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DOI: 10.1055/a-1839-5643
Risk Factors for Maternal Body Mass Index and Gestational Weight Gain in Twin Pregnancies
Risikofaktoren für den mütterlichen Body-Mass-Index und die Gewichtszunahme in der Schwangerschaft bei Zwillingsschwangerschaften- Abstract
- Zusammenfassung
- Introduction
- Materials and Methods
- Results
- Discussion
- Conclusion
- References
Abstract
Objective This retrospective cohort study analyzes risk factors for abnormal pre-pregnancy body mass index and abnormal gestational weight gain in twin pregnancies.
Methods Data from 10 603/13 682 twin pregnancies were analyzed using uni- and multivariable logistic regression models to determine risk factors for abnormal body mass index and weight gain in pregnancy.
Results Multiparity was associated with pre-existing obesity in twin pregnancies (aOR: 3.78, 95% CI: 2.71 – 5.27). Working in academic or leadership positions (aOR: 0.57, 95% CI: 0.45 – 0.72) and advanced maternal age (aOR: 0.96, 95% CI: 0.95 – 0.98) were negatively associated with maternal obesity. Advanced maternal age was associated with a lower risk for maternal underweight (aOR: 0.95, 95% CI: 0.92 – 0.99). Unexpectedly, advanced maternal age (aOR: 0.98, 95% CI: 0.96 – 0.99) and multiparity (aOR: 0.6, 95% CI: 0.41 – 0.88) were also associated with lower risks for high gestational weight gain. Pre-existing maternal underweight (aOR: 1.55, 95% CI: 1.07 – 2.24), overweight (aOR: 1.61, 95% CI: 1.39 – 1.86), obesity (aOR: 3.09, 95% CI: 2.62 – 3.65) and multiparity (aOR: 1.64, 95% CI: 1.23 – 2.18) were all associated with low weight gain. Women working as employees (aOR: 0.85, 95% CI: 0.73 – 0.98) or in academic or leadership positions were less likely to have a low gestational weight gain (aOR: 0.77, 95% CI: 0.64 – 0.93).
Conclusion Risk factors for abnormal body mass index and gestational weight gain specified for twin pregnancies are relevant to identify pregnancies with increased risks for poor maternal or neonatal outcome and to improve their counselling. Only then, targeted interventional studies in twin pregnancies which are desperately needed can be performed.
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Zusammenfassung
Ziel Diese retrospektive Kohortenstudie analysiert die Risikofaktoren für einen abnormalen Body-Mass-Index vor der Schwangerschaft und eine abnormale Gewichtszunahme während der Schwangerschaft bei Zwillingsschwangerschaften.
Methoden Daten aus 10 603/13 682 Zwillingsschwangerschaften wurden mithilfe von univariablen und multivariablen logistischen Regressionsmodellen analysiert, um die Risikofaktoren für einen abnormalen Body-Mass-Index und eine abnormale Gewichtszunahme in der Schwangerschaft zu bestimmen.
Ergebnisse Multiparität war mit vorbestehender Adipositas bei Zwillingsschwangerschaften assoziiert (aOR 3,78; 95%-KI 2,71 – 5,27). Eine akademische Anstellung bzw. eine Führungsposition (aOR 0,57; 95%-KI 0,45 – 0,72) sowie fortgeschrittenes mütterliches Alter (aOR: 0,96, 95%-KI 0,95 – 0,98) waren negativ mit mütterlichem Adipositas assoziiert. Fortgeschrittenes mütterliches Alter war mit einem niedrigeren Risiko für mütterliches Untergewicht assoziiert (aOR 0,95; 95%-KI 0,92 – 0,99). Unerwarteterweise waren fortgeschrittenes mütterliches Alter (aOR 0,98; 95%-KI 0,96 – 0,99) sowie Multiparität (aOR 0,6; 95%-KI 0,41 – 0,88) auch mit einem niedrigeren Risiko für eine starke Gewichtszunahme in der Schwangerschaft assoziiert. Vorbestehendes mütterliches Untergewicht (aOR 1,55; 95%-KI 1,07 – 2,24), Übergewicht (aOR 1,61; 95%-KI 1,39 – 1,86), Adipositas (aOR 3,09; 95%-KI 2,62 – 3,65) und Multiparität (aOR 1,64; 95%-KI 1,23 – 2,18) waren alle mit einer niedrigeren Gewichtszunahme assoziiert. Die Wahrscheinlichkeit, dass Frauen, die als Angestellte (aOR 0,85; 95%-KI 0,73 – 0,98) oder in akademischen Stellungen arbeiteten oder Führungspositionen innehaben, in der Schwangerschaft nur wenig an Gewicht zulegen, war geringer (aOR 0,77; 95%-KI 0,64 – 0,93).
Schlussfolgerung Das Wissen um die Risikofaktoren für einen abnormalen Body-Mass-Index und eine abnormale Gewichtszunahme in der Schwangerschaft bei Zwillingsschwangerschaften ist wichtig, damit Schwangerschaften mit einem erhöhten Risiko eines schlechten mütterlichen oder kindlichen Outcomes frühzeitig identifiziert werden können und die Beratung dieser schwangeren Frauen dementsprechend verbessert werden kann. Nur dann können dringend benötigte gezielte Interventionsstudien bei Zwillingsschwangerschaften durchgeführt werden.
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Schlüsselwörter
Gewichtszunahme in der Schwangerschaft - Zwillingsschwangerschaft - Adipositas - Übergewicht - UntergewichtIntroduction
In 2016, the World Health Organization (WHO) reported that globally more than 1.9 billion individuals (39%) had an increased body mass index (BMI) > 25.0 kg/m2, which means that these are either overweight or obese [1]. In contrast, undernutrition, defined as a BMI < 18.5 kg/m2, affected “only” 462 million adults in the same year [2]. Meanwhile, overweight and obesity have exceeded undernutrition as global public health concern.
It has been demonstrated that, in singleton pregnancies, an abnormal maternal body mass index is associated with pre-, peri- and postnatal risks such as stillbirth [3], gestational diabetes (GDM) [4], hypertensive disorders in pregnancy (HDP) [5], preterm birth [5] or increased rates of cesarean deliveries [4]. Furthermore, epigenetic processes cause rising rates of non-communicable diseases in the offspring [6].
Twin births had increased since the 1980s in most Western countries, mainly due to artificial reproductive techniques [7]. Accordingly, in Germany (Hessen), twin births increased between 2000 and 2015 from 1.5% to 1.9% [8]. Nevertheless, the rates of obesity in the whole population, among pregnant women with singletons and with twin pregnancies continue to increase [8], [9].
To date, studies only investigated the impact of a high BMI in twin pregnancies on pregnancy outcomes such as HDP or GDM [10], [11] or the impact of a low maternal BMI on preterm birth [12].
However, to improve preventive concepts, it is necessary to know risk factors for abnormal BMI and inadequate gestational weight gain (GWG) in twin pregnancies. Therefore, we hereby aim to identify risk factors of abnormal BMI and deviant GWG in twin pregnancies.
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Materials and Methods
Study group
This is a retrospective population-based cohort study of twin pregnancies between 2000 and 2015 in the Federal state of Hessen (Germany) with a population of 6.176 million inhabitants in 2015 [13]. The electronic medical records from all perinatal centers were anonymously stored by the Federal Office for Perinatal Quality Assurance (“Geschäftsstelle Qualitätssicherung Hessen”/HEPE). All data retrieved for this study were extensively reviewed for plausibility and completeness by two reviewers (KN, NT). Since the original data set was organized and registered per twin and not per pregnancy, here, we only examined maternal characteristics from the data sets of first twins.
From the total data base of twin pregnancies (n = 13 682) we excluded data sets with missing or incomplete maternal weight measurements (n = 656), missing height measurements or height < 120 cm (n = 562), first clinical examinations performed after 14 weeks (n = 1771), delivery before 24 gestational weeks (n = 89) and one case with unknown sex of the first twin.
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BMI and GWG
The WHO definitions were applied to categorize the maternal BMI into four groups: underweight < 18.5 kg/m2, normal weight 18.5 – 24.9 kg/m2, overweight 25.0 – 29.9 kg/m2 and obesity ≥ 30 kg/m2. The database contained two weight measurements for each pregnancy: one from the first examination and a second one before birth. The mean maternal GWG per week was calculated by dividing the total GWG in grams during pregnancy by the number of weeks between first examination and delivery assuming a linear weight gain throughout pregnancy. In absence of international or national guidelines for maternal GWG in twin pregnancies, we had classified the maternal GWG per week in quartiles (Q), with the medium quartiles (Q2 and Q3) representing normal GWG. This resulted in cut-offs of GWG < 419.4 g/week for low GWG (Q1), 419.4 – 692.3 g/week for normal GWG (Q2 and Q3) and > 692.3 g/week for high GWG (Q4) [8].
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Statistical analysis
Using uni- and multivariable logistic regression models, the following risk factors for low and high maternal BMI early in pregnancy (“pre-existing”) and low and high GWG were identified: maternal age (continuous variable), nationality (German or other), parity (number of previous deliveries including stillbirths), marital status (mother with a partner, single parent), and maternal socioeconomic status. For the latter, the work characteristics was used as a proxy and was classified in: housewife, in training, workers (untrained workers or temporary employees), employees, and women with academic or leadership positions. For GWG, maternal BMI was included in analyses as a confounder ([Fig. 2]).
Reference groups for all analyses were women with a normal BMI (18.5 – 24.9 kg/m2) and normal GWG (Q2 – Q3). All p-values were two-sided with a significance level of 0.05.
Univariable analyses assessed the association between sociodemographic factors and BMI or GWG, respectively ([Tables 2] and [3]). In multivariable analyses, we assessed the maternal characteristics as risk factors for abnormal BMI and GWG. For all statistical analyses we used the programs R for Windows version 3.5.1, RStudio version 1.1.456 and Microsoft Excel 2013. In accordance with the guidelines of the working group for the survey and utilization of secondary data, AGENS, no ethical approval was required for this study [14].
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Results
Characteristics of the study group
The final study cohort comprises 10 603/13 682 twin pregnancies between 2000 and 2015. Within this cohort, 324/10 603 women (3.1%) were classified as underweight at their first examination, 6321/10 603 women (59.6%) were normal weight, 2489/10 603 women (23.5%) were overweight and 1469/10 603 (13.9%) were obese. The mean maternal age was 32.1 years, 81.3% of mothers were of German nationality, almost 10% were a single parent, more than 50% were primiparous, 38% of the mothers were housewives, and > 50% were either employees or working in an academic or leadership position ([Table 1]).
Underweight (n = 324, 3.06%) |
Normal weight (n = 6321, 59.62%) |
Overweight (n = 2489, 23.47%) |
Obesity (n = 1469, 13.85%) |
Total (n = 10 603) |
Overall p-value |
|
---|---|---|---|---|---|---|
n = 10 603 twin pregnancies, SD = standard deviation, a n = 8767, b n = 10 552, c n = 7471. bold = p < 0.05 |
||||||
Mean maternal age (SD) |
31.1 (5.80) |
32.3 (5.08) |
32.1 (5.02) |
31.5 (5.03) |
32.1 (5.09) |
< 0.001 |
Mothersʼ nationality |
< 0.001 |
|||||
|
248 (76.5%) |
5185 (82.0%) |
1966 (79.0%) |
1222 (83.2%) |
8621 (81.3%) |
|
|
76 (23.5%) |
1136 (18.0%) |
523 (21.0%) |
247 (16.8%) |
1982 (18.7%) |
|
Single parenta |
0.185 |
|||||
|
219 (88.7%) |
4647 (89.6%) |
1886 (90.4%) |
1144 (91.3%) |
7896 (90.1%) |
|
|
28 (11.3%) |
537 (10.4%) |
200 (9.6%) |
106 (8.5%) |
871 (9.9%) |
|
Parityb |
< 0.001 |
|||||
|
201 (62.2%) |
3783 (60.1%) |
1308 (52.8%) |
703 (48.1%) |
5995 (56.8%) |
|
|
89 (27.6%) |
1896 (30.1%) |
750 (30.3%) |
478 (32.7%) |
3213 (30.4%) |
|
|
22 (6.8%) |
451 (7.2%) |
285 (11.5%) |
164 (11.2%) |
922 (8.7%) |
|
|
11 (3.4%) |
160 (2.5%) |
135 (5.5%) |
116 (7.9%) |
422 (4.0%) |
|
Professionc |
< 0.001 |
|||||
|
96 (44.2%) |
1518 (35.0%) |
746 (41.1%) |
486 (44.3%) |
2846 (38.1%) |
|
|
8 (3.7%) |
93 (2.1%) |
29 (1.6%) |
21 (1.9%) |
151 (2.0%) |
|
|
6 (2.8%) |
126 (2.9%) |
51 (2.8%) |
42 (3.8%) |
225 (3.0%) |
|
|
62 (28.6%) |
1595 (36.7%) |
665 (36.7%) |
389 (35.4%) |
2711 (36.3%) |
|
|
45 (20.7%) |
1010 (23.3%) |
323 (17.8%) |
160 (14.6%) |
1538 (20.6%) |
Risk factors |
Underweight |
Overweight |
Obesity |
||||||
---|---|---|---|---|---|---|---|---|---|
OR (95% CI) |
p-value |
Global p-value |
OR (95% CI) |
p-value |
Global p-value |
OR (95% CI) |
p-value |
Global p-value |
|
Univariable analysis, n = 10 603 twin pregnancies, reference: normal BMI (≥ 18.5 < 25.0 kg/m2), OR = odds ratio, 95% CI = 95% confidence interval, a n = 8767, b n = 10 552, c n = 7471. bold = p < 0.05 |
|||||||||
Maternal age |
0.95 (0.93 – 0.98) |
< 0.0001 |
0.99 (0.98 – 1) |
0.0318 |
0.97 (0.96 – 0.98) |
< 0.0001 |
|||
Mothersʼ nationality |
0.0130 |
0.0010 |
0.2957 |
||||||
|
reference |
reference |
reference |
||||||
|
1.4 (1.07 – 1.82) |
1.21 (1.08 – 1.36) |
0.92 (0.79 – 1.07) |
||||||
Single parenta |
0.6232 |
0.3246 |
0.0472 |
||||||
|
reference |
reference |
reference |
||||||
|
1.11 (0.74 – 1.66) |
0.92 (0.77 – 1.09) |
0.8 (0.64 – 1) |
||||||
Parityb |
0.6069 |
< 0.0001 |
< 0.0001 |
||||||
|
reference |
reference |
reference |
||||||
|
0.88 (0.68 – 1.14) |
0.3420 |
1.14 (1.03 – 1.27) |
0.0123 |
1.36 (1.19 – 1.54) |
< 0.0001 |
|||
|
0.92 (0.58 – 1.44) |
0.7102 |
1.83 (1.56 – 2.15) |
< 0.0001 |
1.96 (1.61 – 2.38) |
< 0.0001 |
|||
|
1.29 (0.69 – 2.42) |
0.4207 |
2.44 (1.92 – 3.09) |
< 0.0001 |
3.9 (3.03 – 5.02) |
< 0.0001 |
|||
Professionc |
0.02239 |
< 0.0001 |
< 0.0001 |
||||||
|
reference |
reference |
reference |
||||||
|
1.36 (0.64 – 2.88) |
0.4221 |
0.63 (0.41 – 0.97) |
0.0364 |
0.71 (0.43 – 1.14) |
0.1578 |
|||
|
0.75 (0.32 – 1.75) |
0.5103 |
0.82 (0.59 – 1.15) |
0.2590 |
1.04 (0.72 – 1.5) |
0.8280 |
|||
|
0.61 (0.44 – 0.85) |
0.0035 |
0.85 (0.75 – 0.96) |
0.0105 |
0.76 (0.66 – 0.89) |
0.0004 |
|||
|
0.7 (0.49 – 1.01) |
0.0586 |
0.65 (0.56 – 0.76) |
< 0.0001 |
0.49 (0.41 – 0.6) |
< 0.0001 |
Risk factors |
Low maternal weight gain vs. normal weight gain |
High maternal weight gain vs. normal weight gain |
||||
---|---|---|---|---|---|---|
OR (95% CI) |
p-value |
Global p-value |
OR (95% CI) |
p-value |
Global p-value |
|
Univariable analysis, n = 10 603 twin pregnancies, reference: quartiles Q2–Q3 (“normal weight gain”, 419.4 – 692.3 g/week) within the according population OR = odds ratio, 95% CI = 95% confidence interval, a n = 8767, b n = 10 552, c n = 7471. bold = p < 0.05 |
||||||
Maternal age |
0.99 (0.98 – 1) |
0.0299 |
0.97 (0.96 – 0.98) |
< 0.0001 |
||
Mothersʼ nationality |
0.0391 |
0.7070 |
||||
|
reference |
reference |
||||
|
1.13 (1.01 – 1.27) |
0.98 (0.87 – 1.1) |
||||
Single parenta |
0.3737 |
0.0462 |
||||
|
reference |
reference |
||||
|
0.92 (0.77 – 1.1) |
1.18 (1 – 1.4) |
||||
Parityb |
< 0.0001 |
< 0.0001 |
||||
|
reference |
reference |
||||
|
1.16 (1.05 – 1.29) |
0.0049 |
0.74 (0.67 – 0.83) |
< 0.0001 |
||
|
1.32 (1.12 – 1.55) |
0.0007 |
0.64 (0.53 – 0.76) |
< 0.0001 |
||
|
2.17 (1.75 – 2.7) |
< 0.0001 |
0.68 (0.51 – 0.9) |
0.0068 |
||
Professionc |
< 0.0001 |
0.0255 |
||||
|
reference |
reference |
||||
|
0.75 (0.5 – 1.13) |
0.1672 |
0.99 (0.66 – 1.49) |
0.9780 |
||
|
1.11 (0.8 – 1.54) |
0.5196 |
1.36 (0.97 – 1.9) |
0.0718 |
||
|
0.77 (0.67 – 0.87) |
< 0.0001 |
1.13 (0.99 – 1.29) |
0.0652 |
||
|
0.67 (0.57 – 0.78) |
< 0.0001 |
0.91 (0.78 – 1.06) |
0.2361 |
||
BMI at 1st examination |
< 0.0001 |
0.2849 |
||||
|
reference |
reference |
||||
|
1.63 (1.45 – 1.83) |
< 0.0001 |
1.07 (0.95 – 1.19) |
0.2709 |
||
|
3.7 (3.25 – 4.23) |
< 0.0001 |
1.14 (0.97 – 1.33) |
0.1022 |
||
|
1.43 (1.09 – 1.88) |
0.0090 |
0.93 (0.71 – 1.23) |
0.6294 |
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Risk factors for maternal BMI
The multivariable analysis found that advanced maternal age was negatively associated with maternal underweight (aOR: 0.95, 95% CI: 0.92 – 0.99, p < 0.01). None of the other variables assessed were associated with maternal underweight ([Fig. 1 a]).
Multiparity with 3 or more previous deliveries was associated with overweight in twin mothers (aOR: 2.46, 95% CI: 1.82 – 3.33, p < 0.0001), whereas there was a significantly lower frequency of overweight in women with an academic or leadership position (aOR: 0.74, 95% CI: 0.62 – 0.89, p = 0.001) ([Fig. 1 b]).
Mothers with a nationality other than German were significantly less obese as compared to German women with twins (aOR: 0.66, 95% CI: 0.54 – 0.8, p < 0.001). A parity ≥ 3 was associated with increased risk for obesity (aOR: 3.78, 95% CI: 2.71 – 5.27, p < 0.001). Working in an academic or leadership position (aOR: 0.57, 95% CI: 0.45 – 0.72, p < 0.001) and increasing maternal age were both negatively associated with maternal obesity in the multivariable model (aOR: 0.96, 95% CI: 0.95 – 0.98, p < 0.001) ([Fig. 1 c]).
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Risk factors for maternal GWG
Advanced maternal age (aOR: 0.98, 95% CI: 0.96 – 0.99, p < 0.001) and parity ≥ 3 (aOR: 0.60, 95% CI: 0.41 – 0.88, p = 0.009) were associated with lower risks for high GWG (> 75th centile, Q4) ([Fig. 2 a]). High GWG was not significantly associated with the pre-existing BMI ([Fig. 2 a]).
Accordingly, parity ≥ 3 (aOR: 1.64, 95% CI: 1.23 – 2.18, p < 0.001), maternal underweight (aOR: 1.55, 95% CI: 1.06 – 2.23, p = 0.02), overweight (aOR: 1.61, 95% CI: 1.39 – 1.86, p < 0.0001) and obesity (aOR: 3.09, 95% CI: 2.62 – 3.65, p < 0.0001) were all associated with a low GWG (< 25th centile, Q1). As compared to housewives working as employee (aOR: 0.85, 95% CI: 0.73 – 0.98, p = 0.03) or in an academic or leadership position (aOR: 0.77, 95% CI: 0.64 – 0.93, p < 0.01) was negatively associated with low GWG ([Fig. 2 b]).
The results of the univariable analysis of risk factors for low or high BMI or GWG are demonstrated in [Tables 2] and [3]. After controlling for confounders, the results were similar in the multivariable model. However, within the univariable model working as an employee was significantly associated a lower risk for underweight (OR: 0.61, 95% CI: 0.44 – 0.85, p = 0.0035), overweight (OR: 0.85, 95% CI: 0.75 – 0.96, p = 0.0105) and obesity (OR: 0.76, 95% CI: 0.66 – 0.89, p = 0.0004).
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Discussion
The present study found that, in twin pregnancies, maternal age, multiparity, and mothersʼ profession reflecting her socioeconomic status were risk factors associated with an abnormal maternal BMI and deviant GWG. Additionally, both a high and a low pre-existing BMI in early pregnancy were associated with low GWG. These findings are different from the singleton pregnancies of the German cohort, where high pre-pregnancy BMI is associated with excessive GWG [9]. In singleton pregnancies, it had been described that low GWG was positively associated with regular exercise in week 30, whereas being overweight before pregnancy was inversely associated with regular exercise in week 17, aOR = 0.8 (0.7 – 0.8) and 30, aOR = 0.7 (0.6 – 0.7). Since all women experiencing a multiple pregnancy were less likely to exercise regularly during pregnancy, the impact of lifestyle during pregnancy seems less pronounced [15].
We found a negative association between increasing maternal age and underweight in women with twin pregnancies, which had also been described in Asian and African women of reproductive age [16], [17], [18].
Not only in the whole population, but also in twin gestations a pre-existing BMI ≥ 30 kg/m2 was more frequent in younger women. This can be explained by the increasing prevalence of obesity in Western countries [19]. It is worrisome that even the World Obesity Federation stated that, globally, the defined target of “no increase in obesity beyond the levels of 2010” cannot be realized [20].
The fact that a high parity was associated with increasing risks for maternal overweight and obesity had already been observed in women of childbearing age [18], [21]. One of many causal factors is an excess postpartum weight retention occurring more frequently in women with excessive GWG [22]. While pre-pregnancy BMI was increased in multiparous women, the risk for high GWG was significantly lower in women with a high parity, which had already been observed in singleton pregnancies [23], [24], [25]. While the lower frequency of high GWG we observed among multiparous women is in accordance with recommendations for women with a high BMI [26] to prevent pregnancy and birth complications in singleton pregnancies, their effects differ in twin pregnancies: Even though an association between high maternal BMI and adverse maternal pregnancy such as preeclampsia or gestational diabetes was found in twin pregnancies, the relationship is not as strong as in singletons [12]. In addition, one study even stated that low GWG of overweight women with twin pregnancies does not reduce the risk for maternal complications but causes increased rates of preterm birth [27]. This association still needs further research but we can already conclude that multiparous women should be monitored especially close.
A multivariable analysis of almost 7000 singleton pregnancies had found that a low maternal educational level was associated with increased risks of maternal overweight and obesity [25]. Hughes et al. analyzed the relationship between unemployment and BMI among adults in the UK and similarly observed an association between unemployment and obesity among non-smokers [28].
While the maternal BMI in early pregnancy was not associated with an increased risk for high GWG in this twin cohort, we observed a U-shaped association between maternal BMI and low GWG: women with a BMI ≥ 25 kg/m2 demonstrated a significantly lower GWG as already described by Hutcheon et al. [29]. While Hutcheon et al. did not present results for underweight women, we found that a maternal BMI < 18.5 kg/m2 was also significantly associated with low GWG. Since underweight and low GWG may simultaneously lead to increased risks for SGA infants and preterm birth [30] underweight women with twins need to be closely monitored for early diagnosis of fetal growth restriction.
Overall, the effects of maternal BMI and GWG on the outcome of twin pregnancies require further evaluation. Previous studies found an association between a high maternal BMI and hypertensive disorders and gestational diabetes mellitus [10], [11] in twin pregnancies. Higher risks for hypertensive disorders [31], [32] and Cesarean deliveries [30] were also observed in women with high GWG. A low maternal pre-pregnancy BMI and low maternal GWG during twin pregnancies have been associated with adverse neonatal outcomes like preterm birth [12], [32], [33].
While the risk factors identified in this study can already be a useful tool to help identify women who need a more careful surveillance during twin pregnancy, we have also analyzed the impact of maternal BMI and weight gain on maternal and neonatal outcomes. This will be part of consecutive publications and debates.
The main strength of this study is that the analysis of risk factors for aberrant BMI and GWG might allow improving prevention and a closer surveillance of the twin pregnancies. The large cohort of twin pregnancies enabled us to perform multivariable analyses. Another strength is that we based the analysis in this study on previously defined cut-offs for GWG categories in twin gestations [8]. We are conscious of the fact that we could only show associations, but no causal relationships. A weakness is that the protocol of HEPE did allow neither to differentiate between mono- and dichorionic twins nor to analyse maternal weight continuously. Therefore, we could not specify the cut-off values for weekly maternal GWG for gestational age. Data on the socioeconomic status were not systematically documented causing missing values.
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Conclusion
We identified multiparity and low socioeconomic status as risk factors for pre-existing maternal overweight or obesity in twin pregnancies. Young age and nulliparity were associated with high maternal GWG in twin gestations. Parity ≥ 3 and an abnormally high or low maternal BMI were all associated with increased risks for low GWG.
Our results should help to identify and counsel women pregnant of twins at risk for abnormal GWG, whereby high GWG is strongly associated with adverse maternal and low GWG with poor neonatal outcomes in twin gestations. This issue is part of still unpublished data from the same database investigating the impact of BMI and GWG on maternal and neonatal outcomes. Unfortunately, there are no controlled studies yet on interventions of abnormal GWG specified for twin pregnancies. Our paper might be a new stimulus for future studies to improve surveillance and to investigate which lifestyle interventions might be helpful in twin gestations to improve the outcome in mothers with abnormal BMI or weight gain.
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Conflict of Interest
The authors declare that they have no conflict of interest.
Acknowledgements
The authors would like to thank their colleagues from the hospitals documenting the pregnancy and perinatal data, as well as the Hessen Quality Assurance Centre, especially Dr. Björn Misselwitz, for providing the total database.
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References
- 1 World Health Organization. Fact sheets – Malnutrition, 2022. Accessed June 14, 2022 at: https://www.who.int/news-room/fact-sheets/detail/malnutrition
- 2 World Health Organization. Obesity and overweight, 2022. Accessed June 14, 2022 at: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight
- 3 Flenady V, Koopmans L, Middleton P. et al. Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis. Lancet 2011; 377: 1331-1340
- 4 Poston L, Caleyachetty R, Cnattingius S. et al. Preconceptional and maternal obesity: epidemiology and health consequences. Lancet Diabetes Endocrinol 2016; 4: 1025-1036
- 5 Santos S, Voerman E, Amiano P. et al. Impact of maternal body mass index and gestational weight gain on pregnancy complications: an individual participant data meta-analysis of European, North American and Australian cohorts. BJOG 2019; 126: 984-995
- 6 Fernandez-Twinn DS, Hjort L, Novakovic B. et al. Intrauterine programming of obesity and type 2 diabetes. Diabetologia 2019; 62: 1789-1801
- 7 Boyle B, McConkey R, Garne E. et al. Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984–2007. BJOG 2013; 120: 707-716
- 8 Schubert J, Timmesfeld N, Noever K. et al. Challenges for better care based on the course of maternal body mass index, weight gain and multiple outcome in twin pregnancies: a population-based retrospective cohort study in Hessen/Germany within 15 years. Arch Gynecol Obstet 2020; 301: 161-170
- 9 Noever K, Schubert J, Reuschel E. et al. Changes in Maternal Body Mass Index, Weight Gain and Outcome of Singleton Pregnancies from 2000 to 2015: A Population-based Retrospective Cohort Study in Hesse/Germany. Geburtshilfe Frauenheilkd 2020; 80: 508-517
- 10 Al-Obaidly S, Parrish J, Murphy KE. et al. Maternal pre-gravid body mass index and obstetric outcomes in twin gestations. J Perinatol 2014; 34: 425-428
- 11 Fox NS, Roman AS, Saltzman DH. et al. Obesity and adverse pregnancy outcomes in twin pregnancies. J Matern Fetal Neonatal Med 2014; 27: 355-359
- 12 Ram M, Berger H, Lipworth H. et al. DOH-Net (Diabetes, Obesity and Hypertension in Pregnancy Research Network) and SOON (Southern Ontario Obstetrical Network) Investigators. The relationship between maternal body mass index and pregnancy outcomes in twin compared with singleton pregnancies. Int J Obes (Lond) 2020; 44: 33-44
- 13 Statistik.Hessen. Tabellen Bevölkerung, 2021. Accessed March 12, 2021 at: https://statistik.hessen.de/zahlen-fakten/bevoelkerung-gebiet-haushalte-familien/bevoelkerung/tabellen
- 14 Swart E, Gothe H, Geyer S. et al. Gute Praxis Sekundärdatenanalyse (GPS): Leitlinien und Empfehlungen. Gesundheitswesen 2015; 77: 120-126
- 15 Owe KM, Nystad W, Bø K. Correlates of regular exercise during pregnancy: the Norwegian Mother and Child Cohort Study. Scand J Med Sci Sports 2009; 19: 637-645
- 16 Abrha S, Shiferaw S, Ahmed KY. Overweight and obesity and its socio-demographic correlates among urban Ethiopian women: evidence from the 2011 EDHS. BMC Public Health 2016; 16: 636
- 17 Hashan MR, Rabbi MF, Haider SS. et al. Prevalence and associated factors of underweight, overweight and obesity among women of reproductive age group in the Maldives: Evidence from a nationally representative study. PloS One 2020; 15: e0241621
- 18 He Y, Pan A, Yang Y. et al. Prevalence of Underweight, Overweight, and Obesity Among Reproductive-Age Women and Adolescent Girls in Rural China. Am J Public Health 2016; 106: 2103-2110
- 19 Ng M, Fleming T, Robinson M. et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet 2014; 384: 766-781
- 20 World Obesity Federation. COVID-19 and Obesity: The 2021 Atlas, The cost of not addressing the global obesity crisis. March 2021. Accessed June 14, 2022 at: https://www.worldobesityday.org/assets/downloads/COVID-19-and-Obesity-The-2021-Atlas.pdf
- 21 Weiss JL, Malone FD, Emig D. et al. Obesity, obstetric complications and cesarean delivery rate–a population-based screening study. Am J Obstet Gynecol 2004; 190: 1091-1097
- 22 Gallagher K, Ralph J, Petros T. et al. Postpartum Weight Retention in Primiparous Women and Weight Outcomes in Their Offspring. J Midwifery Womens Health 2019; 64: 427-434
- 23 Paulino DS, Surita FG, Peres GB. et al. Association between parity, pre-pregnancy body mass index and gestational weight gain. J Matern Fetal Neonatal Med 2016; 29: 880-884
- 24 Hermanussen M, Scheffler C. Secular trends in gestational weight gain and parity on birth weight: An editorial. Acta Paediatr 2021; 110: 1094-1096
- 25 Gaillard R, Durmuş B, Hofman A. et al. Risk factors and outcomes of maternal obesity and excessive weight gain during pregnancy. Obesity (Silver Spring) 2013; 21: 1046-1055
- 26 Schaefer-Graf U, Ensenauer R, Gembruch U. et al. Obesity and Pregnancy. Guideline of the German Society of Gynecology and Obstetrics (S3-Level, AWMF Registry No. 015–081, June 2019). Geburtshilfe Frauenheilkd 2021; 81: 279-303
- 27 Liu LY, Zafman KB, Fox NS. Weight gain and pregnancy outcomes in overweight or obese women with twin gestations. J Matern Fetal Neonatal Med 2021; 34: 1774-1779
- 28 Hughes A, Kumari M. Unemployment, underweight, and obesity: Findings from Understanding Society (UKHLS). Prev Med 2017; 97: 19-25
- 29 Hutcheon JA, Platt RW, Abrams B. et al. Pregnancy Weight Gain by Gestational Age in Women with Uncomplicated Dichorionic Twin Pregnancies. Paediatr Perinat Epidemiol 2018; 32: 172-180
- 30 Bodnar LM, Himes KP, Abrams B. et al. Gestational Weight Gain and Adverse Birth Outcomes in Twin Pregnancies. Obstet Gynecol 2019; 134: 1075-1086
- 31 Pettit KE, Lacoursiere DY, Schrimmer DB. et al. Maternal and neonatal outcomes in women with twin pregnancies with excessive gestational weight gain. J Matern Fetal Neonatal Med 2016; 29: 2182-2185
- 32 Lipworth H, Melamed N, Berger H. et al. Diabetes, Obesity, and Hypertension In Pregnancy Research Network Investigators. Maternal weight gain and pregnancy outcomes in twin gestations. Am J Obstet Gynecol 2021; 225: 532.e1-532.e12
- 33 Algeri P, Pelizzoni F, Bernasconi DP. et al. Influence of weight gain, according to Institute of Medicine 2009 recommendation, on spontaneous preterm delivery in twin pregnancies. BMC Pregnancy Childbirth 2018; 18: 6
Correspondence
Publication History
Received: 28 January 2022
Accepted after revision: 27 April 2022
Article published online:
10 August 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 World Health Organization. Fact sheets – Malnutrition, 2022. Accessed June 14, 2022 at: https://www.who.int/news-room/fact-sheets/detail/malnutrition
- 2 World Health Organization. Obesity and overweight, 2022. Accessed June 14, 2022 at: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight
- 3 Flenady V, Koopmans L, Middleton P. et al. Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis. Lancet 2011; 377: 1331-1340
- 4 Poston L, Caleyachetty R, Cnattingius S. et al. Preconceptional and maternal obesity: epidemiology and health consequences. Lancet Diabetes Endocrinol 2016; 4: 1025-1036
- 5 Santos S, Voerman E, Amiano P. et al. Impact of maternal body mass index and gestational weight gain on pregnancy complications: an individual participant data meta-analysis of European, North American and Australian cohorts. BJOG 2019; 126: 984-995
- 6 Fernandez-Twinn DS, Hjort L, Novakovic B. et al. Intrauterine programming of obesity and type 2 diabetes. Diabetologia 2019; 62: 1789-1801
- 7 Boyle B, McConkey R, Garne E. et al. Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984–2007. BJOG 2013; 120: 707-716
- 8 Schubert J, Timmesfeld N, Noever K. et al. Challenges for better care based on the course of maternal body mass index, weight gain and multiple outcome in twin pregnancies: a population-based retrospective cohort study in Hessen/Germany within 15 years. Arch Gynecol Obstet 2020; 301: 161-170
- 9 Noever K, Schubert J, Reuschel E. et al. Changes in Maternal Body Mass Index, Weight Gain and Outcome of Singleton Pregnancies from 2000 to 2015: A Population-based Retrospective Cohort Study in Hesse/Germany. Geburtshilfe Frauenheilkd 2020; 80: 508-517
- 10 Al-Obaidly S, Parrish J, Murphy KE. et al. Maternal pre-gravid body mass index and obstetric outcomes in twin gestations. J Perinatol 2014; 34: 425-428
- 11 Fox NS, Roman AS, Saltzman DH. et al. Obesity and adverse pregnancy outcomes in twin pregnancies. J Matern Fetal Neonatal Med 2014; 27: 355-359
- 12 Ram M, Berger H, Lipworth H. et al. DOH-Net (Diabetes, Obesity and Hypertension in Pregnancy Research Network) and SOON (Southern Ontario Obstetrical Network) Investigators. The relationship between maternal body mass index and pregnancy outcomes in twin compared with singleton pregnancies. Int J Obes (Lond) 2020; 44: 33-44
- 13 Statistik.Hessen. Tabellen Bevölkerung, 2021. Accessed March 12, 2021 at: https://statistik.hessen.de/zahlen-fakten/bevoelkerung-gebiet-haushalte-familien/bevoelkerung/tabellen
- 14 Swart E, Gothe H, Geyer S. et al. Gute Praxis Sekundärdatenanalyse (GPS): Leitlinien und Empfehlungen. Gesundheitswesen 2015; 77: 120-126
- 15 Owe KM, Nystad W, Bø K. Correlates of regular exercise during pregnancy: the Norwegian Mother and Child Cohort Study. Scand J Med Sci Sports 2009; 19: 637-645
- 16 Abrha S, Shiferaw S, Ahmed KY. Overweight and obesity and its socio-demographic correlates among urban Ethiopian women: evidence from the 2011 EDHS. BMC Public Health 2016; 16: 636
- 17 Hashan MR, Rabbi MF, Haider SS. et al. Prevalence and associated factors of underweight, overweight and obesity among women of reproductive age group in the Maldives: Evidence from a nationally representative study. PloS One 2020; 15: e0241621
- 18 He Y, Pan A, Yang Y. et al. Prevalence of Underweight, Overweight, and Obesity Among Reproductive-Age Women and Adolescent Girls in Rural China. Am J Public Health 2016; 106: 2103-2110
- 19 Ng M, Fleming T, Robinson M. et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet 2014; 384: 766-781
- 20 World Obesity Federation. COVID-19 and Obesity: The 2021 Atlas, The cost of not addressing the global obesity crisis. March 2021. Accessed June 14, 2022 at: https://www.worldobesityday.org/assets/downloads/COVID-19-and-Obesity-The-2021-Atlas.pdf
- 21 Weiss JL, Malone FD, Emig D. et al. Obesity, obstetric complications and cesarean delivery rate–a population-based screening study. Am J Obstet Gynecol 2004; 190: 1091-1097
- 22 Gallagher K, Ralph J, Petros T. et al. Postpartum Weight Retention in Primiparous Women and Weight Outcomes in Their Offspring. J Midwifery Womens Health 2019; 64: 427-434
- 23 Paulino DS, Surita FG, Peres GB. et al. Association between parity, pre-pregnancy body mass index and gestational weight gain. J Matern Fetal Neonatal Med 2016; 29: 880-884
- 24 Hermanussen M, Scheffler C. Secular trends in gestational weight gain and parity on birth weight: An editorial. Acta Paediatr 2021; 110: 1094-1096
- 25 Gaillard R, Durmuş B, Hofman A. et al. Risk factors and outcomes of maternal obesity and excessive weight gain during pregnancy. Obesity (Silver Spring) 2013; 21: 1046-1055
- 26 Schaefer-Graf U, Ensenauer R, Gembruch U. et al. Obesity and Pregnancy. Guideline of the German Society of Gynecology and Obstetrics (S3-Level, AWMF Registry No. 015–081, June 2019). Geburtshilfe Frauenheilkd 2021; 81: 279-303
- 27 Liu LY, Zafman KB, Fox NS. Weight gain and pregnancy outcomes in overweight or obese women with twin gestations. J Matern Fetal Neonatal Med 2021; 34: 1774-1779
- 28 Hughes A, Kumari M. Unemployment, underweight, and obesity: Findings from Understanding Society (UKHLS). Prev Med 2017; 97: 19-25
- 29 Hutcheon JA, Platt RW, Abrams B. et al. Pregnancy Weight Gain by Gestational Age in Women with Uncomplicated Dichorionic Twin Pregnancies. Paediatr Perinat Epidemiol 2018; 32: 172-180
- 30 Bodnar LM, Himes KP, Abrams B. et al. Gestational Weight Gain and Adverse Birth Outcomes in Twin Pregnancies. Obstet Gynecol 2019; 134: 1075-1086
- 31 Pettit KE, Lacoursiere DY, Schrimmer DB. et al. Maternal and neonatal outcomes in women with twin pregnancies with excessive gestational weight gain. J Matern Fetal Neonatal Med 2016; 29: 2182-2185
- 32 Lipworth H, Melamed N, Berger H. et al. Diabetes, Obesity, and Hypertension In Pregnancy Research Network Investigators. Maternal weight gain and pregnancy outcomes in twin gestations. Am J Obstet Gynecol 2021; 225: 532.e1-532.e12
- 33 Algeri P, Pelizzoni F, Bernasconi DP. et al. Influence of weight gain, according to Institute of Medicine 2009 recommendation, on spontaneous preterm delivery in twin pregnancies. BMC Pregnancy Childbirth 2018; 18: 6