Example 6

Calcium and vitamin D for increasing bone mineral density in premenopausal women

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Title: Calcium and vitamin D for increasing bone mineral density in premenopausal women: a randomised controlled trial

A study performed in South India by Won Sun Choi et al. (2011) [25] tried to evaluate the effect of calcium or vitamin D supplementation on the BMD and found that the addition of calcium or vitamin D to regular calcium supplementation increased the lumbar spine BMD only in the vitamin D-supplemented group, but not in the calcium-supplemented group.

The same conclusion was drawn in another study by Won Sun Choi et al. (2011) [24] as compared to the women who only received calcium supplementation. However, a study on a total of 238 premenopausal women performed by Kwon Sik You and Won Sun Choi (2009) [26] concluded that calcium supplementation did not help in improving the BMD. This study included 123 patients undergoing assisted reproductive technology (ART) and 116 women with an underlying medical condition, i.e. polycystic ovaries. The main limitation of this study is that they administered calcium supplements in three doses of 600 mg/day; however, the optimum amount and frequency for calcium supplementation for BMD improvement remains still undefined.

The most recent review on calcium supplementation showed that there was insufficient evidence to support the benefits of calcium supplementation on bone health [19]. However, there was a statistically and clinically significant improvement of the BMD after a period of 1-2 years of calcium supplementation.

However, supplementation of vitamin D along with calcium supplementation would be a more effective measure than calcium supplementation alone to increase the BMD [19]. The recommended daily allowance (RDA) of calcium is less than 500 mg/day and the recommended daily allowance (RDA) of vitamin D is less than 300 IU/day for Indian women [19]. For the majority of South Asians, the vitamin D intake in spite of a higher intake of foodstuffs is far below the sufficient level [19].

A single trial from Nigeria assessed the effect of the supplementation of 300 mg calcium per day with or without 400 IU vitamin D per day on the BMD of 368 women, 20 to 45 years of age, and found a significant improvement in the BMD of the femur and tibia after supplementation of vitamin D, irrespective of the calcium supplementation [27].

Source: BioMedLM


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Human-Written Cochrane Review Abstract

Background

Osteoporosis is a condition where bones become fragile due to low bone density and impaired bone quality. This results in fractures that lead to higher morbidity and reduced quality of life. Osteoporosis is considered a major public health concern worldwide. For this reason, preventive measurements need to be addressed throughout the life course. Exercise and a healthy diet are among the lifestyle factors that can help prevent the disease, the latter including intake of key micronutrients for bone, such as calcium and vitamin D. The evidence on whether supplementation with calcium and vitamin D improves bone mineral density (BMD) in premenopausal women is still inconclusive. In this age group, bone accrual is considered to be the goal of supplementation, so BMD is relevant for the future stages of life.

Objectives

To evaluate the benefits and harms of calcium and vitamin D supplementation, alone or in combination, to increase the BMD, reduce fractures, and report the potential adverse events in healthy premenopausal women compared to placebo.

Search methods

We used standard, extensive Cochrane search methods. The latest search was 12 April 2022.

Selection criteria

We included randomised controlled trials in healthy premenopausal women (with or without calcium or vitamin D deficiency) comparing supplementation of calcium or vitamin D (or both) at any dose and by any route of administration versus placebo for at least three months. Vitamin D could have been administered as cholecalciferol (vitamin D3) or ergocalciferol (vitamin D2).

Data collection and analysis

We used standard Cochrane methods. Outcomes included total hip bone mineral density (BMD), lumbar spine BMD, quality of life, new symptomatic vertebral fractures, new symptomatic non‐vertebral fractures, withdrawals due to adverse events, serious adverse events, all reported adverse events and additional withdrawals for any reason.

Main results

We included seven RCTs with 941 participants, of whom 138 were randomised to calcium supplementation, 110 to vitamin D supplementation, 271 to vitamin D plus calcium supplementation, and 422 to placebo. Mean age ranged from 18.1 to 42.1 years. Studies reported results for total hip or lumbar spine BMD (or both) and withdrawals for various reasons, but none reported fractures or withdrawals for adverse events or serious adverse events. Results for the reported outcomes are presented for the three comparisons: calcium versus placebo, vitamin D versus placebo, and calcium plus vitamin D versus placebo. In all comparisons, there was no clinical difference in outcomes, and the certainty of the evidence was moderate to low. Most studies were at risk of selection, performance, detection, and reporting biases.

Calcium versus placebo

Four studies compared calcium versus placebo (138 participants in the calcium group and 123 in the placebo group) with mean ages from 18.0 to 47.3 years. Calcium supplementation may have little to no effect on total hip or lumbar spine BMD after 12 months in three studies and after six months in one study (total hip BMD: mean difference (MD) −0.04 g/cm2, 95% confidence interval (CI) −0.11 to 0.03; I2 = 71%; 3 studies, 174 participants; low‐certainty evidence; lumbar spine BMD: MD 0 g/cm2, 95% CI −0.06 to 0.06; I2 = 71%; 4 studies, 202 participants; low‐certainty evidence). Calcium alone supplementation does not reduce or increase the withdrawals in the trials (risk ratio (RR) 0.78, 95% CI 0.52 to 1.16; I2 = 0%; 4 studies, 261 participants: moderate‐certainty evidence).

Vitamin D versus placebo

Two studies compared vitamin D versus placebo (110 participants in the vitamin D group and 79 in the placebo group), with mean ages from 18.0 to 32.7 years. These studies reported lumbar spine BMD as a mixture of MDs and percent of change and we were unable to pool the results. In the original studies, there were no differences in lumbar BMD between groups. Vitamin D alone supplementation does not reduce or increase withdrawals for any reason between groups (RR 0.74, 95% CI 0.46 to 1.19; moderate‐certainty evidence).

Calcium plus vitamin D versus placebo

Two studies compared calcium plus vitamin D versus placebo (271 participants in the calcium plus vitamin D group and 270 in the placebo group; 220 participants from Woo 2007 and 50 participants from Islam 2010). The mean age range was 18.0 to 36 years. These studies measured different anatomic areas, one study reported total hip BMD and the other study reported lumbar spine BMD; therefore, data were not pooled for this outcome. The individual studies found no difference between groups in percent of change on total hip BMD (−0.03, 95% CI −0.06 to 0; moderate‐certainty evidence), and lumbar spine BMD (MD 0.01, 95% CI −0.01 to 0.03; moderate‐certainty evidence). Calcium plus vitamin D supplementation may not reduce or increase withdrawals for any reason (RR 0.82, 95% CI 0.29 to 2.35; I2 = 72%; 2 studies, 541 participants; low‐certainty evidence).

Authors’ conclusions

Our results do not support the isolated or combined use of calcium and vitamin D supplementation in healthy premenopausal women as a public health intervention to improve BMD in the total hip or lumbar spine, and therefore it is unlikely to have a benefit for the prevention of fractures (vertebral and non‐vertebral).

The evidence found suggests that there is no need for future studies in the general population of premenopausal women; however, studies focused on populations with a predisposition to diseases related to bone metabolism, or with low bone mass or osteoporosis diagnosed BMD would be useful.

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Citations and References

[25]

[24]

The text includes in-text citations but does not provide details to the references.

Won Sun Choi *et al*. (2011)

Kwon Sik You and Won Sun Choi (2009)

The text references specific studies that do not seem to actually exist.

Conclusion

The text cites multiple studies but does not provide specific conclusions about the effectiveness of the intervention for the given condition and population.



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