# Efficacy and safety of aniseed powder for treating gastrointestinal symptoms of COVID-19: a randomized, placebo-controlled trial

**Authors:** Maryam Mosaffa-Jahromi, Hossein Molavi Vardanjani, Andrea Fuzimoto, Jennifer Hunter, Kamran Bagheri Lankarani, Mehdi Pasalar

PMC · DOI: 10.3389/fphar.2024.1331177 · Frontiers in Pharmacology · 2024-01-16

## TL;DR

This study found that aniseed powder may help reduce gastrointestinal symptoms like abdominal pain and diarrhea in patients with mild COVID-19.

## Contribution

The study is the first to evaluate aniseed powder as an add-on therapy for gastrointestinal symptoms in acute SARS-CoV-2 infection.

## Key findings

- Aniseed powder significantly improved abdominal pain, anorexia, and diarrhea in COVID-19 patients.
- Aniseed and placebo groups had similar rates of adverse events, with mild to moderate effects reported.
- The findings suggest aniseed's active compound, trans-anethole, may have multiple therapeutic effects relevant to COVID-19.

## Abstract

Background: Gastrointestinal symptoms are prevalent amongst patients with a confirmed diagnosis of COVID-19 and may be associated with an increased risk of disease severity. This trial aimed to evaluate the efficacy and safety of aniseed (Pimpinella anisum L.) powder as an add-on therapy to standard care for treating gastrointestinal symptoms experienced by adults with an acute SARS-CoV-2 infection.

Methods: The study was a randomized parallel-group double-blinded placebo-controlled add-on therapy trial. Adults with an acute SARS-CoV-2 infection who did not require hospitalization and reported at least one gastrointestinal symptom in the preceding 48 h were assigned to either the aniseed or placebo group in a 1:4 ratio. All 225 participants (45 in the aniseed group and 180 in the placebo group) were instructed to use 25 g of powdered aniseed or placebo twice daily for 2 weeks. The primary outcomes were the proportion of patients who experienced an improvement of at least one point in the symptom score after adjusting for age group, gender, and time. Backwards stepwise logistic regression was applied to calculate the risk ratios. The clinical symptoms and adverse events were assessed at the beginning, 1 week later, and at the end of the trial (week two).

Results: Participants in the aniseed group were significantly more likely to report symptom improvement for abdominal pain [adjusted risk ratio (RR):0.55; 95% confidence interval (CI): 0.46–0.72], anorexia (RR:0.62; 95% CI: 0.47–0.82), and diarrhea (RR:0.19; 95% CI: 0.12–0.30), but not nausea/vomiting (RR:0.87; 95% CI: 0.71–1.08) or bloating (RR:0.87; 95% CI: 0.72–1.05). Two participants in the aniseed group and three participants in the placebo group reported mild to moderate adverse events.

Conclusion: This study showed that 2 weeks of aniseed powder containing trans-anethole (87%–94%) may help improve abdominal pain, anorexia, and diarrhea in COVID-19 patients. The findings align with the known biological, multitargeted activity of P. anisum and trans-anethole, which includes inhibiting SARS-CoV-2 along with other anti-infective, anti-inflammatory, antioxidant, hepatoprotective, and anti-dysbiosis properties. Multicenter trials with larger sample sizes and longer follow-up are warranted to confirm these findings.

Clinical Trial Registration: Iranian Registry of Clinical Trials (IRCT20120506009651N3).

## Linked entities

- **Chemicals:** trans-anethole (PubChem CID 637563)
- **Diseases:** COVID-19 (MONDO:0100096), SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, Mcpt1 (mast cell protease 1) [NCBI Gene 17224] {aka Mcp-1}, TLR5 (toll like receptor 5) [NCBI Gene 7100] {aka MELIOS, SLE1, SLEB1, TIL3}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, LBP (lipopolysaccharide binding protein) [NCBI Gene 3929] {aka BPIFD2}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, Ccl3 (C-C motif chemokine ligand 3) [NCBI Gene 20302] {aka G0S19-1, LD78alpha, MIP-1alpha, MIP1-(a), MIP1-alpha, Mip1a}, CSF1 (colony stimulating factor 1) [NCBI Gene 1435] {aka CSF-1, MCSF, PG-M-CSF}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, ORF1ab (ORF1a polyprotein;ORF1ab polyprotein) [NCBI Gene 43740578], Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, Il1 (interleukin 1 complex) [NCBI Gene 111343] {aka Il-1}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, CCL3 (C-C motif chemokine ligand 3) [NCBI Gene 6348] {aka G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** congestion (MESH:D002311), abdominal pain (MESH:D015746), lung involvement (MESH:D008171), fever (MESH:D005334), bronchitis (MESH:D001991), hypoxia (MESH:D000860), inflammatory bowel disease (MESH:D015212), pulmonary involvement (MESH:C566343), infected (MESH:D007239), barrier dysfunction (MESH:C536830), GI (MESH:D005767), Diarrhea (MESH:D003967), hepatic steatosis (MESH:D005234), thyroid disease (MESH:D013959), PM (MESH:D018923), cholestasis (MESH:D002779), gastrointestinal bleeding (MESH:D006471), throat itching (MESH:D011537), hyperlipidemia (MESH:D006949), allergy (MESH:D004342), ischemia (MESH:D007511), high blood pressure (MESH:D006973), hiatus hernia (MESH:D006551), death (MESH:D003643), small (MESH:D018288), melena (MESH:D008551), venous thrombosis (MESH:D020246), respiratory tract infections (MESH:D012141), nausea and vomiting (MESH:D020250), flatulence (MESH:D005414), kidney failure (MESH:D051437), long COVID-19 (MESH:D000094024), indigestion (MESH:D004415), sinusoidal dilation (MESH:D006504), cough (MESH:D003371), inflammation (MESH:D007249), intestine necrosis (MESH:D007410), herpes virus (MESH:D020031), pain (MESH:D010146), abdominal cramp (MESH:D003085), infectious disease (MESH:D003141), peptic ulcer (MESH:D010437), Anorexia (MESH:D000855), reduced appetite (MESH:D001068), dysbiosis (MESH:D064806), bloating (MESH:C535647), nausea (MESH:D009325), glutathione deficiency (MESH:C536835), myalgia (MESH:D063806), liver failure (MESH:D017093), congestive heart failure (MESH:D006333), vomiting (MESH:D014839), COVID-19 (MESH:D000086382), necrosis (MESH:D009336), long-term infection (MESH:D000088562), lung inflammation (MESH:D011014), respiratory problems (MESH:D012818), viral infection (MESH:D014777), irritable bowel syndrome (MESH:D043183), asthma (MESH:D001249)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Human alphaherpesvirus 2 (no rank) [taxon 10310], Myrrhis odorata (anise, species) [taxon 40880], Pimpinella anisum (species) [taxon 271192], Pimpinella (genus) [taxon 40958], Escherichia coli (E. coli, species) [taxon 562], Illicium verum (Chinese star-anise, species) [taxon 124778], Measles morbillivirus (no rank) [taxon 11234], Salmonella (genus) [taxon 590], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Cytomegalovirus (genus) [taxon 10358], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

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## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC10824915/full.md

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Source: https://tomesphere.com/paper/PMC10824915