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Complementary
and Alternative Medicine Series
Premenstrual Syndrome, Part 2
Tori Hudson, ND
As mentioned in part 1,1 80% of women experience premenstrual
emotional or physical changes, whereas only about 20% to 40% of
these women have difficulties as a result. A much smaller number,
about 2.5% to 5%,2 feel it has a significantly negative
impact on their lives, to the point where work, relationships, and
home life are jeopardized. Nutrition, exercise, and nutritional
supplementation are natural approaches in the management and treatment
of premenstrual syndrome (PMS). What follows is a guide to the botanicals
and natural hormones that have been investigated that also help
symptoms of PMS.
BOTANICALS
Chaste Tree (Vitex agnus castus)
Chaste tree berry has been seen by many alternative practitioners
as one of the most important herbs to treat PMS. The effect of chaste
tree is on the hypothalamus-hypophysis axis. It increases secretion
of luteinizing hormone and also has an effect that favors progesterone.
Two surveys were done covering 1,542 women with PMS who had been
treated with a German liquid extract of chaste tree for periods
of up to 16 years.3 The average dose was 42 drops daily.
Effectiveness as recorded by the patients' doctors was either
very good, good, or satisfactory in 92% of the cases. Comparable
dosing in standardized capsules are one capsule at 175 mg if standardized
to 0.75% agnuside, or one capsule at 215 mg if standardized to 0.6%
aucubin. No certain comparable dose of straight chaste tree tincture
is known, but most practitioners would use 1 to 2 teaspoons daily.
The newest study was a clinical trial on 170 women with PMS,4
the most well-designed trial yet studying the efficacy of chaste
tree in women's health. Women were assigned to take either a tablet
containing an extract of chaste tree berry (20 mg) or a placebo
tablet once daily for 3 months. Subjective reporting of irritability,
mood changes, anger, headache, breast tenderness, and bloating were
recorded. At the end of the 3 months, women taking chaste tree reported
a 52% reduction in PMS symptoms versus 24% reduction for those in
the placebo group. Women in the chaste tree group reported their
significant reduction in all symptoms except for bloating before
the menses. This well designed clinical trial confirms the previous
findings of the uncontrolled studies.
There have been less positive chaste tree and PMS studies. In
one trial, dramatic improvements were seen during the first treatment
cycle with chaste tree, and that improvement was maintained for
the next two remaining cycles.5 However, this pattern
also occurred in the placebo group. Twenty symptoms were assessed
but only one improved significantly more than in the placebo group.
Ginkgo (Ginkgo biloba)
A double-blind, placebo-controlled study was done in 1993 to determine
the effectiveness of ginkgo extract on PMS symptoms. One hundred
sixty-five women were studied and received either a ginkgo extract
of 24% ginkgo flavonglycoside content at 80 mg twice daily or a
placebo from day 16 of their cycle to day 5 of the next cycle. The
ginkgo extract was effective against the congestive symptoms of
PMS, particularly breast pain or tenderness6 but not
other PMS symptoms.
St. John's Wort
A prospective, open, uncontrolled, observational pilot study using
St. John's wort standardized extract, 300 mg three times daily,
was investigated to establish a hypothesis and to test methods for
a future randomized controlled trial.7 Nineteen women
with PMS underwent a preliminary screening interview and completed
a daily symptom rating for one cycle. After taking the St. John's
wort for two complete menstrual cycles, daily symptoms were rated
using the Hospital Anxiety and Depression scale and a modified Social
Adjustment Scale. The degree of improvement in overall PMS scores
between baseline and the end of the trial was 51%, with more than
two thirds of the sample demonstrating at least a 50% decrease in
symptom severity. The mood subscale showed the most improvement
(57%), and the symptoms with the greatest reductions in scores were
crying (92%), depression (85%), confusion (75%), feeling out of
control (72%), nervous tension (71%), anxiety (69%), and insomnia
(69%).
Additional Herbs
Many other herbs that have not been subjected to scientific research
for the treatment of PMS have also been used successfully by women
and practitioners for decades. These include many species of wild
yam, licorice root, dong quai, and black cohosh. Angelica or dong
quai has been primarily regarded as a "female" remedy and used to
treat menopausal symptoms, menstrual cramps, abnormal uterine bleeding,
and premenstrual problems. No one knows exactly how dong quai works
in addressing premenstrual symptoms although it is known to aid
in uterine relaxation, as is needed with premenstrual uterine cramping.
Licorice may be useful in treating PMS because of its ability to
raise progesterone levels. Although abnormal hormone levels in women
with PMS is not yet a proven finding, many women respond to either
more progesterone or herbs that help the body to raise its own progesterone
level. Black cohosh has been shown to reduce premenstrual depression,
anxiety, tension, and mood swings in a study done back in the 1960s.8
Other plants are used because of their benefit with specific symptoms,
and do have scientific efficacy and documentation; for example,
kava extract is used for anxiety, St. John's wort for depression,
dandelion leaf for water weight gain, valerian for sleep problems,
and lemon balm for herpes eruptions. You will often find one or
more of these herbs in a combination herbal and nutritional product
that has been specifically formulated for PMS symptoms relief.
NATURAL HORMONES
Natural Progesterone
Perhaps no other PMS therapy has been the target of so much controversy
as natural progesterone. This has as much to do with the lack of
agreement and scientific research to support a unified theory as
to the cause of PMS as it has to do with the efficacy of natural
progesterone itself. Green and Dalton advanced a theory in the 1950s
that PMS was caused by unopposed estrogen during the luteal phase
of the menstrual cycle. Dalton reported in her book, the Premenstrual
Syndrome and Progesterone Therapy9 that she has used
natural progesterone via injections (25-100 mg daily), vaginal and
rectal suppositories (400-1,600 mg daily), and subcutaneous pellets
(500-1,600 mg every 3-12 months) with results as good as complete
relief of PMS symptoms in 83% of women.10 There have
been several studies that demonstrate a lack of efficacy of rectal
and vaginal suppositories in the treatment of PMS. In 1979, Sampson
conducted the first placebo-controlled, double-blind trial of rectal-vaginal
progesterone. There was no significant difference between progesterone
at either a 200 mg dose twice daily by suppository or pessary, rectally
or vaginally, and placebo.11 In 1983, Van der Meer et
al published results of a randomized clinical trial of rectal progesterone.
Twenty patients received 200 mg progesterone twice daily. Of the
13 who completed the trial, none showed a difference in psychologic
or somatic symptoms.12 In 1986, Maddocks et al restudied
vaginal progesterone for PMS; 200 mg twice daily was delivered vaginally
and compared with placebo in a double-blind trial.13
There were 48 women who entered the study and only 20 completed
it. The somatic and affective symptoms were the same for both progesterone
and placebo. In 1990, Freeman also found progesterone in vaginal
and rectal suppositories to be ineffective.14 Although
the suppository method of delivering natural progesterone for PMS
has not held up to scientific scrutiny, oral micronized natural
progesterone has. A controlled study by Dennerstein and colleagues
in 1985 found an overall beneficial effect using 300 mg/day (100
mg in the morning; 200 mg in the evening) for 10 days of each menstrual
cycle starting 3 days after ovulation.15 A statistically
significant improvement was noted in anxiety, depression, distress,
swelling, fluid retention, and hot flushes. No effect was seen in
libido or restlessness. One subject experienced a severe premenstrual
migraine as a side effect.
Natural progesterone creams have not been subjected to scientific
scrutiny for PMS although tens of thousands of women can attest
to their benefit. Progesterone cream is commonly used in over-the-counter
products that contain up to as much as 400 mg of natural progesterone
per ounce. Using 1/4 teaspoon per dose will deliver approximately
20 mg of United States Pharmacopeia natural progesterone, the same
progesterone that is in oral micronized progesterone. Applying 1/4
to 1/2 teaspoon twice daily starting at midcycle and continuing
for 12 days, stopping the day before the menses is a typical use.
The best sites for rubbing in the cream include the palms, inner
upper arms, chest, and inner thighs.
Prior to the use of selective serotonin reuptake inhibitors (SSRIs)
for the treatment of PMS, conventional mainstream medicine has not
been able to offer women a known cause for PMS nor has it been able
to offer a management approach short of pharmaceuticals with often
as many side effects as relief. Self-care with natural therapies
has been the dominant method of how women manage PMS. Women have
clearly taken this monthly familiar problem into their own hands
and more often than not have determined what works for them. The
astute and well educated practitioner can offer additional therapies
and clinical insights to help most of the remaining women with more
severe symptoms who need more specific and effective dosing regimens
of natural substances as well as a well thought out comprehensive
approach. Select individuals with clearly severe (especially mood
and behavioral) symptoms can then be prescribed SSRIs. Treating
PMS with a natural and holistic approach often serves as a touchstone
for motivating women to make lifestyle changes that have a positive
cascade effect on their general health.
Tori Hudson, ND, is a professor, National College of Naturopathic
Medicine, and director, A Woman's Time, PC, Portland, Ore.
REFERENCES
- Hudson T. Premenstrual Syndrome. The Female Patient. 2002;27(5):47-49,59.
- American College of Obstetrics and Gynecology (ACOG). Committee
opinion. Int J Gynecol Obstet. 1995;50:80.
- Dittmar F. Das pramenstruelle Spannungssyndrome. J Gynakol.
1989; 5(6):4-7.
- Schellenberg R. Treatment for the premenstrual syndrome with
agnus castus fruit extract: prospective, randomized, placebo controlled
study. BMJ. 2001;20:134-137.
- Turner S, Mills S. A double-blind clinical trial on a herbal
remedy for premenstrual syndrome: a case study.Complement Ther
Med. 1993;1:73-77.
- Tamborini A, Taurelle R. "Value of standardized Ginkgo biloba
extract in the management of congestive symptoms of premenstrual
syndrome." Gynecol Obstet. 1993;88: 447-457.
- Stevinson C, Ernst E. A pilot study of Hypericum perforatum
for the treatment of premenstrual syndrome. Br J Obstet Gynaecol.
2000;107:870-876.
- Schildge E. Essay on the treatment of premenstrual and menopausal
mood swings and depressive states. Rigelh Biol Umsch. 1964;19(2):18-22
- Dalton K. The Premenstrual Syndrome and Progesterone Therapy.
2nd ed. Chicago, Ill: Year Book Medical Publishers; 1976.
- Keye W Jr. Medical treatment of premenstrual syndrome. Can
J Psychiatry. 1985;30:483-487.
- Sampson G. Premensrual syndrome: a double-blind controlled trial
of progesterone and placebo. Br J Psychiatry. 1979;135:209.
- Van Der Meer Y, Benedek-Jaszmann L, Van Loenen A. Effect of
high-dose progesterone on the pre-menstrual syndrome; a double-blind
cross-over trial. J Psychosomatic Obstet Gynaecol. 1983;2:220.
- Maddocks S, Hahn P, Moller F, et al. A double-blind placebo-controlled
trial of progesterone vaginal suppositories in the treatment of
premenstrual syndrome. Am J Obstet Gynecol. 1986;154:573.
- Freeman E, Rickels K, Sonheimer S, Polansky M. Ineffectiveness
of progesterone suppository treatment for premenstrual syndrome.
JAMA. 1990;264:349-353.
- Dennerstein L, Spencer-Gardner C, Gotts, G et al. Progesterone
and the premenstrual syndrome: a double blind crossover trial.
Br Med J. 1985;290:1617-1621.
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