logo
Can Turmeric Help You Lose Weight?

Can Turmeric Help You Lose Weight?

Health Line21 hours ago

Turmeric is a widely used spice with several potential health benefits. While it is thought to help with weight loss, further research in humans is needed to verify this.
Turmeric, also known as the golden spice, is popular in Asian cuisine and has been a part of traditional Indian medicine — or Ayurveda — for thousands of years.
Most of turmeric's health properties can be attributed to curcumin, a compound that has strong antioxidant and anti-inflammatory properties.
Recent studies indicate that turmeric may play a role in weight loss.
Learn more about whether turmeric could help with weight loss and how much you would have to take to see results.
Turmeric and weight loss
Recent research has examined turmeric's role in weight loss.
In fact, a 2023 review suggests that curcumin may suppress particular inflammatory markers that play a role in obesity. These markers are typically elevated in people with excess weight or obesity.
A 2022 review noted that curcumin is a promising natural compound that may help with weight loss; however, more studies are needed before turmeric can be recommended as a weight management or preventive measure.
Turmeric safety and adverse effects
In general, turmeric and curcumin are considered safe.
The World Health Organization (WHO) suggests a range of 0-3 mg per kilogram of body weight as a safe daily intake.
Nonetheless, some people who take large doses of this compound may experience adverse effects, such as:
allergic reactions
nausea
vomiting
stomach pain
constipation
skin rash
diarrhea
Also, those with the following conditions should avoid turmeric supplements:
Bleeding disorders. Turmeric may hinder blood clotting, which may cause issues in people with bleeding disorders.
Iron deficiency. Turmeric may hinder iron absorption.
Kidney stones. This spice is high in oxalates, which are compounds that may bind to calcium and contribute to kidney stone formation.
Note that there's insufficient evidence regarding the safety of these supplements among pregnant or breastfeeding people. Therefore, it's recommended that they avoid them.
Moreover, some turmeric products may contain filler ingredients not revealed on the label, so it's best to choose a supplement that has been certified by a third party, such as NSF International or Informed Choice.
A healthcare professional can help determine whether turmeric or curcumin supplements are right for you.
How to use turmeric
Turmeric comes in several forms, though the easiest way to use it is as a cooking spice.
It's also enjoyed in beverages like turmeric ginger tea and golden milk, which is made by heating milk, turmeric, ginger, black pepper, and cinnamon powder.
In Indian cuisine, turmeric is commonly consumed in tea with black pepper and other ingredients like honey, ginger, olive oil, and coconut oil.
That said, most human studies suggest that health benefits are only seen at higher doses, such as those found in turmeric extracts or curcumin supplements.
That's because turmeric contains a very small amount of curcumin, whereas extracts pack a bigger punch of curcumin.
You may want to choose a supplement that includes black pepper, as its compounds significantly improve curcumin absorption.
Although there are no official dosage guidelines for these supplements, recent research suggests that 400–600 mg of a standard curcumin powder can be taken up to three times a day to see potential benefits.
However, you should avoid taking high doses of turmeric for longer than three months at a time, as long-term safety research is unavailable.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Spinach, strawberries top new ‘Dirty Dozen' list of pesticide-laden produce
Spinach, strawberries top new ‘Dirty Dozen' list of pesticide-laden produce

CNN

timean hour ago

  • CNN

Spinach, strawberries top new ‘Dirty Dozen' list of pesticide-laden produce

Agriculture Sustainability Food & health EconomyFacebookTweetLink Follow More than 90% of samples of a dozen fruits and vegetables tested positive for potentially harmful pesticide residues, according to the 2025 Shopper's Guide to Pesticides in Produce. Dubbed the 'Dirty Dozen,' the list is compiled from the latest government testing data on nonorganic produce by the Environmental Working Group, or EWG, a health advocacy organization that has produced the annual report since 2004. Spinach topped the list, with more pesticide residue by weight than any other produce tested, followed by strawberries, kale (along with mustard greens and collards), grapes, peaches, cherries, nectarines, pears, apples, blackberries, blueberries and potatoes. The annual report is not meant to discourage consumers from eating fruits and vegetables, which are key to good health, but instead to provide tools for decisions on whether to buy organic for the fruits or vegetables their families consume the most, said Alexis Temkin, EWG's vice president of science. 'The guide is there to help consumers eat a lot of fruits and vegetables while trying to reduce pesticide exposure,' Temkin said. 'One of the things that a lot of peer-reviewed studies have shown over and over again (is) that when people switch to an organic diet from a conventional diet, you can really see measurable levels in the reduction of pesticide levels in the urine.' The Alliance for Food and Farming, which represents organic and conventional produce farmers, has been a long-standing critic of the annual report. 'We strongly support consumer choice when shopping for fruits and vegetables. But this choice should not be influenced by this list,' Teresa Thorne, the alliance's executive director, said in an email. 'Instead consumers should be reassured by decades of toxicology studies, government data and nutrition research which underscores the importance of a diet rich in fruits and vegetables on health and the safety of both organic and conventionally grown produce,' Thorne added. Blackberries were new to the list, having never been tested before by the US Department of Agriculture, while potatoes joined the rankings after being absent in recent years — mainly due to the use of a plant growth regulator called chlorpropham. The chemical has been banned in the European Union, Temkin said. 'It's applied after harvest to essentially prevent potatoes from sprouting while they're in storage or in transit,' Temkin said. 'Because it's applied so late after harvest and so close to when consumers might be exposed or eating potatoes, that's partially what leads to some of these really high concentrations.' More than 50 different pesticides were detected on each of several crops on the Dirty Dozen section of the Shopper's Guide, which was updated this year to measure pesticide toxicity, Temkin said. 'We still have measurements of the detection frequency of pesticides, how many different pesticides are found on produce, as well as the overall concentration. We also have an indicator of that concentration relative to a dose that might cause harm in an animal study,' she said. 'A lot of the Dirty Dozen produce rank really highly when you look at pesticide toxicity, especially relative to the 'Clean Fifteen' items, which have fewer detections of pesticide residues,' Temkin added. As part of the report, EWG also creates an annual 'Clean Fifteen' — a list of conventional produce with the least amount of pesticide residue. Many of these fruits and vegetables are protected by skins you peel before eating — but not all. Pineapple was the least contaminated produce tested, followed by sweet corn (fresh and frozen), avocados, papaya, onions, frozen sweet peas, asparagus, cabbage, watermelon, cauliflower, bananas, mangos, carrots, mushrooms and kiwi. 'An important aspect of the USDA pesticide testing is they really try to mimic consumer behavior. … They wash fruits or vegetables for about 15 or 20 seconds under running water, and then they also peel something like citrus or a mango or a banana,' Temkin said. 'If there are any pesticides on that outer layer, that is removed, and that might be one of the reasons why some of these fruits or vegetables that are on the Clean Fifteen tend to have less detectable pesticide residues.' More tips: All produce, even organic, should be washed before peeling so dirt and bacteria aren't transferred from a knife onto the fruit or vegetable, according to the US Food and Drug Administration. After washing, dry with a clean cloth or paper towel. Firm produce such as carrots, cucumbers, melons and potatoes can be scrubbed with a clean vegetable brush under running water, the FDA said. All other produce can be gently rubbed while being rinsed. There's no need to use bleach, soap or a produce wash — fruits and vegetables are porous and can absorb the chemicals. Remove the outermost leaves of cabbage, lettuce and other leafy greens and rinse each leaf carefully — but don't blast your greens with water, or you'll bruise them. Experts said it's best to use low-pressure water that is warmer than your produce and a colander to spin the greens dry. Don't forget to wash the colander afterward. Exceptions are 'triple-washed' bagged greens, which the FDA said do not need an additional wash. Pesticides have been linked in studies to premature births, congenital malformations such as neural tube defects, spontaneous abortions and an increase in genetic damage in humans. Exposure to pesticides has also been associated with lower sperm concentrations, heart disease, cancer and other disorders. Farmworkers who use or are exposed to pesticides are at highest risk, according to studies. A 2022 meta-analysis found workers exposed to pesticides were nearly five times as likely to have DNA damage, while a February 2024 study concluded children exposed at an early age showed poorer neurodevelopment from infancy to adolescence. Children are the most suspectable to the dangers of pesticides due to their small size and developing body and brain, experts say. The risk can actually begin in the womb. 'Pesticide exposure during pregnancy may lead to an increased risk of birth defects, low birth weight, and fetal death,' according to the American Academy of Pediatrics. 'Exposure in childhood has been linked to attention and learning problems, as well as cancer.'

From September, Singapore mandates measles shots for helpers in homes with unvaccinated kids
From September, Singapore mandates measles shots for helpers in homes with unvaccinated kids

Yahoo

time2 hours ago

  • Yahoo

From September, Singapore mandates measles shots for helpers in homes with unvaccinated kids

SINGAPORE, June 11 — From September 1, all domestic helpers in Singapore working in homes with children under the age of seven who are not fully vaccinated against measles must themselves be immunised, the country's Ministry of Manpower (MOM) announced yesterday. The move is aimed at safeguarding 'unvaccinated young children who are at higher risk of serious health complications from measles infections', said MOM, as reported by Channel News Asia (CNA). Singapore has already recorded 10 measles infections in 2025 as of the week ending May 10, just one shy of the total 11 cases reported in all of 2024, according to the Ministry of Health. Employers applying for or renewing work permits for migrant domestic workers (MDWs) must now declare: Whether the domestic helper is already vaccinated or immune to measles Whether all children under seven in the household are fully vaccinated If unvaccinated, whether a vaccination appointment has been booked Domestic helpers may be exempted if they are already immune — either through previous infection or past vaccination — or if all children under seven in the home have been fully immunised. Proof of immunity, such as vaccination records or serology test results, may be required. Employers are advised to check their domestic helper's immunity status well before permit renewal. Households with immunocompromised members are also strongly encouraged to verify their helper's measles immunity or arrange for vaccination. To meet the requirement, domestic helpers must receive two doses of the MMR (measles, mumps, and rubella) vaccine, spaced at least 28 days apart. The vaccine is available at private GP clinics, with the cost to be paid by employers. MOM also warned against false declarations. 'If employers with children below seven years old are found with MDWs who are not immune against measles, their work pass privileges may be suspended until vaccination proof is submitted,' the ministry said. Random checks and documentary audits will be conducted to ensure compliance. While Singapore maintains high overall vaccination rates — over 95 per cent for the first MMR dose and 90 per cent for the second among resident two-year-olds — sporadic cases are expected, MOM said, citing the 'highly transmissible nature of the disease'. The Communicable Diseases Agency (CDA) stressed that despite strong local immunity, 'the surge in measles cases globally and regionally continues to pose public health risks, particularly for those without measles immunity'. Measles, which spreads through airborne droplets, has been part of Singapore's compulsory childhood immunisation schedule since 1985.

Kelun-Biotech Announces Breakthrough Therapy Designation Granted for Sacituzumab Tirumotecan (Sac-TMT) in Combination With Tagitanlimab in China for Certain Types of Non-Small Cell Lung Cancer
Kelun-Biotech Announces Breakthrough Therapy Designation Granted for Sacituzumab Tirumotecan (Sac-TMT) in Combination With Tagitanlimab in China for Certain Types of Non-Small Cell Lung Cancer

Yahoo

time2 hours ago

  • Yahoo

Kelun-Biotech Announces Breakthrough Therapy Designation Granted for Sacituzumab Tirumotecan (Sac-TMT) in Combination With Tagitanlimab in China for Certain Types of Non-Small Cell Lung Cancer

CHENGDU, China, June 10, 2025 /PRNewswire/ -- Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. (the "Company") today announced that its TROP2-directed antibody-drug conjugate (ADC) sacituzumab tirumotecan (sac-TMT) (佳泰莱®) in combination with the PD-L1 monoclonal antibody tagitanlimab (科泰莱®) was granted Breakthrough Therapy Designation by the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of China for the first-line treatment of locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) without actionable genomic alterations. Breakthrough Therapy Designation is granted for treatment options that demonstrate significant clinical advantages over currently available treatments and is aimed at expediting the research, development and marketing of innovative treatment options that address clinically urgent medical needs. This designation is based on the efficacy and safety data from the non-squamous cohort of the Phase II OptiTROP-Lung01 study. This marks the fifth Breakthrough Therapy Designation granted to sac-TMT by the NMPA. Sac-TMT has previously received this designation for: Locally advanced or metastatic triple-negative breast cancer (TNBC) in July 2022; EGFR-mutant, locally advanced or metastatic NSCLC after progression on EGFR-TKI therapy in January 2023; Locally advanced or metastatic hormone-receptor positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-) breast cancer (BC) in patients who have previously received at least two lines of systemic chemotherapy in June 2023; First-line treatment of unresectable locally advanced, recurrent or metastatic PD-L1 negative TNBC in March 2024. Results from a Phase 2 OptiTROP-Lung01 study of sac-TMT in combination with tagitanlimab in first-line advanced or metastatic non-squamous NSCLC patients were presented in a poster session at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting[1]. Dr. Michael Ge, CEO of Kelun-Biotech said, "This designation by the NMPA highlights the importance of developing novel therapeutic options for diverse NSCLC subtypes. Sac-TMT in combination with tagitanlimab demonstrated clinically meaningful outcomes in key endpoints for patients with non-squamous NSCLC without actionable genomic alterations as a first-line treatment. We are excited about the therapeutic potential of TROP2 ADC- immunotherapy combinations, and we look forward to working with regulatory authorities in China to bring this combination therapy to patients in need as soon as possible." [1] Abstract #8529: Lung Cancer – Non-Small Cell Metastatic, ASCO Annual Meeting, 2025 About sac-TMT (佳泰莱®)Sac-TMT, a core product of the Company, is a novel human TROP2 ADC in which the Company has proprietary intellectual property rights, targeting advanced solid tumors such as NSCLC, BC, gastric cancer (GC), gynecological tumors, among others. Sac-TMT is developed with a novel linker to conjugate the payload, a belotecan-derivative topoisomerase I inhibitor with a drug-to-antibody-ratio (DAR) of 7.4. Sac-TMT specifically recognizes TROP2 on the surface of tumor cells by recombinant anti-TROP2 humanized monoclonal antibodies, which is then endocytosed by tumor cells and releases KL610023 intracellularly. KL610023, as a topoisomerase I inhibitor, induces DNA damage to tumor cells, which in turn leads to cell-cycle arrest and apoptosis. In addition, it also releases KL610023 in the tumor microenvironment. Given that KL610023 is membrane permeable, it can enable a bystander effect, or in other words kill adjacent tumor cells. In May 2022, the Company licensed the exclusive rights to MSD (the tradename of Merck & Co., Inc., Rahway, NJ, USA) to develop, use, manufacture and commercialize sac-TMT in all territories outside of Greater China (includes Mainland China, Hong Kong, Macao, and Taiwan). To date, two indications for sac-TMT have been approved and marketed in China for the treatment of adult patients with unresectable locally advanced or metastatic TNBC who have received at least two prior systemic therapies (at least one of them for advanced or metastatic setting) and EGFR mutation-positive locally advanced or metastatic non-squamous NSCLC following progression on EGFR-TKI therapy and platinum-based chemotherapy. Sac-TMT became the first domestic ADC with global intellectual property rights to be fully approved for marketing. It is also the world's first TROP2 ADC to be approved for marketing in a lung cancer indication. In addition, two new indication applications for sac-TMT for the treatment of adult patients with EGFR-mutant locally advanced or metastatic NSCLC who progressed after treatment with EGFR-TKI therapy and with unresectable locally advanced, metastatic HR+/HER2- BC who have received prior endocrine therapy and other systemic treatments in the advanced or metastatic setting were accepted by the CDE, and were included in the priority review and approval process. As of today, the Company has initiated 8 registrational clinical studies in China. MSD has initiated 14 ongoing Phase 3 global clinical studies of sac-TMT as a monotherapy or with pembrolizumab2 or other agents for several types of cancer. These studies are sponsored and led by MSD. About Tagitanlimab (科泰莱®)Tagitanlimab is the first PD-L1 mAb globally to receive authorization for the first-line treatment of NPC. Previously, the NMPA has approved the marketing in China of tagitanlimab used in combination with cisplatin and gemcitabine for the first-line treatment of patients with R/M NPC and monotherapy for the treatment of patients with recurrent or metastatic NPC who have failed after prior 2L+ chemotherapy, respectively. About Kelun-BiotechKelun-Biotech ( is a holding subsidiary of Kelun Pharmaceutical ( which focuses on the R&D, manufacturing, commercialization and global collaboration of innovative biological drugs and small molecule drugs. The company focuses on major disease areas such as solid tumors, autoimmune, inflammatory, and metabolic diseases, and in establishing a globalized drug development and industrialization platform to address the unmet medical needs in China and the rest of world. The Company is committed to becoming a leading global enterprise in the field of innovative drugs. At present, the Company has more than 30 ongoing key innovative drug projects, of which 3 projects have been approved for marketing, 1 project is in the NDA stage, and more than 10 projects are in the clinical stage. The company has established one of the world's leading proprietary ADC platforms, OptiDC™, and has 1 ADC project approved for marketing, 1 ADC project in NDA stage, and multiple ADC and novel DC assets in clinical or preclinical research stage. For more information, please visit Media: klbio_pr@ View original content to download multimedia: SOURCE Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store