| |
The diagnosis of polycystic ovary syndrome (PCOS) has become much
more common in recent years. It is now not unusual for women in the
United States to come for consultation having self-diagnosed PCOS.
This awareness is largely the result of the efforts of two
well-organised advocacy groups in the US which communicate via the
Internet, as well as information from recent articles in popular
magazines.
PCOS is extremely common, estimated to occur in 3%-7% of women of
reproductive age.1,2 Because of the
heterogeneous nature of the disorder, there is no universal
consensus on the diagnostic criteria for PCOS. However, the classic
features of the syndrome are well established and include chronic
anovulation and hyperandrogenism (with or without skin
manifestations). In most women, characteristic polycystic ovaries
will be observed on ultrasonography. The criterion of enlarged
ovaries, with 8-10 peripherally oriented cystic structures in a
single sonographic plane,3 is best detected with the use
of a vaginal probe. While many affected women are of normal body
weight, obesity is common, as is the tendency to gain weight easily.
However, there is less agreement about the diagnosis of PCOS in women
who are ovulatory, and the relevance of isolated ultrasonographic
findings in asymptomatic women is uncertain.
The high prevalence of PCOS and its potential for causing significant
morbidity4 has prompted investigators
to call this syndrome a disorder for the "generalist".2 Heightened
awareness and early diagnosis provide the opportunity to intervene
and thus prevent certain sequelae of the disorder. The Figure
provides a crude depiction of the risks associated with PCOS from the
time of early diagnosis (by 20 years of age) throughout life.
Reproductive concerns, which begin in the second to third decade,
relate to infertility because of anovulation and increased
pregnancy wastage, as well as the risks of endometrial disease
(hyperplasia and cancer) and probably also ovarian cancer.
Dysfunctional uterine bleeding and skin manifestations of androgen
excess (acne, hirsutism) are also causes for concern. Among the many
diseases associated with PCOS and shown in the Figure, breast cancer,
although it has been suggested,5 has not been included
because there are no supporting data.
Metabolic risks, particularly in obese women, increase by the time
women reach their mid-30s. Diabetes has been found to occur in 7.5% of
women with PCOS in this age group, and impaired glucose tolerance in
31%.6
Cardiovascular risks include dyslipidaemia, hypertension,
atherosclerosis, and an increased risk of myocardial
infarction,4 although mortality per
se may not be increased, except in women with
diabetes.7 Cardiovascular risks have
been most closely linked to abnormalities of insulin action.
Insulin resistance has been found to occur in most women with PCOS and
is more severe in obese women and in those with greater menstrual
irregularity.1 The insulin resistance in
PCOS may also be associated with -cell
dysfunction, as occurs in type 2 diabetes.8 Insulin resistance in PCOS,
although often subtle, has been found consistently and has been
implicated as the proximate instigating factor leading to the
complications of the syndrome (from endometrial disease to
dyslipidaemia, hypertension and atherosclerotic cardiovascular
disease).
It is generally thought that if insulin status can be normalised many
of the clinical manifestations of the disorder, as well as the
associated risks, may be eliminated. Certainly, the characteristic
symptoms of PCOS in one young woman with an insulinoma were seen to
dissipate when the tumour was removed.9 Reductions in insulin
resistance have been shown to normalise hormonal abnormalities
(luteinising hormone, androgens) and restore normal menstrual
function as well as ovulation in some women with PCOS.
In this issue of the Journal, Norman and colleagues review data on the
use of metformin in PCOS.10 This article, on behalf of
the Endocrine Society of Australia, the Australian Diabetes Society
and the Australasian Paediatric Endocrine Group, is timely in
bringing attention to the metabolic aspects of this very common
disorder. The authors stress the importance of screening all
patients for diabetes, as well as taking note of additional
cardiovascular risk factors. In general, as suggested by the
authors, lifestyle modifications should be the cornerstone of any
therapy for PCOS.11
The review by Norman et al is comprehensive, but there are even more
data emerging in the literature. Metformin is generally well
tolerated, apart from the gastrointestinal disturbance, which
precludes its use in some women. Consistent with the view of Norman et
al, metformin is considered to be most appropriate as a short-term
measure to improve ovulatory function (with or without
ovulation-inducing agents) in women seeking fertility. It has been
suggested that metformin may also help in reducing the high pregnancy
wastage which is characteristic of PCOS.12 However, there is less
consensus about its long-term use. While metformin is increasingly
being used as an adjunct for weight loss13 and to prevent the
development of diabetes in high-risk individuals, there are no data
at present to support this preventive strategy. There is also
uncertainty about how best to monitor patients who are taking
metformin. Norman et al have suggested measuring "clinically useful
endpoints".10 While this is a logical
approach, it is not known which measurements, if any, correlate with
the benefits of metformin treatment. Moreover, it is difficult to
assess insulin resistance in PCOS with simple, non-invasive
outpatient tests.
Unlike the thiazolidinediones, metformin is not a true
insulin-sensitising agent. However, metformin has been reported to
give similar results in terms of ovulatory function to those with the
thiazolidinedione troglitazone. This product has been withdrawn
from the US market because of hepatic toxicity. Other
thiazolidinediones (rosiglitazone and pioglitazone) may be useful
but do not facilitate weight loss. A more natural product,
D-chiro-inositol, which works as a second messenger for
insulin, is well tolerated and offers promise as a new medication for
potential long-term use.14
As noted above, there are hyperandrogenic women with polycystic
ovaries who have normal menstrual cycles. These women may also be
considered to have PCOS, although there is no clear consensus on this
issue. In general, such women have less severe insulin resistance,
and may be at reduced risk of developing the morbid sequelae of PCOS,
although there are no definitive data on this. There is currently a
dilemma about characterising completely asymptomatic women who
have polycystic ovarian morphology only. This ovarian finding may
occur in 16%-20% of the normal population. Recent data suggest that
some women exhibit subtle abnormalities (such as low high-density
cholesterol levels and mild insulin resistance),15 suggesting
that, while the risk is probably low, this phenotype may also require
close monitoring over time.
Although the cause of PCOS remains elusive, it can no longer be denied
that it is a metabolic syndrome with associated morbidities which are
reproductive, metabolic and cardiovascular in nature. Early
diagnosis and monitoring throughout life is imperative. While
low-dose oral contraceptives have a beneficial role earlier in life
and can prevent excess risk of ovarian and endometrial cancer,
screening for diabetes, dyslipidemia and cardiovascular disease
assumes importance by the fourth decade. Diet and exercise are of
paramount importance life-long, and medications to correct insulin
abnormalities are considered important adjuncts which may prove to
be a mainstay of management.
Rogerio A Lobo
Chairman
Department of Obstetrics and Gynecology Columbia University
College of Physicians and Surgeons and New York Presbyterian
Hospital, New York, NY, USA
- Lobo RA, Carmina E. The importance of diagnosing the polycystic
ovary syndrome. Ann Intern Med 2000; 132: 989-993.
-
Nestler JE. Polycystic ovary syndrome: a disorder for the
generalist. Fertil Steril 1998; 70: 811-812.
-
Franks S. Morphology of the polycystic ovary in polycystic ovary
syndrome. In: Dunaif A, Given JR, Haseltine FP, Merriam GR, editors.
Polycystic ovary syndrome. Boston: Blackwell; 1992: 19-28.
-
Carmina E, Lobo RA. Polycystic ovary syndrome (PCOS): arguably the
most common endocrinopathy is associated with significant
morbidity in women. J Clin Endocrinol Metab 1999; 84:
1897-1899.
-
Gammon MD, Thompson WD. Polycystic ovaries and the risk of breast
cancer. Am J Epidemiol 1991; 134: 818-824.
-
Legro RS, Kunselman AR, Dodson WC, et al. Prevalence and predictors
of risk for type 2 diabetes mellitus and impaired glucose tolerance in
polycystic ovary syndrome: a prospective, controlled study in 254
affected women. J Clin Endocrinol Metab 1999; 84: 165-169.
-
Wild S, Pierpoint T, McKeigue P, et al. Cardiovascular disease in
women with polycystic ovary syndrome at long-term follow-up: a
retrospective cohort study. Clin Endocrinol (Oxf) 2000; 52:
595-600.
-
Ehrmann DA, Sturis J, Byrne MM, Karrison T, et al. Insulin secretory
defects in polycystic ovary syndrome. Relationship to insulin
sensitivity and family history of non-insulin-dependent diabetes
mellitus. J Clin Invest 1995; 96: 520-527.
-
Murray RD, Davison RM, Russell RC, et al. Clinical presentation of
PCOS following development of an insulinoma: case report. Hum
Reprod 2000; 15: 86-88.
-
Norman RJ, Kidson WJ, Cuneo RC, Zacharin MR. Metformin and
intervention in polycystic ovary syndrome. Med J Aust 2001;
174: 580-583.
-
Norman R, Clark A. Obesity and reproductive disorders. Reprod
Fertil Develop 1998; 10: 55-63.
-
Glueck CJ, Phillips H, Cameron D, et al. Continuing metformin
throughout pregnancy in women with polycystic ovary syndrome
appears to safely reduce first-trimester spontaneous abortion: a
pilot study. Fertil Steril 2001; 75: 46-52.
-
Pasquali R, Gambineri A, Biscotti D, et al. Effect of long-term
treatment with metformin added to hypocaloric diet on body
composition, fat distribution, and androgen and insulin levels in
abdominally obese women with and without the polycystic ovary
syndrome. J Clin Endocrinol Metab 2000; 85: 2767-2774.
-
Nestler JE, Jakubowicz DJ, Reamer P, et al. Ovulatory and
metabolic effects of D-chiro-inositol in the polycystic
ovary syndrome. N Engl J Med 1999; 340: 1314-1320.
-
Chang PL, Lindheim SR, Lowre C, et al. Normal ovulatory women with
polycystic ovaries have hyperandrogenic pituitary-ovarian
responses to gonadotropin-releasing hormone-agonist testing.
J Clin Endocrinol Metab 2000; 85: 995-1000.
©MJA 2001
Make a
comment
Readers may print a single copy for personal use. No further
reproduction or distribution of the articles
should proceed without the permission of the publisher. For
permission, contact the
Australasian Medical Publishing Company.
Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>".
<URL: http://www.mja.com.au/>
© 2001 Medical Journal of Australia.
|