424.2, 232.9)
−78.0 (− 120.9, 276.9)
86.3 (− 147.7, 320.3)
−21.3 (− 281.6, 239.1)
− 174.1 (− 364.8, 16.5)
−57.2 (− 314.9, 200.5)
Maternal annual income (REF = R30000 and above)
 No personal income
− 108.3 (− 219.2, 2.6)
− 80.2 (− 369.6, 209.2)
76.4 (− 106.1, 258.9)
31.9 (−78.6, 142.4)
82.6 (− 47.4, 212.6)
88.4 (− 56.2, 233.0)
21.2 (− 84.7, 127.1)
39.0 (− 104.1, 182.1)
 Less than R30000
− 153.7* (− 271.3, − 36.1)
− 157.1 (− 464.1, 149.8)
− 62.9 (− 256.5, 130.6)
−23.4 (− 140.6, 93.8)
28.9 (− 108.9, 166.7)
40.1 (− 113..3, 193.5)
− 192.4** (− 304.7, − 80.1)
−61.5 (− 213.3, 90.3)
Infant Gender (REF = Male)
 Female
81.2* (18.2, 144.3)
68.1 (− 96.3, 232.6)
58.2 (− 45.5, 161.9)
− 34.4 (− 97.2, 28.4)
− 106.7** (− 180.6, − 32.9)
− 187.6** (− 269.8, − 105.5)
−219.4** (− 279.5, − 159.2)
−67.8 (− 149.2, 13.5)
Parity (REF = Multiparous)
 Nulliparous
− 246.4** (− 348.5, − 144.3)
−300.1* (− 566.6, − 33.6)
−182.9 (− 350.9, − 14.9)
− 91.1 (− 192.8, 10.7)
−119.6 (− 239.2, 0.1)
− 229.3** (− 362.5, − 96.2)
− 327.3** (− 424.7, − 229.8)
−160.1* (− 291.9, − 28.4)
 Primaparous
− 179.1** (− 274.6, − 83.6)
−228.8 (− 478.1, 20.6)
−130.4 (− 80.1, − 287.6)
25.6 (− 69.6120.8)
58.8 (− 53.1, 170.8)
−47.1 (− 171.6, 77.5)
− 107.4* (− 198.6, − 16.2)
−10.5 (− 133.8, 112.8)
Family Size
−73.6** (− 93.4, − 51.9)
−19.8 (− 74.1, 34.4)
−5.5 (− 39.7, 28.6)
15.8 (−4.9, 36.5)
−3.9 (− 28.2, 20.5)
−9.4 (− 36.5, 17.7)
−51.3** (− 71.1, − 31.5)
−12.6 (− 39.4, 14.2)
Married* employed
314.0** (80.5, 547.5)
97.5 (− 512.0, 706.9)
12.0 (− 372.3, 396.3)
−223.3 (− 456.0, 9.4)
− 190.2 (− 463.8, 83.5)
− 277.5 (− 581.9, 27.1)
− 429.0** (− 651.9, − 206.1)
−65.9 (− 367.4, 235.4)
Living together* Employed
− 172.8 (− 474.1, 128.5)
−318.6 (− 1104.9, 467.8)
−110.6 (− 606.4, 385.2)
288.2 (−12.0, 588.0)
295.6 (− 57.4, 648.7)
218.2 (− 174.7, 611.1)
361.6* (73.9, 649.2)
127.2 (− 261.7, 516.0)
Single*Unemployed (REF)
 Primary or less* Employed
1392.0** (742.8, 2041.2)
1666.0 (28.6, 3360.7)
753.8 (− 314.7, 1822.4)
382.8 (− 264.3, 1029.8)
664.3 (− 96.7, 1425.2)
364.9 (− 481.9, 1211.6)
98.1 (− 521.8, 718.1)
779.1 (− 58.9, 1617.2)
 High school * Employed
237.6* (30.8, 444.5)
634.8* (94.9, 1174.7)
50.5 (−289.9, 391.0)
−137.5 (−343.6, 68.6)
−69.3 (− 311.7, 173.1)
98.9 (− 170.9, 368.6)
296.4** (98.9, 493.8)
76.3 (− 190.6, 343.3)
College or University*Unemployed (REF)
**Significant at 0.01 level*significant at 0.05 level
From Table 3, the confidence intervals of the ordinary regression and the quantile regression at the 50th quantile have a considerable overlap. Otherwise quantile regression estimates confidence intervals lie outside the confidence intervals for the ordinary least squares regression, suggesting that the effects of these covariates may not be constant across the conditional distribution quantiles. And hence justifies the importance of quantile regression to have a better picture in the whole spectrum of the birthweight quantile.
In order to avoid redundancy in the interpretation of the results in Table 3 and Fig. 2, we interpret few. Vegetable rich foods consumption during pregnancy increased birthweight at lower quantiles. This increase was significant at the 5th quantile (p = 0.001). However, in the 95th quantile, increase in consumption of vegetable rich foods had resulted in birthweight reduction. An increased frequency of junk foods intake by mothers was also associated with a slight increase in birthweight at the lower quantiles and significantly higher increase at the 95th quantile (p < 0.001). The results also indicated that consumption of snack and energy foods (p = 0.001), nuts and rice foods (p < 0.001) and junk foods (p < 0.001) during pregnancy increased the infant birthweight at the 95th quantiles of birthweight. Similarly, higher frequency of consuming nuts and rice foods by mothers is associated with increased birthweight in the 50th quantile (p = 0.021).
Mothers who consume protein rich foods with a higher frequency, tend to give birth to infants with significantly lower birthweight, as evidenced in the 5th and 95th quantile (p < 0.001). However, an increased frequency of protein rich foods intake increased birthweight of an infant at the75th and 90th quantiles. Female infants had a lower birthweight at the upper quantiles (p < 0.001) than males.
The two-way significant interactions were maternal employment status with marital status and maternal employment status with maternal education (Fig. 3). Infants born to employed women with marital status of living together weighed less than infants born to married mothers in the lower tail of the birthweight distribution but are more likely to have high birthweight at the upper tail quantiles. The interaction between maternal employment and education had a large positive effect on birth weight, especially in the lower tail; this difference is smaller in the upper quantiles of the distribution. For instance, at the 5th and 10th quantiles, infants from employed mothers with some primary school or less education, had 1670 g (p < 0.001) and 1824 g (p < 0.001) higher birthweights respectively than those from unemployed mothers with college or university education.

Discussion

This study showed, through the use of novel statistical approach, that protein rich foods dietary pattern had significant differential effects in the lower and upper quantiles of birthweight in Durban, South Africa. Our findings further suggest that vegetable rich foods and starch foods dietary patterns showed a protective effect at the 5th quantile of birthweight. Quantile regression models allowed for exploration of differential effects of dietary patterns across quantiles of birthweight adjusting for important demographic and socio-economic factors in MACE birth cohort. The differential effect of dietary patterns on quantiles of birthweight has not been previously described.
Previous studies that examined the association between maternal dietary patterns during pregnancy and birth outcomes, particularly in the presence of a high burden of low birthweights in the data set, used ordinary least square and logistic regression [11, 15, 17, 34]. The quantile regression insight on differential effect of maternal dietary on the different quantiles of birthweight.
Consumption of a traditional dietary pattern (potatoes, meat, vegetables) in early pregnancy, has been found in other studies to reduce the risk of having a low birthweight infant [11, 17]. Our study found further evidence in support of these studies, with consumption of vegetable rich foods and starch foods having a protective effect at the 5th quantile of birthweight. Unlike to these studies, our findings found that consumption of vegetable rich foods had associated with birthweight reduction at the 95th quantile. However, this is consistent with a study among British women that found processed and vegetarian diets were associated with the lowest birthweight [35]. A study in Brazil demonstrated that snack dietary patterns of mothers was associated with increase in birthweight [34]. In line with this, our findings showed increased intake of snack and energy foods by mothers during their pregnancy was associated with increased birthweight at lower and upper tail of birthweight. A review on studies from high-income countries found junk foods dietary pattern is related to low birthweight [13]. On the contrary, the findings of our study indicated that maternal consumption of junk foods during pregnancy was associated with increased offspring birthweight at the 95th quantile. In line with our study, junk food diet characterized by high consumption of fast foods, soft drink, processed meat, or chips frequently during pregnancy was associated increased risk of having a baby with a high birthweight in Australia [36].
In the 5th quantile, our study revealed that consumption of protein rich foods by mothers is associated with decreased birthweight. This is similar to what was found in studies in Ghana and Denmark, which indicated that red and processed meat diets during pregnancy, was associated with an increased risk of infants with lower birthweights [15, 37]. It is also noted that in a low-income cohort of US women, high protein intake was associated with reduced birth weight [38]. Moreover, the quantile regression modeling in our study showed evidence of a varied effect of protein rich foods consumed by mothers, throughout the conditional distribution of birthweight. For instance, women with more frequent consumption of protein rich foods, were associated with giving birth to infants with increased birthweight at the 75th and 90th quantile and these association was with a reduced birthweight at the 95th quantile.
Completing at least upper secondary education was found protective against low birthweight infants [39, 40]. Adverse socio-economic conditions such as maternal unemployment [40] and education level [41] have been linked to low birthweight in other studies. Unlike these studies, our study found an interaction effect of maternal employment with education and marital status. i.e. unemployed women with college or university education were more likely to have a low birthweight infant. The findings of the present study indicated that infants from employed and unmarried women, tend to have lower birthweight in the bottom lower (5th) quantile, but more likely to be macrosomia in the top upper tail (95th) quantile. This may be attributed to the job loadings on women during pregnancy. The quantile regression in this study showed that employment and family size had a differential effect across the different quantiles of birthweight. In higher quantiles of birthweight, female infants had consistently lower birthweight. This results corroborate what other authors who used linear regression [42] and logistic regression [43] found, i.e. male infants were more likely to be heavier at birth, compared with female infants.
An important strength of our study is that we were able to obtain detailed dietary data from an ongoing birth cohort, and using this rich dataset, we were able to describe, through factor analysis, a typical dietary pattern in a developing country, low socio-economic community utilizing both traditional and “western” dietary patterns. The additional strength of this study is that use of novel statistical approach, quantile regression, which is a very useful tool for data that are heterogeneous, in the sense that the tails and the central location of the conditional distributions vary differently with the levels of covariates and it is also robust, as it makes no distributional assumption about the error term in the model. A limitation of the study was the varying description of similar food types among participants (eg. the frequent use of trade names or local terms in describing intake), which may have resulted in high loading at different factors.

Conclusions

Food frequency questionnaires (FFQ) have been used in the study of dietary patterns among pregnant females. The advantage of this approach is that it identifies local dietary intake. In order to minimize the recall bias, the dietary data was collected in the third trimester of pregnancy, not at neonatal. Exploratory factor analysis data reduction was employed to transform the large set of correlated variables into smaller sets of non-correlated variables, known as factors, allowing a better understanding of the dimensions underlying the initial variables. Quantile regression allowed modeling the differential effect of maternal dietary patterns adjusting for socio-demographics on the entire quantile of birthweight spectrum. This would have been missed if traditional regression methods had been employed as it models at the average birthweight. The quantile regression model identified substantially differential effects of protein rich foods, parity and infant gender in the lower and upper distribution of birthweight. Moreover, vegetable rich foods and starch foods dietary patterns showed a protective effect at the 5th quantile of birthweight. Future studies need to consider other indicators such as gestational age, birth length and head circumference as measures of birth outcomes to better explore the effects of maternal dietary patterns.

Acknowledgements

We wish to acknowledge the Mother and Child in the Environment cohort study participants, all study fieldworkers and nursing staff at the participating clinics and hospitals. We also sincerely thank all the international collaborators (Utrecht, Michigan) and local collaborators of the MACE Study.
Written, informed consent was obtained from the mother for the children and provided their own consent. Follow-ups of the study were approved by the respective ethics committees at the University of KwaZulu-Natal Medical School.
Not applicable.

Competing interests

All authors declare that they have no any competing interests.
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Metadaten
Titel
The differential effect of maternal dietary patterns on quantiles of Birthweight
verfasst von
Aweke A. Mitku
Temesgen Zewotir
Delia North
Prakash Jeena
Rajen N. Naidoo
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Erschienen in
BMC Public Health / Ausgabe 1/2020
Elektronische ISSN: 1471-2458
DOI
https://doi.org/10.1186/s12889-020-09065-x

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