Skip to main content
American Journal of Epidemiology logoLink to American Journal of Epidemiology
. 2008 Oct 22;168(12):1374–1380. doi: 10.1093/aje/kwn258

Maternal Calcium Intake During Pregnancy and Blood Pressure in the Offspring at Age 3 Years: A Follow-up Analysis of the Project Viva Cohort

Rachel Bakker , Sheryl L Rifas-Shiman, Ken P Kleinman, Steven E Lipshultz, Matthew W Gillman
PMCID: PMC2727186  PMID: 18945693

Abstract

A previous analysis of the Project Viva cohort (eastern Massachusetts, 1999−2002 recruitment) found an association between higher second-trimester supplemental maternal calcium intake and lower systolic blood pressure in offspring at 6 months. The authors analyzed 5,527 systolic blood pressure measurements from 1,173 mother-child pairs from this same cohort when the children were aged 3 years. They estimated the change in offspring blood pressure for a 500-mg difference in maternal total, dietary-only, and supplemental-only calcium intake during the first 2 trimesters of pregnancy. Mean daily total calcium intake was 1,311 mg (standard deviation, 421) in the first trimester and 1,440 mg (standard deviation, 386) in the second trimester. Mean systolic blood pressure of the offspring at age 3 years was 92.1 mm Hg (standard deviation, 10.3). None of the maternal calcium intake measures during the first and second trimesters was associated with systolic blood pressure in the offspring. For example, for each 500-mg increment in maternal total elemental calcium intake in the second trimester, child's 3-year systolic blood pressure was 0.1 mm Hg lower (95% confidence interval: −0.9, 0.6). Maternal calcium intake during pregnancy was not associated with offspring blood pressure at the age of 3 years.

Keywords: blood pressure, calcium, cardiovascular diseases, child, pregnancy


More than one-quarter of US adults have hypertension (1), a major cardiovascular risk factor (2). Small blood pressure differences in children may progress to larger differences at older ages (3): blood pressure increases with age and tracks over time (2, 4, 5). Thus, finding predictors of childhood blood pressure may aid in preventing hypertension over the long term.

Several studies in children have suggested that higher calcium intake is related to lower blood pressure (68), particularly in children whose calcium intake is low (911). One mechanism by which a diet low in calcium could increase blood pressure is through an increase in 1,25-dihydroxyvitamin D level, which could increase vascular smooth muscle cell intracellular calcium and thus peripheral vascular resistance (12). In addition, the benefits of calcium intake on blood pressure may start in utero (1317). A recent systematic review and meta-analysis by Bergel and Barros (18) estimated that higher maternal calcium intake during pregnancy was associated with 1.92 mm Hg (95% confidence interval (CI): −3.14, −0.71) lower blood pressure in offspring ranging in age from 1 to 9 years. Two randomized controlled trials (13, 15) and 3 observational studies (13, 19, 20) were included in the review. An experiment in rats (15) also showed that a deficit in maternal dietary calcium intake during pregnancy had an increasing effect over age on the offspring's blood pressure. However, a dietary calcium intake much higher than recommended provided no benefits.

Of the studies included in the systematic review by Bergel and Barros (18), 4 had sample sizes smaller than our previously published cohort analysis of 936 children aged 6 months (20). We found that a 500-mg increment in maternal second-trimester calcium intake from supplements was associated with a change in systolic blood pressure of −3.0 mm Hg (95% CI: −4.9, −1.1). However, we found no effect of calcium from foods, and 6 months is a relatively young age at which to study blood pressure outcomes.

Accordingly, the objective of this study was to investigate the association between 1) maternal calcium intake and blood pressure in the offspring at a later age and 2) calcium intake from both foods and supplements in early and midgestation.

MATERIALS AND METHODS

Subjects

The subjects for this study were participants in Project Viva, a prospective cohort study of gestational factors, pregnancy outcomes, and offspring health. Between April 1999 and July 2002, we recruited women attending their initial prenatal visit at 1 of 8 urban and suburban obstetric offices of a multispecialty group practice in eastern Massachusetts.

Eligibility criteria included fluency in English, gestational age less than 22 weeks at the initial prenatal clinical appointment, and singleton pregnancy. Details of recruitment and retention procedures are available elsewhere (21).

Data collection

The first study visit immediately followed recruitment at the woman's initial clinical prenatal visit. During this first visit, we obtained informed consent, carried out a brief interview, and provided a take-home, self-administered questionnaire that included a validated food frequency questionnaire (FFQ) to assess the woman's diet during the first trimester (22). We gathered information about first-trimester vitamin and supplement use during a brief interview.

We performed the second study visit at 26–28 weeks of gestation. During this visit, we again conducted a brief interview and provided a questionnaire that included a similar FFQ about the woman's diet during the second trimester. At that time, the FFQ itself included questions about vitamin and supplement use during the second trimester.

Within 3 days after delivery, we conducted a brief interview with the mother in the hospital. We also took anthropometric and blood pressure measurements of the newborn.

When the children reached 3 years of age, we invited all mothers with their eligible children for an in-person visit. During this visit, we updated information on the mother; took anthropometric, skinfold thickness, and blood pressure measurements from both mother and child; and administered an FFQ to the mother about the child's diet.

The human subject review committees of Harvard Pilgrim Health Care, Brigham and Women's Hospital, and Beth Israel Deaconess Medical Center (all in Boston, Massachusetts) approved the study protocols.

Measurements

Details of the data collected for Project Viva during pregnancy are described elsewhere (21). In summary, in addition to the FFQ assessment, we obtained demographic, social, economic, behavioral, and health information at the 2 prenatal visits. At the first prenatal visit, we administered a brief maternal interview to collect information on prepregnancy weight and height as well as father's weight and height. We used these data to calculate prepregnancy body mass index (BMI; weight (kg)/height (m)2) of the mother and BMI of the father. We estimated gestational age at birth from the number of days between the first day of the last menstrual period and the date of delivery, and we compared these estimates with ultrasound measurements made between 16 and 20 weeks of gestation. If the difference was more than 10 days, we used the ultrasound-based gestational age. At the 3-year visit, we measured the BMI of the child.

We measured systolic and diastolic blood pressures in both mother and child with a Dinamap (Critikon, Inc., Tampa, Florida) Pro 100 automated oscillometric recorder. For each of 5 measurements of the child taken 1 minute apart, we recorded child position (sitting, semireclining, reclining, or standing), arm used, cuff size, child state (asleep, quiet awake, crying, or active awake), ambient temperature, blood pressure machine used, pulse, and which research assistant obtained the readings.

We measured nutrient intake with a validated FFQ during the first and second trimesters of pregnancy (23). The dietary period assessed during the first-trimester FFQ was “during this pregnancy” (the date of the last menstrual period until the date of assessment). For the second-trimester FFQ, the dietary period was “in the past 3 months.” We also assessed the child's diet with a validated FFQ during the 3-year visit (24). To calculate calcium intake from foods and supplements, we used the Harvard nutrient database, which contains food composition values from the US Department of Agriculture, supplemented by other sources (25). From the maternal and child's FFQs, we also estimated intakes of vitamin D, which is important in calcium absorption. We used the nutrient residuals method to energy-adjust nutrients (26).

Statistical analysis

The main explanatory variable in this study was maternal calcium intake. We studied 3 different calcium estimates for both the first and second trimesters: total calcium intake, calcium intake from foods only, and calcium intake from supplements only.

Our main outcome was systolic blood pressure in the offspring at age 3 years. We focused on systolic blood pressure rather than diastolic blood pressure because it is a better predictor of later outcomes and is more accurately measured (3, 27). Although the first blood pressure measurement tends to be higher than the following ones, we did include the first measurement in the analysis because it tends to improve precision when absolute levels are not as important as differences (28).

We used mixed models to assess associations between predictors and blood pressure (29). The mixed-model method fits each of the as many as 5 blood pressure measurements of every child as repeated outcome measures. An advantage of this modeling approach over using the average measure for each child as an outcome is that children with more measurements and less variability in their measurements are assigned more weight than those with fewer measurements, more variability, or both.

We evaluated confounding by examining the association of calcium intake with systolic blood pressure before and after adding covariates to the regression model. All models were controlled for blood pressure measurement conditions of body position, child state, arm used, cuff size, measurement sequence number, and blood pressure machine to increase precision of the measurements. The “crude” models were also adjusted for child's age and sex. Ambient temperature did not add information, so we did not include it in the models. We used energy-adjusted nutrients for total and food-derived calcium intake only (25). The reason for not adjusting for energy intake at the supplement nutrients level is because supplements do not contribute to total daily caloric intake.

In subsequent models, we adjusted for ethnicity, education, prepregnancy BMI, and third-trimester systolic blood pressure of the mother; BMI of the father; and child's BMI z score at the 3-year visit. We calculated linear regression effect estimates and 95% confidence intervals for a 500-mg increment in elemental calcium intake, which approximates the difference in total elemental calcium intake between the 25th and 75th percentiles during the first and second trimesters (20). We used SAS version 9.1 software (SAS Institute, Inc., Cary, North Carolina) for all analyses.

RESULTS

Of the 2,128 women who delivered live infants, 1,579 were eligible for 3-year follow-up by virtue of having prenatal FFQ data and consent available for child follow-up. We collected follow-up information on 1,402 participants, including in-person examinations of 1,294. For this analysis, we excluded 101 participants with missing blood pressure data (7 because the machine was not working and 94 because the participant declined blood pressure measurement), 1 with invalid blood pressure measurements, and 19 with no or an invalid FFQ during pregnancy (energy intake lower than 600 or higher than 6,000 kcal). Thus, the cohort for analysis comprised 1,173 mother-child pairs (74% of 1,579). In total, 1,017 children had 5 systolic blood pressure measurements, 67 had 4, 28 had 3, 29 had 2, and 32 had 1, for a total of 5,527 measurements.

Compared with mothers eligible for the 3-year in-person visit but excluded from the analysis (n = 406), mothers in this analysis had a higher educational status (34% vs. 24% had a graduate degree), were more likely to be white (73% vs. 57%), were more likely to be married or cohabitating (94% vs. 87%), and reported higher household income (>$70,000: 65% vs. 52%), but they were similar regarding parity (≥1: 53% vs. 50%). Age at enrollment (32.5 vs. 30.8 years), prepregnancy BMI (24.6 vs. 25.3 kg/m2), gestational age at delivery (39.5 vs. 39.3 weeks), and birth weight (3.499 vs. 3.414 kg) were slightly different.

Mean first-trimester maternal daily total calcium intake was 1,311 mg (standard deviation (SD), 421; 5th–95th percentile: 684–2,037). Mean calcium intake was 1,109 mg/day (SD, 338; 5th–95th percentile: 592–1,676) from foods only and 195 mg/day (SD, 237; 5th–95th percentile: 0–643) from supplements only. Second-trimester intakes were slightly higher; daily total calcium intake was 1,440 mg (SD, 386), with 1,170 mg/day (SD, 341) from foods only and 264 mg/day (SD, 191) from supplements only. Total mean caloric intake increased from 2,095 kcal/day (SD, 657) in the first trimester to 2,158 kcal/day (SD, 645) in the second trimester (Table 1). These results were similar to those for the cohort as a whole (30).

Table 1.

Characteristics of 1,173 Mother-Child Pairs Participating in Project Viva, Eastern Massachusetts, 1999–2002 and Analyzed for Any Relation Between Maternal Calcium Intake During Pregnancy and Systolic Blood Pressure in the Offspring at Age 3 Years

Characteristics Mean (SD) No. %
Prenatal maternal characteristics
    Daily calcium intake, mg
        First trimester
            Total 1,311 (421)
            From foods only 1,109 (338)
            From supplements only 195 (237)
        Second trimester
            Total 1,440 (386)
            From foods only 1,170 (341)
            From supplements only 264 (191)
    Calorie intake, kcal
        First-trimester total 2,095 (657)
        Second-trimester total 2,158 (645)
    Daily vitamin D intake, μg
        First-trimester total 277 (165)
        Second-trimester total 368 (138)
Other maternal factors
    Age at enrollment, years 32.5 (5.0)
    Prepregnancy body mass index, kg/m2 24.6 (5.2)
    Mean third-trimester systolic blood pressure, mm Hg 111.5 (8.3)
    Race/ethnicity
        White 856 73
        Black 136 12
        Hispanic 71 6
        Asian 58 5
        Other 51 4
    Educational level
        High school diploma at most 86 7
        Some college 243 21
        Bachelors degree 439 37
        Graduate degree 404 34
    Marital status
        Married or cohabitating 1,099 94
        Divorced/separated/never married/other 72 6
    Parity
        0 550 47
        1 423 36
        2 153 13
        ≥3 47 4
    Household income, $
        <40,000 136 12
        40,001 to 70,000 249 23
        >70,000 719 65
Paternal characteristics
    Body mass index, kg/m2 26.4 (3.9)
Child characteristics
    Gestational age at birth, weeks 39.5 (1.8)
    Birth weight, kg 3.499 (0.558)
    Boys 590 50
    Breastfeeding duration, months
        0 131 11
        >0 to <12 668 57
        ≥12 313 27
        Unknown 61 5
Child characteristics at 3-year visit
    Age, years 3.3 (0.3)
    Anthropometrics
        Body mass index, kg/m2 16.5 (1.5)
        Body mass index z score 0.46 (1.04)
    Blood pressure
        Systolic blood pressure, mm Hg 92.1 (10.3)
        Diastolic blood pressure, mm Hg 58.2 (8.1)
        Pulse, beats/minute 106 (12)
    Nutrient intake
        Total calcium, mg 968 (273)
        Total vitamin D, μg 245 (111)

Abbreviation: SD, standard deviation.

About half of the children were girls. Mean gestational age at birth was 39.5 weeks (SD, 1.8). Approximately 6% of the children were born at a gestational age of less than 37 weeks. Mean birth weight was 3.499 kg (SD, 0.558). At the follow-up visit, the mean age of the children was 3.3 years (SD, 0.3). Mean systolic blood pressure was 92.1 mm Hg (SD, 10.3), which is similar to published blood pressure levels at this age (31). Mean calcium intake of the children at the 3-year visit was 968 mg/day (SD, 273), and mean vitamin D intake was 245 μg/day (SD, 111) (Table 1).

Crude models showed no association between first- or second-trimester total maternal calcium intake and systolic blood pressure in the child at age 3 years: the change associated with a 500-mg difference in calcium intake was 0.2 mm Hg (95% CI: −0.4, 0.8) during the first trimester and −0.2 mm Hg (95% CI: −0.9, 0.4) during the second trimester) (Table 2). This lack of association persisted after covariate adjustment (first trimester: 0.1 mm Hg (95% CI: −0.5, 0.7), second trimester: −0.1 mm Hg (95% CI: −0.9, 0.6)) (Table 2). We found no associations between calcium from supplements only or from foods only in the first (data not shown) or second trimester (adjusted model for calcium from supplements: −0.1 mm Hg (95% CI: −1.4, 1.2), adjusted model for calcium from foods only: −0.2 mm Hg (95% CI: −1.0, 0.6)) (Table 3). We repeated the same analysis for diastolic blood pressure measurements of the children; we also found no association with maternal calcium intake (data not shown).

Table 2.

Estimates From Multivariate Mixed Regression Models Predicting Offspring Blood Pressure From Maternal Total Dietary Calcium Intake During Pregnancy in 1,173 Mother-Child Pairs Participating in Project Viva, Eastern Massachusetts, 1999–2002

Model Covariates Estimated Change in Systolic Blood Pressure at Age 3 Years for a 500-mg Difference in Maternal Calcium Intake, mm Hg
First Trimester
Second Trimester
Change 95% CI Change 95% CI
Adjusted for maternal energy intakea and child's blood pressure measurement conditions,b sex, and age at 3-year visit 0.2 −0.4, 0.8 −0.2 −0.9, 0.4
Model 1 + maternal ethnicity, education, prepregnancy BMI, third-trimester systolic blood pressure, and paternal BMI 0.0 −0.6, 0.7 −0.2 −0.9, 0.5
Model 2 + child BMI z score at 3-year visit 0.1 −0.5, 0.7 −0.1 −0.9, 0.6

Abbreviations: BMI, body mass index; CI, confidence interval.

a

The nutrient residuals method was used to energy-adjust total calcium intake.

b

Blood pressure measurement conditions are body position, child state (asleep, quiet awake, crying, or active awake), arm used, cuff size, measurement sequence number, and blood pressure machine.

Table 3.

Estimates From Multivariate Mixed Regression Models Predicting Offspring Blood Pressure From Maternal Calcium Intake From Foods Only and Supplements Only During the Second Trimester of Pregnancy in 1,173 Mother-Child Pairs Participating in Project Viva, Eastern Massachusetts, 1999–2002

Model Covariates Estimated Change in Systolic Blood Pressure at Age 3 Years for a 500-mg Difference in Maternal Calcium Intake, mm Hg
Second-Trimester Calcium Intake From Supplements Only
Second-Trimester Calcium Intake From Foods Only
Change 95% CI Change 95% CI
Adjusted for maternal energy intakea and child's blood pressure measurement conditions,b sex, and age at 3-year visit −0.1 −1.5, 1.3 −0.3 −1.0, 0.5
Model 1 + maternal ethnicity, education, prepregnancy BMI, third-trimester systolic blood pressure, and paternal BMI −0.1 −1.5, 1.3 −0.2 −1.0, 0.6
Model 2 + child BMI z score at 3-year visit −0.1 −1.4, 1.2 −0.2 −1.0, 0.6

Abbreviations: BMI, body mass index; CI, confidence interval.

a

The nutrient residuals method was used to energy-adjust calcium intake from foods only.

b

Blood pressure measurement conditions are body position, child state (asleep, quiet awake, crying, or active awake), arm used, cuff size, measurement sequence number, and blood pressure machine.

Additional adjustment for total maternal vitamin D intake again revealed no association between total maternal calcium intake and systolic blood pressure in the offspring (fully adjusted model, first trimester: −0.1 mm Hg (95% CI: −0.8, 0.7), second trimester: −0.3 mm Hg (95% CI: −1.2, 0.6)) or for diastolic blood pressure (fully adjusted model, first trimester: 0.1 mm Hg (95% CI: −0.5, 0.7), second trimester: −0.2 mm Hg (95% CI: −0.9, 0.5)). Similarly, adjusting for calcium intake and vitamin D intake of the child at age 3 years did not change the estimates (data not shown).

DISCUSSION

We found no association between maternal calcium intake during the first or second trimester of pregnancy and blood pressure in the child at age 3 years. With the relatively large sample size, the confidence intervals were narrow enough to rule out any clinically meaningful association. In no analysis of total calcium intake was a 95% confidence limit greater than 1.3 or less than −1.5 mm Hg (Table 3). Thus, the inverse association we previously found between second-trimester supplemental calcium intake and systolic blood pressure at the age of 6 months in the same cohort (20) was not present when the children were 2.5 years older.

One of the reasons for this difference could be the change in the child's diet between the age of 6 months and 3 years. At age 6 months, a substantial proportion of children were receiving their entire calcium intake from breast milk or infant formula. At age 3 years, the amounts of calcium consumed through the child's own diet could overwhelm any prenatal influence. However, adjusting for 3-year calcium intake made no difference in our results. Additionally, we did not find a cross-sectional association between children's 3-year calcium intake and their blood pressures (data not shown).

Another possible explanation for the lack of an association could be that the effect of maternal calcium intake on offspring blood pressure reappears after 3 years. In rats, Bergel and Belizán (15) found that a maternal diet deficit in calcium during pregnancy had an increasing effect over age on the offspring's blood pressure. In humans, Silverman et al. (32) found early (at birth) and late (after 4 years), but not intermediate, effects of diabetes in utero on obesity in childhood. Therefore, an association between maternal calcium intake and blood pressure in the offspring might become evident again when the children are older.

Our null results were similar to those of at least 1 other study. Morley et al. (19) found no association between maternal calcium supplementation and blood pressure in twins at age 9 years. However, whether data from twin studies can be generalized to singletons is still debated (33, 34).

Misleading null associations between diet and disease can occur in several circumstances (26). Nutrients can interact. Vitamin D interacts with calcium, affecting calcium absorption in the intestines, and it may affect the development of cardiovascular disease (26, 35). Chan et al. (36) found that calcium supplementation during pregnancy is associated with increased cord blood 25-hydroxyvitamin D levels, the active part of vitamin D. However, adjusting the multivariate models for vitamin D intake in the first and second trimesters of the mother did not change our results. Also adjusting for child's dietary vitamin D intake did not change our results.

Another possibility is that the range of calcium intake was too narrow to see an effect. Calcium supplementation has the greatest blood-pressure-lowering effect in individuals with the lowest habitual intakes of calcium, in most studies less than about 900 mg/day (9, 11, 37). Approximately 19% of women in the first trimester and 16% in the second trimester had such low intakes. However, the lowest calcium intakes found in our data were not associated with higher blood pressures.

One of the strengths of this study was the prospective data collection, which started in early pregnancy. None of the other observational studies (13, 19) collected dietary data during pregnancy; rather, they collected recalled nutrient and covariate data after delivery. Another strength was collection of a wider range of potential confounding factors than in previous studies. In addition, we had a relatively large sample size of 1,173 participants. Published studies were conducted in smaller samples, varying from 57 children (16) to 591 children (14), as reviewed by Bergel and Barros (18). We measured maternal calcium intake in both the first and second trimesters. In addition, the blood pressure measurements in this study were very precise. For 87% of the children at the age of 3 years, we collected 5 blood pressure measurements. Finally, the FFQ is an appropriate method to measure calcium intake in large studies measuring long-term dietary intake.

Several limitations of this study should be mentioned. The participating mothers in this study were relatively older and highly educated, and all were residents of eastern Massachusetts. Thus, findings may not be generalizable to other populations (38). Loss to follow-up may cause selection bias; several characteristics were different between the analysis group and the participants not included in this analysis.

In conclusion, the results of this study do not confirm findings from earlier studies that higher maternal calcium intake is associated with lower childhood blood pressure. Nevertheless, following the children in this and other cohorts is warranted to investigate whether an association between maternal calcium intake and offspring blood pressure exists at later stages of the life course.

Acknowledgments

Author affiliations: The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands (Rachel Bakker); Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands (Rachel Bakker); Obesity Prevention Program, Department of Ambulatory Care and Prevention, Harvard Medical School/Harvard Pilgrim Health Care, Boston, Massachusetts (Sheryl L. Rifas-Shiman, Ken P. Kleinman, Matthew W. Gillman); Department of Pediatrics, Leonard M. Miller School of Medicine, University of Miami, Miami, Florida (Steven E. Lipshultz); and Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts (Matthew W. Gillman).

This work was supported by grants from the US National Institutes of Health (HD034568, HL064925, and HL068041) and by Harvard Medical School and Harvard Pilgrim Health Care Foundation.

The authors thank the staff of Project Viva.

Conflict of interest: none declared.

Glossary

Abbreviations

BMI

body mass index

CI

confidence interval

FFQ

food frequency questionnaire

SD

standard deviation

References

  • 1.National Center for Health Statistics. Hyattsville, MD: US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics; 2007. Health, United States, 2007—With Chartbook on Trends in the Health of Americans. (DHHS publication 2007-1232). ( http://www.cdc.gov/nchs/hus.htm). Table 70. Hypertension and elevated blood pressure among persons 20 years of age and over, by sex, age, race and Hispanic origin, and poverty level: United States, 1988–94 and 2001–2004. ( http://www.cdc.gov/nchs/data/hus.hus07.pdf#listtables) [Google Scholar]
  • 2.Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003;42(6):1206–1252. doi: 10.1161/01.HYP.0000107251.49515.c2. [DOI] [PubMed] [Google Scholar]
  • 3.Barker DJP, Bagby SP. Developmental antecedents of cardiovascular disease: a historical perspective. J Am Soc Nephrol. 2005;16(9):2537–2544. doi: 10.1681/ASN.2005020160. [DOI] [PubMed] [Google Scholar]
  • 4.Celermajer DS, Ayer JGJ. Childhood risk factors for adult cardiovascular disease and primary prevention in childhood. Heart. 2006;92(11):1701–1706. doi: 10.1136/hrt.2005.081760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Levine RS, Hennekens CH, Klein B, et al. Tracking correlations of blood pressure levels in infancy. Pediatrics. 1978;61(1):121–125. [PubMed] [Google Scholar]
  • 6.Gillman MW, Oliveria SA, Moore LL, et al. Inverse association of dietary calcium with systolic blood pressure in young children. JAMA. 1992;267(10):2340–2343. [PubMed] [Google Scholar]
  • 7.Cappuccio FP, Elliott P, Allender PS, et al. Epidemiologic association between dietary calcium intake and blood pressure: a meta-analysis of published data. Am J Epidemiol. 1995;142(9):935–945. doi: 10.1093/oxfordjournals.aje.a117741. [DOI] [PubMed] [Google Scholar]
  • 8.Griffith LE, Guyatt GH, Cook RJ, et al. The influence of dietary and nondietary calcium supplementation on blood pressure. An updated meta-analysis of randomized controlled trials. Am J Hypertens. 1999;12(1 pt 1):84–92. doi: 10.1016/s0895-7061(98)00224-6. [DOI] [PubMed] [Google Scholar]
  • 9.Gillman MW, Hood MY, Moore LL, et al. Effect of calcium supplementation on blood pressure in children. J Pediatr. 1995;127(2):186–192. doi: 10.1016/s0022-3476(95)70293-8. [DOI] [PubMed] [Google Scholar]
  • 10.van Mierlo LAJ, Arends LR, Streppel MT, et al. Blood pressure response to calcium supplementation: a meta-analysis of randomized controlled trials. J Hum Hypertens. 2006;20(8):571–580. doi: 10.1038/sj.jhh.1002038. [DOI] [PubMed] [Google Scholar]
  • 11.Hofmeyr GJ, Atallah AN, Duley L. Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems [electronic article] Cochrane Database Syst Rev. 2006 doi: 10.1002/14651858.CD001059.pub2. (3):CD001059. [DOI] [PubMed] [Google Scholar]
  • 12.Zemel MB. Calcium modulation of hypertension and obesity: mechanisms and implications. J Am Coll Nutr. 2001;20(5 suppl):428S–435S. doi: 10.1080/07315724.2001.10719180. [DOI] [PubMed] [Google Scholar]
  • 13.McGarvey ST, Zinner SH, Willett WC, et al. Maternal prenatal dietary potassium, calcium, magnesium, and infant blood pressure. Hypertension. 1991;17(2):218–224. doi: 10.1161/01.hyp.17.2.218. [DOI] [PubMed] [Google Scholar]
  • 14.Belizán JM, Villar J, Bergel E, et al. Long term effects of calcium supplementation during pregnancy on the blood pressure of offspring: follow up of a randomised controlled trial. BMJ. 1997;315(7103):218–285. doi: 10.1136/bmj.315.7103.281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Bergel E, Belizán JM. A deficient maternal calcium intake during pregnancy increases blood pressure of the offspring in adult rats. BJOG. 2002;109(5):540–545. [PubMed] [Google Scholar]
  • 16.Hatton DC, Harrison-Hohner J, Coste S, et al. Gestational calcium supplementation and blood pressure in the offspring. Am J Hypertens. 2003;16(10):801–805. doi: 10.1016/s0895-7061(03)01027-6. [DOI] [PubMed] [Google Scholar]
  • 17.Hiller JE, Crowther CA, Moore VA, et al. Calcium supplementation in pregnancy and its impact on blood pressure in children and women: follow up of a randomised controlled trial. Aust N Z J Obstet Gynaecol. 2007;47(2):115–121. doi: 10.1111/j.1479-828X.2007.00696.x. [DOI] [PubMed] [Google Scholar]
  • 18.Bergel A, Barros AJD. Effect of maternal calcium intake during pregnancy on children blood pressure: a systematic review of the literature [electronic article] BMC Pediatr. 2007;7:15. doi: 10.1186/1471-2431-7-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Morley R, Carlin JB, Dwyer T. Maternal calcium supplementation and cardiovascular risk factors in twin offspring. Int J Epidemiol. 2004;33(6):1304–1309. doi: 10.1093/ije/dyh284. [DOI] [PubMed] [Google Scholar]
  • 20.Gillman MW, Rifas-Shiman SL, Kleinman KP, et al. Maternal calcium intake and offspring blood pressure. Circulation. 2004;110(14):1990–1995. doi: 10.1161/01.CIR.0000143199.93495.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Gillman MW, Rich-Edwards JW, Rifas-Shiman SL, et al. Maternal age and other predictors of newborn blood pressure. J Pediatr. 2004;144(2):240–245. doi: 10.1016/j.jpeds.2003.10.064. [DOI] [PubMed] [Google Scholar]
  • 22.Oken E, Taveras EM, Popoola FA, et al. Television, walking, and diet associations with postpartum weight retention. Am J Prev Med. 2007;32(4):305–311. doi: 10.1016/j.amepre.2006.11.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Fawzi WW, Rifas-Shiman SL, Rich-Edwards JW, et al. Calibration of a semi-quantitative food frequency questionnaire in early pregnancy. Ann Epidemiol. 2004;14(10):754–762. doi: 10.1016/j.annepidem.2004.03.001. [DOI] [PubMed] [Google Scholar]
  • 24.Blum RE, Wei EK, Rockett HR, et al. Validation of a food frequency questionnaire in Native American and Caucasian children 1 to 5 years of age. Matern Child Health J. 1999;3(3):167–172. doi: 10.1023/a:1022350023163. [DOI] [PubMed] [Google Scholar]
  • 25.Huh SY, Rifas-Shiman SL, Kleinman KP, et al. Maternal protein intake is not associated with infant blood pressure. Int J Epidemiol. 2005;34(2):378–384. doi: 10.1093/ije/dyh373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Willett WC. [Google Scholar]
  • 27.Miura K, Daviglus ML, Dyer AR, et al. Relationship of blood pressure to 25-year mortality due to coronary heart disease, cardiovascular diseases, and all causes in young adult men: the Chicago Heart Association Detection Project in Industry. Arch Intern Med. 2001;161(12):1501–1508. doi: 10.1001/archinte.161.12.1501. [DOI] [PubMed] [Google Scholar]
  • 28.Gillman MW, Cook NR. Blood pressure measurement in childhood epidemiological studies. Circulation. 1995;92(4):1049–1057. doi: 10.1161/01.cir.92.4.1049. [DOI] [PubMed] [Google Scholar]
  • 29.Laird NM, Ware JH. Random-effects models for longitudinal data. Biometrics. 1982;38(4):963–974. [PubMed] [Google Scholar]
  • 30.Rifas-Shiman SL, Rich-Edwards JW, Willett WC, et al. Changes in dietary intake from the first to the second trimester of pregnancy. Paediatr Perinat Epidemiol. 2006;20(1):35–42. doi: 10.1111/j.1365-3016.2006.00691.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. Pediatrics. 2004;114:555–576. [PubMed] [Google Scholar]
  • 32.Silverman BL, Rizzo TA, Cho NH, et al. Long-term effects of the intrauterine environment. The Northwestern University Diabetes in Pregnancy Center. Diabetes Care. 1998;21(suppl 2):B142–B149. [PubMed] [Google Scholar]
  • 33.Morley R, Dwyer T. Studies of twins: what can they tell us about the fetal origins of adult disease? Paediatr Perinat Epidemiol. 2005;19(suppl 1):2–7. doi: 10.1111/j.1365-3016.2005.00608.x. [DOI] [PubMed] [Google Scholar]
  • 34.Morley R. Can we generalize from findings in twins? Paediatr Perinat Epidemiol. 2005;19(suppl 1):54–59. doi: 10.1111/j.1365-3016.2005.00610.x. [DOI] [PubMed] [Google Scholar]
  • 35.Zittermann A. Vitamin D and disease prevention with special reference to cardiovascular disease. Prog Biophys Mol Biol. 2006;92(1):39–48. doi: 10.1016/j.pbiomolbio.2006.02.001. [DOI] [PubMed] [Google Scholar]
  • 36.Chan GM, McElligott K, McNaught T, et al. Effects of dietary calcium intervention on adolescent mothers and newborns: a randomized controlled trail. Obstet Gynecol. 2006;108(3 pt 1):565–571. doi: 10.1097/01.AOG.0000231721.42823.9e. [DOI] [PubMed] [Google Scholar]
  • 37.Hofmeyr GJ, Duley L, Atallah A. Dietary calcium supplementation for prevention of pre-eclampsia and related problems: a systematic review and commentary. BJOG. 2007;114(8):933–943. doi: 10.1111/j.1471-0528.2007.01389.x. [DOI] [PubMed] [Google Scholar]
  • 38.Oken E, Huh SY, Taveras EM, et al. Associations of maternal prenatal smoking with child adiposity and blood pressure. Obes Res. 2005;13(11):2021–2028. doi: 10.1038/oby.2005.248. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Epidemiology are provided here courtesy of Oxford University Press

RESOURCES