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Review

Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

by
Hee-Jeong Yoo
1,2,†,
Ha-Young Yoon
1,†,
Jeong Yee
1,* and
Hye-Sun Gwak
1,*
1
College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Korea
2
Department of Pharmacy, National Medical Center, Seoul 04564, Korea
*
Authors to whom correspondence should be addressed.
†
These authors contribute equally to this work.
Pharmaceuticals 2021, 14(11), 1198; https://doi.org/10.3390/ph14111198
Submission received: 18 October 2021 / Revised: 11 November 2021 / Accepted: 20 November 2021 / Published: 22 November 2021
(This article belongs to the Section Natural Products)
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Abstract

:
Ephedrine, the main active ingredient of mahuang, may lead to weight loss; however, it can also induce cardiovascular side effects. As ephedrine use remains controversial, this study aimed to systematically review previous studies on ephedrine-containing products and perform meta-analysis of the existing evidence on weight, blood pressure (BP), heart rate, and lipid change effects of ephedrine-containing products. We searched for placebo-controlled randomized studies in PubMed, Web of Science, and EMBASE until July 2021 using the following search terms: (ephedr* OR mahuang) AND (“weight loss” OR obes* OR overweight). Mean differences (MDs) and 95% confidence intervals (CIs) were calculated to evaluate the effects of ephedrine-containing products on weight, BP, heart rate, and lipid profiles. A total of 10 articles were included. Compared with the placebo group, the ephedrine-containing product group was associated with greater weight loss, with an MD of −1.97 kg (95% CI: −2.38, −1.57). In the ephedrine-containing product group, the mean heart rate was 5.76 beats/min higher than in the placebo group (95% CI: 3.42, 8.10), whereas intergroup differences in systolic and diastolic BP were not statistically significant. The ephedrine-containing product group had a significantly higher mean high-density lipoprotein cholesterol level (MD: 2.74 mg/dL; 95% CI: 0.94, 4.55), lower mean low-density lipoprotein cholesterol level (MD: −5.98 mg/dL; 95% CI: −10.97, −0.99), and lower mean triglyceride level (MD: −11.25 mg/dL; 95% CI: −21.83, −0.68) than the placebo group. Compared with placebo, the ephedrine-containing products showed better effects on weight loss and lipid profiles, whereas they caused increased heart rate. The ephedrine-containing products may be beneficial to obese or overweight patients; however, close monitoring is needed, especially heart rate monitoring.

1. Introduction

Obesity is a pathological condition in which excess fat in the body accumulates due to metabolic imbalance [1]. Obesity is recognized as one of the most important challenges facing public health and economies [2]. The prevalence of obesity has been continuously increasing. According to National Health and Nutrition Examination Survey (NHANES) data, over 40% of the American population is obese [1]. Additionally, obesity can lead to various diseases, such as diabetes mellitus, cardiovascular or musculoskeletal diseases, cancers, and psychiatric disorders [3,4,5,6].
Lifestyle modification, including calorie restriction and physical exercise, is the primary approach to weight loss [7]. Along with lifestyle changes, pharmacotherapy can be used to manage obesity, especially when body mass index (BMI) exceeds 30 kg/m2 or in the context of comorbid diseases and a BMI exceeding 27 kg/m2 [8]. Several drugs have been approved for obesity treatment, with sufficient evidence of safety and efficacy, including orlistat, phentermine–topiramate, naltrexone–bupropion and liraglutide [9]. Various herbal medicines and extracts (e.g., chitosan, garcinia, green tea, guar gum, mahuang, psyllium, and pyruvate) are also available for weight loss; however, unlike approved drugs, the clinical evidence for these products is not clear [10].
Mahuang, Ephedra sinica, is one of the most widely used herbal medicines for the treatment of obesity. Ephedrine promotes sympathetic neuronal actions, causing the heart to beat more strongly and quickly [11]. It also increases metabolism and suppresses appetite, thus promoting body fat decomposition [12,13]. Several studies have shown that single or mixed preparations of ephedrine can lead to weight loss and increased energy [14,15,16,17]. According to Douglas et al., patients taking ephedrine-containing capsules had a greater weight loss than those taking placebo (−3.1 kg vs. −2.1 kg in 8 weeks) [15]. Hackman et al. also showed that the ephedrine-treated groups lost more body weight than control groups (−3.0 kg vs. −1.0 kg in 3 months and −7.2 kg vs. −2.3 kg in 9 months) [17]. However, excessive ephedrine doses may cause adverse reactions, such as increased blood pressure and pulse rate, palpitations, insomnia, headaches, and nausea [18,19,20].
Several systematic reviews and meta-analyses have evaluated the effectiveness of herbal medicines for weight loss [21,22,23]. However, most studies have assessed the short-term efficacy of herbal medicines or have focused only on body weight and fat mass changes. Therefore, this systematic review and meta-analysis of studies investigating ephedrine-containing products aimed to summarize existing evidence regarding the effects of ephedrine-containing products on weight, in addition to new outcomes including blood pressure, heart rate, and lipid profiles.

2. Results

2.1. Literature Search

A detailed flow chart of the article selection process is presented in Figure 1. A total of 1882 articles were identified from searches of the three databases. After the removal of 630 duplicates, 1252 records were initially identified, of which the titles and abstracts were screened for inclusion. From this initial review, 74 articles were selected for full-text reviews and assessed for eligibility. Of these articles, 64 were excluded for the following reasons: not original research (n = 27), not a clinical trial (n = 15), not in English (n = 1), participants ineligible by age (n = 2), study duration less than 4 weeks (n = 2), ineligible outcomes (n = 10), ineligible drug interventions (n = 4), not amenable to data extraction (n = 2), and overlapping population (n = 1). Ultimately, 10 articles were selected for this systematic review [24,25,26,27,28,29,30,31,32,33].
The characteristics of the included articles are presented in Table 1. The articles were published between 1985 and 2015. Six of the studies were conducted in America, three in Europe, and one in Oceania. Daily ephedrine doses ranged from 60 to 150 mg and caffeine was co-administered in most studies. Study duration ranged between 4 and 24 weeks. The risk of bias was rated as “some concern” for two articles and “low” for eight articles.

2.2. Weight Loss

Nine studies with 534 patients were evaluated to investigate the weight loss effect of ephedrine-containing products in obese or overweight individuals. The weight mean difference (MD) between the ephedrine-containing product group and the placebo group was −1.97 kg (95% confidence interval (CI): −2.38, −1.57; p < 0.00001; I2 = 80%) (Figure 2). Neither Begg’s test nor Egger’s test revealed significant publication bias (Begg’s test: p = 0.677; Egger’s test: p = 0.356; Figure S1, Supplementary Materials).

2.3. Blood Pressure and Heart Rate

Four studies assessed the effects of ephedrine-containing products on blood pressure and heart rate. There were no significant differences in systolic blood pressure (SBP) and diastolic blood pressure (DBP) between the ephedrine-based treatment group and the placebo group (Figure 3A,B, respectively). In contrast, the mean heart rate of the ephedrine-containing product group was 5.76 beats/min higher than that of the placebo group (95% CI: 3.42, 8.10; p < 0.00001; I2 = 94%) (Figure 3C). No significant publication biases were detected in any blood pressure or heart rate analyses, and all p values of the Begg’s and Egger’s tests were >0.05 (Figure S2, Supplementary Materials).

2.4. Lipid Levels

Three studies investigated the influence of ephedrine-containing products on high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), triglyceride (TG), or total cholesterol (TC). The ephedrine-containing products group had a higher mean HDL-C concentration, with an MD of 2.74 mg/dL (95% CI: 0.94, 4.55; p = 0.003; I2 = 0%) (Figure 4A). Additionally, the ephedrine-containing product group had significantly lower mean concentrations of LDL-C (Figure 4B) and TG (Figure 4C) than the placebo group: the MDs were −5.98 mg/dL (95% CI: −10.97, −0.99; p = 0.02; I2 = 0%) and −11.25 mg/dL (95% CI: −21.83, −0.68; p = 0.04; I2 = 20%), respectively. In terms of TC, there was no significant intergroup difference, but the ephedrine-containing product group had a lower mean TC concentration (MD: −3.00; 95% CI: −8.84, 2.83; p = 0.31; I2 = 0%, Figure 4D). Neither Begg’s test nor Egger’s test showed significant publication bias in any of the lipid level analyses (Figure S3, Supplementary Materials).

2.5. Subgroup Analysis

Among the included studies, six studies were published after the year 2000; there were five studies for weight loss and three studies for change of blood pressure and heart rate. In terms of lipid levels, all studies were published after the year 2000. The weight MD between the ephedrine-containing product group and the placebo group was −2.25 kg (95% CI: −2.81, −1.69; p < 0.00001; I2 = 88%; Figure S4, Supplementary Materials). The SBP of the ephedrine-containing product group was 1.16 mmHg lower than that of the placebo group (95% CI: −1.69, −0.63; p < 0.0001; I2 = 12%), whereas there was no significant difference in DBP between the ephedrine-based treatment group and the placebo group. In terms of heart rate, the ephedrine-containing product group had 5.90 beats/min higher heart rate than that of the placebo group (95% CI: 2.18, 9.63; p = 0.0008; I2 = 86%).

3. Discussion

In this systematic review and meta-analysis, we demonstrated the effects of ephedrine-containing products on weight loss, BP, heart rate, and lipid profiles in obese or overweight patients. The main results are as follows: compared with placebo, the ephedrine-containing products in daily dose from 60 to 150 mg for 4 to 24 weeks (1) significantly decreased the body weight with an MD of −2.0 kg, (2) increased the heart rate by 5.8 beats/min, and (3) were associated with better lipid profiles (decreased LDL-C, TG, and TC with an MD of −6.0 mg/dL, −11.3 mg/dL, and −3.0 mg/dL, respectively, and increased HDL-C by 2.7 mg/dL). The subgroup analysis with studies published after the year 2000 showed a similar trend as the main results. As the subgroup analysis included only three to five studies, it should be further validated.
Several meta-analyses have investigated the weight loss effects of prescription drugs and complementary medicines for weight management. A recent network meta-analysis showed that, compared with placebo, orlistat and lorcaserin were associated with mean weight loss of around 3 kg over 1 year, and naltrexone–bupropion and phentermine–topiramate were associated with mean weight loss of 5 kg and 9 kg in a year, respectively [34]. Another meta-analysis investigated the weight loss effects of complementary medicines and found that green tea-containing and garcinia-containing herbal medicines achieved 1.6 kg and 0.4 kg of weight loss, respectively. However, single preparations of each herbal extract were not associated with statistically significant changes [22]. Our study revealed that ephedrine-containing products were associated with around 2 kg of weight loss, which was greater than the extent of weight reduction associated with other herbal medicines but lower than that associated with weight loss drugs. Although a clinically significant weight loss is usually regarded as 2.5 kg or more, which is known to be sufficient for reducing cardiovascular events and mortality in large trials [35], the weight loss effect of ephedrine-containing products was quite beneficial for obesity management.
Ephedrine, a mixed sympathomimetic agent, stimulates α- and β-adrenergic receptors and increases the release of norepinephrine [36]. It has been known to increase myocardial contractility and heart rate and raise BP [37]. Due to its adverse cardiovascular effects, the U.S. Food and Drug Administration (FDA) prohibited the sale of dietary supplements containing ephedrine alkaloids in 2004 [38]. However, 1 year later, the U.S. District Court overturned the FDA’s ban [39], and the cardiovascular safety of ephedrine remained to be clarified. Our meta-analysis results show that patients taking ephedrine-containing products had faster heart rates, which was consistent with previous studies showing that ephedrine-containing dietary supplements were associated with a 2-fold higher risk of palpitations [20]. However, our review failed to demonstrate statistical significance in terms of ephedrine’s effects on SBP and DBP, possibly due to the small number of included studies. Further research is warranted in this regard.
Ephedrine-containing products were also shown to be associated with improved lipid profiles. This finding was similar to that reported after an in vivo study in which the ephedra group had lower TG and higher HDL levels [40]. This can be explained by the differential expression of lipid metabolism-related genes. Matteis et al. report that ephedrine with caffeine increases the expression of the β3-adrenergic receptor in adipocytes, which are involved in lipolysis [41]. It has also been shown that mice treated with ephedra extracts have elevated expression of PPAR-α and adiponectin, which are known to regulate lipid and lipoprotein metabolism [40]. Accordingly, ephedrine is likely to decrease fat accumulation, thereby leading to weight loss.
This review had several limitations. First, the daily dose of ephedrine varied from study to study, leading to clinical heterogeneity. Second, most studies co-administered caffeine, which is also known to be beneficial for weight control by increasing energy expenditure and decreasing energy intake [42,43]. There may be synergistic effects on weight loss, which makes it difficult to distinguish their own effects on weight loss. Third, some potential confounders, such as age, baseline body weight, and comorbidities, could not be adjusted for in the analysis. Fourth, as we did not limit the publication year of studies, some studies were quite old, with around half of them performed before the year 2000. Last, this meta-analysis only included articles reporting on studies of obese or overweight adults; therefore, the results should be interpreted with caution, especially for adolescents, older adults, and non-obese populations.

4. Materials and Methods

4.1. Literature Search Strategy and Inclusion Criteria

This meta-analysis was conducted according to the checklist outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [44]. An extensive search was performed using three electronic databases (PubMed, Web of Science, and EMBASE) until July 2021 using the following search terms: (ephedr* OR mahuang) AND (“weight loss” OR obes* OR overweight).
Articles were eligible for inclusion if they (i) reported on original research and were published in peer-reviewed journals; (ii) involved obese or overweight adults (>18 years of age); (iii) compared ephedrine-containing products with placebo; (iv) evaluated one or more clinical outcomes, including weight, heart rate, blood pressure (SBP or DBP), or lipid levels (HDL-C, LDL-C, TG, or TC); (v) followed participants for at least 4 weeks; and (vi) were randomized controlled trials, including parallel or crossover designs. Articles were excluded if they (i) were in vitro or animal studies, (ii) were not published in English, or (iii) were not amenable to data extraction. If multiple articles had overlapping data, only the one article that included the most comprehensive data was included in the meta-analysis.

4.2. Data Extraction and Study Quality Assessment

Two reviewers independently extracted data, and discrepancies were resolved by discussions until consensus was reached. The following information was extracted: first author’s name, publication year, country, number of patients, percentage of males, mean age and baseline body weight, intervention, and study duration.
Two researchers independently assessed the selected articles according to the revised Cochrane risk-of-bias tool for randomized trials (RoB 2.0) [45] with the following five domains: (1) randomization process, (2) deviations from intended interventions, (3) missing outcome data, (4) measurement of the outcome, and (5) selection of the reported result. Articles were rated as “high”, “low”, or “some concerns” in terms of each of these domains. Any disagreement was resolved through discussion between the two assessors or, when necessary, in consultation with a third investigator.

4.3. Statistical Analysis

MDs and 95% CIs were calculated to identify the effects of ephedrine-containing products on weight, blood pressure, heart rate, and lipid levels. Heterogeneity across studies was estimated by way of chi-square and I² analyses. An I² value ≥50% indicated significant heterogeneity. A fixed-effects model was used if I² was <50%, and a random-effects model was used if I² was ≥50% [46]. Both Begg’s rank correlation test and Egger’s regression test of the funnel plot were conducted to detect publication bias [47,48]. A subgroup analysis was performed with studies published after the year 2000. Statistical analyses were performed using Review Manager (version 5.3; The Cochrane Collaboration, Copenhagen, Denmark) and R Studio software (version 3.6.0; R Foundation for Statistical Computing, Vienna, Austria). A p-value <0.05 was considered statistically significant.

5. Conclusions

This systematic review and meta-analysis provides sufficient evidence concerning the weight loss and lipid-modifying effects of ephedrine-containing products, along with the possibility of increasing heart rate. Ephedrine-containing products may benefit obese or overweight individuals; however, close monitoring is crucial, particularly heart rate monitoring.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ph14111198/s1, Figure S1: Funnel plot demonstrating the association between ephedrine-containing products and weight loss (kg), Figure S2: Funnel plots demonstrating the association between ephedrine-containing products and vital sign change, Figure S3: Funnel plots demonstrating the association between ephedrine-containing products and lipid level change, Figure S4: Forest plots of subgroup analysis with studies published after the year 2000: (A) weight loss (kg); (B) systolic blood pressure (mmHg); (C) diastolic blood pressure (mmHg); (D) heart rate (beats/min).

Author Contributions

Conceptualization, H.-J.Y., H.-Y.Y., J.Y. and H.-S.G.; methodology, H.-J.Y., H.-Y.Y., J.Y. and H.-S.G.; formal analysis, H.-J.Y. and H.-Y.Y.; writing—original draft preparation, H.-J.Y. and H.-Y.Y.; writing—review and editing, J.Y. and H.-S.G.; supervision, H.-S.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Ethical review and approval were waived for this study due to the nature of the review article.

Informed Consent Statement

Patient consent was waived due to the nature of the review article.

Data Availability Statement

Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflict of interest.

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Pharmaceuticals 14 01198 g001 550
Figure 1. Article selection flow chart.
Figure 1. Article selection flow chart.
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Figure 2. Forest plot to compare weight loss (kg) between ephedrine-containing products and placebo in obese or overweight patients.
Figure 2. Forest plot to compare weight loss (kg) between ephedrine-containing products and placebo in obese or overweight patients.
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Pharmaceuticals 14 01198 g003 550
Figure 3. Forest plots to compare blood pressure and heart rate changes between ephedrine-containing products and placebo in obese or overweight patients. (A) Systolic blood pressure (mmHg); (B) diastolic blood pressure (mmHg); (C) heart rate (beats/min).
Figure 3. Forest plots to compare blood pressure and heart rate changes between ephedrine-containing products and placebo in obese or overweight patients. (A) Systolic blood pressure (mmHg); (B) diastolic blood pressure (mmHg); (C) heart rate (beats/min).
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Pharmaceuticals 14 01198 g004 550
Figure 4. Forest plots to compare lipid profile changes between ephedrine-containing products and placebo in obese or overweight patients. (A) High-density lipoprotein cholesterol (mg/dL); (B) low-density lipoprotein cholesterol (mg/dL); (C) triglycerides (mg/dL); (D) total cholesterol (mg/dL).
Figure 4. Forest plots to compare lipid profile changes between ephedrine-containing products and placebo in obese or overweight patients. (A) High-density lipoprotein cholesterol (mg/dL); (B) low-density lipoprotein cholesterol (mg/dL); (C) triglycerides (mg/dL); (D) total cholesterol (mg/dL).
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Table
Table 1. Summary of included articles.
Table 1. Summary of included articles.
StudyCountryPopulation (Male %)Age (year)Baseline Body Weight (kg)Experimental GroupDurationRisk of Bias
Astrup 1992Denmark135 (16.3)28.3 ± 7.095.1 ± 14.4Ephedrine 20 mg and caffeine 200 mg tid, ephedrine 20 mg tid24 weeksLow
Bogacka 2007USA41 (17.1)37.5 ± 7.894.1 ± 11.4Ephedrine 25 mg and caffeine 200 mg tid16 weeksSome concerns
Boozer 2001USA67 (14.9)41.1 ± 8.789.4 ± 10.3Ephedrine 24 mg and caffeine 80 mg tid8 weeksLow
Boozer 2002USA167 (18.0)45.3 ± 12.388.0 ± 14.3Ephedrine 30 mg and caffeine 64 mg tid6 monthsLow
Buemann 1994Denmark32 (0.0)N/A93.3 ± 2.9Ephedrine 20 mg and caffeine 200 mg tid8 weeksLow
Carey 2015Australia23 (100.0)22.5 ± 1.677.1 ± 2.6Day 1: ephedrine 2.5 mg/kg, day 2–28: ephedrine 1.5 mg/kg/day28 daysSome concerns
Coffey 2004USA102 (13.7)43.5 ± 10.092.8 ± 12.0Ephedrine 10 mg, caffeine 60 mg, and salicin 15 mg (N/A)12 weeksLow
Greenway 2004USA40 (17.5)46.1 ± 2.483.0 ± 2.7Ephedrine 24 mg and caffeine 60 mg tid3 monthsLow
Krieger 1990USA24 (8.3)35.4 ± 7.5N/AWeek 1–4: ephedrine 25 mg, caffeine 50 mg, and aspirin 100 mg tid, week 5–8: ephedrine 50 mg, caffeine 50 mg, and aspirin 100 mg tid8 weeksLow
Pasquali 1985Italy46 (30.4)36.3 ± 3.8N/AEphedrine 25 mg tid, ephedrine 50 mg tid3 monthsLow
N/A: not available, qd: once a day, tid: three times a day, USA: United States of America.
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Yoo, H.-J.; Yoon, H.-Y.; Yee, J.; Gwak, H.-S. Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Pharmaceuticals 2021, 14, 1198. https://doi.org/10.3390/ph14111198

AMA Style

Yoo H-J, Yoon H-Y, Yee J, Gwak H-S. Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Pharmaceuticals. 2021; 14(11):1198. https://doi.org/10.3390/ph14111198

Chicago/Turabian Style

Yoo, Hee-Jeong, Ha-Young Yoon, Jeong Yee, and Hye-Sun Gwak. 2021. "Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials" Pharmaceuticals 14, no. 11: 1198. https://doi.org/10.3390/ph14111198

APA Style

Yoo, H. -J., Yoon, H. -Y., Yee, J., & Gwak, H. -S. (2021). Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Pharmaceuticals, 14(11), 1198. https://doi.org/10.3390/ph14111198

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