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Medicine and the Community
Vitamin D deficiency in veiled or dark-skinned pregnant women
Sonia R Grover and Ruth Morley
MJA 2001; 175: 251-252
For editoral comment, see Mason and Diamond; see also Nozza and Rodda
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Abstract -
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Objectives: To determine the vitamin D status of
veiled or dark-skinned pregnant women, because of their known
increased risk of vitamin D deficiency.
Design: An audit of vitamin D status.
Setting: An antenatal clinic in a major metropolitan
teaching hospital, Melbourne, Victoria.
Participants: Pregnant women attending the clinic
who agreed to be screened.
Main outcome measures: Serum 25-hydroxyvitamin
D3 (25OHD3) level at first visit to the
antenatal clinic.
Results: Of 94 women, 82 were screened. Sixty-six
women (80%) had 25OHD3 values below the test reference
range (22.5-93.8 nmol/L).
Conclusions: Our findings are a cause for concern,
because vitamin D deficient women are at risk of bone disease and their
children at risk of neonatal hypocalcaemia and rickets.
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Most of our vitamin D comes from the action of ultraviolet light on
skin.1 People with a darker skin
produce less vitamin D for a given sunlight exposure,1,2 and veiled
women, regardless of the climate, are at a high risk of vitamin D
deficiency because of their reduced skin exposure to
sunlight.3-6 In pregnant women there is
the added risk of vitamin D deficiency in the baby.
We screened veiled or dark-skinned pregnant women attending an
antenatal clinic at a major metropolitan teaching hospital in
Melbourne, Victoria, to determine their vitamin D status.
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Subjects
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Veiled and/or dark-skinned women attending the antenatal clinic at
the Royal Women's Hospital, Melbourne, were advised that they were at
increased risk of vitamin D deficiency, putting them at risk of
osteomalacia and their children at risk of vitamin D deficiency
related problems. Over a 10-month period (July 1999 - April 2000), all
such women were asked to provide a blood sample so that their serum
level of 25-hydroxyvitamin D3 (25OHD3)
could be measured. Those who consented were given a pathology request
form for a blood sample to be taken.
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Assay
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Serum samples were stored at - 20ºC, and the 25OHD3 assays
were performed in batches in the complex chemistry laboratory at the
Royal Children's Hospital, Melbourne, using the Incstar
radioimmunoassay kit (Dade Behring, Melbourne). The reference
range for this test was 22.5-93.8 nmol/L. The coefficient of
variation between successive assays at a mean concentration of 43.9
nmol/L was 11.7%. The assay fulfilled the acceptability
criteria of the Royal College of Pathologists of Australasia
endocrinology quality assurance program.
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Risk assessment
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We recorded the date the blood sample was taken (summer was defined as
November to April, and winter as May to October); the patient's facial
skin colour (fair, intermediate or very dark skinned); and the degree
and consistency of skin covering (women who covered their arms and
wore a veil or scarf over their hair and neck at all times when outdoors
were coded as "consistently covered"; those who uncovered in a
private, outdoor environment as "inconsistently covered"; and
those who did not generally cover their arms, hair and neck when
outdoors as "uncovered").
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Of 94 veiled or dark-skinned women attending the clinic during the
study period, 82 had a blood sample taken. Two did not agree to be
tested, and the remaining women did not go to have a blood sample taken.
Serum levels of 25OHD3 are shown in Box 1. The median value
was 14 nmol/L (range, 3-77 nmol/L). In 66 women (80%) the vitamin D
level was below the reference level (< 22.5 nmol/L).
Of the women with values below 22.5 nmol/L, 66% (21/32) had blood
samples collected in summer and 90% (45/50) in winter (95% CI for
difference, 6%-43%; P < 0.01 by 2 test).
Information on skin colour and covering was complete for 70 of the 82
women. The proportion of women with serum 25OHD3 values
below 22.5 nmol/L, according to skin colour and covering, is shown in
Box 2. Although numbers in some subgroups were extremely small, it did
not appear that this additional information was helpful for clinical
management. Among the 12 women with missing information, 11 (92%) had
vitamin D levels under 22.5 nmol/L, and nine were tested in winter.
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Of the dark-skinned and/or veiled pregnant women we tested, 80% were
at high risk of vitamin D deficiency, with serum 25OHD3
values below the reference range. The number of veiled and/or
dark-skinned pregnant women attending the Royal Women's Hospital
each year is not recorded, but, if they were evenly distributed among
the five weekly clinics (as appears likely), we estimate that around
560 such women would attend each year.
Inadequate sunlight exposure can occur even in Australia,
especially among women with a modest dress code or those who limit
sunlight exposure for other reasons (eg, valid concerns about the
risk of skin cancer). However, vitamin D deficiency can be prevented
or treated with dietary supplements. Dark-skinned or veiled women
should be screened for vitamin D deficiency and those who are
deficient should be given vitamin D supplements, whether or not they
are pregnant, because of their high risk of bone disease. Their
children are also at risk of vitamin D deficiency and their infants, if
breast fed, should be given suitable infant vitamin D supplements
(Penta-vite, Roche).
We did not measure maternal parathyroid hormone (PTH) levels during
the period of this audit, but now do so routinely. PTH is an important
marker of bone health in the mother, and there is some evidence that
fetal growth is inversely related to maternal PTH level and
positively related to maternal calcium level at
delivery.7
Research is needed to determine the optimal
vitamin D level in pregnant women, in terms of outcome for themselves
and their offspring, and to determine whether other groups of women
are also vitamin D deficient. Data from Queensland (Associate
Professor John McGrath, Director, Department of Psychiatry,
University of Queensland, Brisbane, personal
communication8) and from the
Geelong Osteoporosis Study (Dr Julie Pasco, Study Coordinator,
personal communication) suggest that vitamin D deficiency in women
of reproductive age is not limited to specific ethnic or cultural
groups.
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We thank Peter Vervaart and Rhonda Greaves for undertaking the
laboratory assays and staff in the Monday clinic at the Royal Women's
Hospital for their help. Ruth Morley is supported by the Victorian
Health Promotion Foundation (VicHealth).
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- Norman AW. Sunlight, season, skin pigmentation, vitamin D, and
25-hydroxyvitamin D: integral components of the vitamin D endocrine
system. Am J Clin Nutr 1998; 67: 1108-1110.
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Feleke Y, Abdulkadir J, Mshana R, et al. Low levels of serum
calcidiol in an African population compared with a North European
population. Eur J Endocrinol 1999; 141: 358-360.
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el-Sonbaty MR, Abdul-Ghaffar NU. Vitamin D deficiency in veiled
Kuwaiti women. Eur J Clin Nutr 1996; 50: 315-318.
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Ghannam NN, Hammami MM, Bakheet SM, Khan BA. Bone mineral density of
the spine and femur in healthy Saudi females: relation to vitamin D
status, pregnancy, and lactation. Calcif Tissue Int 1999;
65: 23-28.
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Taha SA, Dost SM, Sedrani SH. 25-Hydroxyvitamin D and total
calcium: extraordinarily low plasma concentrations in Saudi
mothers and their neonates. Pediatr Res 1984; 18: 739-741.
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Gannage-Yared MH, Chemali R, Yaacoub N, Halaby G. Hypovitaminosis
D in a sunny country: relation to lifestyle and bone markers. J Bone
Miner Res 2000; 15: 1856-1862.
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Brunvand L, Quigstad E, Urdal P, Haug E. Vitamin D deficiency and
fetal growth. Early Hum Dev 1996; 45: 27-33.
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McGrath JJ, Kimlin MG, Saha S, et al. Vitamin D insufficiency in
south-east Queensland [letter]. Med J Aust. 2001; 174:
150-151.
(Received 14 Aug 2000, accepted 2 May 2001)
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Royal Women's Hospital, Melbourne, VIC.
Sonia R Grover, MD, FRACOG, Obstetrician.
Clinical Epidemiology and Biostatistics Unit, Murdoch Children's
Research Institute, and University of Melbourne Department of
Paediatrics, Royal Children's Hospital, Melbourne, VIC.
Ruth Morley, MB BChir, FRCPCH, Senior Research Fellow.
Reprints will not be available from the authors. Correspondence: Dr
Ruth Morley, Clinical Epidemiology and Biostatistics Unit, Murdoch
Children's Research Institute, and University of Melbourne
Department of Paediatrics, Royal Children's Hospital, Flemington
Road, Parkville, VIC 3052.
morleyrATcryptic.rch.unimelb.edu.au
©MJA 2001
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| 2:
Proportion of women with serum vitamin D (25-hydroxyvitamin D3) levels under
22.5nmol/L, according to skin covering and skin colour |
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Skin
colour |
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| Skin
covering* |
Very
dark |
Intermediate |
Light |
Total |
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| Consistently
covered |
6/6
(100%) |
1/2
(50%) |
23/25
(92%) |
30/33
(91%) |
| Inconsistently
covered |
3/5
(60%) |
1/3
(33%) |
18/24
(75%) |
22/32
(69%) |
| Uncovered |
2/2
(100%) |
2/3
(67%) |
0 (0) |
4/5
(80%) |
| Total |
11/13
(85%) |
4/8
(50%) |
41/49
(84%) |
56/70
(80%) |
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| *Consistently
covered - women always covered up, including arms, hair and neck, when outdoors;
inconsistently covered - women did not usually cover fully in their own
garden; and uncovered - women did not generally cover their arms, hair and
neck when outdoors. |
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