Cindy,
a 34 year old flight attendant had been taking birth control pills for
17 years because of PCOS (Polycystic Ovary Syndrome). The chief
complaint was acne and hirsutism from high testosterone levels, for
which the birth control pills had been prescribed. Cindy had married a
year ago, and was now ready to start a family, so she had discontinued
the birth control pills on her own a few months before arriving to my
office. Cindy had one normal menstrual period in the last four months
since stopping the BCP's. Cindy came for an office visit because she
wanted a treatment that would restore normal menstrual cycles,
fertility, as well eliminate the excess facial hair, acne and other
androgenic effects of elevated testosterone levels.
Laboratory workup showed absent progesterone production on Day 19 of her cycle indicating anovulation. Genetic testing for CYP21A was
negative for nonclassical congentital adrenal hyperplasia. Her DHEA
and testosterone levels were mildly elevated. Baseline 17
hydrocyprogesterone was normal. Treatment was started (see below).
Three months later Cindy called to report that she was pregnant.
Above left image: Many women with PCOS are frustrated by mainstream
medical treatment, and may feel like this photo of Janet Leigh from the
Alfred Hitchcock movie, Psycho, (c) copyright 1960 Paramount Pictures.
Treatment program for PCOS to induce ovulation:
1) Treatment was started with progesterone capsules 100 mg twice a day for days 12-26 of the cycle.
2) Metformin 500 mg tabs twice a day with meals.
3) Clomid 50 mg tabs for 5 days on days 3-7 of the cycle.
4) If the above is ineffective at inducing ovulation , Dexamethazone 2 mg per day for days 3-12 of the cycle.
How Does This Work ?
The
defining hallmark of PCOS is lack of ovulation, which in turn causes
progesterone deficiency. Progesterone for PCOS was pioneered by John R
Lee MD who wrote extensively about his experience treating PCOS with
cyclic progesterone. This is covered in Part One.
Cyclic progesterone is thought to reset the hypothalamic-pituitary axis
which controls ovulation, thus helping restart normal ovulation in the
PCOS patient when taken over a 3-6 months of use.
Progesteroneinhibits 5 alpha reductase
(the enzyme that converts testosterone to its stronger metabolite,
DHT), and thus my reduce hirsutism and serve as an anti-androgen. (1)
Spironolactone,
(Aldactone 50 mg BID) another commonly used drug used as a blood
pressure pill, diuretic pill, and also has anti-androgen effects, it
inhibits 5 alpha reductase conversion of testosterone to DHT, and is
commonly used to treat hirsutism in PCOS patients. (2)
Metformin
In obese women with the polycystic ovary syndrome, decreasing
serum insulin concentrations with metformin reduces ovarian cytochrome
P450c17 alpha activity and ameliorates hyperandrogenism.(3)(13)
Dexamethasone
Some cases of anovulation are the result of a genetic enzyme
deficiency in the adrenal gland with inadequate conversion of 17
hydroxyprogesterone into cortisol. This leads to overproduction of
androgenic hormones such as DHEA and Testosterone. This is the CYP 21A
genetic mutation, also called the 21 hydroxylase deficiency, also called
Non-Classical CAH (congential adrenal hyperplasia) .
This genetic
abnormality may be associated with anovulation and hirsutism in a
clinical presentation which may mimic PCOS. In this scenario,
Dexamethasone may be added to the Clomid. (Dexamethasone 2 mg per day for days 3-12 of the cycle.)
The Dexamethasone inhibits
ACTH production by the pituitary and prevents the adrenal from making
excess testosterone, and is in fact curative of the hirsutism and acne
symptoms, and in many cases restores ovulation and fertility.(6-11)(14-20)
Dexamethasone for Hirsutism and Acne- Relief of Androgenic Symptoms
Some
authors report success with low dose Dexamethasone (0.25 mg tab PO Qhs)
given every night before sleep. This was originally described in an article by Maria New MD in treatment of hirsutism and acne in NON-Classical CAH (congential adrenal hyperplasia) (Maria New MD,
JCEM Nov 1, 2006
vol. 91
no. 11
4205-4214)
(6-11)(14-20)(21)
Above Left Image: Before and After. Acne Resolves after 3 months of Dexamethasone (0.25 mg Qhs) courtesy of Maria New, JCEM Nov 2006 (21)
Clomid to Induce Ovulation
Clomiphene
is the first drug of choice to induce ovulation in the PCOS patient.
Clomid blocks the estrogen receptors in the hypothalamus, causing an LH,
FSH surge, which induces ovulation. Clomid is usually given over 5
days during the luteal phase of the cycle, for days 3-7 or 4-8 at a
dose starting at 50 mg per day. This may be increased by 100 mg if the
lower dosage is unsuccessful and fails to induce ovulation. (4,5)
(12,13)
OCP's, Birth Control Pills and other Synthetic Hormones
OCPs
are commonly prescribed to the PCOS patient to mask the androgenic
symptoms of acne and hirsutism. This form of therapy is ill advised and
misplaced, since it does not address the underlying problem of lack of
ovulation with disordered hormone production. In other words, OCPs are
symptomatic treatment which does not address the root cause of the
problem, which is anovulation with imbalance in ovarian and adrenal
hormone regulation. OCP's further suppress and prevent ovulation,
rather than restore this normal physiological function in the female.
Obstet Gynecol. 1991 Jul;78(1):103-7.
Effects of sex steroids on skin 5 alpha-reductase activity in vitro.
Cassidenti DL, Paulson RJ, Serafini P, Stanczyk FZ, Lobo RA.
Department of Obstetrics and Gynecology, University of Southern California School of Medicine, Los Angeles.
Skin 5 alpha-reductase activity is the major factor influencing the manifestation of androgen excess. Although oral contraceptives
have been useful for the treatment of androgen excess, little is known
of the independent effects of the various progestins and estrogens on
inhibition of skin 5 alpha-reductase activity. We incubated minces of
normal genital and pubic skin with physiologic concentrations of
3H-testosterone to assess 5 alpha-reductase activity by its conversion
to 3H-dihydrotestosterone.
In separate experiments, 5 alpha-reductase activity was assessed before and after the addition of progesterone, medroxyprogesterone acetate, levonorgestrel, norethindrone, 17 beta-estradiol, and ethinyl estradiol.
Progesterone, levonorgestrel, and norethindrone demonstrated 97 +/- 5.3%, 47.9 +/- 6.3%, and 59 +/- 4.6% inhibition, respectively, of genital skin 5 alpha-reductase activity at 10(-4) mol/L (P less than .01).
Medroxyprogesterone acetate, however, failed to affect 5 alpha-reductase activity at similar doses.
Estradiol
exhibited 40.8 +/- 14.2% inhibition at 10(-4) mol/L (P less than .01),
whereas ethinyl estradiol at concentrations from 10(-8) to 10(-4) mol/L
failed to inhibit 5 alpha-reductase activity.
We conclude that progesterone
and the 19-nor-derivatives inhibit 5 alpha-reductase activity at high
doses, whereas medroxyprogesterone acetate does not. Therefore, the
19-nor-progestin component may expand the usefulness of oral
contraceptives in the treatment of hirsutism by an inhibitory action on
skin 5 alpha-reductase activity.
Spironolactone for Hirsutism
2) http://www.ncbi.nlm.nih.gov/pubmed/12749435
Fertil Steril. 2003 Apr;79(4):942-6. Use of cyproterone acetate, finasteride, and spironolactone to treat idiopathic hirsutism. Lumachi F, Rondinone R.
Department of Surgical and Gastroenterological Sciences, University of Padua, School of Medicine, Padova, Italy.
To compare the effectiveness of cyproterone acetate, finasteride, and spironolactone in the treatment of idiopathic hirsutism.
DESIGN: Prospective randomized clinical study.
SETTING:University hospital.
PATIENT(S): Forty-one women (median age, 21 years [range, 18-34 years]) with idiopathic hirsutism who had requested to use an oral contraceptive.
INTERVENTION(S):
Patients were randomly assigned to receive cyproterone acetate (12.5
mg/d for the first 10 days of the cycle), finasteride (5 mg/d), or spironolactone (100 mg/d) for 12 months. Follow-up was done at the end of therapy.
MAIN
OUTCOME MEASURE(S): Ferriman-Gallwey score before treatment, at 6 and
12 months of treatment, and 1 year after the end of treatment, and
androgenic profile before and after treatment.
RESULT(S): At the end
of therapy, the Ferriman-Gallwey score decreased by 38.9%, 38.6%, and
38.5% in patients who used cyproterone acetate, finasteride, and
spironolactone, respectively. One year after therapy, the
Ferriman-Gallwey score of patients who used spironolactone was
significantly lower (6.74 +/- 1.41) than that of patients who used
either cyproterone acetate (7.92 +/- 1.08), or finasteride (9.08 +/-
0.99). The androgenic profile did not change significantly during
treatment.
CONCLUSION(S):
In patients with idiopathic
hirsutism, the short-term results of treatment with cyproterone acetate,
finasteride, and spironolactone are similar, but spironolactone is
effective for a longer time.
Metformin Decreases Insulin, and decreases Testosterone
N Engl J Med. 1996 Aug 29;335(9):617-23.
Decreases in ovarian cytochrome P450c17
alpha activity and serum free testosterone after reduction of insulin
secretion in polycystic ovary syndrome. (using Metformin) Nestler JE,
Jakubowicz DJ. Department of Internal Medicine, Medical College of
Virginia, Virginia Commonwealth University, Richmond, VA 23298-0111,
Insulin resistance and increased ovarian cytochrome P450c17 alpha activity are both features of the polycystic ovary syndrome.
P450c17 alpha, which is involved in androgen biosynthesis, has both 17
alpha-hydroxylase and 17,20-lyase activities. Increased activity of this
enzyme results in exaggerated conversion of progesterone to 17
alpha-hydroxyprogesterone in response to stimulation by gonadotrophin.
We hypothesized that hyperinsulinemia stimulates ovarian P450c17 alpha
activity.
METHODS: We measured fasting serum steroid
concentrations and the response of serum 17 alpha-hydroxyprogesterone to
leuprolide, a gonadotrophin-releasing hormone agonist, and performed
oral glucose-tolerance tests before and after oral administration of
either metformin (500 mg three times daily) or placebo for four to eight weeks in 24 obese women with the polycystic ovary syndrome.
RESULTS: In the 11 women given metformin, the
mean (+/- SE) area under the serum insulin curve after oral glucose
administration decreased from 9303 +/- 1603 to 4982 +/- 911 microU per
milliliter per minute (56 +/- 10 to 30 +/- 6 nmol per liter per minute)
(P = 0.004).
This decrease was associated with a reduction in the basal serum 17 alpha-hydroxyprogesterone concentration from 135 +/- 21 to 66 +/-
7 ng per deciliter (4.1 +/- 0.6 to 2.0 +/- 0.2 nmol per liter) (P =
0.01) and a reduction in the leuprolide-stimulated peak serum 17
alpha-hydroxyprogesterone concentration from 455 +/- 54 to 281 +/- 52 ng
per deciliter (13.7 +/- 1.6 to 8.5 +/- 1.6 nmol per liter) (P = 0.01).
The serum 17 alpha-hydroxyprogesterone values increased slightly in the
placebo group.
In the metformin group, the basal serum luteinizing
hormone concentration decreased from 8.5 +/- 2.2 to 2.8 +/- 0.5 mlU per
milliliter (P = 0.01), the serum free testosterone concentration
decreased from 0.34 +/- 0.07 to 0.19 +/- 0.05 ng per deciliter (12
+/- 3 to 7 +/- 2 pmol per liter) (P = 0.009), and the serum sex
hormone-binding globulin concentration increased from 0.8 +/- 0.2 to 2.3
+/- 0.6 microgram per deciliter (29 +/- 7 to 80 +/- 21 nmol per liter)
(P < 0.001). None of these values changed significantly in the
placebo group.
CONCLUSIONS: In obese women with the polycystic ovary syndrome, decreasing
serum insulin concentrations with metformin reduces ovarian cytochrome
P450c17 alpha activity and ameliorates hyperandrogenism.
the
administration of metformin reduced the serum insulin concentration
during fasting and the insulin response to oral glucose administration.
Concomitantly,
ovarian cytochrome P450c17a activity decreased, as demonstrated by a
substantial reduction in the response of serum 17a-hydroxyprogesterone
to
the administration of leuprolide (to increase luteinizing hormone
secretion). The reduction in P450c17a activity was accompanied by a
decline in the serum free testosterone concentration.
Establishing "Day One" of the Menstrual Period
•Day one is counted as the first day of menstrual bleeding
•The period can be from a spontaneous menstrual period or from a
period induced with a progestin medication such as Provera
(medroxyprogesterone acetate)
Inducing a Period (if needed)
•In order to induce a period, Provera is given for 5 to 10 days at a dose of 5 or 10mg daily
•The period usually starts within 2-7 days after the last Provera pill is taken
Starting Clomid
•Clomid is started early in the menstrual cycle and is taken for five days either from cycle days 3 through 7, or from day 5 through 9
•Clomid is usually started at a dose of one tablet (50mg) daily - taken any time of day
Increasing Clomid Dosage (if needed)
•If the patient does not ovulate on the starting dose, Provera is
often given to induce a period - then a 100mg dose of Clomid is tried
•That means that a woman taking Clomid on days 5-9 will often ovulate on about day 16-20 of the cycle
•However, there is significant variation in how long it takes
ovulate using Clomid. Some will ovulate much later - as late as two or
three weeks after the
last clomiphene tablet.
--------------------------------------------------------------------------------
How long should I try Clomid before moving on to other treatment options?
There is no set number of cycles of Clomid that should be
done before moving on to other fertility treatments. Several variables
are involved in the decision
about moving on to more aggressive therapy.
No Ovulation Results After increasing Clomid Dosage
•If a woman is not ovulating on a low dose of Clomid, the dose should be increased
•If not ovulating at 150 mg then other therapies should be attempted
Female age and Clomid treatment and when to be more aggressive
•Relatively fewer cycles should be done with an older female partner
•Clomid probably should not be used at all if the female age is 40
or older because of the significantly reduced fertility potential
•Women 38 or older should probably start fertility treatment with a fertility specialist - rather than with their gynecologist
•If the female is under 38 years old and the sperm is good then
usually 3-6 months of Clomid cycles (with good ovulation) are often
tried
Clomid and Metformin for PCOS
Glucophage Plus Clomiphene for Fertility Treatment and Pregnancy with Polycystic Ovarian Syndrome
Page author Richard Sherbahn MD
Metformin and Clomid Use with PCOS
•Women who do not ovulate often have polycystic ovarian
syndrome, or PCOS
•Clomid, also called Serophene, or clomiphene citrate is the most
commonly used medication to try to induce ovulation in women that do not
ovulate on their
own
•Metformin (Glucophage) is an oral medication that is mainly used to
treat diabetes
•However, it can also be used with PCOS to help women ovulate and
achieve pregnancy.
•Some women with PCOS that do not ovulate when treated with
Clomid or metformin alone could ovulate and have success when glucophage
and Clomid are used
together
Metformin alone for PCOS
A relatively small percentage of women that do not ovulate
regularly and have polycystic ovarian disease will ovulate regularly and
become pregnant from
treatment with metformin alone.
For those women that are taking metformin for PCOS and are not achieving
pregnancy, a reasonable option is to add Clomid to the metformin
treatment
An Alternative to Injectable FSH Medications, or IVF
Using clomiphene and metformin together can be beneficial for
the women with polycystic ovarian syndrome. If they can ovulate and get
pregnant with this
medication combination, they can avoid the more expensive and invasive
treatments such as using injectable FSH medications or in vitro
fertilization for
PCOS.
Side Effects of Glucophage / Metformin and Clomid for PCOS
About one fourth of women taking metformin have gastrointestinal side effects such as abdominal discomfort, diarrhea and nausea. We do not know of any
serious complications from metformin treatment of PCOS.
•Details about side effects of Clomid
Treatment Protocol for for Taking Metformin and Clomid to Induce Ovulation
The benefit of metformin on ovulation in women with polycystic
ovaries is not seen right away. There is some benefit starting about a
month after beginning
metformin.
•Metformin has a more substantial benefit for fertility when the woman has been taking it for at least 60 to 90 days.
Metformin Dosing
Metformin is taken in a dose that the woman can tolerate. Most people can tolerate 500 mg three times daily, if they build up to that dose gradually.
•We usually start metformin at 500 mg once daily, then increase
to 500 mg twice a day after one week, then to 500 mg three times daily
after another week.
•If the three times daily dose cannot be tolerated due to side effects, we remain on the twice-daily dose.
Clomid Dosing
•Clomiphene is usually started at a dose of one tablet (50 mg) daily for five days
•It is started early in the menstrual cycle, usually either days 3 - 7 or days 5 - 9
•Women that have very irregular cycles usually need to have a period induced with a progestin medication such as Provera
•If 50 mg of clomiphene per day does not result in ovulation, we increase the dose in the next cycle to 100 mg per day
•If there is not ovulation at 100 mg, we either try 150 mg per
day - or we give up on Clomid and move on to other fertility treatments
-------------------------------------------------------------------------
Clomid for PCOS
Metformin
Dexamethazone
Induction of Ovulation
Hum Reprod. 2006 Jul;21(7):1805-8. Epub 2006 Mar 16.
Clomiphene citrate and dexamethazone in treatment of clomiphene citrate-resistant polycystic ovary syndrome: a prospective placebo-controlled study.
Elnashar A, Abdelmageed E, Fayed M, Sharaf M.
Department of Obstetrics and Gynecology, Benha University Hospital, Benha, Egypt.
The aim of this work was to evaluate the efficacy of adding
dexamethazone (DEX) (high dose, short course) to clomiphene citrate (CC)
in CC-resistant
polycystic ovary syndrome (PCOS) with normal dehydroepiandrosterone
sulphate (DHEAS) in induction of ovulation.
METHODS: Eighty infertile women with CC-resistant PCOS were randomly assigned into two groups.
Group I:
Clomiphene citrate100 mg/day was given from day 3 to day 7 of the cycle and
DEX 2 mg/day from day 3 to day 12 of the cycle.
Group II: Same protocol of CC combined with placebo (folic acid tablets) was given from day 3 to day 12 of the cycle.
The main outcome was ovulation.
Secondary measures included number of follicles >18 mm endometrial
thickness and pregnancy rate. Ovarian follicular response was monitored
by transvaginal
ultrasound. HCG 10,000 U was given when at least one follicle measured
18 mm, and timed intercourse was advised.
RESULTS: There were no statistically significant differences between
groups as regards age, duration of infertility, BMI, waist-hip ratio
(WHR), menstrual
pattern, hirsutism, serum DHEAS or day of HCG administration.
The mean number of follicles>18 mm at the time of HCG administration and the mean endometrial
thickness were significantly higher in the DEX group than in the placebo group (P<0.05).
Similarly, there were significantly higher rates of ovulation (75
versus 15%) (P<0.001) and pregnancy (40 versus 5%) (P<0.05) in the DEX group.
Dexamethazone was very well tolerated as no patients complained of any
side
effect. There was a significant difference between the responders and
non-responders in the presence of oligomenorrhea, amenorrhea or
hirsutism.
CONCLUSION: Induction of ovulation by adding DEX (high dose, short
course) to CC in CC-resistant PCOS with normal DHEAS is associated with
no adverse anti-
estrogenic effect on the endometrium and higher ovulation and pregnancy
rates in a significant number of patients. Induction with DEX appears to
be
independent on age, period of infertility, BMI or WHR.
Use of dexamethasone and clomiphene citrate in the treatment of clomiphene citrate-resistant patients with polycystic ovary syndrome and normal
dehydroepiandrosterone sulfate levels: a prospective, double-blind, placebo-controlled trial.
Parsanezhad ME, Alborzi S, Motazedian S, Omrani G.
Source
Division of Infertility, Department of Obstetrics and Gynecology, School
of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
To evaluate the effects of short-course administration of dexamethasone
(DEX) combined with clomiphene citrate (CC) in CC-resistant patients
with polycystic
ovary syndrome (PCOS) and normal DHEAS levels.
DESIGN:
Prospective, double-blind, placebo-controlled, randomized study.
SETTING:
Referral university hospitals.
PATIENT(S):
Two hundred thirty women with PCOS and normal DHEAS who failed to ovulate after a routine protocol of CC.
INTERVENTION(S):
The treatment group received 200 mg of CC from day 5 to day 9 and 2 mg of DEX from day 5 to day 14 of the menstrual cycle. The control group received the
same protocol of CC combined with placebo.
MAIN OUTCOME MEASURE(S):
Follicular development, hormonal status, ovulation rate, pregnancy rate.
RESULT(S):
Mean follicular diameters were 18.4124 +/- 2.4314 mm and 13.8585 +/-
2.0722 mm for the treatment and control groups, respectively.
Eighty-eight percent of
the treatment group and 20% of the control group had evidence of
ovulation. The difference in the cumulative pregnancy rate in the
treatment and control
groups was statistically significant.
CONCLUSION(S):
Hormonal levels, follicular development, and cumulative pregnancy rates
improved with the addition of DEX to CC in CC-resistant patients with
PCOS and normal
DHEAS. This regimen is recommended before any gonadotropin therapy or
surgical intervention.
Clomiphene-dexamethasone treatment of clomiphene-resistant women with and without the polycystic ovary syndrome.
Singh KB, Dunnihoo DR, Mahajan DK, Bairnsfather LE.
Department of Obstetrics and Gynecology, Louisiana State University School of Medicine, Shreveport 71130.
We used clomiphene and dexamethasone in 40 infertile women to treat chronic anovulation resistant to the use of clomiphene alone. Eighteen (45%) of the women
had the polycystic ovary (PCOS) syndrome; the remaining 22 (55%)
had clomiphene-resistant anovulation from idiopathic causes. Both groups
of women were
similar in regard to age, parity, duration of infertility and absence of
other causes of infertility besides chronic anovulation.
Ovulation could be induced
in approximately 90% of the women in each group. Altogether, 19 of 36 women (52.8%) conceived without any side effects or complications. The cumulative
probability of conception at nine months of treatment was 87.5% in PCOS patients and 46% in the non-PCOS group.
Clomiphene plus dexamethasone was highly
effective in the treatment of clomiphene-resistant anovulation associated with infertility in women with and without the PCO syndrome.
Zentralbl Gynakol. 1980;102(12):645-50.
[Combined clomiphene-dexamethasone therapy in cases with resistance to clomiphene (author's transl)].
[Article in German]
Lisse K.
Abstract
Combined clomiphene-dexamethasone treatment was applied to 13 patients with clomiphene-resistant anovulation which had been caused by androgenic
hyperactivity of ovarian or adrenal origin.
The women, following induced withdrawal bleeding,
received
200 mg/die clomiphene over five days,
from the fifth through the ninth days of their cycles,
plus 2 mg/die dexamethasone over ten days,
from the fifth to 14th days of cycle, after they had failed to conceive in response to clomiphene alone administered in rising doses up to 200 mg/die.
Nine
pregnancies
were successfully induced by that treatment. Two of them ended in
abortion and one in premature twin delivery. Combined
clomiphene-dexamethasone
treatment is recommended for clomiphene-resistant cases with ovarian or
adrenal hyperandrogenism, particularly for patients with polycystic
ovaries (Stein-
Leventhal syndrome).
--------------------------------------
1982
11) www.ncbi.nlm.nih.gov/pubmed/6214735
Obstet Gynecol. 1982 Oct;60(4):497-501.
Clomiphene and dexamethasone in women unresponsive to clomiphene alone.
Lobo RA, Paul W, March CM, Granger L, Kletzky OA.
Twelve oligomenorrhic women with polycystic ovary syndrome (PCO)
in whom
clomiphene (250 mg daily for 5 days) and 10,000 IU human chorionic
gonadotropin had failed to induce ovulation were treated with clomiphene and
dexamethasone. Eight of the 12 women underwent complete hormonal
assessment during treatment. Six of the 12 ovulated and 1 conceived.
Serum total and unbound
estradiol and testosterone (T), serum dehydroepiandrosterone sulfate
(DHEA-S), sex hormone binding-globulin binding capacity (SHBG-BC),
luteinizing hormone
(LH), follicle-stimulating hormone (FSH) and prolactin (PRL) were
measured during clomiphene and dexamethasone therapy. SHBG-BC increased
in response to
clomiphene whether or not ovulation occurred. After treatment with
clomiphene and dexamethasone there was a significant decrease in serum
T, unbound T, and
DHEA-S 2 weeks after dexamethasone administration, but there were no
change in LH, FSH, or PRL. In patients who ovulated after clomiphene and
dexamethasone,
T and unbound T increased again after clomiphene was begun despite the
continuation of dexamethasone. The women who ovulated after clomiphene
and
dexamethasone treatment had significantly higher pretreatment levels of
DHEA-S than those who did not ovulate. Clomiphene and dexamethasone
treatment may be
beneficial to women who have elevated levels of DHEAS and who fail to
ovulate with maximum doses of clomiphene.
[Treatment of anovulation in polycystic ovary syndrome with clomiphene citrate in 10-day cycles].
[Article in Spanish]
Porcile A, Venegas E, Gallardo E.
Abstract
The efficacy of a new schedule for the use of Clomiphene citrate (50 mg daily, during the first ten days of the cycle) is reported, in relation to ovulation
induction and fertility. We treated 41 patients with the syndrome of polycystic ovary, who were anovulant and desired fertility. Ovulation was successfully
induced in 35 of them (85.4%). Pregnancy was achieved in 28 patients (68.3%).
In
87.5% of those becoming pregnant, gestations was achieved with less
than 6
months of treatment. Our results are equally good or better than those
reported in the literature with conventional treatment. Pregnancies
obtained were
normal. No congenital malformations were observed. There were only two
abortions, spontaneous. No patient presented ovarian hyperstimulation
syndrome. This
new schedule is recommended because it is effective and it may give less
complications. Also, it is not necessary to increase progressively the
dose of
clomiphene citrate.
Fertil Steril. 2009 Feb;91(2):514-21. Epub 2008 Mar 5.
Comparison of clomiphene citrate, metformin, or the combination of both for first-line ovulation induction, achievement of pregnancy, and live birth in Asian
women with polycystic ovary syndrome: a randomized controlled trial.
Zain MM, Jamaluddin R, Ibrahim A, Norman RJ.
Source
Department of Obstetric and Gynaecology, Alor Setar Hospital, Kedah, Malaysia.
To
determine the first-line medication to be used in anovulatory patients
with polycystic ovary syndrome (PCOS) for ovulation induction and
pregnancy
achievement.
DESIGN:
Randomized controlled trial.
SETTING:
Infertility unit of a public hospital.
PATIENT(S):
One hundred fifteen newly diagnosed patients with PCOS based on ESHRE/ASRM criteria.
INTERVENTION(S):
These patients were assigned to three groups: group 1 (38 patients)
received 500 mg of metformin three times a day; group 2 (39 patients)
received clomiphene
citrate (CC) at an incremental dose; group 3 (38 patients) received both
medications.
MAIN OUTCOME MEASURE(S):
Rates of ovulation, pregnancy (PR), and live birth.
RESULT(S):
The ovulation rate was 23.7% in the metformin group,59% in the CC group, and 68.4% in the combination treatment group. This was translated into a similar PR
and live birth rate, which were higher in the CC and combination groups compared to the metformin group (PR: 7.9%, 15.4%, and 21.1%; live birth rate: 7.9%,
15.4%, and 18.4% in metformin, CC, and combination treatment groups,
respectively), although statistically the differences were not
significant. There were
no multiple pregnancies and the rate of spontaneous first trimester loss
was similar to the general population.
CONCLUSION(S):
Clomiphene citrate should be the first-line treatment for ovulation induction in anovulatory patients with PCOS.
------------------------------------------------------------------------------
Textbook on Androgen Excess Disorders in Women free online
Dexamethasone Reduces Androgen Levels in PCOS patients
2004 NORWAY
14) http://humrep.oxfordjournals.org/content/19/3/529.full
http://humrep.oxfordjournals.org/content/19/3/529.full.pdf
Hum. Reprod.
(2004)
19
(3):
529-533.
Six‐ month
treatment with low‐dose dexamethasone further reduces androgen levels in
PCOS women treated with diet and lifestyle advice, and metformin
E.
Vanky1,3,K.Å. Salvesen1 and S.M. Carlsen2 1Department of Obstetrics
and Gynecology and 2Section of Endocrinology, Department of Medicine, St
Olavs Hospital, University Hospital of Trondheim, Trondheim, Norway.
BACKGROUND:
The purpose of this study was to investigate the effect of low‐dose
dexamethasone on androgen levels in women with polycystic ovary syndrome
(PCOS) treated with diet and lifestyle counselling, and metformin.
METHODS:
A prospective, randomized, double blind, placebo‐controlled study was
carried out. Thirty‐eight women with PCOS were randomized to either
dexamethasone 0.25 mg daily or placebo for 26 weeks. All received diet
and lifestyle counselling at inclusion and metformin 850 mg three times
daily during the whole study. Main outcome measures were: androgen
levels, body mass index (BMI), insulin c‐peptide, fasting glucose and
serum lipids. Two‐tailed t‐tests and Pearson’s statistics were used.
RESULTS: Compared with the placebo, dexamethasone reduced testosterone
by 27%, androstenedione by 21%, dehydroepiandrosterone sulphate by 46%
and free testosterone index by 50% in women with PCOS treated with diet
and lifestyle advice, and metformin. BMI, fasting glucose, insulin
c‐peptide and serum lipid levels were unaffected.
CONCLUSIONS: Six‐month, low‐dose dexamethasone treatment further reduces androgen levels in metformin‐trated PCOS women. 2003 MAYO CLINIC ROCHESTER MINN
15) http://www.jfponline.com/pages.asp?aid=3059
February 2003 · Vol. 15, No. 2 EXAMINING THE EVIDENCE
Dexamethasone-clomiphene citrate (CC) treatment in CC-resistant PCOS patients
DANIEL
DUMESIC, MD CONSULTANT, REPRODUCTIVE ENDOCRINOLOGY AND INFERTILITY MAYO
CLINIC . ROCHESTER, MINN The question: Does dexamethasone-clomiphene
citrate (CC) treatment improve ovulation rates in CC-resistant patients
with polycystic ovary syndrome?
Two hundred thirty infertile PCOS
patients who failed to ovulate during CC therapy (250 mg/day orally for
5 days) and human chorionic gonadotropin (hCG) administration (10,000
units, intramuscularly) were randomized to CC (200 mg/day, cycle days
5-9) with or without DEX (2 mg/day, cycle days 5-14).
2011 EGYPT Review Article
16) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039006/
Int J Womens Health. 2011; 3: 25–35.
Published online 2011 February 8. doi: 10.2147/IJWH.S11304
PMCID: PMC3039006
Treatment options for polycystic ovary syndrome
Ahmed Badawy1 and Abubaker Elnashar2
1Department of Obstetrics and Gynecology, Mansoura University, Mansoura, Egypt;
2Department of Obstetrics and Gynecology, Benha University, Benha, Egypt
Glucocorticoids
such as prednisone and dexamethasone have been used to induce
ovulation. Elnashar et al demonstrated that induction of ovulation by
adding dexamethasone (high dose, short course) to CC in CC-resistant
PCOS with normal DHEAS is associated with no adverse antiestrogenic
effect on the endometrium and higher ovulation and pregnancy rates in a
significant number of patients.34
In PCOS patients with high adrenal androgen, low-dose dexamethasone (0.25–0.5 mg) at bedtime can be used.35
In a study of 230 women with PCOS who failed to ovulate with 200 mg of CC for 5 days, addition of 2 mg of dexamethasone from days 5–14
is associated with a higher ovulation rate and cumulative pregnancy
rate.36 Enthusiasm for their use is dampened, however, by their
potential adverse effects on insulin sensitivity; therefore, prolonged
use should be discouraged.
2006 EGYPT
17) humrep.oxfordjournals.org/content/21/7/1805.long
,,,
http://www.ncbi.nlm.nih.gov/pubmed/16543255
Hum Reprod. 2006 Jul;21(7):1805-8. Epub 2006 Mar 16.
Clomiphene citrate and dexamethazone in treatment of clomiphene citrate-resistant polycystic ovary syndrome: a prospective placebo-controlled study.
Elnashar A, Abdelmageed E, Fayed M, Sharaf M.
SourceDepartment of Obstetrics and Gynecology, Benha University Hospital, Benha, Egypt.
BACKGROUND:The
aim of this work was to evaluate the efficacy of adding dexamethazone
(DEX) (high dose, short course) to clomiphene citrate (CC) in
CC-resistant polycystic ovary syndrome (PCOS) with normal
dehydroepiandrosterone sulphate (DHEAS) in induction of ovulation.
METHODS:Eighty
infertile women with CC-resistant PCOS were randomly assigned into two
groups. Group I: Clomiphene citrate 100 mg/day was given from day 3 to
day 7 of the cycle and DEX 2 mg/day from day 3 to day 12 of the cycle.
Group II: Same protocol of CC combined with placebo (folic acid tablets)
was given from day 3 to day 12 of the cycle. The main outcome was
ovulation. Secondary measures included number of follicles >18 mm
endometrial thickness and pregnancy rate. Ovarian follicular response
was monitored by transvaginal ultrasound. HCG 10,000 U was given when at
least one follicle measured 18 mm, and timed intercourse was advised.
RESULTS:there
were no statistically significant differences between groups as regards
age, duration of infertility, BMI, waist-hip ratio (WHR), menstrual
pattern, hirsutism, serum DHEAS or day of HCG administration. The mean
number of follicles>18 mm at the time of HCG administration and the
mean endometrial thickness were significantly higher in the DEX group
than in the placebo group (P<0.05). Similarly, there were
significantly higher rates of ovulation (75 versus 15%) (P<0.001) and
pregnancy (40 versus 5%) (P<0.05) in the DEX group. Dexamethazone
was very well tolerated as no patients complained of any side effect.
There was a significant difference between the responders and
non-responders in the presence of oligomenorrhea, amenorrhea or
hirsutism.
CONCLUSION:Induction of ovulation by adding DEX
(high dose, short course) to CC in CC-resistant PCOS with normal DHEAS
is associated with no adverse anti-estrogenic effect on the endometrium
and higher ovulation and pregnancy rates in a significant number of
patients. Induction with DEX appears to be independent on age, period of
infertility, BMI or WHR.
http://www.ncbi.nlm.nih.gov/pubmed/12788885
J Clin Endocrinol Metab. 2003 Jun;88(6):2760-6.
Beyond
adrenal and ovarian androgen generation: Increased peripheral 5
alpha-reductase activity in women with polycystic ovary syndrome.
Fassnacht M, Schlenz N, Schneider SB, Wudy SA, Allolio B, Arlt W.
Source Department of Medicine, Endocrine and Diabetes Unit, University of Würzburg, 97080 Würzburg, Germany.
Abstract
Hyperandrogenism, a main clinical feature of polycystic ovary syndrome
(PCOS), is thought to result from enhanced ovarian and adrenal androgen
generation. To investigate the contribution of peripheral
steroidogenesis, we used an oral challenge with dehydroepiandrosterone
(DHEA) and analyzed its downstream conversion toward androgens in eight
women with PCOS (age, 20-32 yr; body mass index, 20-41 kg/m(2)) and
eight healthy women matched for age and body mass index. They underwent
frequent serum sampling and urine collection for 8 h on three occasions:
at baseline, and after 4 d of dexamethasone (Dex; 4 x 0.5 mg/d),
followed by ingestion of 100 mg DHEA or placebo. Dex induced similar
significant suppression of circulating steroids in both groups. The oral
DHEA challenge led to similar significant increases in the area under
the concentration-time curve (0-8 h after Dex) of serum DHEA, DHEA
sulfate, androstenedione, and testosterone. However, after oral DHEA,
PCOS women had significantly higher increases in serum 5
alpha-dihydrotestosterone (P < 0.01), its main metabolite
androstanediol glucuronide (P < 0.05), and the 5 alpha-reduced
urinary androgen metabolite androsterone (P < 0.05). PCOS women also
had significantly higher baseline excretion of 5 alpha-reduced
glucocorticoid (P < 0.01) and mineralocorticoid metabolites (P <
0.05). Taken together, these data indicate enhanced peripheral 5
alpha-reductase activity in PCOS. Thus, not only ovary and adrenal, but
also liver and peripheral target tissues, significantly contribute to
steroid alterations in PCOS.
The
Value of the Low-Dose Dexamethasone Suppression Test in the
Differential Diagnosis of Hyperandrogenism in Women Gregory A.
Kaltsas, Andrea M. Isidori, Blerina P. Kola, Rob H. Skelly,
Shern L. Chew, Paul J. Jenkins, John P. Monson, Ashley B.
Grossman and G. Michael Besser Department of Endocrinology, St.
Bartholomew’s Hospital, London ECIA 7BE, United Kingdom
Therapeutic
effects of metformin, rosiglitazone, and dexamethasone in reproductive
women with PCOS Hajder M.1, Hajder E.2, Kudumovic A.3 1 University
Clinical Center Tuzla, Internal clinic, department of Endocrinology,
Bosnia and Herzegovina,
2 University Clinical Center Tuzla,
Gynecology and Obstetrics clinic, Bosnia and Herzegovina, 3 Medical
Faculty of the University of Sarajevo, Bosnia and Herzegovina
The Journal of Clinical Endocrinology & Metabolism November 1, 2006 vol. 91 no. 11 4205-4214
Nonclassical
21-Hydroxylase Deficiency Maria I. New Department of Pediatrics,
Mount Sinai School of Medicine, New York, New York 10029
Context:
Nonclassical congenital adrenal hyperplasia (CAH) owing to steroid
21-hydroxylase deficiency (NC21OHD) is the most frequent of all
autosomal recessive genetic diseases, occurring in one in 100 persons in
the heterogeneous New York City population. NC21OHD occurs with
increased frequency in certain ethnic groups, such as Ashkenazi Jews, in
whom one in 27 express the disease. NC21OHD is underdiagnosed in both
male and female patients with hyperandrogenic symptoms because hormonal
abnormalities in NC21OHD are only mild to moderate, not severe as in the
classical form of CAH. Unlike classical CAH, NC21OHD is not associated
with ambiguous genitalia of the newborn female.
Main Outcome
Measures: The hyperandrogenic symptoms include advanced bone age, early
pubic hair, precocious puberty, tall stature, and early arrest of growth
in children; infertility, cystic acne, and short stature in both adult
males and females; hirsutism, frontal balding, polycystic ovaries, and
irregular menstrual periods in females; and testicular adrenal rest
tissue in males.
Conclusions: The signs and symptoms of hyperandrogenism are reversed with dexamethasone treatment.
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