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Eastern Mediterranean Health Journal |
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Volume 12 Nos 1&2 January - March , 2006 |
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Effect of menopause and renal function on vitamin D status in Iranian women
G.R. Omrani,1 S.M. Masoompour,1 A. Sadegholvaad1 and B. Larijani1
تأثير الإياس ووظيفة الكُلى على حالة الفيتامين D في النساء الإيرانيات
علي عبد الله الجابري، أتسو دورفلو، سامية الرحبي، جيهان العبري، سمير العدوي
الخلاصـة: درس الباحثون تأثيرات الإياس ووظيفة الكُلَى على المتثابتات المصلية التي تعبِّر عن العلاقة بين الفيتامين D وبين جهاز الغدد الصم، وذلك في عينة مستعرضة من 676 امرأة موفورة الصحة في الفئة العمرية 20 – 74 عاماً، في مدينة شيراز. وبيَّنت الدراسة انخفاض الـ 25 - هيدروكسي فيتامين D في المصل في 52.9% من النساء. ولوحظ ازدياد ملموس في هرمون الدُّرَيْقَات في المصل مع تقدُّم عمر النساء في الفترة السابقة للإياس (معامل الترابـط 0.13 = r، 0.02 = P). أما النسـاء في الفترة السابقــة للإياس والفـترة التاليـة للإيـاس، فكان مستــوى الـ 25 - هيدروكسي فيتامين D في المصل والفوسفور، والكالسيوم ثابتاً مع تقدُّم العمر. ولم يُلاحَظ ترابط يُعْتَدُّ به إحصائياً بين تصفية الكرياتينين أو الهرمون الدريقي في المصل (معامل الترابُط = - 0.016 = r، 0.66 = P) وبين مستوى الـ 25 - هيدروكسي فيتامين D في المصل (معامل الترابُط = 0.012 = r، 0.74 = P). وهذا الانتشار المرتفع لعَوَز الفيتامين D يدعو إلى التفكير في إعطاء مكملات غذائية.
ABSTRACT: The effects of menopause and renal function on serum parameters of the vitamin D- endocrine system were studied in a cross-sectional sample of 676 healthy women aged 20–74 years in Shiraz. Low serum 25-hydroxyvitamin D (25-OHD) was found in 52.9% of the women. Serum parathyroid hormone (PTH) increased significantly over the age span in premenopausal women (r = 0.13, P = 0.02). In premenopausal and postmenopausal women, serum levels of 25-OHD, phosphorus and calcium were stable across the age span. There was no significant correlation between creatinine clearance or serum PTH (r = –0.016, P = 0.66) and 25-OHD (r = 0.012, P = 0.74). The high prevalence of vitamin D deficiency warrants consideration of dietary supplementation.
Effet de la ménopause et de la fonction rénale sur le statut en vitamine D chez des femmes iraniennes
RÉSUMÉ: Les effets de la ménopause et de la fonction rénale sur les paramètres sériques du système endocrinien de la vitamine D ont été étudiés dans un échantillon transversal de 676 femmes en bonne santé âgées de 20-74 ans à Chiraz. On a constaté une faible concentration sérique en 25-hydroxyvitamine D (25-OHD) chez 52,9 % des femmes. Le taux d’hormone parathyroïde (PTH) dans le sang augmentait de manière significative avec l’âge chez les femmes préménopausées (r = 0,13, p = 0,02). Chez les femmes préménopausées et postménopausées, la concentration sérique en 25-OHD, en phosphore et en calcium était stable dans la fourchette d’âge. Il n’y avait aucune corrélation significative entre la clairance de la créatinine ou la PTH sérique (r = - 0,016, p = 0,66) et la
25-OHD (r = 0,012, p = 0,74). La forte prévalence de la carence en vitamine D justifie la prise en compte d’une supplémentation alimentaire.
1Endocrine and Metabolism Research Centre, Shiraz University of Medical Sciences, Shiraz, Islamic Republic of Iran (Correspondence to G.R. Omrani: hormone@sums.ac.ir).
Received: 09/12/03; accepted: 06/07/04
Introduction
Vitamin D metabolites and parathyroid hormone (PTH) participate in the
regulation of calcium homeostasis and bone metabolism. It is well known that
vitamin D deficiency causes rickets in children and osteomalacia in adults [1].
It is believed that compromises in vitamin D status and/or a reduced capability
of the kidney to synthesize 1,25-dihydroxyvitamin D [1,25-(OH)2D] are
responsible for impairment in dietary calcium absorption. These deficits lead to
compensatory hypersecretion of parathyroid hormone, which results in bone loss
[2,3]. The serum level of 25-hydroxyvitamin D (25-OHD) has been accepted as an
index for vitamin D status [4].
Ruker et al. reported an inverse relationship between 25-OHD and body mass index
(BMI) [1]. In addition, they found that PTH increased with increasing BMI.
Few investigators have examined the relationship of vitamin D status to key
parameters of bone mineral homeostasis in healthy subjects in our country [5].
In addition, there is no consensus concerning the relationship of age to serum
calcium, phosphorus and PTH levels. Knowledge of these relationships is vital to
understanding changes in the levels of the bone
mineral-regulating hormones and other related homeostatic variations.
The objective of this study, therefore, was to determine the relationship
between age, renal function (serum creatinine and estimated creatinine
clearance) and BMI and parameters of the vitamin D-endocrine system in healthy
women.
Methods
Participants
The study was carried out from January to March 2001. Women aged 20–74 years
were selected by cluster randomized sampling. The Shiraz city map was divided
into 40 areas. In each area, homes whose postal code ended in 0 were selected.
These addresses were visited and 1 woman from each was invited to participate in
the study. The exclusion criteria were: history of fracture or metabolic bone
disease; any malignancy at any age; history of thyroid, parathyroid or adrenal
disease; history of drug abuse or alcoholism; any hepatic or renal disease; use
of drugs which may affect bone and calcium metabolism, including estrogen,
calcium, vitamin D supplements and anticonvulsant medication; oophorectomy; and
gastrointestinal resection; 34 women did not meet these criteria.
The women were asked to come in a fasting state to the Endocrine and Metabolism
Research Centre in Nemazi Hospital in the centre of Shiraz. We invited 880 women
to participate and 710 came for the assessment (170 women refused to
participate), a response rate of 80.7%. Of the 710 women, 36 were excluded
leaving a final sample of 676 women. After informed consent was obtained,
history was taken, blood samples were collected and a physical examination
(thyroid, heart, lung, abdomen plus height and weight) carried out.
Biochemical tests
All blood samples were obtained from the women under fasting conditions between
08.00 and 10.00. The sera were stored at –20 °C until analysis was done in the
laboratory of the Endocrine and Metabolism Research Centre.
Serum calcium (mg/dL; reference range 8.6–10.3 mg/dL), phosphorus (mg/dL;
reference range 2.6–4.5 mg/dL), alkaline phosphatase (IU/L; reference range
< 211 IU/L) and creatinine (mg/dL; reference range 0.6–1.1 mg/dL) were measured
with enzyme kits (Pars Azmun, Tehran) and a Hitachi 902 autoanalyser (Boehringer
Mannheim, Mannheim, Germany). Serum albumin (g/dL; reference range 3.4–4.7 mg/dL)
was measured by turbidimetric assay using a specific antibody.
Serum 25-OHD (reference range 23.1–
113.0 nmol/L) level was measured using immunoradiometric assay with the IDS
gamma-B 25-hydroxyvitamin D kit (IDS, Fountain Hills, Arizona). Serum intact
parathyroid hormone (PTH pg/mL; normal range 13–54 pg/mL) was quantified using
the immunoradiometric assay (DiaSorin, Stillwater, Minnesota).
Creatinine clearance was estimated by the Cockcroft and Gault formula [6], which
takes serum creatinine (mg/dL), weight (kg), age (years) and sex into account:
creatinine clearance (mL/min) = [(140 – age) × weight]/[72 × serum creatinine]
× 0.85 (for women).
Height and weight were measured with a stadiometer and balance scale after
participants had removed their shoes. All measurements were done on the same
equipment. Body mass index was calculated as weight divided by the square of
height (kg/m2).
Statistical analysis
Data were presented as mean and standard deviation (SD). Pearson and partial
correlation coefficients were used to determine the association among variables.
Mean values were compared by student t-test. Statistical analyses were performed
using SPSS, version 9.0. P-value < 0.05 (2-sided test) was considered
statistically significant.
Results
The mean age of the participants in the study was 42.3 years (SD 13.4). Of the
total of 676 women, 183 were postmenopausal, mean age 56.7 years (SD 8.6). Mean
anthropometrical and biochemical measurements of participants are shown in Table
1.

25-hydroxyvitamin D
There was no relationship between age or body mass index and 25-OHD levels in
the participants (premenopausal or postmenopausal) (Table 2). There was no
statistically significant difference between the mean values for 25-OHD in
premenopausal women and postmenopausal women (P = 0.93) (Table 1). We found
53.9% of premenopausal and 51.4% of postmenopausal women in the study had low
levels of 25-OHD (≤ 23 nmol/L).
Parathyroid hormone
Mean serum PTH concentration was 33.1 pg/mL (SD 18.4) in premenopausal women and
34.5 pg/mL (SD 20.0) in postmenopausal women (P = 0.42) (Table 1). There was a
statistically significant inverse relationship between serum PTH and 25-OHD
(r = –0.10, P = 0.009) (Table 2). This relationship was independent of age
(r = –0.08, P = 0.047).
Serum calcium and phosphorus
Total serum calcium was stable across the age span, mean 9.7 mg/dL (SD 0.8). In
both the premenopausal and postmenopausal groups, the level of serum phosphorus
was stable across the age span, r = –0.005, P = 0.9 and r = 0.06, P = 0.37
respectively (Table 2).

Alkaline phosphatase activity
Serum alkaline phosphatase was significantly correlated with age in the women we
studied (r = 0.23, P < 0.01) (Table 2). Serum alkaline phosphatase level was
significantly correlated with serum PTH and phosphorus in premenopausal
(r = 0.2, P = 0.01 and r = 0.14, P = 0.001) and postmenopausal women (r = 0.2,
P = 0.004 and r = 0.19, P = 0.007) (Table 2). The serum alkaline phosphatase
level was significantly higher in postmenopausal women, 209.6 IU/L (SD 65.3),
than in premenopausal women, 174.7 IU/L (SD 70.3), (P < 0.0001) (Table 1).
Creatinine clearance
There was a significant decline in creatinine clearance with age (r = –0.13,
P = 0.001). There was no significant correlation between serum PTH (r = –0.016,
P = 0.66) or 25-OHD (r = 0.012, P = 0.74) and creatinine clearance.
Discussion
The most important finding in our study was the high rate (53.9% of
premenopausal and 51.4% of postmenopausal women) of vitamin D deficiency in the
participants. Lower rates of vitamin D deficiency have been reported in Iranian
postmenopausal women (36%) and the general Saudi Arabian population (35%)
[5,7,8]. But in North America, owing to oral vitamin D intake, hypovitaminosis D
is rarely, if ever, reported in healthy young adults [9–11]. In Scandinavian
countries, vitamin D deficiency has been reported in about 4%–9% of young adults
during winter, and in up to 5% during summer [12,13].
Diet and sunlight are 2 sources of vitamin D in humans. Individuals in Iran have
a limited intake of milk, and milk in Iran is generally not enriched with
vitamin D. On the other hand, Shiraz is located in a subtropical area (latitude
29° N) and has abundant bright sunshine. So a low rate of hypovitaminosis D was
expected in our general population. However, the extent of solar-ultraviolet
(UV) exposure is determined primarily by lifestyle rather than ambient UV
irradiation. The type of clothing used outdoors and the shorter amount of time
spent outdoors are the most probable causes of greater hypovitaminosis D in
women than expected. El-Sonbaty and Abdul-Ghaffar reported a similar finding in
veiled Kuwaiti women [14].
Low level of serum 25-OHD, with normal calcium concentration and absence of
osteomalacia necessitate the measurement of the active form of vitamin D,
1,25-(OH)2D, for reliable interpretation of the results [15,16]. This was a
limitation of our study.
The absence of a decline in 25-OHD levels with age in our sample does not
support the belief that a compromise in either vitamin D status or the hormonal
form of the vitamin is a normal concomitant of the ageing process [17,18].
The age-related increase in serum PTH in this study, similar to that found in
other studies [1,19,20], cannot be attributed to an age-related decline in
vitamin D status because serum 25-OHD levels were stable with age. However, the
inverse relationship of serum PTH with serum 25-OHD, which is independent of
age, suggests that vitamin D status may be a potentially important determinant
of serum PTH levels. It has been hypothesized that elevated serum 25-OHD levels
may decrease serum PTH secretion via direct interaction with 1,25-(OH)2D
receptors in the intestine to enhance calcium absorption and thereby normalize
serum calcium levels and/or in the parathyroid gland to produce feedback
inhibition of PTH secretion [21].
The absence of a correlation between serum PTH and creatinine clearance in the
women we studied (r = –0.01, P = 0.6) does not corroborate the view that
declining renal function is the primary mechanism responsible for the
age-related increase in intact PTH [19]. It is likely that deficits in
glomerular filtration rates substantially greater than those observed in our
healthy participants may be necessary to produce the strong relationship between
creatinine clearance and PTH observed by others [22].
We found relatively stable levels of total serum calcium and phosphorus in
postmenopausal women. Some studies show no decline in total serum calcium
[23,24] while others show a fall [18,25]. Reports concer-ning the effect of age
on serum phosphorus level in women are also contradictory [25,26]. In both the
premenopausal and the postmenopausal women in our study, serum phosphorus levels
were constant with increasing age: this is not compatible with age-related
increase in serum PTH.
Serum alkaline phosphatase activity rose with age in the women we studied; this
is similar to the findings of Marcus, Madvig and Young [19] and Villareal et al.
[27]. The serum alkaline phosphatase level was significantly higher in
postmenopausal women, most probably as a result of hormonal changes during
menopause which increases the effect of PTH on bone. On the other hand, there
was a significant correlation between serum PTH and alkaline phosphatase level.
We conclude that in our healthy premenopausal or postmenopausal Iranian women,
the prevalence of vitamin D deficiency is high, warranting consideration of
dietary vitamin D supplementation.
Acknowledgements
This study was supported by a grant from the Tehran Endocrine and Metabolism
Research Centre, Tehran University of Medical Sciences. The authors thank M.
Moayedfar and M. Monjazeb for their sincere cooperation.
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