| Copyright © 2012. National Academy of Sciences. All rights reserved. Terms of Use and Privacy Statement |
Below are the first 10 and last 10 pages of uncorrected machine-read text (when available) of this chapter, followed by the top 30 algorithmically extracted key phrases from the chapter as a whole.
Intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text on the opening pages of each chapter.
Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.
Do not use for reproduction, copying, pasting, or reading; exclusively for search engines.
OCR for page 318
16
Calcium, Vitamin D, and Magnesium
Calcium and magnesium are both present in the diet and the body at
levels much higher than those of trace minerals such as iron. Approximately
99% of the calcium and magnesium in the human body is located in
the skeleton. For many years, women have been advised to increase
their calcium intake substantially during pregnancy, and there has been
concern that many pregnant women do not ingest enough calcium to
maintain their own skeletons while providing for fetal needs. Vitamin D
is discussed in this chapter since calcium metabolism is dependent on this
vitamin. Although calcium and phosphorus metabolism are closely linked,
phosphorus is not discussed in this report, since usual intakes of the nutrient
are well above the Recommended Dietary Allowance (RDA). Neither
inadequate nor excessive intake appears to be a problem in pregnant women
(NRC, 1989), and phosphorus is not ordinarily contained in multivitamin-
mineral supplements.
CALCIUM
Metabolism
Several changes in calcium metabolism associated with pregnancy facil-
itate the transfer of calcium from mother to fetus while protecting calcium
levels in maternal serum and bone. These include changes in calcium-
regulating hormones, which affect intestinal absorption, renal reabsorption,
and bone turnover of calcium.
318
OCR for page 319
CALCIUM, VITAMIN D, AND MAGNESIUM
319
Total serum calcium decreases gradually throughout pregnancy. This
is associated with and parallels the drop in serum albumin (to which
60% of the serum calcium is attached) that results from expansion of the
extracellular fluid volume. When adjustments are made for changes in
serum albumin or protein concentration, little or no change in the total
serum calcium level is apparent during pregnancy. Serum ionic calcium
changes are minimal (Pitkin et al., 1979~.
Early studies indicated that the level of parathyroid hormone (PTH) in-
creases progressively; in late pregnancy, it was reported to be approximately
50% higher than prepregnancy levels (Pitkin et al., 1979~. However, more
recent research indicates that the previously reported hyperparathyroidism
of pregnancy may be an artifact of earlier radioimmunoassay methods. A
relatively new immunoradiometric assay that is highly specific for the intact,
and presumably biologically active, form of PTH indicated that the mean
serum PTH level in 81 pregnant women was 14.4 ~ 6.3 compared with 24.8
it 9.0 (standard deviation) ng/ml in 11 nonpregnant women (Davis et al.,
1988), indicating a decline during pregnancy.
A calcium-mobilizing peptide that is similar to PTH has been identified
in both rat and human mammary tissue and milk (Budayr et al., 1989;
Thiede and Rodan, 1988~. The partially purified peptide stimulates calcium
transport in the sheep placenta (Rodda et al., 1988), but its role in human
pregnancy remains to be determined. Changes in maternal calcitonin have
been reported to be inconsistent (Pitkin et al., 1979) or increased in
early pregnancy and then stable throughout the remainder of pregnancy
(Whitehead et al., 1981~. A rise in calcitonin may protect the maternal
skeleton against resorption. A substantial amount of the calcium needed
by the fetus is provided by the increased maternal efficiency of dietary
calcium absorption. Elevated 1,25-dihydroxycholecalciferol levels account
for some of this increase, but other as yet unidentified factors may be
involved (Halloran and DeLuca, 19804.
Placental transfer of calcium is an active process that occurs against
a concentration gradient and involves placental calcium-binding protein
(Lester, 1986; Umeki et al., 1981~. Total and ionized serum calcium levels
in the fetus and newborn are substantially higher than those in the mother.
Calcium Balance
Calcium and phosphorus are deposited in the fetus mainly in the last
trimester, but the efficiency of maternal intestinal absorption is increased
by at least the second trimester (Heaney and Skillman, 1971; Shenolikar,
1970~. In a balance study, true absorption of calcium increased from 27%
in nonpregnant women to 54% at 5 to 6 months of gestation and 42%
at term (Heaney and Skillman, 1971~. Urinary calcium increases during
OCR for page 320
320
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
pregnancy, probably because of the higher glomerular filtration rate (Pitkin,
1985~.
Fetal calcium levels suggest that ionized calcium is transferred from
the mother to the fetus at a rate of 50 mg/day at 20 weeks of gestation to
a maximum of 330 mg/day at 35 weeks of gestation (Forbes, 1976~. The
few calcium balance studies that have been conducted in pregnant women
fail to show a positive balance this large, suggesting that calcium may be
withdrawn from maternal bone or that there are inaccuracies in the studies.
Ashe et al. (1979) studied healthy pregnant white women who consumed
an average of 1,390 mg of calcium per day from self-selected diets and
reported that they had sufficient calcium intake to balance urinary and
fecal losses over the course of pregnancy but not to achieve the anticipated
positive balance. Young women with a daily intake of approximately 800 mg
of calcium retained an estimated 14 g of calcium during pregnancy only
half the amount needed for the fetus (Heaney and Skillman, 1971~. In the
third trimester, Scottish women had a positive balance of 142 mg/day when
intake was 1 g and 305 mg/day when intake was 2 g (Duggin et al., 1974~.
Interpretation of these balance data is difficult due to the different levels
of calcium intake, stage of pregnancy, and duration of the various studies.
Maternal Bone Loss
It is unclear whether the increased efficiency of intestinal calcium
absorption during pregnancy prevents a net loss of calcium from the mother.
Calcium balance would be expected to be strongly positive in late pregnancy,
but as discussed above, the amount of calcium retained has been reported
to be insufficient to supply the estimated total fetal needs (Duggin et al.,
1974; Heaney and Skillman, 1971), suggesting that some is withdrawn from
the mother's bones.
Substantial increases in absorptive efficiency and positive balance begin
in the first trimester. This must represent maternal accumulation of calcium,
since the fetal calcium content is negligible at this time. It is possible that
calcium added to maternal bone during early pregnancy is transferred to
the fetus in later gestation. Perhaps because of their inability to detect
small changes in skeletal calcium, measurements of maternal bone mineral
changes have failed to support this possibility. An increase in the amount
of bone alkaline phosphatase activity that is apparent by 10 to 12 weeks of
gestation provides indirect evidence that maternal bone formation may be
increased (Valenzuela et al., 1987~.
Evidence of bone loss during pregnancy is negative in most studies
(Christiansen et al., 1976; Frisancho et al., 1971; Goldsmith and Johnston,
1975; Walker et al., 1972~. X-ray spectrophotometry of the forearm showed
a 4.2% average loss of trabecular bone and a 2% gain in cortical bone
OCR for page 321
CALCIUM, VITAMIN D, AND MAGNESIUM
321
over the course of gestation (Lamke et al., 1977~. Measurement of bone
mineral density by the photon absorption method applied to the distal
radius revealed a significant positive association (R = .77) between parity
and bone density in 1,053 black and white women in California who were
uncontrolled for the extent of lactation (Goldsmith and Johnston, 1975~.
In a retrospective study conducted in New York State, a 1.1% decrease in
femoral neck density per live birth was found, but no association was ob-
served between lumbar spine density and parity (Hreshchyshyn et al., 1988~.
In Bantu and Caucasian South African women, cortical bone thickness in
those with seven or more children was similar to that of women with zero
to two children, even though the Bantu's daily intake of calcium averaged
less than 400 mg (Walker et al., 1972~. Bone density of these two groups
was not compared. Since the total amount of calcium transferred to the
fetus is 30 g, which is equivalent to only 2.5% of maternal skeletal calcium,
bone loss would be difficult to detect even with more precise techniques
such as dual photon beam absorptiometry.
Severe calcium and phosphorus restriction in rats increases maternal
PTH synthesis, plasma 1,25-dihydroxycholecalciferol, and intestinal calcium
absorption and reduces urinary calcium excretion. Consequently, the fetal
mineralization process remains normal (Verhaeghe et al., 1988~. There are
few data on the effect of maternal calcium intake on bone mineralization
in human fetuses. In malnourished women in India, either 300 or 600
mg of supplemental calcium administered daily from week 20 of gestation
significantly increased the density of fetal bones (Reman et al., 1978~. The
clinical importance of this is not clear, however, because there was no
evidence of skeletal abnormalities in infants born to the placebo group.
Usual calcium intakes of the women were reported as low but were not
quantified.
Supplementation and Hypertension
An inverse relationship between calcium intake and blood pressure
has been found in recent studies of nonpregnant adults. Recently, this
finding has been extended to pregnant women in small-scale randomized
clinical trials conducted in the United States (Maryland) and Argentina
(Belizan et al., 1988) as well as in Ecuador (Lopez-Jaramillo et al., 1987~.
Daily calcium supplementation ranging from 1,500 to 2,000 mg reduced the
incidence of pregnancy-induced hypertension in the two South American
countries but not in Maryland. A dose-response relationship was suggested
by one of the studies (Belizan et al., 1988~. In further support of a possible
relationship between calcium metabolism and preeclampsia (pregnancy-
induced hypertension with proteinuria) are data demonstrating that the
presence of hypocalciuria is a diagnostic aid in differentiating preeclampsia
OCR for page 322
322
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
from other forms of gestational hypertension (Taufield et al., 1987~. The
pathophysiologic basis for these associations is unclear, as is the effect of
calcium supplementation on pregnancy outcome. More extensive clinical
trials are needed to explore this relationship further.
Supplementation and Leg Cramps
Leg cramps in pregnant women are sometimes attributed to calcium
deficiency or disturbances in calcium metabolism. The effectiveness of
calcium therapy for treating this complaint is doubtful. Treatment with 2 g
of calcium per day for 3 weeks produced no improvement in the incidence
of leg cramps compared with that in a placebo group given 2 g of ascorbic
acid per day (Hammer et al., 1987~.
Recommendations
Although pregnant women, on average, drink more milk than those
who are neither pregnant nor lactating, the amounts of calcium recom-
mended for pregnancy are often not achieved by dietary sources alone,
especially in blacks, Hispanics, and American Indians (see Chapter 13~.
No adverse consequences of low calcium intake during pregnancy have
been documented. However, there is justifiable concern about the possible
effects of inadequate calcium intake by pregnant women under age 25 in
whom some mineral is most likely still being added to their bones. The
subcommittee defined a low calcium intake to be less than 600 mg/day;
below this level of intake the average U.S. adult develops a negative cal-
cium balance (Marshall et al., 1976~. This is approximately the amount of
calcium in a diet that includes only one small serving of a calcium-rich food
in addition to nondairy foods.
The subcommittee recommends, therefore, that younger women with
low calcium intakes should either increase their intake of food sources of
calcium, such as milk or cheese, or, less preferably, add a supplement that
provides 600 mg of calcium per day. In the United States, however, there
have been no reports on the effect of maternal calcium supplementation
on bone mineralization of the mother or the fetus.
Women with lactose intolerance need careful assessment of their cal-
cium intake because they tend to drink little milk and to have relatively
low calcium intakes. This condition is most prevalent among women of
black, Hispanic, American Indian, and Asian background. These women
can usually tolerate sufficient milk to meet their calcium requirements if
taken in amounts less than one glass at a time. Alternative strategies are to
consume calcium in yogurt, cheese, or low-lactose milk foods that contain
OCR for page 323
CALCIUM, VITAMIN D, AND MAGNESIUM
323
relatively low amounts of lactose. A glass of mild and a slice of hard cheese
each contain approximately 300 mg of calcium.
The adsorbability of calcium from the most commonly used supple-
ments is similar to that from dairy products. Absorption is improved by
consuming calcium supplements with or at the end of a light meal (Heaney
et al., 1989), although the possible inhibitory effects of a meal high in phy-
tate or fiber on calcium absorption have not been adequately investigated.
It is unlikely that pregnant women over age 35 would benefit from
calcium supplementation to a greater extent than younger women would.
Accelerated bone loss does not occur until menopause.
VITAMIN D
Metabolism
Most vitamin D is synthesized from a precursor in the skin after ex-
posure to ultraviolet light from the sun. Relatively few foods are good
sources of this vitamin; the major source in the United States is vita-
min D-fortified milk. After vitamin D is ingested or synthesized in the
skin, the liver converts it to 25-hydroxycholecalciferol, which is the major
circulating form and the best indicator of vitamin D nutritional status.
In the kidney, it is converted into 1,25-dihydroxycholecalciferol, the bio-
logically active form of the vitamin. Levels of the active metabolite are
not highly correlated with 25-hydroxycholecalciferol levels in the physio-
logic range. The 1,25-dihydroxycholecalciferol circulates both bound to a
protein and in a free form; both forms are elevated during pregnancy (Paul-
son and DeLuca, 1986~. Total levels are approximately doubled at term
(Markestad et al., 1986~. The extent to which the increase is stimulated
by PTH, prolactin, or other hormones is unclear. Levels of the precursor
25-hydroxycholecalciferol have been reported as both unchanged (Hillman
et al., 1978) and decreased (Reiter et al., 1979) in pregnant women, but in
animal studies they have been found to be lower when diet and exposure
to ultraviolet light were controlled (Danan et al., 1980~. Both of these
metabolites, as well as 24,25-dihydroxycholecalciferol, which has no known
function, are able to cross the placenta.
Fetal vitamin D status may be influenced by maternal vitamin D status,
placental transfer and synthesis, or fetal synthesis of the vitamin. The rela-
tive importance of each to fetal vitamin D status has not been determined
in humans. Maternal plasma 25-hydroxycholecalciferol levels are higher
than levels in the umbilical vein or in the newborn, although levels of the
free hormone may be higher in the fetus (Bouillon et al., 1981~. Mater-
nal and fetal levels of 25-hydroxycholecalciferol are positively correlated
(Delvin et al., 1982), since the fetus obtains this form of the vitamin from its
OCR for page 324
324
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
mother. In rats, a placental transport mechanism transfers vitamin D, 25-
hydroxycholecalciferol, and 24,25-dihydroxycholecalciferol in similar pro-
portions to the fetus, especially in the third trimester (Clements and Fraser,
1988~. In the fetus, the vitamin is stored mainly as 25-hydroxycholecalciferol
in muscle. Clements and Fraser (19~) demonstrated that the vitamin D
molecules obtained in utero, rather than from maternal milk, are the main
source of the vitamin during the first 10 days postpartum in the rat. This
implies that, at least in rats, the vitamin D status of the neonate is affected
by the maternal vitamin D status during gestation.
Although 1,25-dihydroxycholecalciferol levels are higher in pregnant
than in nonpregnant women, this may have little effect on fetal levels,
since this metabolite is produced by both the placenta and the fetal kidneys
(Delvin et al., 1985~. Although most investigators have found no relation-
ship between maternal and fetal levels of 1,25-dihydroxycholecalciferol, a
positive correlation has been reported by Gertner et al. (1980~. Deficient
maternal levels of 1,25-dihydroxycholecalciferol impair placental calcium
transport to the fetus in sheep (Lester, 1986) but not in rats (Brommage
and DeLuca, 1984~. Human placental calcium-binding protein is believed
to facilitate placental calcium transport but is not very responsive to 1,25-
dihydroxycholecalciferol (Bruns and Bruns, 1983~. Thus, the extent to
which maternal vitamin D status regulates the placental transport of cal-
cium is not clear, although the vitamin is necessary for the maintenance of
maternal calcium status.
Requirements
The dietary requirement for vitamin D is highly dependent on exposure
of the skin to ultraviolet light. In winter, the ultraviolet light reaching the
earth's surface is insufficient for vitamin D synthesis in the skin at the
latitudes of Britain (51°N; Lawson, 1981~; Edmonton, Alberta, Canada
(52°N; Webb et al., 1988~; and Massachusetts (42°N; Webb et al., 1988~.
Further south (e.g., in Los Angeles; 34°N), some synthesis does occur in
winter, but not as much as it does in Puerto Rico (18°N; Webb et al., 1988~.
Prevalence of Deficiency
Only a few studies have provided evidence relevant to the prevalence
of vitamin D deficiency in the United States. Because of differences in
exposure to ultraviolet light, there are seasonal differences in susceptibility
to and prevalence of deficiency.
OCR for page 325
CALCIUM, VITAMIN D, AND MAGNESIUM
325
Seasonal Differences
In New York City, a low vitamin D intake (2.5 to 5 fig, or 100 to 200
IU, per day) combined with a lack of sunlight exposure in winter resulted
in reduced plasma levels of 25-dihydroxycholecalciferol in both the mother
and the umbilical cord (Rosen et al., 1974~. In St. Louis, Missouri, maternal
serum 25-hydroxycholecalciferol concentrations were three times higher in
August than they were in February (42.1 compared with 15.4 ng/ml) in both
black and white women (Hillman and Haddad, 1976~.
Studies from outside of the United States are more informative. In
autumn, both maternal and fetal 25-hydroxycholecalciferol concentrations
are substantially higher than they are in spring in Finland (Kuoppala et al.,
1986), England (Verity et al., 1981), and even Israel (Nehama et al., 1987~.
Reported maternal levels in the fall and spring averaged 17.7 and 10.6
ng/ml in Finland, 25.1 and 16.7 ng/ml in England, and approximately 25
and 16.9 ng/ml in Israel, respectively. Respective newborn levels were 11.5
and 7.5 ng/ml, 16.7 and 10.6 ng/ml, and 18.1 and 11.3 ng/ml. These were
positively correlated with maternal values (Nehama et al., 1987; Verity et
al., 1981~. The prevalence of deficiency (<6.8 ng/ml) in the Israeli women
was 7% in spring and zero in fall. No British women had levels this low.
A much higher prevalence of maternal deficiency (defined as <5 ng/ml)
occurred in Finland 47% in spring and 33% in fall. In all countries, the
reported prevalence of borderline values, i.e., between 5 and 8 ng/ml, was
relatively high after winter.
Racial, Ethnic, and Dietary Differences
In Cleveland, Ohio, vitamin D levels were higher in white mothers
and their infants than they were in their black counterparts (Hollis and
Pittard, 1984), probably because the rate of vitamin D synthesis is slower
in the skin of blacks (Clemens et al., 1982~. On the other hand, a study by
Hillman and Haddad (1976) in St. Louis, Missouri, showed no differences
in the 25-hydroxycholecalciferol levels in black and white pregnant women
in either summer or winter. There are numerous examples of low 25-
hydroxycholecalciferol levels resulting from clothing that restricts exposure
to ultraviolet light, e.g., in Bedouin (Biale et al., 1979) and Saudi Arabian
(Serenius et al., 1984) pregnant women.
A disturbingly high prevalence of vitamin D deficiency has been re-
ported among pregnant Asian (mainly Indian and Pakistani) women living
in Britain (Maxwell et al., 19814. Vitamin D deficiency was indicated by
low plasma 25-hydroxycholecalciferol levels, osteomalacia, elevated alka-
line phosphatase levels, and a high incidence of neonatal hypocalcemia.
On average, 35% of the women and 32% of the infants had undetectable
levels of 25-hydroxycholecalciferol in the first week postpartum (Maxwell et
OCR for page 326
326
DIETARY INTAKE AND NUTRIENT SUPPl AMENS
al., 1981~. Vegetarian women in this group were at a special disadvantage:
71% of them had undetectable levels of 25-hydroxycholecalciferol in the
first week postpartum. This, together with a lack of seasonal fluctuation in
the prevalence of deficiency, suggests that diet was a major factor in the
etiology of their deficiency.
Effects of Deficiency
Maternal vitamin D deficiency has been associated with neonatal
hypocalcemia and tetany in Europe (Paunier et al., 1978), tooth enamel
hypoplasia that is more prevalent in British infants born in late winter or
spring (Cockburn et al., 1980; Purvis et al., 1973), and maternal osteoma-
lacia (Brooke et al., 1980~.
Evidence for Supplementation
Although there are no concomitant seasonal changes in maternal or
fetal 1,25-dihydroxycholecalciferol, calcium, or alkaline phosphatase, the
evidence of strong seasonal fluctuations in serum 25-hydroxycholecalciferol
has provoked suggestions that pregnant women in northern latitudes should
receive vitamin D supplementation during pregnancy, at least during winter
months (Kuoppala et al., 1986; Nehama et al., 1987; Verity et al., 1981~.
Supplementation of British women with approximately 10 fig (400 IU) of vi-
tamin D per day increased maternal and newborn 25-hydroxycholecalciferol
levels in both spring and fall (Verity et al., 1981~. In Finland, supplementa-
tion given because of low 25-hydroxycholecalciferol levels quickly improved
plasma levels of the vitamin (Kuoppala et al., 1986~. Maternal and fetal
25-hydroxycholecalciferol but not 1,25-dihydroxycholecalciferol levels were
increased by supplementation of pregnant French women (Mallet et al.,
1986~.
The ability of supplements to increase maternal and fetal plasma levels
of 25-hydroxycholecalciferol is not sufficient justification to recommend
their use. However, other beneficial effects of such supplements have been
reported. In Britain, for example, daily supplementation of vitamin D-
deficient pregnant women of Asian background with 10 fig (400 IU) per
day lowered (but did not eliminate) the incidence of neonatal hypocalcemia
and convulsions, and it reduced maternal osteomalacia (Brooke et al., 1980~.
The women supplemented with 25 fig (1,000 IU) per day gained weight
faster (63 g/day) than did unsupplemented controls (46 g/day) (Maxwell et
al., 1981~. Reported effects of supplementation on birth weight range from
nonexistent in France (Mallet et al., 1986) to a halving of the incidence
of low birth weight among Asian immigrants in London (Maxwell et al.,
1981) and an increase in birth weight of 100 to 300 g among infants born
OCR for page 327
CALCIUM, VITAMIN D, AND MAGNESIUM
327
in India (Marya et al., 1981~. Infants born to Asian women in Britain given
25 fig (1,000 IU) per day during the last trimester weighed significantly
more between 3 and 12 months after birth, and they were taller between 9
and 12 months, (Brooke et al., 1981) compared with those born to similar
women given placebos.
Dosage
If supplementation with vitamin D is indicated, careful consideration
should be given to selecting a dose that is safe and effective. An excessive
vitamin D intake can result in hyperabsorption of calcium, hypercalcemia,
and calcification of soft tissues. It is not possible to define a minimal toxic
dose (Food and Nutrition Board, 1975) because interindividual sensitivity
to excess vitamin D intake is quite variable. Toxicity in nonpregnant adults
has been reported after repeated 15-mg (600,000-IU) doses (von Beuren et
al., 1966~.
In human pregnancy, high maternal intakes of vitamin D were impli-
cated as the cause of a syndrome that included mental and physical growth
retardation and hypercalcemia in British infants between 1953 and 1957
(Seelig, 1969~. In an animal model, Friedman and Mills (1969) gave high
amounts of vitamin D to pregnant rabbits and induced fetal hypercalcemia,
aortic stenosis, and abnormal skull development. These symptoms are
similar to those caused by excessive vitamin D intake in pregnant women
(Friedman and Roberts, 1966~.
However, high doses of vitamin D given to pregnant women with hypo-
parathyroidism produced no fetal abnormalities (Goodenday and Gordan,
1971~. Very high doses of 1,25-dihydro~ycholecalciferol 17 to 36 mg
(680,000 to 1,444,000 IU) per day produced no harmful effects in a
pregnant woman with vitamin D-resistant rickets, although her infant had
hypercalcemia (Marx et al., 1980~. Thus, it is clear that vitamin D is
potentially toxic to the fetus if given in large doses during pregnancy, but
the level of intake at which this occurs is uncertain.
The relative efficacy of maternal supplementation with vitamin D is
greatest during the third trimester (Clements and Fraser, 1988~. Supple-
ments of vitamin D2(ergocalciferol) and D3 (cholecalciferol) are processed
similarly by the mother and fetus (Markestad et al., 1984~.
Daily 10- to 12.5-,ug (400- to 500-IU) vitamin D supplements have
been reported to be adequate and safe (Cockburn et al., 1980; Markestad
et al., 1986; Paunier et al., 1978~. In Britain, therapeutic use of 25 ,ug
(1,000 IU) per day administered in the last trimester reduced signs of
deficiency without toxicity (Brooke et al., 1980; Heckmatt et al., 1979~.
In other countries, a few large doses rather than small daily doses have
been provided to reduce the need for patient compliance. In northern
OCR for page 328
328
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
France, for example, a single 5-mg (200,000-IU) oral dose of vitamin D2
in the seventh month of pregnancy increased maternal and umbilical cord
levels of 25-hydroxycholecalciferol to the same extent that 25 fig (1,000
IU) of vitamin D2 daily throughout the last trimester did (Mallet et al.,
1986~. In India, 30 fig (1,200 IU) per day given to women in their third
trimester was less effective than two very large doses of 15 mg (600,000 IU)
given in the seventh and eighth months, based on increased serum calcium,
reduced alkaline phosphatase, and increased birth weight (Marya et al.,
1981~. There is a higher risk of overdose when a few large doses are used
in place of daily small doses, and there has been insufficient study of when
during pregnancy to administer large doses of vitamin D for maximum
effectiveness and safety. This approach to the prevention of vitamin D
deficiency is not recommended for use in the United States.
Recommendations
The subcommittee does not recommend routine supplementation with
vitamin D during pregnancy. The preceding discussion illustrates that vita-
min D deficiency is common among pregnant women in Europe and that the
consequences are harmful. In most regions of the United States, however,
exposure to sunlight is greater than in Europe, and unlike the milk in most
European countries, most milk in the United States is fortified with the vi-
tamin. Nevertheless, daily supplementation with 10 fig of vitamin D should
be considered for complete vegetarians, whose 25-hydroxycholecalciferol
levels are low due to their avoidance of milk, eggs, and fish (Dent and
Gupta, 1975; Maxwell et al., 1981~. Supplementation with 5 fig of vitamin
D per day should be considered for pregnant women whose consumption
of vitamin D-fortified mild is low. This concern is compounded during low
exposures to ultraviolet light in winter at the most northern latitudes.
MAGNESIUM
Metabolism
The metabolism of magnesium is not regulated by any known hormone.
Magnesium is essential for the release of PTH and its action on the
intestine, bone, and kidney. A mild magnesium deficiency increases PTH
secretion; administration of large doses of PTH stimulates the intestinal
absorption and renal retention of magnesium. Magnesium participates in
the 25-hydroxylation of cholecalciferol to form 25-hydroxycholecalciferol.
The maternal serum magnesium concentration rises slightly in early
pregnancy, returning to nonpregnant levels by late pregnancy (Reitz et al.,
1977~. Maternal levels are slightly below and correlated with those of the
OCR for page 329
CALCIUM, VITAMIN D, AND MAGNESIUM
329
infant at delivery (Cockburn et al., 1980~. Seasonal fluctuations (e.g., 5%
lower in summer) in maternal blood levels were reported in some studies
(Hillman and Haddad 1976), but not in others (Kuoppala et al., 1986;
Verity et al., 1981~. Vitamin D supplementation has no effect on maternal
or umbilical cord blood magnesium concentrations (Cockburn et al., 1980;
Verity et al., 1981~.
Magnesium is probably actively transported to the fetus (Reitz et al.,
1977~. The normal fetus contains 1 g of magnesium, which is acquired
primarily during the last two trimesters at a rate of about 6 mg/day.
Adequacy of Intake
Magnesium is widely distributed among foods, especially grains, sea-
food, and green vegetables. The average U.S. diet contains approximately
120 mg/1,000 kcal. When magnesium intake is low, the efficiency of its
absorption increases and relatively more of the mineral is retained by the
kidneys.
As indicated in Chapter 13, usual magnesium intakes by pregnant
women in the United States are substantially lower than the RDA of 300
mg (NRC, 1989~. In one study, 10 healthy, white pregnant women living at
home consumed 269 mg/day from their usual diet. For only 6% of 47 one-
week-long balance periods were they in a positive magnesium balance (Ashe
et al., 1979~. On average, balance was negative ~-40 mg/day). Intake may
have been underestimated, however, since magnesium in drinking water
was not measured and there were no signs of magnesium deficiency. In
fact, magnesium deficiency has never been reported to occur in healthy
individuals consuming ordinary diets (Shils, 1988~.
On the basis of a medical records study, Conradt et al. (1984) reported
that magnesium supplementation during pregnancy was associated with
lower frequencies of fetal growth retardation and preeclampsia. This was
reevaluated in a double-blind prospective study in Switzerland (Spading
and Spatting, 1988~. Before 16 weeks of pregnancy, women were randomly
allocated to either an aspartic acid placebo group or to a group receiving
a magnesium supplement providing 360 mg/day as magnesium-aspartate-
hydrochloride. The investigators reported that the supplemented group had
30% fewer hospitalizations (for any cause), approximately 50% as many
premature births and cases of incompetent cervix, and 25% more perinatal
hemorrhages than the placebo group. The rate of infant referral to the
neonatal intensive care unit was half as high for infants of magnesium-
supplemented mothers as for infants of the placebo group. These results
were obtained only when the analysis was limited to women who followed
the protocol (thus the sample was no longer random), and they require
confirmation from other investigators.
OCR for page 330
330
DIETARY INTAKE AA/D NUTRIENT SUPPLEMENTS
Recommendations
Data are insufficient to support a recommendation of magnesium
supplementation for pregnant women. Because of the negative balances
found in healthy women consuming usual diets and the potential beneficial
effects of supplementation observed in one study, however, research on
the effects of magnesium supplementation during pregnancy should receive
high priority.
Dosage
There are no reported studies on the safety of different doses of
magnesium supplements given during pregnancy. Large doses (e.g., 3 to
5 g) of magnesium salts cause catharsis, but there is no evidence of any
other adverse effects in nonpregnant adults (Mordes and Wacker, 1978~. In
studies of iron absorption in nonpregnant women who took vitamin-mineral
supplements containing 60 mg of iron as ferrous fumarate, Seligman et al.
(1983) report that 100 mg of magnesium as magnesium oxide added to
supplements significantly reduced the absorption of the iron.
SUMMARY
There is no evidence that routine calcium, vitamin D, or magnesium
supplementation is beneficial to pregnant women in the United States.
Inadequate calcium intake by women under age 25 is more likely to affect
maternal bone accretion than to cause inadequate calcification of the fetus.
Increased intake of calcium-rich foods is preferred to supplementation
because such foods are also a source of other valuable nutrients, e.g.,
riboflavin and vitamin D.
The vitamin D status of pregnant women is influenced not only by
dietary vitamin D (especially in winter) but also by geographic location and
season because of the low amounts of ultraviolet radiation in winter months
in northern latitudes. Consumption of vitamin D-fortified mild is especially
important in winter since that is the main dietary source of vitamin D.
CLINICAL IMPLICATIONS
.
Ill effects of low maternal calcium intakes on the mother or fetus
have not been reported. Nevertheless, there is some concern that low
calcium intakes during pregnancy might impair bone mineral deposition,
especially in women under age 25.
OCR for page 331
CALCIUM, VITAMIN D, AND MAGNESIUM
331
· A pregnant woman whose calcium intake is less than 600 mg/day-
the approximate amount provided by a diet that includes only one small
serving of a calcium-rich food should be advised to increase her consump-
tion of milk cheese, yogurt, or other food sources of calcium or to take
a calcium supplement at mealtimes that provides 600 mg of calcium per
day. The strategy of increasing dairy product intake is preferred since such
products also supply energy, protein, minerals, and vitamins-all of which
are needed in increased amounts by pregnant women. Special attention
should be directed toward the adequacy of intake of black, Hispanic, and
American Indian women and complete vegetarians.
· For pregnant women who are milk intolerant because of the lack of
the enzyme lactase, strategies should be directed to increase calcium intake
through the use of low-lactose, calcium-rich foods before supplementation
is considered.
· Older pregnant women do not need higher calcium intakes than
do those who are younger.
Evidence does not support the practice of prescribing calcium for
leg cramps during pregnancy.
· There is insufficient evidence to support routine supplementation
with large amounts of calcium as a possible means of preventing pregnancy-
induced hypertension.
· Women who avoid drinking milk have low dietary intakes of vitamin
D, since fortified milk is one of the few dietary sources of this nutrient.
This is of special concern in winter months, when there is less synthesis
of the vitamin in the skin even at southern latitudes and no synthesis
at northern latitudes. Based on the known adverse effects of vitamin D
deficiency during pregnancy, such women should be counseled to increase
their intake of vitamin D-fortified mink or to take supplements providing
10 ,ug (400 IU) of vitamin D per day.
.
There is no justification for routine supplementation with magne
. .
slum ~ urlng pregnancy.
· The subcommittee does not recommend routine supplementation
of pregnant women in the United States with calcium, magnesium, or
vitamin D.
The subcommittee does not recommend the routine use of lab-
orato~y tests to assess the calcium, magnesium, or vitamin D status
in pregnant women. Assessment of vitamin D status using serum 25-
hydroxycholecalciferol levels is recommended for research purposes and,
specifically, to evaluate the prevalence of maternal vitamin D deficiency in
the United States.
.
OCR for page 332
332
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
REFERENCES
Ashe, J.R., F.A. Schofield, and M.R. Gram. 1979. The retention of calcium, iron,
phosphorus, and magnesium during pregnancy: the adequacy of prenatal diets with
and without supplementation. Am. J. Clin. Nutr. 32:286-291.
Belizan, J.M., J. Villar, and J. Repke. 1988. The relationship between calcium intake
and pregnaney-indueed hypertension: up-to-date evidence. Am. J. Obstet. Gyneeol.
158:898-902.
Biale, Y., S. Shany, M. Levi, R. Shainkin-Kestenbaum, and G.M. Berlyne. 1979. 25-
Hydro~eholeealeiferol levels in Beduin women in labor and in cord blood of their
infants. Am. J. Clin. Nutr. 32:2380-2382.
Bouillon, R., F.A. Van Assehe, H. Van Baelen, W. Heyns, and P. De Moor. 1981. Influence
of the vitamin D-binding protein on the serum concentration of 1,25-dihydro~v,itamin
D3. J. Clin. Invest. 67:589-Sg6.
Brommage, R., and H.F. DeLuea. 1984. Placental transport of calcium and phosphorus is
not regulated by vitamin D. Am. J. Physiol. 246:F526-F529.
Brooke, O.G., I.R.F. Brown, C.D.M. Bone, N.D. Carter, H.J.W. Cleeve, J.D. Maxwell, VP.
Robinson, and S.M. Winder. 1980. Vitamin D supplements in pregnant Asian women:
effects on calcium status and fetal growth. Br. Med. J. 280:751-754.
Brooke, O.G., F. Butters, and C. Wood. 1981. Intrauterine vitamin D nutrition and
postnatal growth in Asian infants. Br. Med. J. 283:1024.
Bruns, M.E., and D.E. Bruns. 1983. Vitamin D metabolism and function during pregnancy
and the neonatal period. Ann. Clin. Lab. Sei. 13:521-530.
Budayr, AA., B.P. Halloran, J.C. King, D. Diep, R.A. Nissenson, and G.J. Strewler. 1989.
High levels of a parathyroid hormone-like protein in milk. Proe. Natl. Aead. Sei.
U.S.A. 86:7183-7185.
Christiansen, C., P. R0dbro' and B. Heinild. 1976. Unchanged total body calcium in normal
human pregnancy. Aeta Obstet. Gynecol. Scand. 55:141-143.
Clemens, T.L., J.S. Adams, S.L. Henderson, and M.F. Holiek. 1982. Increased skin pigment
reduces the capacity of skin to synthesise vitamin D3. Lancet 1:74-76.
Clements, M.R., and D.R. Fraser. 1988. Vitamin D supply to the rat fetus and neonate. J.
Clin. Invest. 81:1768-1773.
Coekburn, F., N.R. Belton, R.J. Pubis, M.M. Giles, J.K Brown, T.L. Turner, E.M. Wilkinson,
J.O. Forfar, W.J.M. Barrie, G.S. McKay, and S.J. Pocock 1980. Maternal vitamin D
intake and mineral metabolism in mothers and their newborn infants. Br. Med. J.
281:11-14.
Conradt, A., H. Weidinger, and H. Algayer. 1984. On the role of magnesium in fetal
hypotrophy, pregnancy induced hypertension, and pre-eclampsia. Mag. Bull. 6:68-76.
Danan, J.L, A.C. Delorme, C. Benassayag, G. Vallette, and P. Cuisinier-Gleizes. 1980.
25-Hydroxyvitamin D and 24,25-dihydroxy~itamin D in maternal plasma, fetal plasma
and amniotic fluid in the rat. Biochem. Biophys. Res. Commun. 95:453-460.
Davis, O.K., D.S. Hawkins, L.P. Rubin, J.T. Posillico, E.M. Brown, and I. SchifE. 1988. Serum
parathyroid hormone (PTH) in pregnant women determined by an immunoradiometric
assay for intact PTH. J. Clin. Endocrinol. Metab. 67:850-852.
Delvin, E.E., F.H. Glorieux, B.L. Salle, L. David, and J.P. Varenne. 1982. Control of
vitamin D metabolism in preterm infants: feto-maternal relationships. Arch. Dis.
Child. 57:754-757.
Delvin, E.E., A. Arabian, F.H. Glorieux, and O.A. Mamer. 1985. In vitro metabolism of
25-hydroxycholecaleiferol by isolated cells from human decidua. J. Clin. Endocrinol.
Metab. 60:880-885.
Dent, C.E., and M.M. Gupta. 1975. Plasma 25-hydroxyvitamin-D levels during pregnancy
in Caucasians and in vegetarian and non-vegetarian Asians. Lancet 2:1057-1060.
Duggin, G.G., N.E. Dale, R.C. Lyneham, R.A. Evans, and D.J. Tiller. 1974. Calcium
balance in pregnancy. Lancet 2:926-927.
Food and Nutrition Board. 1975. Hazards of overuse of vitamin D. Am. J. Clin. Nutr.
28:512-513.
Forbes, G.B. 1976. Calcium accumulation by the human fetus. Pediatrics 57:976-977.
OCR for page 333
CALCIUM, VITAMIN D, AND MAGNESIUM
333
Friedman, W.F., and OF. Mills. 1969. The relationship between vitamin D and the
craniofacial and dental anomalies of the supravalvular aortic stenosis syndrome.
Pediatrics 43:12-18.
Friedman, W.F., and WC. Roberts. 1966. Vitamin D and the supravalvar aortic stenosis
syndrome: the transplacental effects of vitamin D on the aorta of the rabbit.
Circulation 34:77-86.
Frisancho, A.R., S.M. Garn, and W. Ascoli. 1971. Unaltered cortical area of pregnant
and lactating women: studies of the second metacarpal bone in North and Central
American populations. Invest. Radial. 6:119-121.
Gertner, J.M., M.S. Glassman, D.R. Coustan, and D.B.P. Goodman. 1980. Fetomaternal
vitamin D relationships at term. J. Pediatr. 97:637 640.
Goldsmith, N.F., and J.O. Johnston. 1975. Bone mineral: effects of oral contraceptives,
pregnancy, and lactation. J. Bone Jt. Surg. 57:657-668.
Goodenday, L^S., and G.S. Gordan. 1971. No risk from vitamin n in nre~nnn~v Ann
Intern. Med. 75:807-808.
Halloran, B.P., and H.F. DeLuca. 1980. Calcium transport in small intestine during
pregnancy and lactation. Am. J. Physiol. 239:E64-E68.
Hammar, M., G. Berg, F. Solheim, and L" Larsson. 1987. Calcium and magnesium status
in pregnant women. A comparison between treatment with calcium and vitamin C in
pregnant women with leg cramps. Int. J. Vitam. Nutr. Res. 57:179-183.
Heaney, R.P., and T.G. Skillman. 1971. Calcium metabolism in normal human pregnancy.
J. Clin. Endocrinol. Metab. 33:661~70.
Heaney, R.P., K.T. Smith, R.R. Recker, and S.M. Hinders. 1989. Meal effects on calcium
absorption. Am. J. Clin. Nutr. 49:372-376.
Heckmatt, J.~, M. Peacock, A.E.J. Davies, J. McMurray, and D.M. Isherwood. 1979.
Plasma 25-hydroxyvitamin D in pregnant Asian women and their babies. Lancet
2:546-549.
Hillman, L^S., and J.G. Haddad. 1976. Perinatal vitamin D metabolism. III. Factors
influencing late gestational human serum 25-hydroxyvitamin D. Am. J. Obstet. Gynecol.
125:196-200.
Hillman, LS ., E. Slatopolsky, and J. G. Haddad. 1 978. Perinatal vitamin D metabolism .
IV. Maternal and cord serum 24,25-dihydroxyvitamin D concentrations. J. Clin.
Endocrinol. Metab. 47:1073-1077.
Hollis, B.W., and W.B. Pittard III. 1984. Evaluation of the total fetomaternal vitamin D
relationships at term: evidence for racial differences. J. Clin. Endocrinol. Metab.
59:652~57.
Hreshchyshyn, M.M., ~ Hopkins, S. Zylstra, and M. Anbar. 1988. Associations of parity,
breast-feeding, and birth control pills with lumbar spine and femoral neck bone
densities. Am. J. Obstet. Gynecol. 159:318-32Z
Kuoppala, T., R. Ibimala, M. Parviainen, T. Koskinen, and M. Ala-Houhala. 1986.
Serum levels of vitamin D metabolites, calcium, phosphorus, magnesium and alkaline
phosphatase in F~nnish women throughout pregnangy and in cord serum at delivery.
Hum. Nutr.: Clin. Nutr. 40C:287-293.
I>mke, B., J. Brundin, and P. Moberg. 1977. Changes of bone mineral content during
pregnan~y and lactation. Acta Obstet. Gynecol. Scand. 56:217-219.
Lawson, D.E.M. 1981. Dietary vitamin D: is it necessary? J. Hum. Nutr. 35:61~3.
Lester, G.E. 1986. Cholecalciferol and placental calcium transport. Fed. Proc., Fed. Am.
Soc. Exp. Biol. 45:2524-2527.
Lopez-Jaramillo, P., M. NaIvaez, and R. Yepez. 1987. Effect of calcium supplementation on
the vascular sensitivity to angiotensin II in pregnant women. Am. J. Obstet. Gynecol.
156:261-26Z
Mallet, E., B. Gugi, P. Brunelle, ~ Henocq, J.P. Basuyau, and H. Lemeur. 1986. Vitamin
D supplementation in pregnangy: a controlled trial of two methods. Obstet. Gynecol.
68:300-3(~4.
Markestad, T., L~ Aksnes, M. Ulstein, and D. Aarskog. 1984. 25-Hydroxyvitamin D
and 1,25-dihydroxyvitamin D of D2 and D3 origin in maternal and umbilical cord
- ~~~ r--c>--~ ~
OCR for page 334
334
DIETARY INTAKE AND NUTRIENT SUPPLEMENTS
serum after vitamin D2 supplementation in human pregnancy. Am. J. Clin. Nutr.
40:1057-1063.
Markestad, T., M. Ulstein, L. Aksnes, and D. Aarskog. 1986. Serum concentrations of
vitamin D metabolites in vitamin D supplemented pregnant women. A longitudinal
study. Aeta Obstet. Gyneeol. Seand. 65:63-67.
Marshall, D.H., B.E.C. Nordin, and R. Speed. 1976. Caleium, phosphorus and.magnesium
requirement. Proe. Nutr. Soe. 35:163-173.
Marx, SJ., E.G. Swart, Jr., AJ. Hamstra, and H.F. DeLuea. 1980. Normal intrauterine
development of the fetus of a woman receiving extraordinarily high doses of 1,25-
dihydroxyvitamin D3. J. Clin. Endoerinol. Metab. 51:1138-1142.
Marya, R.K., S. Rathee, V. Lata, and S. Mudgil. 1981. Effects of vitamin D supplementation
in pregnancy. Gyneeol. Obstet. Invest. 12:155-161.
Maxwell, J.D., Lo Ang, O.G. Brooke, and I.R.F. Brown. 1981. Vitamin D supplements
enhance weight gain and nutritional status in pregnant Asians. Br. J. Obstet. Gynaeeol.
88:987-991.
Mordes, J.P., and W.E.C Waeker. 1978. Excess magnesium. Pharmaeol. Rev. 29:273-300.
Nehama, H., S. W~entroub, Z Eisenberg, A. Birger, B. Milbauer, and Y. Weisman.
1987. Seasonal variation in paired maternal-newborn serum 25-hydroxyvitamin D and
24,25-dihydroxyvitamin D concentrations in Israel. Isr. J. Med. Sei. 23:274-277.
NRC (National Research Council). 1989. Recommended Dietary Allowances, 10th ed.
Report of the Subcommittee on the Tenth Edition of the RDAs, Food and Nutrition
Board, Commission on Life Sciences. National Academy Press, Washington, D.C. 284
PPe
Paulson, S.K., and H.F. DeLuea.
7:331-336.
Paunier, L^, G.
1986. Vitamin D metabolism during pregnancy. Bone
Laeourt, P. Pilloud, P. Sehlaeppi, and P.C. Sizonenko. 1978. 25-
Hydroxyvitamin D and calcium levels in maternal, cord and infant serum in relation
to maternal vitamin D intake. Helv. Paediatr. Aeta 33:95-103.
Pitkin, R.M. 1985. Caleium metabolism in pregnancy and the perinatal period: a review.
Am. J. Obstet. Gyneeol. 151:99-109.
Pitkin, R.M., WA. Reynolds, G.A. Williams, and G.K. Hargis. 1979. Caleium metabolism
in normal pregnancy a longitudinal study. Am. J. Obstet. Gynecol. 133:781-790.
Pubis, RJ., WJ. MeK. Barrie, G.S. Mackay, E.M. Wilkinson, F. Coekburn, N.R. Belton,
and J.O. Forfar. 1973. Enamel hypoplasia of the teeth associated with neonatal
tetany: a manifestation of maternal vitamin-D deficiency. Lancet 2:811-814.
Raman, L^, K Rajalakshmi, KAV.R. Krishnamaehari, and J.G. Sastry. 1978. Effect of
calcium supplementation to undernourished mothers during pregnancy on the bone
density of the neonates. Am. J. Clin. Nutr. 31:466-469.
Reiter, E.O., G.D. Braunstein, A. Vargas, and A W. Root. 1979. Changes in 25-
hydroxyvitamin D and 24,25-dihydro~yvitamin D during pregnancy. Am. J. Obstet.
Gyneeol. 135:227-229.
Reitz, R.E., T.A. Daane, J.R. Woods, and R.L. Weinstein. 1977. Caleium, magnesium,
phosphorus, and parathyroid hormone interrelationships in pregnancy and newborn
infants. Obstet. Gynecol. 50:701-705.
Rodda, CP., M. Kubota, J.A. Heath, P.R. Ebeling, J.M. Moseley, A.D. Care, I.W. Caple,
and TJ. Martin. 1988. Evidence for a novel parathyroid ho~mone-related protein in
fetal lamb parathyroid glands and sheep placenta: comparisons with a similar protein
implicated in humoral hypercalcaemia of malignancy. J. Endocrinol. 117:261-271.
Rosen, J.F., M. Roginsky, G. Nathenson, and L" Finberg. 1974. 25-Hydroxyvitamin D.
Plasma levels in mothers and their premature infants with neonatal hypocalcemia.
Am. J. Dis. Child. 127:220-223.
Seelig, M.S. 1969. Vitamin D and cardiovascular, renal, and brain damage in infancy and
childhood. Ann. N.Y. Aead. Sei. 147:539-582.
Seligman, P.A., J.H. Caskey, J.L~ Frazier, R.M. Zueker, E.R. Podell, and R.H. Allen. 1983.
Measurements of iron absorption from prenatal multivitamin-mineral supplements.
Obstet. Gyneeol. 61:356-362.
OCR for page 335
CALCIUM, VITAMIN D, AND MAGNESIUM
335
Serenius, F., A.T. Elidnssy, and P. Dandona. 1984. Vitamin D nutrition in pregnant women
at term and in newly born babies in Saudi Arabia. J. Clin. Pathol. 37:444 447.
Shenolikar, I.S. 1970. Absorption of dietary calcium in pregnancy. Am. J. Clin. Nutr.
23:63-67.
Shils, M.E. 1988. Magnesium in health and disease. Annul Rev. Nutr. 8:429-460.
Spatting, L^, and G. Spatting. 1988. Magnesium supplementation in pregnancy. A double-
blind study. Br. J. Obstet. Gynaecol. 95:120-125.
Taufield, P.A., K.L. Ales, L^M. Resnick, M.L. Druzin, J.M. Gertner, and J.H. Laragh. 1987.
Hypocalciuna in preeclampsia. N. Engl. J. Med. 316:715-718.
Thiede, M.A., and G.A. Rodan. 1988. Expression of a calcium-mobilizing parathyroid
hormone-like peptide in lactating mammary tissue. Science 242:278-280.
Umeki, S., S. Nagao, and Y. Nozawa. 1981. The purification and identification of
calmodulin from human placenta. Biochim. Biophys. Acta 674:319-326.
Valenzuela, GJ., L^A. Munson, N.M. lbrbaux, and J.R. Farley. 1987. Time-dependent
changes in bone, placental, intestinal, and hepatic alkaline phosphatase activities in
serum during human pregnancy. Clin. Chem. 33:1801-1806.
Verhaeghe, J., M. Thomasset, ~ Brehier, F.A. van Assche, and R. Bouillon. 1988.
1,25(OH)2D3 and Ca-binding protein in fetal rats: relationship to the maternal
vitamin D status. Am. J. Physiol. 254:E505-E512.
Verity, C.M., D. Burman, P.C. Beadle, J.B. Holton, and A. Morris. 1981. Seasonal changes
in perinatal vitamin D metabolism: maternal and cord blood biochemistry in normal
pregnancies. Arch. Dis. Child. 56:943-948.
von Beuren, AL., J. Apitz, J. Stoermer, H. Schlange, B. Kaiser, W. v. Berg, and G.
Jorgensen. 1966. Vitamin-D-hypercalcamische Hertz- und GefaBerkankung. Dtsch.
Med. Wochenschr. 19:881-883.
Walker, A R.P., B. Richardson, and F. Walker. 1972. The influence of numerous pregnancies
and lactations on bone dimensions in South African Bantu and Caucasian mothers.
Clin. Sci. 42:189-196.
Webb, A.R., L Kline, and M.F. Holick. 1988. Influence of season and latitude on
the cutaneous synthesis of vitamin D3: exposure to winter sunlight in Boston and
Edmonton will not promote vitamin D3 synthesis in human skin. J. Clin. Endocrinol.
Metab. 67:373-378.
Whitehead, M., G. Lane, O. Young, S. Campbell, G. Abeyasekera, C.J. Hillyard, I.
MacIntyre, KG. Phang, and J.C. Stevenson. 1981. Interrelations of calcium-regulating
hormones during normal pregnancy. Br. Med. J. 283:10-12.
Representative terms from entire chapter:
calcium intake