| Literature DB >> 35814725 |
Abigail Perry1, Anna Stephanou1, Margaret P Rayman1.
Abstract
Pre-eclampsia affects 3%-5% of pregnant women worldwide and is associated with a range of adverse maternal and fetal outcomes, including maternal and/or fetal death. It particularly affects those with chronic hypertension, pregestational diabetes mellitus or a family history of pre-eclampsia. Other than early delivery of the fetus, there is no cure for pre-eclampsia. Since diet or dietary supplements may affect the risk, we have carried out an up-to-date, narrative literature review to assess the relationship between nutrition and pre-eclampsia. Several nutrients and dietary factors previously believed to be implicated in the risk of pre-eclampsia have now been shown to have no effect on risk; these include vitamins C and E, magnesium, salt, ω-3 long-chain polyunsaturated fatty acids (fish oils) and zinc. Body mass index is proportionally correlated with pre-eclampsia risk, therefore women should aim for a healthy pre-pregnancy body weight and avoid excessive gestational and interpregnancy weight gain. The association between the risk and progression of the pathophysiology of pre-eclampsia may explain the apparent benefit of dietary modifications resulting from increased consumption of fruits and vegetables (≥400 g/day), plant-based foods and vegetable oils and a limited intake of foods high in fat, sugar and salt. Consuming a high-fibre diet (25-30 g/day) may attenuate dyslipidaemia and reduce blood pressure and inflammation. Other key nutrients that may mitigate the risk include increased calcium intake, a daily multivitamin/mineral supplement and an adequate vitamin D status. For those with a low selenium intake (such as those living in Europe), fish/seafood intake could be increased to improve selenium intake or selenium could be supplemented in the recommended multivitamin/mineral supplement. Milk-based probiotics have also been found to be beneficial in pregnant women at risk. Our recommendations are summarised in a table of guidance for women at particular risk of developing pre-eclampsia. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.Entities:
Keywords: blood pressure lowering; dietary patterns; nutrient deficiencies; nutritional treatment; weight management
Year: 2022 PMID: 35814725 PMCID: PMC9237898 DOI: 10.1136/bmjnph-2021-000399
Source DB: PubMed Journal: BMJ Nutr Prev Health ISSN: 2516-5542
Search terms used for article selection
| Factor | Key search terms |
| Antioxidants | preeclampsia AND antioxidants |
| Calcium | preeclampsia AND calcium |
| Dietary pattern | preeclampsia AND ‘dietary pattern’ |
| Fibre | preeclampsia AND fibre OR fiber |
| Folate/folic acid | preeclampsia AND folate OR preeclampsia AND ‘folic acid’ |
| Iodine | preeclampsia AND iodine |
| Magnesium | preeclampsia AND magnesium |
| Maternal weight | preeclampsia AND ‘gestational weight gain’ OR preeclampsia AND ‘maternal BMI’ |
| Multivitamins/multiminerals | preeclampsia AND multivitamin OR preeclampsia AND multimineral |
| Omega-3 long-chain polyunsaturated fatty acids | preeclampsia AND omega-3 long-chain polyunsaturated fatty acids |
| Salt | preeclampsia AND salt |
| Selenium | preeclampsia AND selenium |
| Vitamin B12 | preeclampsia AND ‘vitamin B12’ |
| Vitamin D | preeclampsia AND ‘vitamin D’ |
| Zinc | preeclampsia AND zinc |
Evidence from different studies on nutrients that show a lack of benefit on pre-eclampsia risk or prevention
| Nutrient and citation | Type of study | Participants (n) | Main outcomes | Findings | Conclusion |
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| Poston | RCT with 1000 mg C and 400 IU E | 2404 UK women at increased risk of PE | PE, low birth weight, small size for gestational age | Women treated with vitamins C and E did not have a reduced risk; RR 0.97, 95% CI 0.80 to 1.17. | Vitamin C and E supplementation in the 2nd trimester did not reduce the risk of PE in women at risk. |
| Klemmensen | Prospective cohort study of vitamin intake | n=49 373 Danish women | Vitamin intake from diet and supplement from previous 4 weeks estimated from 25-week FFQ. PE, eclampsia, HELLP. | Vitamin C was not associated with an increased risk of any type of PE. For severe PE/eclampsia/HELLP, there was a decreasing trend with increasing dietary vitamin C intake (p=0.01). | Vitamin C showed an increased incidence of severe pre-eclampsia, eclampsia and HELLP. Vitamin E increased the risk of disease. |
| Rumbold | Cochrane Database of Systematic Reviews/meta-analysis | 10 eligible studies | PE, severe PE (HELLP), preterm birth, SGA, baby death | No significant difference between antioxidant and control groups in risk of PE (RR 0.73, 95% CI 0.51 to 1.06) and severe PE (RR 1.25, 95% CI 0.89 to 1.76). | No difference in PE risk. Women reported abdominal pain, required antihypertensive therapy and hospital admission. |
| Basaran | Systematic review/meta-analysis of the effectiveness of combined vitamin C/E versus placebo supplement | 9 studies, | PE, gestational hypertension, placental abruption | PE incidence in vitamin C/E was 9.7% (949/9833) and 9.5% (946/9842) in placebo group. | Vitamin C/E supplementation does not reduce the risk of PE and should not be recommended to prevent PE. |
| Salles | Systematic review of RCTs that evaluated the use of antioxidants versus placebo | 15 studies with 21 012 women and 21 647 | PE | No significant difference in PE incidence was observed; RR 0.92, 95% CI 0.82 to 1.04. | Prevention of PE and other outcomes was not observed. |
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| Williams | Case–control study | 22 PE women, | Polyunsaturated fatty acids in women’s erythrocytes were measured. | Women with the lowest levels of ω-3 fatty acids were 7.6 times more likely to have had their pregnancies complicated by pre-eclampsia than women with the highest levels of ω-3 fatty acids (95% CI 1.4 to 40.6). | Low levels of ω-3 fatty acids and high levels of some ω-6 fatty acids, particularly AA, were associated with an increased PE risk. |
| Oken | Prospective cohort study of intake | n=1718 women | First-trimester intake of Ca, ω-3/ω-6/trans fatty acids, folate, Mg, vitamins C, D, E with PE/PIH | A somewhat lower risk of PE was associated with higher intake of the elongated ω-3 fatty acids DHA and EPA (OR 0.84, 95% CI 0.69 to 1.03 per 100 mg/day). There were no effects of other nutrients on PE. | There was a |
| Szajewska | Systematic review of RCTs comparing ω-3 LC-PUFA supplementation with placebo/no supplementation | 6 eligible studies | PE, eclampsia, pregnancy duration, preterm delivery, low birth weight | No significant difference was observed in PE rate between supplemented group and placebo group; RR 0.73, 95% CI 0.22 to 2.37. | ω-3 supplementation increases the duration of pregnancy and head circumference but does not decrease the rate of PE. |
| Makrides | Systematic review of RCTs of supplement with fish oil/other prostaglandin precursor with placebo/no treatment | 6 eligible studies | PE, preterm birth, low birth weight, SGA | No difference on the risk of PE between supplemented and placebo groups. | There is not enough evidence to support the use of fish oils or prostaglandins on the risk of PE. |
| Horvath | RCT meta-analysis comparing ω-3 LC-PUFA supplement with placebo or no supplementation | 4 studies; | Duration of pregnancy, birth weight, PIH, PE | The rate of PE was similar in both groups. | There is no evidence to support the use of ω-3 LC-PUFA to reduce the rate of PE. |
| Imhoff-Kunsch | Systematic review of RCTs where ω-3 LC-PUFAs were provided to pregnant women for ≤1 trimester | 15 eligible studies | PE, maternal BP, gestational duration, preterm birth | ω-3 LC-PUFA supplementation was not associated with maternal blood pressure, infant death, stillbirth or PE risk. However, women receiving ω-3 LC-PUFA had a 26% lower risk of early preterm delivery. | There was no benefit of the use of ω-3 LC-PUFA on the risk of PE. |
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| Duley | Systematic review | 2 studies, | PE | No difference was observed between dietary salt restriction and a normal diet on the risk of pre-eclampsia; OR 1.11, 95% CI 0.46 to 2.66. | Evidence is low to assess whether advice to restrict salt during pregnancy is beneficial. |
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| Makrides | Systematic review of RCTs and quasi-RCTs that assessed the effects of dietary Mg supplement | 10 eligible studies in 9090 women | Perinatal mortality, SGA, maternal mortality, PE | There was no association between magnesium supplementation and the risk of perinatal mortality or small for gestational age. There was no effect on PE (RR 0.87, 95% CI 0.58 to 1.32; three trials, 1042 women). | The evidence is of low quality to show that magnesium supplementation can be beneficial during pregnancy. |
| de Araújo | RCT. 300 magnesium citrate/placebo per day given from 12 to 20 weeks until delivery. | n=318 women | PE | 18.1% of women in magnesium group and 19.7% of women in the control group developed PE; OR 0.90, 95% CI 0.48 to 1.69. | Magnesium supplementation does not reduce the risk of PE. |
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| Zahiri Sorouri | RCT with 400 µg folic acid and 30 mg ferrous sulfate, with/without 15 mg zinc sulfate per day from the 16th gestational week | n=540 | PE, low birth weight, macrosomia, head circumference, length, preterm delivery, gestation at birth | No significant differences were found between the zinc-supplemented group and the no-zinc group on the risk of PE. | Zinc supplementation at 15 mg/day does not improve pregnancy outcomes. |
AA, arachidonic acid; BP, blood pressure; DHA, docosahexaenoic acid; EPA, eicosapentaenoic acid; FFQ, Food Frequency Questionnaire; HELLP, haemolysis-elevated liver enzymes and low platelet count; PE, pre-eclampsia; PIH, pregnancy-induced hypertension; RCT, randomised controlled trial; RR, risk ratio; SGA, small for gestational age.
Figure 1The OR for pre-eclampsia and the percentage of women with pre-eclampsia against maternal pre-pregnancy body mass index (BMI).8 Values are ORs (95% CIs) on a log scale from multilevel binary logistic regression models that reflect the risk of pregnancy complications per pre-pregnancy BMI group compared with the reference group (largest group, 20.0–22.4 kg/m2). The bars represent the percentage of pre-eclampsia per BMI group. Models are adjusted for maternal age, educational level, parity and smoking habits during pregnancy8 (adapted from Santos et al 8).
Recommendations for total weight gain during pregnancy, by pre-pregnancy BMI24
| Pre-pregnancy BMI (kg/m2) | Recommended total weight gain (kg) |
| Underweight <18.5 | 12.5–18 |
| Healthy weight 18.5–24.9 | 11.5–16 |
| Overweight 25.0–29.9 | 7–11.5 |
| Obese ≥30 | 5–9 |
BMI, body mass index.
Figure 2Relationship between total dietary fibre intake (g/day) and the risk of pre-eclampsia (solid line), with 95% CI (dotted lines). Arrows indicate previous Recommended Dietary Allowance of 20–30 g/day of total fibre for pregnant women in the USA. The vertical bars along the dietary fibre axis indicate the density of the data (adapted from Frederick et al 37).
Figure 3(A) Correlation between incidence of pre-eclampsia in various countries and serum/plasma selenium concentration (adapted from Vanderlelie and Perkins [119]). (B) Distribution of toenail selenium concentrations in pre-eclamptic and control subjects. Horizontal bars, median values (adapted from Rayman et al 127).
Factors implicated in reducing the risk of pre-eclampsia (Recommended Dietary Allowance (RDA) included in column 1)
| Factor | Recommendation | Further relevant advice |
| Maternal weight | Excessive weight gain during pregnancy and between pregnancies should be avoided. Women should ideally be of a healthy body weight (BMI) prior to conception. Recommendations are that underweight women (BMI ≤18.5) should put on between 13 and 18 kg; normal-weight women (BMI 18.5–24.9) should put on between 11.5 and 16 kg; overweight women (BMI 25–29.9) should put on between 7 and 11.5 kg and obese women (BMI ≥30) should put on no more than 5–9 kg. | A woman aiming to reduce her BMI prior to pregnancy should do so safely preferably with the help of a suitable healthcare professional. |
| Fibre | A high-fibre diet is recommended for pregnant women and those at risk of pre-eclampsia. Women should aim for a fibre intake of 25–30 g/day to reduce the risk of pre-eclampsia. | Higher fibre intake can reduce blood cholesterol, blood pressure and inflammation and may also aid in weight management. |
| Prebiotics and | Consume milk-based probiotics where possible as part of a normal diet. | Further research is required to determine the quantity, timing and efficacy of probiotics to reduce pre-eclampsia risk. |
| Dietary patterns | Pregnant women should aim to consume ≥400 g of fruits and vegetables per day and ≥250 mg/day of docosahexaenoic/eicosapentaenoic acid by consuming ~230 g (8 ounces) of mixed seafood per week. High fat, salt, sugar foods and red and processed meats should be limited. | Avoid raw fish and fish with a high mercury content (shark, swordfish, king mackerel, tilefish, marlin, orange roughy, bigeye tuna) during pregnancy. |
| Vitamin D | Daily vitamin D supplement of 10–25 µg (400–1000 IU); stay well away from the upper limit of 100 μg (4000 IU). | A woman’s current vitamin D status can be measured and may be helpful in defining optimum dosage. |
| Calcium | All pregnant women to be supplemented with 1 g calcium per day from 20 weeks’ gestation to delivery. Women at heightened risk of pre-eclampsia and/or with a low dietary calcium intake should take a calcium supplement of 1–2 g/day during pregnancy. | Calcium supplement, for example, carbonate or citrate. Women are likely to have low dietary calcium intake if they do not consume dairy products which are a major calcium source. |
| Selenium | Women who are likely to have low selenium status (eg, in the UK), should increase their intake of selenium-rich foods, such as fish/shellfish. Alternatively, they should take a multivitamin/multimineral containing selenium as soon as they know they are pregnant and preferably when planning pregnancy. | Brazil nuts are a good source of selenium but the dose can be very high, so it is a risky way of supplementing selenium. Keep intake down to four per week if taking regularly. |
| Multivitamins/multiminerals | Women should take a multivitamin/multimineral supplement containing folic acid, vitamin D (unless taking separately) and selenium (if status is low) if they are planning on becoming pregnant. If pregnancy is unplanned, the woman should start the supplement as soon as possible. The supplement should be taken for at least the first trimester. | This supplement may be of particular importance for those who are overweight. Iodine is important for fetal brain development and should be included for a woman who does not eat dairy products or fish in a country that does not have iodised salt. The usual dose in pregnancy is 150 μg/day, usually as potassium iodide. Avoid taking a kelp supplement. |
BMI, body mass index.