Does rooibos tea improve cholesterol and blood sugar?
Rooibos tea may improve cholesterol (one 40-person trial, six cups daily), but blood sugar, bone and allergy claims rest on lab and animal studies.
Rooibos (pronounced "ROY-boss") is a herbal tea made from the leaves of Aspalathus linearis, a shrub that grows only in the Cederberg region of South Africa. It is naturally caffeine-free, low in tannins, and has a mild, slightly sweet flavor that works well on its own or with milk.
If you are looking for an alternative to regular tea or coffee -- especially in the evening -- rooibos is an excellent option. It will not interfere with sleep, it does not have the bitter edge that tannin-heavy teas can have, and it brings some unique antioxidants not found in any other food.
For people who need to avoid caffeine entirely (during pregnancy, with certain medications, or by preference), rooibos is one of the most satisfying substitutes available.
What you can do
- Drink rooibos in the evening as a caffeine-free swap for tea or coffee; it is low in tannins and mild on the stomach1.
- If you try it for cholesterol, the study used six cups a day for six weeks4.
- Choose unfermented 'green' rooibos for more aspalathin; fermented red rooibos still has meaningful bioactive compounds2.
Be careful if
Go deeper
How it works What it does in your body, in plain words 2 min
What makes rooibos scientifically interesting is aspalathin, a dihydrochalcone found exclusively in the Aspalathus linearis plant1. No other commercially available food or drink contains this compound. Aspalathin is a potent antioxidant, but its health relevance goes beyond simple free-radical scavenging.
Research has focused on aspalathin's effects on glucose metabolism and insulin sensitivity. In cell and animal studies, aspalathin has been shown to stimulate glucose uptake in muscle cells and improve insulin secretion from pancreatic beta cells3. These findings have generated interest in rooibos as a supportive dietary choice for people managing blood sugar.
Rooibos also contains nothofagin, orientin, isoorientin, vitexin, and isovitexin -- a flavonoid profile distinct from Camellia sinensis teas2.
Low Tannin Advantage
Traditional black and green teas contain significant tannins, which can inhibit iron absorption and cause stomach discomfort in sensitive individuals. Rooibos is notably low in tannins, making it gentler on the stomach and less likely to interfere with mineral absorption1. This makes it a practical choice for people with iron deficiency or those who drink several cups per day.
Cardiovascular and Metabolic Research
A human intervention study by Marnewick et al. (2011) found that six weeks of rooibos consumption (six cups per day) in adults at risk for cardiovascular disease significantly improved lipid profiles -- LDL cholesterol and triglycerides decreased while HDL cholesterol increased4. The study also showed reduced markers of oxidative stress and lipid peroxidation.
Bone Health and Allergy Relief
Preliminary research suggests that rooibos flavonoids may support bone metabolism. In vitro studies have shown that orientin and luteolin (both present in rooibos) can promote osteoblast activity and inhibit osteoclast formation1. These findings are early-stage but suggest potential relevance for bone health, particularly in postmenopausal populations.
Rooibos has also been traditionally used in South Africa as a remedy for allergies and skin conditions. Some evidence supports an antihistamine-like effect of its flavonoids, though rigorous clinical trials are lacking2.
The evidence The studies, what they found, and how much to trust them 2 min · 4 sources
Aspalathin and Metabolic Health
Johnson et al. (2018) provided a comprehensive review of aspalathin's therapeutic potential for metabolic syndrome3. The compound has demonstrated multiple relevant mechanisms in preclinical models:
- Glucose uptake: Aspalathin increases glucose uptake in muscle cells via AMPK activation, independent of insulin signaling.
- Insulin secretion: It enhances glucose-stimulated insulin secretion from pancreatic beta cells.
- Lipid metabolism: Aspalathin suppresses hepatic lipogenesis and reduces triglyceride accumulation.
- Anti-inflammatory: It attenuates NF-kB-mediated inflammation in adipose tissue.
These effects have been demonstrated primarily in cell culture and rodent models. While the mechanistic evidence is robust, human clinical trials specifically testing aspalathin supplementation are still limited. The metabolic effects observed with whole rooibos tea consumption4 may be attributable to aspalathin working synergistically with other rooibos flavonoids.
Cardiovascular Evidence
The Marnewick et al. (2011) trial is the most cited human study on rooibos4. Forty adults at risk for heart disease consumed six cups of rooibos daily for six weeks in a controlled study. Key findings:
- LDL cholesterol decreased significantly (p < 0.001)
- Triglycerides decreased significantly
- HDL cholesterol increased significantly
- Plasma conjugated dienes (a marker of lipid peroxidation) decreased
- Glutathione (an endogenous antioxidant) levels improved
The effect sizes were clinically meaningful, comparable to moderate dietary interventions. However, six cups per day represents high consumption, and whether lower doses produce proportional benefits is unknown.
Bioavailability Considerations
Joubert and de Beer (2011) addressed the critical question of whether rooibos compounds are bioavailable when consumed as tea1,2. Aspalathin is absorbed in the gut and detectable in plasma, but its bioavailability is relatively low. However, metabolites of aspalathin may retain biological activity, and the consistent results from whole-tea studies suggest that sufficient quantities reach target tissues at typical consumption levels.
Notably, unfermented ("green") rooibos retains significantly more aspalathin than the traditional fermented ("red") rooibos. The fermentation process oxidizes much of the aspalathin. For those seeking maximum antioxidant benefit, green rooibos is the better choice, though fermented rooibos still contains meaningful amounts of bioactive compounds2.
Limitations
The evidence base for rooibos health effects is smaller than for green or black tea. Most mechanistic work comes from a concentrated group of South African research institutions, and independent replication would strengthen the findings. Human trials are few and generally small. The bone health and allergy claims rest on preclinical evidence and traditional use rather than clinical data.
Rooibos is considered very safe. No significant adverse effects have been reported in clinical studies or from its long history of consumption in South Africa. Rare case reports of hepatotoxicity exist but have not established causation, and the overall safety profile is reassuring1.
More on Tea
- Is drinking tea good for your health? 4 min Why tea is one of the most studied beverages in the world, and what makes it good for you.
- Is loose leaf tea healthier than tea bags? 5 min Why loose leaf tea is the better choice for health, quality, and avoiding microplastics.
- Does drinking green tea protect your heart? 7 min EGCG, catechins, and what the science says about green tea and heart health, metabolism, and cancer
Sources
- A review of the bioactivity of South African herbal teas: rooibos (Aspalathus linearis) and honeybush (Cyclopia intermedia). McKay DL, Blumberg JB. Phytotherapy Research, 2007. PubMed 16927447
- Rooibos (Aspalathus linearis) beyond the farm gate: From herbal tea to potential phytopharmaceutical. Joubert E, de Beer D. South African Journal of Botany, 2011. Source
- Aspalathin from Rooibos (Aspalathus linearis): A Bioactive C-glucosyl Dihydrochalcone with Potential to Target the Metabolic Syndrome. Johnson R, de Beer D, Dludla PV, Ferreira D, Muller CJF, Joubert E. Planta Medica, 2018. PubMed 29388183
- Effects of rooibos (Aspalathus linearis) on oxidative stress and biochemical parameters in adults at risk for cardiovascular disease. Marnewick JL, Rautenbach F, Venter I, Neethling H, Blackhurst DM, Wolmarans P, Macharia M. Journal of Ethnopharmacology, 2011. PubMed 20833235