In a previous post I discussed the potential for excess vitamin D to cause heart issues in people with certain vitamin D receptor (VDR) gene polymorphisms. This post focuses on VDR genes, and vitamin D’s important role in producing and maintaining healthy bones.
I discussed the action of the VDR gene and protein in greater detail in the previous post but here’s a quick refresher.
VDR Genes: a Summary
Through binding with the VDR protein, vitamin D increases the uptake of calcium from the intestine into the blood stream, which can then be used to increase bone density.
At the genetic level the VDR gene contains several polymorphisms which have been widely researched. VDR polymorphisms were first described before the human genome had been fully sequenced and so have modern Reference SNP (RS) identifications along with older names, and different allele names, which can lead to some confusion when trying to understand your genetics.
The SNP rs2228570 (T/C) is also known as FokI, is located at the beginning of the VDR gene, and results in the substitution of a methionine (M, Met) for a threonine (T, Thr) amino acid at position 1 of the protein (Met1Thr). As a result, the ‘C’ allele produces a shorter version of the VDR protein of 424 amino acids, whereas the ‘T’ allele produces a normal length protein of 427 amino acids.
The SNPs rs1544410, rs7975232 and rs731236; traditionally known as BsmI, ApaI and TaqI respectively do not result in changes in amino acid; but importantly, they are located so closely together that they are inherited together in specific combinations.
The ‘G’ allele of BsmI (b), ‘G’ allele of ApaI (a) and ‘T’ allele of TaqI (T) are commonly observed together giving rise to the term baT. The association of other alleles (‘A’ BsmI, ‘T’ ApaI and ‘C’ TaqI) gives rise to the term BAt. The baT and Bat combinations are the most frequent in the population, there are also of course, other, rarer combinations.
Confusing, I know!
But understanding how these three SNPs are named and associate with each other is key to understanding the role of vitamin D in bone health.
To help, this is all summarized in the table below, and if you’re interested I discuss it in more depth in my previous post.
|Reference SNP ID||rs2228570||rs1544410||rs7975232||rs731236|
|Traditional Name Variant||f||F||b||B||a||A||T||t|
Summary table of the various different names for VDR polymorphisms and the effect they have on protein coding. For BsmI, AapI and TaqI the alleles which are commonly associated have been coloured giving rise to the baT and BAt terminology which is often seen.
VDR polymorphisms and bone health
Healthy bones are strong but with a surprising degree of flexibility. Osteoporosis is the medical condition that arises when bones become brittle and fragile making them more susceptible to fracture. This is often associated with a deficiency of vitamin D, or calcium, but also correlates strongly with age, especially in postmenopausal women who are at high risk.
So, knowing that calcium absorption is linked to proper vitamin D activity and that vitamin D binds to the VDR protein to induce this effect, a key question is are any VDR gene polymorphisms associated with bone health?
rs2228570 (FokI) ‘C’ allele associated with greater calcium uptake and improved bone health
As I discussed in my previous VDR post, several studies have shown that the shorter VDR protein produced by the presence of the rs2228570 (FokI) ‘C’ allele is more transcriptionally active. This means that given the same levels of vitamin D, someone with the short ‘C’ allele VDR protein will display increased expression of vitamin D dependent genes (1, 2). This increased activation of vitamin D dependent genes results in a greater uptake of calcium from the gut, and has shown to increase bone density, which is associated with improved bone health (3, 4).
However, for the rs1544410 (BsmI), rs7975232 (ApaI) and rs731236 (TaqI) SNPs, it is more difficult to determine an effect. Several small studies investigated each SNP generating conflicting results; for example the rs7975232 (ApaI) ‘G’ allele was been shown to have a negative effect on bone health in one population but no effect in another (5, 6). More recently it has been proposed that it is not the individual polymorphism which may have an impact on bone health but rather the association of the three together. A meta-analysis (a study which pools the data from many smaller previous studies) of the data identified that whilst individual polymorphisms alone did not confer a risk of poor bone health, the ‘Bat’ and ‘BAt’ groups (based on the old naming standards) were associated with poor bone health (7).
Using the table above we can see that ‘Bat’ refers to someone carrying the rs1544410 (BsmI) ‘G’ allele, the rs7975232 (ApaI) ‘G’ allele and the rs731236 (TaqI) ‘C’ allele. ‘BAt’ is the same with the exception of rs7975232 (ApaI) which carries the ‘T’ allele.
Caffeine and bone health
There have been numerous observations that an increase in caffeine intake associates with poor bone health and a risk of developing osteoporosis, but a conclusive effect has never been defined. However, with an aging population and our ever-increasing caffeine intakes the area is being more thoroughly investigated, especially in relation to older or elderly women for whom osteoporosis can be a serious issue.
Understanding your coffee intake
A lot of the studies I discuss below refer to caffeine intake as milligrams (mg); but before we get started I thought it would be a good idea to see just how much caffeine is present in typical hot, soft and energy drinks. As an additional note, whilst there is no firm guidance on upper caffeine intake 400 mg/day is widely accepted to be a safe maximum.
|Decaf Espresso *||0-15|
|Soft & Energy Drinks|
Amount of caffeine in mg present in 8 oz (240 mL) serving. * 1oz (30 mL)
Does caffeine impact bone health?
Now that we know how much caffeine is contained in common drinks, let’s investigate how it is thought to impact on bone health. Firstly, the diuretic effect of caffeine has been proposed to lead to an increase in urinary calcium excretion and decrease in absorption from the intestine. Secondly, it has been proposed that caffeine may itself directly inhibit the production of new bone (8, 9, 10).
Based on these proposed mechanisms studies have been performed investigating the impact of caffeine on bone health with varying results. However, a recent meta-analysis of the data available has described a noticeable effect. Relative risk of fracture increased by 4.9% in women overall and conversely, there was a 9% drop in relative risk of bone fracture for men for each cup of coffee per day. Interestingly, they did not observe any age-related effects even in postmenopausal women who had been identified as being at high risk of developing osteoporosis.
One important note is that there have been relatively few studies looking at the response of men to caffeine so the authors of the paper suggest that the beneficial effect of caffeine in men may be overstated.
But what does this relative risk actually mean?
Well in this instance it refers to the risk of a person who drinks one cup of coffee a day suffering a fracture, compared to someone who drinks no coffee. But without knowing the actual risk this data is meaningless. Luckily the graph below can help with this. As you can see the actual risk of fractures in those below the age of 65 is very low and roughly equal between the sexes.
For example, in the 18-44 category about 10 women in 10,000 will suffer a fracture each year. A 4.9% increase in relative risk would raise this to 10.5 women so the effect is tiny. However, if we look at the 75-84 age group we can see that over 200 women per 10,000 will suffer a fracture each year, a 4.9% increase would increase this to 208. So still a small effect, but importantly this is based on drinking a single cup of coffee, with the risk doubling for each additional serving (11). This effect was confirmed by a later study (12).
Occurrence of fractures per 10,000 people in 2009-10 in the US split by age and sex.
Bringing it all together
Can we link everything together? We know that VDR gene polymorphisms can effect general bone health. We know that increased caffeine intake is related to a decrease in bone health in women, which has more impact in those already at risk of poor bone health.
This study from 2001 by Rapuri et al., showed that postmenopausal women homozygous for the rs731236 (TaqI) ‘C’ allele who ingested over 300mg of caffeine a day showed a 9% decrease in bone density in the spine compared to those with low caffeine intakes, as you can see in the graph below.
Postmenopausal women homozygous for the rs731236 (TaqI) ‘C’ with a caffeine intake over 300 mg per day showed a 9% decrease in bone density compared to women with a low caffeine intake.
Based on the table, about 300mg of caffeine is equivalent to a couple of cups of filter coffee so well within reach as a daily intake (13). However, as yet, there are no reports of this study being repeated or of similar investigations into other VDR gene polymorphisms.
We’ve covered quite a lot here so for a summary I think a list of simple bullet points may be best:
- Vitamin D is important to promote calcium uptake from the gut, which promotes healthy bone formation.
- VDR polymorphisms can negatively affect general bone health;
- Seen for the rs2228570 ‘T’ allele alone and the rs1544410 ‘G’ allele, the rs7975232 ‘G or T’ allele and the rs731236 ‘C’ allele when carried together.
- Carriers of these alleles may want to assess their vitamin D intake and may benefit from additional supplementation.
- High caffeine intake is associated with reduced bone health, particularly in postmenopausal women who are already at high risk.
- A single study investigating VDR gene polymorphisms, caffeine intake and bone health found that high doses of caffeine and the rs731236 ‘C’ allele did correlate with poor bone health but there has been no follow up study to date.
The very latest on genetics, nutrition and supplements delivered to your inbox!
Have a question?
We’re experimenting with QA rather than a comments section.