Passiflora incarnata in Neuropsychiatric Disorders-A Systematic Review.
تصميم الدراسة
- نوع الدراسة
- Systematic Review
- المجتمع المدروس
- Adults ≥18 years with neuropsychiatric disorders (anxiety, insomnia, depression); 9 clinical trials from 1 day to 30 days duration
- التدخل
- Passiflora incarnata in Neuropsychiatric Disorders-A Systematic Review. Various Passiflora incarnata preparations (doses not specified in abstract)
- المقارن
- Placebo or active comparator (varies by trial)
- النتيجة الأولية
- Anxiety levels, insomnia, depression in neuropsychiatric patients
- اتجاه التأثير
- Positive
- خطر التحيز
- Moderate
الملخص
BACKGROUND: Stress is a natural response of the body, induced by factors of a physical (hunger, thirst, and infection) and/or psychological (perceived threat, anxiety, or concern) nature. Chronic, long-term stress may cause problems with sleep, concentration, and memory, as well as affective disorders. The passionflower (Passiflora incarnata) is a perennial plant with documented therapeutic properties. The literature data suggest that the passionflower itself, as well as its preparations, helps reduce stress and can therefore be helpful in the treatment of insomnia, anxiety, and depression. The objective of this systematic review was to evaluate Passiflora incarnata in terms of its neuropsychiatric effects. METHODS: The scientific databases PubMed, ClinTrials.gov, and Embase were searched up to 22 October 2019. The search identified randomized clinical trials describing the effects of Passiflora incarnata in neuropsychiatric disorders. RESULTS: The systematic review included nine clinical trials. The duration of the studies included in the analysis varied widely, from one day up to 30 days. Study participants were no less than 18 years old. In each of the papers, the effects of passionflower were measured by using a number of different tests and scales. The majority of studies reported reduced anxiety levels following the administration of Passiflora incarnata preparations, with the effect less evident in people with mild anxiety symptoms. No adverse effects, including memory loss or collapse of psychometric functions, were observed. CONCLUSION: Passiflora incarnata may be helpful in treating some symptoms in neuropsychiatric patients.
باختصار
The majority of studies reported reduced anxiety levels following the administration of Passiflora incarnata preparations, with the effect less evident in people with mild anxiety symptoms, and some symptoms in neuropsychiatric patients.
النص الكامل
1. Introduction
The passionflower (
Stress is a natural response of the body. It can be induced by factors of a physical (hunger, thirst, infection) and/or psychological (perceived threat, anxiety or concern) nature—namely stressors. Stress has been linked to cellular inflammation. Physiologically, the body’s response to stress causes an immediate activation of the adrenergic system and the sympathetic–adrenomedullary axis (SAM axis), followed by the hypothalamic–pituitary–adrenal axis (HPA axis). Chronic, long-term stress is a pathological condition, which may impair concentration and memory, as well as lead to affective disorders, such as depression, schizophrenia, and the post-traumatic stress disorder [
The objective of this systematic review was to evaluate the efficacy of
2. Materials and Methods
2.1. Search Strategy, Inclusion Criteria
At least two independent authors (K.W., J.A. and K.S.Z.) searched PubMed/MEDLINE/Embase, from database inception until 22 October 2019, without language restrictions. Randomized clinical trials have been found to describe the effect of the use of passion flower in neuropsychiatric disorders. The following search string in Pub Med was used: (“passiflora” OR “passion fruit” OR “passion” OR “passion flower”) AND (anxiety OR depression OR insomnia OR somatoform); Embase (“passiflora”/exp OR “passiflora”) AND (“depression”/exp OR “central depression” OR “clinical depression” OR “depression” OR “depressive disease” OR “depressive disorder” OR “depressive episode” OR “depressive illness” OR “depressive personality disorder” OR “depressive state” OR “depressive symptom” OR “depressive syndrome” OR “mental depression” OR “parental depression” OR “anxiety disorder”/exp OR “anxiety disorder” OR “anxiety disorders” OR “insomnia”/exp OR “agrypnia” OR “hyposomnia” OR “insomnia” OR “sleep initiation and maintenance disorders” OR “sleeplessness” OR” somatoform disorder”/exp OR “somatoform disorder” OR “somatoform disorders”), oraz ClinTrials.gov (
We utilized the following inclusion criteria: (i) original studies, (ii) studies with access to full text, (iii) studies in which the treatment included any products (supplements, tinctures, extracts, infusions, raw materials, etc.) containing
2.2. Data Abstraction
Data for country in which the study was conducted, information about the sponsors, type of blindness, duration of the study, and main purpose of the study, as well as the name of the preparation used during therapy, were extracted. During data abstraction, detailed data on the studied population were looked for, i.e., the average age and standard deviation of studied persons, the number and percentage of men participating in the study, and the number of people randomized to the study. Data extraction was performed based on the guidelines contained in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) protocol, but with no study protocol registration. If data were missing, authors were contacted via email, to ask for additional information. Inconsistencies were resolved by consensus, with the corresponding author being involved. The results that were compared in the systematic review involved various scales and tests, such as the Hamilton Rating Scale for Depression (HRSD), Visual Analogue Scale (VAS), Numerical Rating Scale (NRS), Observers Assessment of Alertness and Sedation Scale (OAA/S), Corah’s Dental Anxiety Scale, Revised (DAS-R), Ramsey Scale, Digit symbol substitution test (DSST), Concentration Endurance Test, (The d2 test), Memory test, Continuous Performance Task/Test (CPT), Trieger Dot Test (TDT), Perceptive Accuracy Test (PAT), Finger Tapping Test (FTT), and State-Trait Anxiety Inventory (STAI-S, STAI-T). Data from charts and figures were extracted by means of WebPlotDigitizer software (
2.3. Outcomes
The primary outcome was to evaluate the effects of a
3. Results
3.1. Search Results
The first search in PubMed and Embase databases resulted in 417 hits. Among them, 305 studies were excluded as duplicates and/or after evaluation at the title/abstract level. After excluding 305 studies, 112 full-text articles were eventually reviewed, 103 of which were excluded due to the failure to meet previously established inclusion criteria. The main reasons for exclusion were as follows: review (
3.2. Study Characteristics
Nine studies carried out between 2017 and 2019 were included in this systematic review.
The objective of this systematic review was to evaluate
3.3. Effect of Passiflora Treatments on Neuropsychiatric Parameters
The systematic review included nine studies. In each of the works, different criteria were taken into account: the Hamilton Rating Scale for Depression (HRSD), Observers Assessment of Alertness and Sedation Scale (OAA/S), Corah’s Dental Anxiety Scale, Revised (DAS-R), Ramsey Scale, Digit symbol substitution test (DSST), Continuous Performance Task/Test (CPT), Trieger Dot Test (TDT), Perceptive Accuracy Test (PAT), Finger Tapping Test (FTT), State-Trait Anxiety Inventory (STAI), Visual Analogue Scale (VAS), memory test, and Concentration Endurance Test (d2 test). The results of the use of the
The Hamilton Depression (HAM-D) Scale is a numerical scale consisting of 21 points (or 17 points in some cases). It is a tool used in general psychiatry, to assess the diagnosis of depression and to clinically evaluate the use of antidepressants. The HAM-D score level of depression is as follows: 10–13, mild; 14–17, mild to moderate; and >17, moderate to severe [
3.4. Risk of Bias Assessment
The bias analysis showed that the three studies were of low quality and received less than 5 points in the risk of bias (ROB) evaluation [
4. Discussion
Neuropsychiatric disorders, such as schizophrenia, bipolar affective disorder, major depressive disorder, and attention-deficit hyperactivity disorder, are a common and, regrettably, increasingly prevalent problem. Around the world, depression affects some 322 million people, while 264 million live with anxiety [
Nine clinical trials were included in this paper. The reviewed studies analyzed the effects of passionflower preparations on anxiety levels experienced by patients during medical interventions, including spinal anesthesia, dental procedures, or surgery, as well as on sleep quality and cognitive functions. In eight papers, the study subjects were healthy, and, in one,
Akhondzadeh et al. [
Aslanargun et al. [
The objective of the study by Azimaraghi et al. [
To compare the anxiolytic action of
Dimpfel et al. [
The objective of the study by Kaviani et al. [
Movafegh et al. [
Ngan and Conduit [
The objective of the study by Rokhtabnak et al. [
This systematic review has some limitations. First, there are few studies on the effects of
Another limitation may be the lack of information on which part of the plant was used in the research. Traditional medicine uses the leaves, stamps, seeds, and flowers (aerial parts) of
In conclusion, the authors of the works included in this systematic review all agree that
5. Conclusions
Passionflower has the potential to alleviate some symptoms of neuropsychiatric origin. No adverse effects, including memory loss or collapse of psychometric functions, have been linked to passionflower administration. The anti-anxiety effect of
الأشكال
Study flowchart.
الجداول
Table 4
Risk of bias (ROB).
| Reference/Country | Publication Year | Random Generation of The Error Sequence (Selection Error) | Hiding the Allocation (Selection Variation) | Blinding of Participants and Staff (Biased Evaluation) | Performance Evaluation Blindness (Detection Error) | Incomplete Result Data | Selective Reporting (Reporting Error) | Other Biases | Number of Indications with Low Risk of Bias |
|---|---|---|---|---|---|---|---|---|---|
| Akhondzadeh et al. (Iran) [ | 2001 | L | ? | L | ? | L | L | L | 5 |
| Aslanargun et al. (Turkey) [ | 2012 | ? | ? | L | ? | L | L | L | 4 |
| Azimaraghi et al. (Iran) [ | 2017 | L | L | L | L | L | L | L | 7 |
| Dantas et al. (Brazil) [ | 2017 | L | L | L | L | L | L | L | 7 |
| Dimpfel et al. (Germany) [ | 2011 | L | ? | ? | ? | L | L | L | 4 |
| Kaviani et al. (Iran) [ | 2013 | L | ? | H | ? | L | L | L | 4 |
| Movafegh et al. (Iran) [ | 2008 | L | L | L | L | L | L | L | 7 |
| Ngan and Conduit (Australia) [ | 2011 | ? | L | L | L | L | L | L | 6 |
| Rokhtabnaket al. (Iran) [ | 2017 | L | L | L | L | L | L | L | 7 |
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