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Table 3 The effect of herbal medicine for premenstrual syndrome

From: Effects and treatment methods of acupuncture and herbal medicine for premenstrual syndrome/premenstrual dysphoric disorder: systematic review

#

Intervention

Frequency

Sample

2 cycles of pre-rating

Initial state M

Outcome

Control

Adverse

P-value

(dosage/day) -form

(Tx Duration)

Size

(Improved rate or end-of-Tx score)

(no of CG)

Events

10

Vitex Agnus castus17** (VAC, BNO 1095) 40 mg -Tablet

1/day

33

Confirmed

PMSD sum score 29.38 ± 7.63 (p = 0.752)

PMSD sum score 14.66 ± 0.52

Placebo

No notable AE observed

=0.0001

(3 cycles)

(34)

11

Vitex Agnus castus18 (VAC, BNO 1095, 4.0 mg of dried ethanolic (70%)) 40 mg -Tablet

2/day

101

Confirmed

PMSD 29.13 ± 7.88 (p = 0.4017)

PMSD 6.41 ± 7.94

Placebo

No serious AE observed

<0.05

(3 cycles)

PMTS 26.17 ± 4.79 (p = 0.1649)

PMTS 9.92 ± 9.01

(101)

12

Vitex Agnus castus extract19** (AC extract)

1/day

19

Confirmed

DSR 171.758.1 (p > 0.05) HAM-D 15.24.7 (p > 0.05) CGI-SI 4.11.4 (p > 0.05)

DSR 82.849.5

Fluoxetine

No serious AE observed from TG

>0.1

HAM-D 7.64.3

(19)

20-40 mg –Tablet

(2 cycles)

CGI-I 1.20.7 five symptoms diminished 50% or more

2CG: Sexual dysfunction

13

Vitex Agnus castus20 (Vitex agnus extract)

1/day

62

Confirmed

DSR 30% higher score @ LP

Better than CG

Placebo

No serious AE observed

<0.0001

@ LP

(66)

40 drops (4.5 mg) -Liquid

(6 cycles)

14

Hypericum Perforatum21

2/day

17

Confirmed

DSR score in LP 12.6

DSR score 5.80 (F [1,30] = 4.82; p = 0.04; partial Z2 = 0.14)

Placebo

No serious AE observed

>0.05

(Li 160 (80% methanolic dry extract, 0.18% hypericin, 3.38% hyperforin) 900 mg -Tablet

(2 cycles)

(15)

15

Hypericum Perforatum22 (St. John’s wart extract, 300 mg of extract, 900 ug of hypericin) 1800ug hypericin (600 mg) -Tablet

2/day

64

Confirmed

MD score 326.33§

MD score 230.28 (p ≤ 0.007)

Placebo

No serious AE observed

<0.007

(61)

(2 cycles)

16

Hypericum Perforatum23

2/day

85

Confirmed

DSR 149.07

DSR 86.13

2 Cellulose

No serious AE observed

<0.05

(extract N/A) two 1340 ug hypericin -Tablet

(2 cycles)

Anxiety 41.15 ± 9.74 Crying 20.52 ± 11.73 Depression 29.26 ± 7.49 Craving 22.01 ± 11.03 Hydration 36.13 ± 8.50

Anxiety 23.08 ± 14.78 (p = 0.223) Crying 5.87 ± 10.23 (p = 0.001, 71% reduction) Depression 13.82 ± 6.48 (p < 0.001, 52% reduction) Craving 17.26 ± 7.41 (p < 0.001) Hydration 26.10 ± 10.18 (p < 0.090)

Tablets

(85)

17

Xiao Yao San or Dan Zhi Xiao Yao San8 -Powder form

3/day

31

Confirmed

Diagnosed as PMS

Physical MDQ 68.9% reduction

Placebo

No AE

<0.001

@ LP

Physical MDQ psychological MDQ BDI ANX ANG PSS diagnosed as PMS (p < 0.005)

Psychological MDQ 74.8% reduction

(30)

(3 cycles)

BDI 43.1% reduction ANX 23.8% reduction ANG 39.3% reduction PSS 16.4% reduction (p < 0.001)

18

Crocus sativus (saffron) 24 30 mg -Tablet

2/day

24

Confirmed

DSR < 50 PMS diagnosed by HDRS

50% reduction in severity of symptoms by DSR and HDRS (P < 0.001)

Placebo

No severe AE reported

<0.001

(2 cycles)

(23)

19

Elsholtzia splendens 25 120 mg -Tablet

1/day

10

Not recorded

BDI 33.50 ± 5.82

BDI 23.60 ± 4.79 (p < 0.01) STAI 48.10 ± 5.20 (p < 0.05) STAI 52.00 ± 6.18

Placebo

None reported

<0.01

 

(3 cycles)

STAI 58.40 ± 7.30

(10)

PAF 270.20 ± 82.61

PAF 176.7 ± 61.33 (p = 0.530)

20

Cirsium japonicum25 120 mg -Tablet

1/day

10

Not recorded

BDI 33.60 ± 8.8

BDI 30.40 ± 5.40

Placebo

None reported

<0.01

(3 cycles)

STAI 50.90 ± 9.50

STAI 52.00 ± 6.18

(10)

PAF 257.30 ± 74.81

PAF 185.6 ± 53.65

21

Ginkgo biloba L.26 40 mg -Tablet

3/day

45

Confirmed

Overall score 34.80 (p = 0.930) Severity of psychological symptoms 38.41 (p = 0.899)

Overall score 11.11 (p < 0.001) Severity of psychological symptoms 10.89 (p < 0.001)

Placebo

No severe AE reported

<0.001

@ LP

(45)

(2 cycles)

  1. Literatures yield 11 studies and 7 different herbs. It includes total dosage per day, number of times the herbs were taken per day dither at all phases or only during luteal phase (@ LP), the duration of the studies by menstrual cycles, sample size (Treatment Group: TG), two menstrual cycles of prospective ratings, baseline score using assessment tools used at each studies, the outcome measures and results, control types with number of analyzed: CG), and p-value.
  2. *M, Measurement; PMSD, Premenstrual Syndrome Diary (four-point rating scale); PMTS, The Premenstrual Tension Syndrome Self-Rating Scale; DSR, Daily Symptom Report; PAF, Premenstrual Assessment Form;HDRS, Hamilton Depression Rating Scale (17-item); MD, Menstrual Diary(made up of 25 symptoms); MDQ, menstrual distress questionnaire); BDI, Beck Depression Inventory; ANX, state-anxiety; ANG, state-anger(ANX, ANG were measured with the Spielberger State Trait Personality Inventory; PSS, perceived stress scale; STAI.
  3. **Study 10 [17] is the analysis of a sub-population of Study11 [18]. Study 12 is the analysis of a sub-population of a study within a systematic review of clinical trials [27].