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Ru(II)-Based Amino Acid Complexes Show Promise for Leukemia Treatment: Cytotoxicity and Some Light on their Mechanism of Action.
Biological Trace Element Research (2019) 192:91–97
https://doi.org/10.1007/s12011-019-1654-5
The Possibilities of Using Chromium Salts as an Agent Supporting
Treatment of Polycystic Ovary Syndrome
Anna Piotrowska 1
Gabriel Nowak 2,3
1
1
1
2
2
& Wanda Pilch & Olga Czerwińska-Ledwig & Roxana Zuziak & Agata Siwek & Małgorzata Wolak &
Received: 14 November 2018 / Accepted: 24 January 2019 / Published online: 4 February 2019
# The Author(s) 2019
Abstract
The polycystic ovary syndrome (PCOS) is the most frequent endocrinopathy in women in reproductive age with the so far
undetermined causes of development. In the etiopathogenesis of PCOS, the role of insulin resistance is emphasised, which was an
indication for the attempts at using chromium III salts (Cr) in augmenting pharmacotherapy applied in patients. The analysis of
the usefulness and efficacy of this approach was the direct goal of this thesis. Animal tests confirmed the efficacy of chromium in
maintaining the appropriate level of glycaemia and insulinaemia, normalisation of plasma concentrations of microelements and
also a correlation between the Cr level, insulin and dehydroepiandrosterone (DHEA) was found. A decrease in the expression of
3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase was identified in adipose tissue. Clinical studies,
although sparse, show that the supplementation with chromium can improve BMI and the parameters evaluating the control of
glycaemia and increase the chances for ovulation and regular menstruation. However, the small number and a variability in study
protocols makes comparing them very difficult. A completely new subject that has not been yet studied is the possibility of using
chromium in levelling mood disorders in patients with PCOS. Currently, there are still no sufficient proofs for introducing
chromium as a standard in treating and preventing insulin resistance in patients with PCOS. However, this direction remains
open, and treating insulin resistance is an important challenge in clinical practice.
Keywords Chromium picolinate . Obesity . Insulin sensitivity . Mood disorders . Dietary nutrient . Physiological benefits
Introduction
Polycystic ovary syndrome (PCOS) is one of the most frequent
endocrinopathies in women in reproductive age and in adolescence. In accordance with American data, this disorder is diagnosed in 4–12% of women; however, according to European
data, this condition may occur twice as frequent [1–3]. The
frequency of diagnosing in a given country is influenced by
the prevalence of obesity and also ethnic and racial differences,
as described in the epidemiological literature and in the clinical
* Anna Piotrowska
anna.piotrowska@awf.krakow.pl
1
Department of Biochemistry and Basics of Cosmetology, University
of Physical Education, Kraków, Poland
2
Department of Pharmacobiology, Jagiellonian University Medical
College, Kraków, Poland
3
Department of Neurobiology, Laboratory of Trace Elements
Neurobiology, Institute of Pharmacology PAS, Kraków, Poland
image of this disorder [4]. The causes of PCOS are still being
studied; there is an ongoing search for the genes responsible for
the manifestation of the disease, and the clinical image is
extraordinarily heterogeneous [2, 5]. There are gynaecological
and metabolic symptoms; all of them influence patient’s
psychological condition and self-esteem [6, 7].
One of the most important elements of the image of the
observed metabolic disorders is insulin resistance and a whole
set of glycaemic disorders. In patients with PCOS, obesity and
dyslipidaemia are more frequent [8, 9]. This led to the hypothesis that the application of supplementation with chromium
(III) indicated as an microelement facilitating in maintaining
normal glycaemia and normal level of lipoprotein in plasma
and dealing with obesity [10].
Review Method
A review of Internet databases (PubMed, Ebsco and
ScienceDirect) and medical journals was performed,
Piotrowska et al.
92
PCOS was described for the first time by Stein and Leventhal
in 1935. The first name of the condition was based on both
their names. The current terminology is derived from the characteristic image of an ovary with peripherally located cysts.
PCOS is characterised by hyperandrogenism and ovary function and changes in their structure [2, 11]. Other names of the
syndrome include functional ovary androgenism, chronic
hyperandrogenic lack of ovulation, ovary dysmetabolic syndrome, sclerotic ovary syndrome, polycystic ovaries or the
aforementioned historical name: Stein–Leventhal syndrome.
and under breasts [15, 16]. More than half of the women
suffering from PCOS experience overweight and obesity, usually of the androidal type [8]. Increased body weight has negative influence on carbohydrate economy, which causes insulin resistance, leading also to hyperinsulinaemia. It is thought
that high concentration of circulating insulin contributes to the
increased production of androgen in an ovary and to ovulation
disorders. In a significant part of patients, an abnormal lipid
profile is observed. Patients with PCOS are at high risk of
developing cardiovascular disease being its distant consequence [17, 18].
PCOS is a condition strongly affecting mental health and
social functioning. In women with PCOS, an increased number of anxiety and/or depression incidents is reported [6, 7]. In
great majority of cases, this is connected with the clinical
image of this disorder, deteriorating the quality of life [6,
19]. It has been concluded that the increased level of free
testosterone in the plasma, one of the main anomalies in
PCOS, is correlated with the increased risk of depression.
There are studies reporting even sevenfold increase in the
frequency of suicides among patients [20]. Patients often have
a problem with their identity and social functioning. They feel
the difference between their appearance and the image of the
woman created by media. They withdraw from social life.
Also, the infertility present in 72% of patients contributes to
the development of serious psychosocial problems [8, 19, 21].
PCOS Symptoms and Course of the Disease
Dietary Treatment and Supplementation in PCOS
Currently, in order to diagnose PCOS, the Rotterdam criteria
were approved by the American Society for Reproductive
Medicine and the European Society of Human Reproduction
and Embryology, in accordance with which PCOS is indicated
by two of the three symptoms: menstruation disorders or
amennorrhea with ovulation disorder or lack thereof; clinical
and/or biochemical signs of hyperandrogenism; presence of
polycystic ovaries in ultrasound, after prior elimination of other conditions related to hyperandrogenism [12].
PCOS frequently presents with acne, hirsutism, hair loss,
irregular menstruation and infertility. It increases the risk of
endometriosis and breast cancer, and it is also related to the
following disorders: dyslipidaemia, hypertension, cardiovascular diseases and diabetes, fitting the consequences of a metabolic syndrome [13]. Hyperandrogenism manifests by androgenic alopecia, hirsutism, acne lesions, increased hair loss,
oily skin, seborrhoeic lesions and clitoromegaly. Hirsutism,
one of the most frequent symptoms, assessed according to
the Ferriman–Gallwey score, is the presence of gruff, thick
and pigment-saturated hair in women in places typical for
men, e.g. upper lip, chin, chest, nape of the neck, lumbar
region, abdomen, thighs and feet [14]. A frequently appearing
skin symptom in women with PCOS is also acanthosis
nigricans, usually located on elbows, nape of the neck, armpits
In the aspect of direct correlation between obesity and the
frequency of PCOS, it seems that diet therapy should play
the major role in managing the condition [22]. Studies revealed disorders in the metabolism of many nutrients, such
as vitamin D, numerous minerals and omega-6 fatty acid
[23]. Therefore, dietary strategies and supplementation have
become points of interest of persons studying the problems of
women with PCOS [24]. Among others, the effects of dietary
supplementation with the application of inositol and folic acid
have been indicated [25, 26], and also interesting effects have
been observed regarding 12-week probiotic supplementation
[27].
Minimising insulin resistance can play a significant role in
controlling PCOS [28]. The development and understanding of
the phenomenon of insulin resistance in the pathogenesis of this
syndrome were an indication to search for new methods,
including adjusting the diet of patients [29]. One of the methods
leading to this effect was supposed to be chromium (III).
searching for papers in Polish and in English from years
2000–2018. The following keywords and their combinations
were used: polycystic ovary syndrome (PCOS, zespół
policystycznych jajników), chromium (chrom), chromium
picolinate (pikolinian chromu), chromium chloride (chlorek
chromu), glucose intolerance (nietolerancja glukozy), lean
body mass (beztłuszczowa masa ciała), lipid profile (profil
lipidowy), mood disorders (zaburzenia nastroju) and depression (depresja). The analysis included original, case studies
and review papers related to the studied subject.
Results
Polycystic Ovary Syndrome
Chromium
Chromium (Cr) can be present at different levels of oxidation;
however, only Cr (III) is responsible for beneficial effects
[10]. The first publication on the biochemical role of Cr in
The Possibilities of Using Chromium Salts as an Agent Supporting Treatment of Polycystic Ovary Syndrome
mammal organisms was published in 1959 [30], and since that
time, it has been placed on the list of the elements necessary
for optimal functioning of living organisms. This was the result of observations indicating that the amount of Cr in the
structures of hair, plasma and sweat has negative correlation
with age, which differentiates it from most contaminations
accumulated in organisms with the passing of time. In patients
subjected to long-term parenteral nutrition, symptoms of Cr
deficiency were observed, manifested mainly by glucose intolerance. These changes were easily treated after supplementation [31, 32]. Indications for its supplementation used to be
very broad; however, currently, Cr is one of the elements
causing the greatest controversies. It is argued that it does
not belong to the necessary microelements, but it evokes a
potential benefit and/or adverse effects. Adequate intake
(AI) was set based on estimated mean intakes and amounts
35 μg/day and 25 μg/day for young men and women, respectively. In Poland, there are no separate recommendations for
this biometal AI, and no detailed guidelines on doses of PCOS
supplementation have been set.
Chromium, Glycaemic Level and Insulin Sensitivity
The first studies of the influence of Cr on maintaining the
proper glucose tolerance in rats were conducted in the late
1950s [30]. These observations were confirmed also in clinical setting, in patients subjected to long-term parenteral nutrition [33]. Chromium has become a popular subject of studies
regarding glucose intolerance and insulin resistance.
Currently, the conclusions are that only supplements including
yeast enriched with this metal have influence on the decrease
of concentration of glucose or glycated haemoglobin in blood
[34]. However, in the paper of Yin et al. comparing the studies
from years 2000–2012, it was shown that supplementation
can cause decrease of fasting glycaemia, but it has no influence on the concentration of glycated haemoglobin [35]. It is
indicated that Cr takes part in insulin signalling and increases
sensitivity to insulin of insulin-sensitive cells [36–38], and
deficiency, rare as it is, increases the risk of metabolic diseases
and diabetes [38].
93
and the improvement of lipid indicators in the blood was
shown. The lack of influence of supplementation is also confirmed by the later studies with the use of yeast enriched with
Cr [34] and chromium picolinate (CrP) [43].
Chromium and Body Mass Control
Chromium dietary supplements were very popular in the
1990s and later, as products facilitating weight loss and increasing muscle mass. To this day, many of them are still
offered by pharmacies and drugstores, which, in the context
of the frequency of obesity in women with PCOS, is another
indication at the necessity of analysing the activity and efficacy of such supplementation. Unfortunately, so far there have
not been any scientific reports proving the efficacy of supplementation with Cr in decreasing the content of adipose tissue
and increasing muscle mass, against the marketing claims of
the manufacturers of dietary supplements [10]. A paper
summarising the results of publications regarding the application of supplementation with Cr in persons with overweight
and obesity indicates that there have been a relatively small
number of studies with proper protocols: high heterogeneity
of intervention types and sample sizes, which usually were
small or moderate (622 subjects evaluated in total) [44]. The
intervention time was 12–16 weeks, and the observation for
potential adverse effects: 8–24 weeks. The results show that
Cr supplements in all doses have some influence on losing
weight after 12–16 weeks of supplementation, but the effective dosage cannot be yet determined. No decisive proofs in
the form of significant changes of BMI, waist circumference
or percentage content of adipose tissue were found. This is
significant in the light of the studies conducted by Pazderska
et al., which indicate that waist circumference in patients with
PCOS is suggested as a predictor of glucose and lipid metabolism disorders [45]. In the review of 10 studies performed by
Pitter [46], a significant differential effect to the benefit of CrP
was indicated; however, the clinical significance of this effect
is still disputed. Also, the safety of supplementation with CrP
in persons with overweight and obesity is still being determined, although reports on adverse effects of supplementation
with Cr are more casuistic in nature [47].
Chromium and Lipid Metabolism
Supplementation with Chromium in PCOS
Animal study results confirm the positive influence of Cr on
lipid profile change [39] and the influence of supplementation
with this microelement on full cholesterol concentrations,
LDL and HDL cholesterol and triglycerides [40]. However,
clinical studies provide ambiguous results. Despite positive
observations from the turn of the twentieth and twenty-first
centuries [41], the studies of Kleefstra et al. [42] did not
achieve positive results of a 6-month supplementation with
chromium picolinate (III) (500 and 1000 μg/day). Only a
slight dependence between the content of Cr (III) in the serum
Due to the concomitance of PCOS and insulin resistance, an
attempt was made to apply supplementation with Cr in this
disorder. Studies conducted in animals showed the efficacy of
the increased supply of Cr in maintaining the proper level of
insulin and glucose in fasting conditions, an improvement of
the microelement levels in plasma, which were disturbed due
to a disease [48], and they confirmed the dependence between
the concentration of Cr, insulin and dehydroepiandrosterone
(DHEA) [48, 49]. Thanks to the mouse model of PCOS, the
94
influence of the syndrome on phenotypical characteristics was
demonstrated: the mice developed abdominal obesity,
hyperandrogenism, hyperinsulinaemia, follicular atresia and
light hepatic steatosis. The model mice with Cr supplementation showed a tendency to decrease body weight gain, liver
mass and its steatosis was significantly lower in these animals;
however, Cr did not improve the morphology of ovaries. In
the adipose tissue of the supplemented animals, a decrease of
3β-hydroxysteroid and 17β-hydroxysteroid dehydrogenases
was revealed. In model animals, a reverse correlation between
the concentration of Cr in serum and in muscles and the concentration of insulin was noted, which points to the fact that
PCOS can cause a low level of Cr in serum and in muscles,
and it seems to lead to hyperinsulinaemia [47]. The analysis of
plasma concentrations of selected metals, including Cr, was
the subject of several papers and was reviewed in detail in
2016 [50]. Two studies evaluating plasma chromium levels
selected by Spritzer et al. did not indicate differences between
women with PCOS and controls.
As of now, several randomised placebo-controlled clinical
studies have been conducted in patients with PCOS. Amr and
Abdel-Rahim evaluated the influence of supplementation in
adolescents (age range, 14–17 years old) [51]. Thirty-five adolescent girls with histories of menstruation disorders were
qualified for the study. In 6 months, subjects were given
1000 μg of CrP. After this period, the lack of significant
change of BMI was indicated; however, the number of subjects with oligomenorrhoea/amenorrhoea decreased in the
supplemented group, and also a significant decrease of the
mean ovary volume and the total number of ovarian cysts
was observed. What is important, in the supplemented group,
the level of free testosterone in the serum was significantly
lower. However, no significant improvement was noted in the
image of acne and hirsutism.
The rest of the studies of the application of therapy or
supporting therapy of PCOS with Cr were conducted in mature women, and the meta-analysis of the results is presented
in review studies [52–55]. In Heshmati’s work [53], the final
meta-analysis included only five properly randomised and
placebo (or an approved drug)-controlled studies, with 137
women with PCOS in total. The authors indicated three studies assessing Cr as a single supplement [56–58]. Two of them
assessed Cr in comparison to metformin [59, 60]. Populations
of the studied groups were from 6 to 46 women, and the
applied diagnostics of PCOS complied with the criteria of
the Rotterdam consensus [12]. These studies were conducted
in the USA, Egypt and Iran. All the women were in reproductive age, and the intervention time was from 6 weeks to
6 months. Chromium, in comparison to placebo or other therapies, caused significant changes in the insulin resistance
markers (summary data analysis from five studies indicated
significantly lower HOMA-IR values in the group supplemented with chromium). The study describing the influence
Piotrowska et al.
of supplementation on HOMA-B showed a significant difference. In this study, after 8 weeks of supplementation in women with PCOS, also a significant decrease in HOMA-IR and
an increase of the QUICKI result were reported, in comparison to placebo [57]. Comparing Cr with metformin treatment,
it was indicated that supplementation of diet with Cr was not
related to insulin concentration [59, 60]. Meta-analysis conducted by Tang et al. [55] indicates the improvement in insulin
sensitivity; however, it has failed to show a beneficial effect of
Cr supplementation on the level of total and free testosterone.
Data analysis showed no effect of supplementation on body
mass, fasting insulin and glucose or serum lipid levels. Also,
there were no significant differences in luteinizing hormone
(LH), follicle-stimulating hormone (FSH) and prolactin
(PRL). Maleki concludes that a longer period of supplementation is required to obtain a significant effect of Cr intake on
the level of sex hormones in the plasma [54]. The conducted
studies and their meta-analyses do not provide an unequivocal
answer regarding the efficacy of supplementation, and the
observed effects are too poor to allow for the implementation
of such an approach to the standard therapy of patients with
PCOS.
Chromium and Treatment of Mood Disorders in PCOS
According to Kurek and Babiarczyk, due to the multidimensional character of the problems related to PCOS in women,
they should be provided complex care including the physical
and psychosocial problems [6]. Treatment of physical disorders should be conducted in accordance with the current
needs, which is aimed at reaching the goals they have chosen.
The psychosocial disorders, which are very often skipped in
the process of treatment, should be paid special attention, and
these women should be provided psychological help in fighting depression, which often appears in this condition [6, 7].
The first information indicating the possibility of antidepressant activity of Cr is from the 1990s. It was described that the
symptoms of atypical depression, dysthymia, seasonal affective disorders and daily mood swings decreased. Due to the
fact that in some women with PCOS depressive states related
to unsuccessful attempts at getting pregnant, high BMI and
low self-esteem, preparations with Cr can have positive influence; however, this has not been studied so far.
The mechanism of antidepressant activity of Cr seems to be
of pharmacological nature [61–63], as deficiency of this metal
is rare [64, 65], and the effective doses are relatively high both
in animal tests [61–63] and in clinical application: Cr salt,
administered in dose 400–600 μg/day, was effective in patient
with depression [66–68].
The antidepressant activity of Cr studied in animal models
of depression depends (to various degrees) on noradrenergic,
dopaminergic and serotonin signalling. It was shown that the
antidepressant activity of chromium chloride (CrCl3) is
The Possibilities of Using Chromium Salts as an Agent Supporting Treatment of Polycystic Ovary Syndrome
partially dependent on serotonin receptors 5-HT1A and 5HT2A [63]. On the other hand, the noradrenergic mechanism
was indicated in the studies with the application of adrenergic
receptor antagonists (propranolol, prazosin, yohimbine) and
the reinforcement of the antidepressant activity of reboxetine
(selective inhibitor of noradrenaline uptake) [63]. Also, the
role of dopaminergic system was indicated [63]. The involvement of the monoamine systems was also indicated by
Franklin and Odontiadis [69], who demonstrated increase in
the level of serotonin and its metabolites, as well as a change
in the number of 5HT2A receptors of the downregulation type.
Glutamatergic system takes part in the antidepressant activity
of Cr through receptors AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor) and NMDA (N-methyl-D-aspartate receptor) [62]. Additionally, Khanam and Pillai
[70] suggested the involvement of K+ channels; however, this
has never been confirmed. The complex mechanism in correlation with an interesting clinical profile (activity in dysthymic, seasonal disorders and atypical depression) and the influence on carbohydrate metabolism, and perhaps also lipid metabolism, makes Cr supplementation in patient with PCOS a
still interesting study subject.
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References
1.
2.
3.
4.
Summary
5.
Chromium gained its greatest popularity by the end of the
twentieth century. In scientific literature, one can find an enormous number of studies concerning the influence of supplementation on carbohydrate–lipid economy of the body, but not
only on that aspect. The indications regarding the influence on
the markers describing insulin resistance allowed to presume
the efficacy of such supplementation in PCOS.
The indicated mechanisms of action for Cr confirmed in
animal tests are unfortunately not always confirmed in the
conducted clinical studies. The efficacy of supplementation
in diabetes and dyslipidaemias is undermined, in maintaining
appropriate body weight—negated. The available reports on
the role of Cr are often contradictory, and the state of knowledge does not confirm the previous assumptions fully, which,
unfortunately, often is the result of poor planning of research
works and especially using very small patient groups.
The role of Cr supplementation in PCOS remains unsolved.
An interesting phenomenon is especially the possibility of this
element influencing the mood, which constitutes a big challenge in the discussed condition. A significant factor for using
Cr supplementation in patients with PCOS can be also the fact
that in animal tests, low Cr level was observed in serum and in
muscles with concomitant hyperinsulinaemia. Nevertheless,
in order to unequivocally assess the efficacy of Cr supplementation in the discussed condition, it is necessary to conduct
further studies in this direction of sufficient sample size for
sufficient duration in well-defined populations.
95
6.
7.
8.
9.
10.
11.
12.
13.
March WA, Moore VM, Willson KJ, Phillips DIW, Norman RJ,
Davies MJ (2010) The prevalence of polycystic ovary syndrome in
a community sample assessed under contrasting diagnostic criteria.
Hum Reprod 25(2):544–551. https://doi.org/10.1093/humrep/
dep399
Azziz R, Woods KS, Reyna R, Key TJ, Knochenhauer ES, Yildiz
BO (2004) The prevalence and features of the polycystic ovary
syndrome in an unselected population. J Clin Endocrinol Metab
89:2745–2749
Norman RJ, Dewailly D, Legro RS, Hickey TE (2007) Polycystic
ovary syndrome. Lancet 370:685–697. https://doi.org/10.1016/
S0140-6736(07)61345-2
Carmina E, Koyama T, Chang L, Stanczyk FZ, Lobo RA (1992)
Does ethnicity influence the prevalence of adrenal
hyperandrogenism and insulin resistance in polycystic ovary syndrome? Am J Obstet Gynecol 167:1807–1812
Legro RS, Arslanian SA, Ehrmann DA, Hoeger KM, Murad MH,
Pasquali R, Welt CK, Endocrine Society (2013) Diagnosis and
treatment of polycystic ovary syndrome: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 98:4565–4592.
https://doi.org/10.1210/jc.2013-2350
Kurek G, Babiarczyk B (2017) Biopsychosocial problems experienced by women at reproductive age suffering from polycystic
ovary syndrome. Pol Prz Nauk Zdr 1(50):7–15. https://doi.org/10.
20883/ppnoz.2017.1 (Polish)
Cooney LG, Lee I, Sammel MD, Dokras A (2017) High prevalence
of moderate and severe depressive and anxiety symptoms in polycystic ovary syndrome: a systematic review and meta-analysis.
Hum Reprod 32(5):1075–1091. https://doi.org/10.1093/humrep/
dex044
Joham AE, Teede HJ, Ranasinha S, Zoungas S, Boyle J (2015)
Prevalence of infertility and use of fertility treatment in women with
polycystic ovary syndrome: data from a large community-based
cohort study. J Women Health 24:299–307. https://doi.org/10.
1089/jwh.2014.5000
Sirmans SM, Pate KA (2013) Epidemiology, diagnosis, and management of polycystic ovary syndrome. Clin Epidemiol 6:1–13.
https://doi.org/10.2147/CLEP.S37559
Piotrowska A, Pilch W, Tota Ł, Nowak G (2018) Biological significance of chromium III for the human organism. Med Pr 69(2):211–
223. https://doi.org/10.13075/mp.5893.00625 (Polish)
Kruszyńska A, Słowińska-Srzednicka J (2008) Progress in diagnosis and treatment of Polycystic Ovary Syndrome. Post Nauk Med
21(3):148–153 (Polish)
Rotterdam ESHRE/ASRM-Sponsored PCOS consensus workshop
group (2004) Revised 2003 consensus on diagnostic criteria and
long-term health risks related to polycystic ovary syndrome
(PCOS). Hum Reprod 19(1):41–47
Ollila MM, Piltonen T, Puukka K et al (2015) Weight gain and
dyslipidemia in early adulthood associate with polycystic ovary
Piotrowska et al.
96
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
syndrome: prospective cohort study. J Clin Endocrinol Metab 101:
739–747. https://doi.org/10.1210/jc.2015-3543
Bumbuliene Ż, Alisauskas J (2009) Evaluation and treatment of
adolescent girls with hirsutism. Ginekol Pol 80:374–378 (Polish)
Housman E, Reynolds RV (2014) Polycystic ovary syndrome: a
review for dermatologists: part I. Diagnosis and manifestations. J
Am Acad Dermatol 71:847.e1–847.e10. https://doi.org/10.1016/j.
jaad.2014.05.007
Dong Z, Huang J, Huang L, Chen X, Yin Q, Yang D (2013)
Associations of acanthosis nigricans with metabolic abnormalities
in polycystic ovary syndrome women with normal body mass index. J Dermatol 40(3):188–192. https://doi.org/10.1111/13468138.12052
Kuligowska-Jakubowska M, Dardzińska J, Rachoń D (2012)
Disorders of carbohydrate metabolism in women with polycystic
ovary syndrome (PCOS). Diabetol Klin 1(5):185–195 (Polish)
Spritzer PM (2014) Polycystic ovary syndrome: reviewing diagnosis and management of metabolic disturbances. Arq Bras
Endocrinol Metab 58(2):182–187
Podfigurna-Stopa A, Luisi S, Regini C, Katulski K, Centini G,
Meczekalski B, Petraglia F (2015) Mood disorders and quality of
life in polycystic ovary syndrome. Gynecol Endocrinol 31(6):431–
434. https://doi.org/10.3109/09513590.2015.1009437
Krępuła K, Bidzińska-Speichert B, Lenarcik A, TworowskaBardzińska U (2012) Psychiatric disorders related to polycystic
ovary syndrome. Endokrynol Pol 63(6):488–491
Specjalski R (2013) Psychosexual disorder in women with polycystic ovary syndrome. Piel Pol 3(49):230–234 (Polish)
Mendoza N, Cancelo M (2014) Diabetes mellitus and polycystic
ovary syndrome: implications for diet and nutrition. Handbook of
diet and nutrition in the menstrual cycle, periconception and fertility, vol 32. Academic Publishers, Wageningen, pp 521–532. https://
doi.org/10.3920/978-90-8686-767-7_32
Rondanelli M, Perna S, Faliva M, Monteferrario F, Repaci E, Allieri
F (2014) Focus on metabolic and nutritional correlates of polycystic
ovary syndrome and update on nutritional management of these
critical phenomena. Arch Gynecol Obstet 290:1079–1092. https://
doi.org/10.1007/s00404-014-3433-z
Arentz S, Smith CA, Abbott J, Bensoussan A (2017) Nutritional
supplements and herbal medicines for women with polycystic ovary syndrome; a systematic review and meta-analysis. BMC
Complement Altern Med 17(1):500. https://doi.org/10.1186/
s12906-017-2011-x
Facchinetti F, Bizzarri M, Benvenga S, D’Anna R, Lanzone A,
Soulage C, di Renzo GC, Hod M, Cavalli P, Chiu TT, Kamenov
ZA, Bevilacqua A, Carlomagno G, Gerli S, Oliva MM, Devroey P
(2015) Results from the international consensus conference on
myo-inositol and d-chiro-inositol in obstetrics and gynecology:
the link between metabolic syndrome and PCOS. Eur J Obst
Gynecol Reprod Biol 195:72–76. https://doi.org/10.1016/j.ejogrb.
2015.09.024
Regidor PA, Schindler AE, Lesoine B, Druckman R (2018)
Management of women with PCOS using myo-inositol and folic
acid. New clinical data and review of the literature. Horm Mol Biol
Clin Investig. https://doi.org/10.1515/hmbci-2017-0067
Samimi M, Dadkhah A, Haddad Kashani H, Tajabadi-Ebrahimi M,
Seyed Hosseini E, Asemi Z (2018) The effects of synbiotic supplementation on metabolic status in women with polycystic ovary
syndrome: a randomized double-blind clinical trial. Probiotics
Antimicrob Proteins. https://doi.org/10.1007/s12602-018-9405-z
Moghetti P (2016) Insulin resistance and polycystic ovary syndrome. Curr Pharm Design 22:5526–5534
Geller DH, Pacaud D, Gordon CM, Misra M (2011) State of the art
review: emerging therapies: the use of insulin sensitizers in the
treatment of adolescents with polycystic ovary syndrome (PCOS).
Int J Pediatr Endocrinol. https://doi.org/10.1186/1687-9856-2011-9
30.
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
Schwarz K, Mertz W (1959) Chromium (III) and the glucose tolerance factor. Arch Biochem Biophys 85:292–295
Brown RO, Forloines-Lynn S, Cross RE, Heizer WD (1986)
Chromium deficiency after long-term total parenteral nutrition.
Dig Dis Sci 31(6):661–664
Jeejeebhoy KN, Chu RC, Marliss EB, Greenberg GR, BruceRobertson A (1977) Chromium deficiency, glucose intolerance,
and neuropathy reversed by chromium supplementation, in a patient receiving long-term total parenteral nutrition. Am J Clin Nutr
30(4):531–538
Moukarzel A (2009) Chromium in parenteral nutrition: too little or
too much? Gastroenterology 137:18–28. https://doi.org/10.1053/j.
gastro.2009.08.048
Racek J, Sindberg C, Moesgaard S et al (2013) Effect of chromiumenriched yeast on fasting plasma glucose, glycated haemoglobin
and serum lipid levels in patients with type 2 diabetes mellitus
treated with insulin. Biol Trace Elem Res 155(1):1–4. https://doi.
org/10.1007/s12011-013-9758-9
Yin R, Phung O (2015) Effect of chromium supplementation on
glycated hemoglobin and fasting plasma glucose in patients with
diabetes mellitus. Nutr J. https://doi.org/10.1186/1475-2891-14-14
Hummel M, Standl E, Schnell O (2007) Chromium in metabolic
and cardiovascular disease. Horm Metab Res 39:743–751. https://
doi.org/10.1055/s-2007-985847
Hua Y, Clark S, Ren J, Sreejayan N (2012) Molecular mechanisms
of chromium in alleviating insulin resistance. J Nutr Biochem 23:
313–319. https://doi.org/10.1016/j.jnutbio.2011.11.001
Wang ZQ, Cefalu WT (2010) Current concepts about chromium
supplementation in type 2 diabetes and insulin resistance. Curr
Diabetes Rep 10:145–151. https://doi.org/10.1007/s11892-0100097-3
Cefalu W, Wang Z, Zhang X et al (2002) Oral chromium picolinate
improves carbohydrate and lipid metabolism and enhances skeletal
muscle glut-4 translocation in obese, hyperinsulinemic (JCR-LA
corpulent) rats. J Nutr 132:1107–1114. https://doi.org/10.1093/jn/
132.6.1107
Sun Y, Clodfelder BJ, Shute AA, Irvin T, Vincent JB (2002) The
biomimetic [Cr3O(O2CCH2CH3)6(H2O)3]+ decreases plasma insulin, cholesterol, and triglycerides in healthy and type II diabetic
rats but not type I diabetic rats. J Biol Inorg Chem 7:852–862.
https://doi.org/10.1007/s00775-002-0366-y
Rabinovitz H, Friedensohn A, Leibovitz A, Gabay G, Rocas C,
Habot B (2004) Effect of chromium supplementation on blood
glucose and lipid levels in type 2 diabetes mellitus elderly patients.
Int J Vitam Nutr Res 74:178–182. https://doi.org/10.1024/03009831.74.3.178
Kleefstra N, Houweling S, Jansman F et al (2006) Chromium treatment has no effect in patients with poorly controlled, insulin-treated
type 2 diabetes in an obese Western population. Diabetes Care 29:
321–325. https://doi.org/10.2337/diacare.29.03.06.dc05-1453
Yazaki Y, Faridi Z, al AY (2010) A pilot study of chromium
picolinate for weight loss. J Altern Complement Med 16(3):291–
299. https://doi.org/10.1089/acm.2009.0286
Tian H, Guo X, Wang X, He Z, Sun R, Ge S, Zhang Z, Cochrane
Metabolic and Endocrine Disorders Group (2013) Chromium
picolinate supplementation for overweight or obese adults.
Cochrane Database Syst Rev 29(11):CD010063. https://doi.org/
10.1002/14651858.CD010063.pub2
Pazderska A, Kyaw Tun T, Phelan N, McGowan A, Sherlock M,
Behan LA, Boran G, Gibney J (2018) In women with PCOS, waist
circumference is a better surrogate of glucose and lipid metabolism
than disease status per se. Clin Endocrinol 88(4):565–574. https://
doi.org/10.1111/cen.13542
Pittler M, Ernst E (2004) Dietary supplements for body-weight
reduction: a systematic review. Am J Clin Nutr 79(4):529–536.
https://doi.org/10.1093/ajcn/79.4.529
The Possibilities of Using Chromium Salts as an Agent Supporting Treatment of Polycystic Ovary Syndrome
47.
48.
49.
50.
51.
52.
53.
54.
55.
56.
57.
58.
Suksomboon N, Poolsup N, Yuwanakorn A (2014) Systematic review and meta-analysis of the efficacy and safety of chromium
supplementation in diabetes. J Clin Pharm Ther 39(3):292–306.
https://doi.org/10.1111/jcpt.12147
Chen T, Chen Y, Liu C et al (2015) Effect of chromium supplementation on element distribution in a mouse model of polycystic ovary
syndrome. Biol Trace Elem Res 168(2):472–480. https://doi.org/
10.1007/s12011-015-0384-6
Chen T, Chen Y, Liu C et al (2017) Steroidogenic enzymes of
adipose tissue in modulation of trivalent chromium in a mouse
model of PCOS. Gynecol Endocrinol 33(1):48–52. https://doi.org/
10.1080/09513590.2016.1205579
Spritzer PM, Lecke SB, Fabris VC, Ziegelmann PK, Amaral L
(2016) Blood trace element concentrations in polycystic ovary syndrome: systematic review and meta-analysis. Biol Trace Elem Res
175(2):254–262. https://doi.org/10.1007/s12011-016-0774-4
Amr N, Abdel-Rahim HE (2015) The effect of chromium supplementation on polycystic ovary syndrome in adolescents. J Pediatr
Adolesc Gynecol 28(2):114–118. https://doi.org/10.1016/j.jpag.
2014.05.005
Fazelian S, Rouhani MH, Bank SS, Amani R (2017) Chromium
supplementation and polycystic ovary syndrome: a systematic review and meta-analysis. J Trace Elem Med Biol 42:92–96. https://
doi.org/10.1016/j.jtemb.2017.04.008
Heshmati J, Omani-Samani R, Vesali S, Maroufizadeh S,
Rezaeinejad M, Razavi M, Sepidarkish M (2018) The effects of
supplementation with chromium on insulin resistance indices in
women with polycystic ovarian syndrome: a systematic review
and meta-analysis of randomized clinical trials. Horm Metab Res
50(3):193–200. https://doi.org/10.1055/s-0044-101835
Maleki V, Izadi A, Farsad-Naeimi A, Alizadeh M (2018)
Chromium supplementation does not improve weight loss or metabolic and hormonal variables in patients with polycystic ovary
syndrome: a systematic review. Nutr Res 56:1–10. https://doi.org/
10.1016/j.nutres.2018.04.003
Tang XL, Sun Z, Gong L (2018) Chromium supplementation in
women with polycystic ovary syndrome: systematic review and
meta-analysis. J Obstet Gynaecol Res 44(1):134–143. https://doi.
org/10.1111/jog.13462
Ashoush S, Abou Gamrah A, Bayoumy H, Othman N (2016)
Chromium picolinate reduces insulin resistance in polycystic ovary
syndrome: randomized controlled trial. J Obstet Gynaecol Res 42:
279–285. https://doi.org/10.1111/jog.12907
Jamilian M, Asemi Z (2015) Chromium supplementation and the
effects on metabolic status in women with polycystic ovary syndrome: a randomized, double-blind, placebo-controlled trial. Ann
Nutr Metab 67:42–48. https://doi.org/10.1159/000438465
Lucidi RS, Thyer AC, Easton CA, Holden AEC, Schenken RS,
Brzyski RG (2005) Effect of chromium supplementation on insulin
97
resistance and ovarian and menstrual cyclicity in women with polycystic ovary syndrome. Fertil Steril 84:1755–1777. https://doi.org/
10.1016/j.fertnstert.2005.06.028
59. Amooee S, Parsanezhad ME, Shirazi MR et al (2013) Metformin
versus chromium picolinate in clomiphene citrate-resistant patients
with PCOs: a double-blind randomized clinical trial. Iran J Reprod
Med 11:611–618
60. Fogle RH, Baker MB, Patel SK, Korst LM, Stanczyk FZ, Sokol RZ
(2007) A prospective, randomized clinical trial comparing chromium picolinate to metformin for the treatment of insulin resistance in
obese, Hispanic women with polycystic ovarian syndrome. Fertil
Steril 88:S181
61. Attenburrow MJ, Odontiadis J, Murray BJ (2002) Chromium treatment decreases the sens itivity of 5HT2A receptors.
Psychopharmacology 159:432–436. https://doi.org/10.1007/
s00213-001-0960-7
62. Piotrowska A, Młyniec K, Siwek A, Dybała M, Opoka W, Poleszak
E, Nowak G (2008) Antidepressant-like effect of chromium chloride in the mouse forced swim test: involvement of glutamatergic
and serotonergic receptors. Pharmacol Rep 60(6):991–995
63. Piotrowska A, Siwek A, Wolak M, Pochwat B, Szewczyk B, Opoka
W, Poleszak E, Nowak G (2013) Involvement of the monoaminergic system in the antidepressant-like activity of chromium chloride
in the forced swim test. J Physiol Pharmacol 64(4):493–498
64. Czerwińska D, Zadrużna M (2003) Estimation of chrome and its
main sources in the diets of people at advanced age suffering from
diabetes. Żyw Człow Metab 30:816–821 (Polish)
65. Skibniewska K, Wyszkowska M, Kot W et al (2007) The content of
chromium in the food rations of UWM students in Olsztyn. Żyw
Człow Metab 34:788–791 (Polish)
66. Davidson JR, Abraham K, Connor KM, McLeod MN (2003)
Effectiveness of chromium in atypical depression: a placebocontrolled trial. Biol Psychiatry 53:261–264
67. Docherty JP, Sack DA, Hoffman M et al (2005) A double-blind,
placebo-controlled, exploratory trial of chromium picolinate in
atypical depression: effect on carbohydrate craving. J Psychiat
Pract 11:302–314
68. McLeod MN, Golden RN (2000) Chromium treatment of depression. Int J Neuropsychopharmacol 3:311–314
69. Franklin M, Odontiadis J (2003) Effects of treatment with chromium picolinate on peripheral amino acid availability and brain monoamine function in the rat. Pharmacopsychiatry 36:176–180. https://
doi.org/10.1055/s-2003-43046
70. Khanam R, Pillai KK (2006) Effect of chromium picolinate on
modified forced swimming test in diabetic rats: involvement of
serotonergic pathways and potassium channels. Basic Clin
Pharmacol Toxicol 98:155–159. https://doi.org/10.1111/j.17427843.2006.pto_288.x