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Premenstrual Syndrome

Premenstrual syndrome (PMS) refers to the different kinds of symptoms experienced by some women during the luteal and menstrual phase of the estrus cycle. It affects upwards of 75% of all women of menstruating age in varying degrees. The most common physical symptoms of PMS are abdominal distension, breast swelling and tenderness, headaches, changes in appetite, food cravings, fatigue, dizziness, weight gain, fluid retention, joint pain, pelvic congestion, poor immunity, constipation or diarrhea, herpes outbreak, and acne. Psychological symptoms might include insomnia, poor memory, grief, irritability, anger, anxiety, poor concentration, and confusion. Such symptoms, when recognized by the physicians of the middle ages, gave rise to all kinds of interesting ideas, such as the concept of a “wondering womb” that searched the body looking for a baby, and in its journey caused the myriad symptoms that we now define as PMS. The modern medical approach to this condition is little better however, and the prevailing notion is that PMS is nothing but a kind of female nervous tension best treated by sedation. (Trickey 1998 35-37; Berkow 1992, 1791)

Although the causes of PMS are varied, in her book Women, Hormones and the Menstrual Cycle, author Ruth Trickey illustrates some common themes, all of which are related to neuroendocrine control:

  • Estrogen- Elevated levels of estrogen relative to progesterone 5 – 10 days prior menses is thought to cause feelings of irritability and aggression by elevating norepinepherine in the brain.
  • Progesterone- A relative deficiency of progesterone 5 – 10 days prior menstruation allows for the elevation of aldosterone, enhancing sodium retention and the resulting edema. The progesterogenic effects of the luteal phase are also inhibited by elevated norepinepherine from emotional stress and elevated estrogen.
  • Aldosterone- Aldosterone is a cause of premenstrual fluid retention, and is enhanced with stress, low progesterone, high estrogen, and a deficiency of magnesium.
  • Prolactin- Women with PMS are thought to have an excessive sensitivity to, or mildly elevated levels of, prolactin. Prolactin is normally secreted in high levels during lactation, and prolactin is implicated in the increased breast sensitivity and swelling of some forms of PMS.
  • Endorphins- Endorphins are natural opiates that elevate mood, and when decreased, can give rise to symptoms of depression. Additionally, endorphins appear to regulate the secretion of the gonadotropins.
  • Dopamine- Dopamine in a prolactin antagonist, and is decreased under the influence of estrogen and a deficiency of magnesium and vitamin B6. Dopamine also appears to regulate mood, and a deficiency is implicated in anxiety, irritability, and emotional lability. (Trickey 1998, 109-118)

Other factors in PMS include a prostaglandin imbalance and the overgrowth of Candida albicans, the latter of which is linked to a relative estrogen excess. A deficiency of vitamin B6 is often implicated in PMS, and treatment with this nutrient may provide relief from depression and anxiety. The breast swelling and tenderness associated with elevated prolactin levels may be relieved by supplementation of vitamin B6 through the enhanced synthesis of dopamine. Vitamin B6 is also a cofactor in the production of the series 1 prostaglandins and can normalize cellular magnesium levels. Magnesium too is a factor in dopamine synthesis, and a deficiency can lead to depression, anxiety, and cyclic breast pain. (Trickey 1998, 109-118)

There are five different subcategories of PMS, first devised by G.E. Abraham, and each of these subtypes have a unique set of symptoms and metabolic abnormalities associated with them. The following chart describes these subtypes and the mechanisms that could cause them. It is important to note that a woman with PMS may experience more than one subtype.

Subgroup

Symptoms

Mechanisms

PMS A

A = anxiety

Anxiety

Nervousness

Mood Swings

Nervous tension

Estrogen excess

Progesterone deficiency

Liver congestion

PMS C

C = craving

Craving for sweets

Increased appetite

Palpitations

Fatigue

Dizziness

Headaches

Hypoglycemia

Magnesium deficiency

Prostaglandin imbalance

Often occurs in association with PMS A


PMS H

H= hydration

Breast tenderness

Bloating

Weight gain

Edema

Elevated aldosterone

Estrogen excess

Progesterone deficiency

Elevated prolactin

PMS D

D= depression

Depression

Poor memory

Grief

Confusion

Insomnia

Estrogen deficiency

PMS P

P= pain

Lower back pain

Abdominal pain

Joint pain

Headaches

Estrogen excess

Prostaglandin imbalance

(Trickey 1998, 118-121)

Treatment of PMS A

The primary treatment of PMS A is to enhance progesterone levels, best accomplished with Chasteberry (Vitex agnus castus), 40 gtt. of a 1:3 extract taken every morning for at least 6 months. Vitamin B6, at a dose between 100-600 mg daily, taken with 50-100 mg of a full spectrum B-complex, is best used 10-14 days prior menses. Magnesium is an important supplement as well, taken at a dosage between 200-800 mg throughout the cycle can be helpful. Botanicals that reduce anxiety and pain, as well as promote a feeling of well-being are an important aspect of treatment, and include relaxing nervines such as Valerian (Valeriana officinalis), Skullcap (Scutellaria lateriflora), Passionflower (Passiflora incarnata), Vervain (Verbena officinalis), and anodynes such as Kava (Piper methysticum) and Pasqueflower (Anenome occidentalis). Adaptogens are particularly indicated in anxiety with exhaustion, including Ashvagandha (Withania somnifera), Shatavari (Asparagus racemosa), Dang gui (Angelica sinensis), Peony root (Paeonia lactiflora), and Siberian Ginseng (Eleuthrococcus senticosus). Hepatics can be useful to enhance the excretion of conjugated estrogens, and include Buplerum (Buplerum chinensis), Barberry (Berberis vulgaris), and Dandelion root (Taraxacum officinalis). Phytoestrogenic herbs that compete with estrogen-binding are useful, such as Red Clover (Trifolium pratense), as well as phytoestrogen-containing foods such as fermented and sprouted legumes. Fiber intake should be enhanced, and greasy fatty foods and refined carbohydrate intake should be curtailed. In particularly recalcitrant cases, natural progesterone creams can be used to enhance serum progesterone levels, 1/4 tsp (equal to 20 mg natural progesterone) applied over the extremities once daily before bedtime.

Treatment of PMS C

The primary treatment of PMC C is to regulate blood sugar levels, best accomplished by enhancing protein intake, especially in the morning, and decreasing refined carbohydrate intake throughout the day. Smaller, more frequent meals can help, as will the elimination of methylxanthine-containing beverages such as coffee and tea that promote labile blood sugar levels. Supplementation with magnesium is useful (800-1000 mg daily), as is chromium (250 mcg thrice daily with meals). To correct the prostaglandin imbalance that can accompany this condition, supplementing with cold water fish oil is very useful, 2-3 grams EPA/DHA daily taken mid cycle until menstruation, or throughout the cycle on a daily basis. Additionally, vitamin B6 (100-300 mg daily, taken with a B-complex), vitamin E (200 600 IU daily), and zinc citrate (50 mg daily) can facilitate the production of PGE1.

Treatment of PMS H

The treatment of PMS H is essentially the same as it is for PMS A, with the addition of treatments to correct aldosterone levels and the sodium-potassium balance. To this end botanicals that are rich in potassium such as Dandelion leaf (Taraxacum officinalis), Catnip (Nepeta cataria), and Skullcap (Scutellaria lateriflora) are helpful when taken as an infusion, as are potassium-rich foods such as kelp, raisins, avocados, apricots, potato skins, cantaloupe, and broccoli. Although the treatment for PMS-H is similar to that of PMS A, the use of Licorice root (Glycyrrhiza glabra) as a phytoestrogen is contraindicated because of its aldosterone-like activity.

Treatment of PMS D

As PMS D relates to a relative estrogen deficiency, therapies that enhance estrogen production or facilitate the cellular activities of estrogen are all helpful. It appears that lead, found in some fuels, paints, and other household products can accumulate in the body and interfere with the activity of estrogen receptors, and thus agents that decrease lead absorption and retention such as magnesium, iron, copper, and zinc. A diet high in fiber can promote the excessive excretion of estrogen and thus fiber intake should be reduced. Foods high in phytoestrogens should be emphasized in the diet, as well as botanicals such as Red Clover (Trifolium pratense), Wild Yam (Dioscorea villosa), False Unicorn root (Chamaelirium luteum), and True Unicorn root (Aletris farinosa). And, just as for PMS A, botanicals that reduce anxiety and pain, as well as promote a feeling of well-being are an important aspect of treatment. For severe pain, follow the recommendations under PMS P. Serotinergic foods such as those high in tryptophan (e.g. turkey and hard cheeses) can also be taken to enhance serotonin levels, or with severe depression the biological precursor to serotonin, 5-HTP (100-300 mg daily).

Treatment of PMS P

PMS P relates to an increased sensitivity to pain, perceived to be an imbalance of the proinflammatory and pain-promoting prostaglandins, facilitated by elevated estrogen and poor estrogen clearance. Supplements that help reduce pain and pain sensitivity include magnesium, vitamin B6, zinc and omega 3 fats rich in EPA/DHA are all here, following the dosage ranges described under PMS C. The additional usage of herbs that have a phytoestrogenic property are helpful, as is increasing dietary fiber. Herbs that inhibit the inflammatory cascade include hepatics such as Feverfew (Tanacetum parthenium), Turmeric (Curcuma longa), Devil’s Claw (Harpagophytum procumbens), and Baical Skullcap (Scutellaria baicalensis). Astringent botanicals help to tone the uterus and promote reguklar contractions, including Red Raspberry (Rubus idaues), Lady’s Mantle (Alchemilla) and Bethroot (Trillium erectum). Botanicals that have potent analgesic and anodyne properties are Crampbark (Viburnum opulus), Black Haw (Viburnum prunifolium), Kava (Piper methysticum), Wild Lettuce root (Lactuca virosa), Jamaican Dogwood (Piscidia erythrina), White Willow bark (Salix alba), California Poppy (Eschscholzia californica), and Pasqueflower (Anenome occidentalis).