Abstract
Endometriosis is a serious health problem character ized by the
persistence and growth of vascularized tissue at va rious ectopic sites such
as ovaries, bowel, or bladder. Despite decades of i ntensive research, we are
not making significant progress toward the etiology or treatment of this
disease. The question of risk factor is similarly u nclear, with one possible
factor being diet-particularly the intake of vitami n D. In addition, as
endometriosis has some similarities and clear conne ctions to cancer, where
vitamin D is heavily studied, this relation started to be a subject of intensive
research in this field, too. The overall aim of thi s study is to review possible
links between vitamin D intake and endometriosis.
Introduction
Endometriosis is a chronic disease with estimated
prevalence of 10% (Missmer and Cramer, 2003).
Despite the seriousness and long-term research
interests, the etiology of endometriosis is still p oorly
understood. However, immunological aspects are
gaining more and more attention (Kralickova and
Vetvicka, 2015) and the search for reliable markers is
still ongoing, with few clearly defined markers
(Kralickova and Vetvicka, 2016). The question of ri sk
factor is similarly unclear, with one possible fact or
being diet-particularly the intake of vitamin D.
Vitamin D
Vitamin D is an essential steroid pro-hormone
playing an important role in maintenance of phospha te
and calcium homeostasis. Despite the “vitamin” name ,
its source is not completely dietary and over 85% i s
generated in the skin following exposure to ultravi olet
light. For detailed description of chemistry and
biological effects of vitamin D, see an excellent
review by Nandi et al. (2016). Besides the principal
role in bone homeostasis, vitamin D is involved in
additional biological processes such as modulation of
cell growth, immune functions and reduction of
inflammation. In addition, vitamin D affects in vitro
insulin and follicle-stimulating, hormone-induced
secretion of progesterone (Smolikova et al ., 2013).
Vitamin D is also heavily involved in human
reproduction, from fertility outcome to semen quali ty
(for review, Anagnostis et al ., 2013). Proposed roles of
vitamin D in women’s reproduction are summarized in a
report by Grundmann and von Versen-Hoynck (2011).
A clinical study found small and nonsignificant
increase in 1,25-hydroxyvitamin D levels in patient s
with endometriosis with a slight trend towards high er
levels according to the severity of the disease
(Somigliana et al ., 2007). Later, a prospective cohort
study of 70,556 women with endometriosis, evaluated
over the period of 14 years, investigated whether t he
plasma 1,25-hydroxyvitamin D levels were associated
with the disease. The results suggested that greate r
plasma levels of vitamin D and higher intake of dai ry
foods are clearly associated with decreased risk of
endometriosis (Harris et al ., 2013). This study, which
estimated serum values of 1- α,25-hydroxyvitamin D3
and calculated variables such as race, age, physica l
activity or alcohol intake, showed inverse associat ion
between 1- α,25-hydroxyvitamin D3 values and
endometriosis and women with the highest levels had
Králíčková Milena and Vetvicka Vaclav / American Journa l of Immunology 2017, 13 (2): 127.130
DOI: 10.3844/ajisp.2017.127.130
128
24% lower risk of endometriosis (Harris et al ., 2013).
On the other hand, a recent study found 1- α,25-
hydroxyvitamin D3 levels significantly lower in ser um
of patients with severe endometriosis (Miyashita et al .,
2016), further confusing the question of whether vi tamin
D levels are important.
The importance of 1- α,25-hydroxyvitamin D3 levels
was confirmed using experimental model of rats with
endometriotic implants. Animals with 1- α,25-
hydroxyvitamin D3 showed significantly lesser
symptoms, leading to the conclusion that this molec ule
resulted in regression via altering implant levels of
VEGF, TIMP-2 and MMP-9 (Yildirim et al ., 2014).
Human clinical trials will be needed to confirm the
possibility of treatment. An interesting observatio n by
Agic et al. (2007) of very high metabolism of vitamin D
in the endometrium suggested possible paracrine act ion
of vitamin D. This hypothesis was supported by find ings
that Elocalcitol, a vitamin D receptor agonist, can
reverse endometriotic implants in animal models
(Mariani et al ., 2012).
An in vitro study focusing on the possible effects of
1-α,25-hydroxyvitamin D3 on human endometriotic
stromal cells isolated from ovarian endometrioma
demonstrated that the addition of 1- α,25-
hydroxyvitamin D3 resulted in reduction of IL-1 β-
and TNF- α-induced inflammatory responses and
reduction of numbers of viable stromal cells
(Miyashita et al ., 2016). If these results are
confirmed, supplementation with vitamin D might
represent a novel strategy. Another hypothesis
suggested that endometriosis is an autoimmune
disease. With the known autocrine/paracrine action of
vitamin D and established relation between
autoimmune diseases and vitamin D, Peterlik and
Cross (2005) focused their attention on vitamin D a s
an immunomodulator. The problems with any clear
relations result from the fact that endometriosis i s
associated with normal or elevated levels of 1- α,25-
hydroxyvitamin D3 and not with any deficiency. The
only possibility would be local effects, which woul d be
missed on fluid evaluation such as serum. Additiona l
hypotheses about vitamin D and endometriosis are
summarized in a recent review (Sayegh et al., 2014).
Vitamin D-Binding Protein
Vitamin D-binding protein (also called Gc-globulin
or DBP) is a multifunctional protein deeply involve d in
transport of vitamin D sterols and in modulation of
inflammation and defense reactions. Due to the
suspected role of inflammation and several immune
aspects in the development of endometriosis, this
protein was also evaluated in women with
endometriosis. However, the levels of this protein both
in serum and in peritoneum were not significantly
different between control and endometriosis groups
(Borkowski et al ., 2008).
2-D electrophoresis was used for evaluation of DBP
levels in peritoneal fluid and plasma. One isoform
(DBPE) showed lower levels in sampled peritoneal fl uid,
but when the patients were treated with oral
contraceptive, the levels of DBPE returned to norma l
(Ferrero et al ., 2005), making the possibility of DBP
involvement even more confusing.
Using proteomics, elevated levels of vitamin D-
binding protein were found in urine of women with
endometriosis (Cho et al ., 2012), suggesting that urine
samples might be utilized in further investigations and
that this protein might play a role in endometriosi s. A
different experimental approach, combining 2-DE gel
electrophoresis with mass spectrometry, was later
used to compare endometrial protein in ectopic
endometrial tissue and normal endometrial tissue.
Among fifteen other proteins, levels of vitamin D-
binding protein were found to be significantly incr eased
in ectopic endometrium, suggesting that this protei n can
have a direct role in the progression of this disea se
(Hwang et al ., 2013).
Human cycling endometrium has been shown to
express vitamin D receptor (Vigano et al ., 2006). This
receptor is a nuclear ligand-inducible transcriptio n factor
and in complex with vitamin D, it regulates express ion
of more than 900 different genes (Carlberg, 2003).
A comparative histological study showed strong
staining for vitamin D receptor in endometriosis an d
endometrial cancer, with the strongest staining in
epithelial cells. In addition, these samples also s howed
stronger expression of vitamin D 1 α-hydroxylase
(Agic et al ., 2007). The authors hypothesized that
vitamin D might affect local action of immune cells
and/or secretion of cytokines involved in developme nt
of endometriosis.
Elocalcitol, a selective vitamin D receptor agonist ,
reduced endometriosis development in mouse model vi a
inhibition of peritoneal inflammation (Mariani et al .,
2012), demonstrated by inhibition of macrophage inf lux
and inhibition of secretion of inflammatory cytokines.
Genetic alterations in the Vitamin D Receptor
(VDR) gene might lead to biologically relevant
defects in gene activation with subsequent changes in
immune functions. Detailed analysis of vitamin D
receptor gene polymorphism in women suffering from
endometriosis revealed no changes between patients
and controls, strongly demonstrating that VDR
polymorphism is not involved in endometriosis
(Lima Vilarino et al ., 2011).
Proteolytic analysis of serum found 3x higher level of
vitamin D-binding protein in patients with
Králíčková Milena and Vetvicka Vaclav / American Journa l of Immunology 2017, 13 (2): 127.130
DOI: 10.3844/ajisp.2017.127.130
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endometriosis. Subsequent analysis of specific alle le
products showed that the most commonly expressed
protein is GC*2 allele product. As this product is not
converted to a macrophage-stimulating factor, the
authors hypothesize that the inability to stimulate
macrophages to optimally phagocytose-invading
Material
results in allowing the endometriotic tiss ue to
seed the peritoneal cavity (Faserl et al ., 2011).
Gene Level
Endometrium is a target of 1- α,25-hydroxyvitamin
D3 actions via regulation of specific genes, most
probably HOXA10 gene expression. This gene is
cyclically expressed in adult endometrium in respon se to
estrogens. 1- α,25-hydroxyvitamin D3 can induce
HOXA10 transcription through VDR binding to its
responsive elements in the HOXA10 gene 5 region,
which might subsequently induce differentiation of
endometrial cells to decidual cells (Du et al ., 2005).
Lower expression of this gene was found in the euto pic
and ectopic endometrium of endometriosis (Deng et al .,
2011). However, a study evaluating VDR
polymorphism found no association between this
polymorphism and endometriosis or infertility
(Villarino et al ., 2011). Another vitamin D-regulated
gene is osteopontin gene, with higher expression in
eutopic endometrium (Cho et al ., 2009).
The 1 α-hydroxylase (enzyme necessary to catalyze
the synthesis of 1- α,25-hydroxyvitamin D3) mRNA is
expressed in ectopic endometrium and its levels are
increased in proliferative phase cultures derived f rom
women with endometriosis. These data suggested that
cycling endometrium might be included among the
extrarenal sites able to synthesize vitamin D
(Vigano et al ., 2006).
Conclusion
Endometriosis was first described more than 150
years ago (Von Rokitansky, 1860), but the causes an d
treatments remain enigmatic and the search for
responsible molecules is still ongoing. Numerous
studies suggest some kind of vitamin D involvement
in the pathogenesis of endometriosis, but direct pr oof
is still elusive. Several studies have found altere d
levels of vitamin D in patients suffering from
endometriosis; however, no clear benefits from
supplementation with vitamin D have been
established. On the other hand, despite intensive
research, we are not closer to understanding the
pathogenesis of endometriosis than we were decades
ago and there is still a need to fully confirm or d isprove
the functional role of the vitamin D system at the
endometrial level. The hopes that vitamin D will
represent the Golden Fleece seem to be unsubstantiated.
Financial Support and Sponsorship
Nil.
Author’s Contributions
Milena Kralickova: Designed the article, wrote the
manuscript.
Vaclav Vetvicka: Designed the article, wrote the
manuscript.
Conflicts of Interest
There are no conflicts of interest.
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