Diabetes Mellitus, Type 2, Interaction, Adverse Herb-Drug
Conditions
Keywords
pharmacokinetics, natural product-drug interactions, transporters
Brief summary
Supplements containing goldenseal, a perennial herb native to North America, have consistently ranked among the top 20 highest selling natural products throughout the last decade. Goldenseal products are marketed as licensed natural health products in Canada and as dietary supplements in the United States. Natural products made from dried roots of the goldenseal plant are purported to have therapeutic value and are used to self-treat a range of medical complications, including the common cold, allergic rhinitis, and digestive disorders, such as diarrhea and constipation. Based on a previous clinical study, goldenseal have been shown to precipitate pharmacokinetic interactions with metformin in healthy volunteers. This follow-up study aims to evaluate the goldenseal-metformin interaction in type 2 diabetic patients. Results from this proposed clinical study will (1) characterize the pharmacokinetic interaction between the botanical dietary supplement goldenseal and anti-diabetic drug metformin, (2) provide evidence-based recommendations to mitigate drug interaction risks, and (3) contribute to the development of a comprehensive strategy for effectively assessing other potential natural-product drug interactions.
Detailed description
Many patient groups, including those afflicted with cardiovascular disease, cancer, HIV/AIDS, hepatitis C, and diabetes, often supplement their prescribed pharmacotherapeutic regimens with herbal and other natural products, raising concern for adverse interactions. Unlike for drug-drug interactions, rigorous, harmonized guidelines for assessing the risk of natural product-drug interactions do not exist. The NCCIH-funded Center of Excellence for Natural Product Drug Interaction (NaPDI) Research was established in September 2015. The mission of the NaPDI Center is to provide leadership in the identification, evaluation, and dissemination of potential clinically meaningful pharmacokinetic natural product-drug interactions. Goldenseal is one of four high priority natural products selected by the NaPDI Center for further evaluation for drug interaction potential. A recent clinical study completed by researchers at the NaPDI center showed that a well-characterized, adulterant- and contaminant-free goldenseal product administered to 16 healthy volunteers (3 g daily by mouth for 6 consecutive days) resulted in a significant decrease (23%) in metformin systemic exposure \[area under the plasma concentration-time curve (AUC)\] with no change in half-life or renal clearance. Based on these clinical observations, along with complementary in vitro data, the current working hypothesis is that goldenseal interacts with intestinal organic cation transporter 1 to alter metformin disposition. These observations may have clinical implications for diabetic patients, as metformin is the first-line treatment and most prescribed anti-diabetic medication for type 2 diabetes. The objective of this study is to assess the potential for goldenseal to alter the pharmacokinetics and clinical effects of standard metformin treatment in well-controlled adult type 2 diabetic patients. Transporter inhibition represents an understudied mechanism of natural product-drug interactions. The proposed clinical study will be the first of its kind to evaluate whether such pharmacokinetic interactions can potentially affect clinical outcomes. The knowledge gained from these efforts will ultimately build upon a systematic framework for effectively studying other transporter-mediated natural product-drug interactions.
Interventions
0.5 mL of an intravenous solution (1 mg/mL) will be administered.
Goldenseal (Solaray; Lot #1020199) is supplied as dried root powder in vegetable capsules, each containing 550 mg of herbal content. Goldenseal capsules will be administered with 240 mL of water.
Sponsors
Study design
Eligibility
Inclusion criteria
* are 18-65 years old and healthy * have been medically diagnosed with Type 2 diabetes and currently taking metformin (1- 2 g daily), but otherwise healthy as determined by the study physician * have an HbA1c \< 8% as determined by laboratory analysis on initial screening * are not taking any medications, dietary/herbal supplements, or citrus juices that can interfere with your ability to eliminate the study drugs and goldenseal from your body * are willing to stop consuming alcohol, caffeinated beverages or other caffeine- containing products the evening before and the morning of the first day of each study arm * are female and are willing to use an acceptable method of birth control that does not include oral birth control pills or patches (such as abstinence, copper IUD, condom) * can provide written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for the subject to comply with the requirements of the study
Exclusion criteria
* have an HbA1c ≥ 8% * have other chronic illnesses other than type 2 diabetes (e.g., type 1 diabetes, kidney disease, hepatic disease, uncontrolled hypertension, coronary artery disease, chronic obstructive pulmonary disease, cancer, or HIV/AIDS) * have a hematologic (blood) disorder * have a history of drug or alcohol abuse * have any major psychiatric illness * are pregnant or breastfeeding * have a history of intolerance or allergy to midazolam or goldenseal products * are taking concomitant medications, both prescription and non-prescription (including dietary supplements/herbal products) known to alter the pharmacokinetics of either study drug or goldenseal constituents
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Metformin AUC | Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration. | Area under the plasma concentration time curve of metformin |
| Metformin Cmax | Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration. | maximum concentration of metformin |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Midazolam AUC | Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration. | area under the concentration vs. time curve of midazolam |
| Metformin Half-Life | 0-24h | half-life of metformin |
| Metformin Renal Clearance | 0-24h | renal clearance of metformin |
Countries
United States
Participant flow
Pre-assignment details
A washout period of ≥7 days between each arm was implemented in the study design.
Participants by arm
| Arm | Count |
|---|---|
| Midazolam Alone - Washout - Midazolam + Acute Goldenseal - Washout - Midazolam + Chronic Goldenseal Twenty-two adults (12 males, 10 females) with type 2 diabetes participated in this three-arm, crossover study to assess a pharmacokinetic natural product-drug interaction. In arm 1 (midazolam alone), participants were administered a single dose of midazolam (0.5 mg) intravenously via a peripherally inserted catheter; at this time, participants were instructed to co-administer their entire daily dose of metformin orally. For Arm 2 (midazolam + acute goldenseal exposure), the same 22 participants were administered a single dose of goldenseal (3.3 g) orally 30 minutes prior to administration of midazolam and metformin. For Arm 3 (chronic goldenseal exposure), participants self-administered goldenseal (1.1 g) orally three times daily for 27 days. On the 28th day, participants were administered the goldenseal three times daily, as well as the single dose of midazolam and metformin. Plasma and urine were collected from 0-24 hours post-midazolam administration for all 3 arms of the study. A washout period of 7 days separated each arm to ensure appropriate washout of midazolam. Participants continued their routine administration of metformin as prescribed throughout the duration of the study without interruption in pharmacotherapy.
Midazolam HCl 1mg/mL inj: 0.5 mL of intravenous solution
Goldenseal (Hydrastis canadensis) 550 mg capsules: dried root powder in vegetable capsules (Solaray; Lot #1020199) | 22 |
| Total | 22 |
Baseline characteristics
| Characteristic | Midazolam Alone - Washout - Midazolam + Acute Goldenseal - Washout - Midazolam + Chronic Goldenseal |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 0 Participants |
| Age, Categorical Between 18 and 65 years | 22 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 2 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 17 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 3 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 1 Participants |
| Race (NIH/OMB) Asian | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 1 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 20 Participants |
| Sex: Female, Male Female | 10 Participants |
| Sex: Female, Male Male | 12 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 22 | 0 / 22 | 0 / 22 |
| other Total, other adverse events | 9 / 22 | 4 / 22 | 2 / 22 |
| serious Total, serious adverse events | 0 / 22 | 0 / 22 | 0 / 22 |
Outcome results
Metformin AUC
Area under the plasma concentration time curve of metformin
Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.
Population: All 22 participants completed the 3 arms of the study (baseline, acute goldenseal exposure, and chronic goldenseal exposure).
| Arm | Measure | Value (GEOMETRIC_MEAN) |
|---|---|---|
| Study Arm 1: Baseline | Metformin AUC | 59.6 mcg*hr/mL |
| Study Arm 2: Acute Goldenseal Exposure | Metformin AUC | 54.5 mcg*hr/mL |
| Study Arm 3: Chronic Goldenseal Exposure | Metformin AUC | 57.3 mcg*hr/mL |
Metformin Cmax
maximum concentration of metformin
Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.
| Arm | Measure | Value (GEOMETRIC_MEAN) |
|---|---|---|
| Study Arm 1: Baseline | Metformin Cmax | 8.92 nM |
| Study Arm 2: Acute Goldenseal Exposure | Metformin Cmax | 8.36 nM |
| Study Arm 3: Chronic Goldenseal Exposure | Metformin Cmax | 8.26 nM |
Metformin Half-Life
half-life of metformin
Time frame: 0-24h
| Arm | Measure | Value (GEOMETRIC_MEAN) |
|---|---|---|
| Study Arm 1: Baseline | Metformin Half-Life | 4.73 hours |
| Study Arm 2: Acute Goldenseal Exposure | Metformin Half-Life | 4.70 hours |
| Study Arm 3: Chronic Goldenseal Exposure | Metformin Half-Life | 4.79 hours |
Metformin Renal Clearance
renal clearance of metformin
Time frame: 0-24h
| Arm | Measure | Value (GEOMETRIC_MEAN) |
|---|---|---|
| Study Arm 1: Baseline | Metformin Renal Clearance | 259 mL / min |
| Study Arm 2: Acute Goldenseal Exposure | Metformin Renal Clearance | 249 mL / min |
| Study Arm 3: Chronic Goldenseal Exposure | Metformin Renal Clearance | 250 mL / min |
Midazolam AUC
area under the concentration vs. time curve of midazolam
Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.
| Arm | Measure | Value (GEOMETRIC_MEAN) |
|---|---|---|
| Study Arm 1: Baseline | Midazolam AUC | 31.9 mcg*hr/mL |
| Study Arm 2: Acute Goldenseal Exposure | Midazolam AUC | 31.1 mcg*hr/mL |
| Study Arm 3: Chronic Goldenseal Exposure | Midazolam AUC | 29.7 mcg*hr/mL |