Sleep Disorders Health Center
Work the Night Shift? Beware Diabetes
March 3, 2009 -- By pitting the time clock against the body's internal clock, night-shift work may cause diabetes and obesity.
The 8.6 million Americans who work the night shift are at increased risk of obesity, diabetes, and heart disease. Why?
A new study shows that much of the body's biological clock -- its circadian rhythm -- keeps day-shift time even when a person goes on the night shift.
Harvard/Brigham and Women's Hospital researcher Frank A.J.L. Scheer and colleagues studied five women and five men who volunteered to undergo a kind of progressive jet lag.
For eight "days," the participants ate and slept on a 28-hour schedule, during which they ate four identical-calorie meals.
When their cycle shifted about 12 hours out of phase -- when they were sleeping during the day and up at night -- the participants' bodies got seriously out of rhythm:
- After meals, three of eight participants tested had blood sugar spikes and insulin resistance similar to those seen in people with diabetes or prediabetes.
- The participants' bodies made more insulin, yet their blood sugar went up.
- Blood levels of leptin went down. Long term, this would increase obesity risk, as decreased leptin makes people burn less energy while craving more food.
- Sleep efficiency -- the time one actually sleeps while in bed -- decreased.
- Blood pressure got higher.
- Cortisol -- the so-called stress hormone that affects blood pressure and blood sugar -- rose and dropped at the wrong time.
The study participants went back to their normal sleep schedules after the experiment. That's not an option for shift workers. Long term, the changes seen in the Scheer study may have ominous consequences.
Animals studies, the researchers note, show that "internal desynchronization" from repeated shifts in the day/night cycle cause premature death.
Scheer and colleagues report their findings in the March 2 early online edition of the Proceedings of the National Academy of Sciences.
Important Safety Information
- KAPIDEX may not be right for everyone. You should not take KAPIDEX if you are allergic to KAPIDEX or any of its ingredients. Severe allergic reactions have been reported.
- Symptom relief does not rule out other serious stomach conditions.
- The most common side effects of KAPIDEX were diarrhea (4.8%), stomach pain (4.0%), nausea (2.9%), common cold (1.9%), vomiting (1.6%), and gas (1.6%). KAPIDEX and certain other medicines can affect each other. Before taking KAPIDEX, tell your doctor if you are taking ampicillin, atazanavir, digoxin, iron, ketoconazole, or tacrolimus. If you are taking KAPIDEX with warfarin, you may need to be monitored because serious risks could occur.
Uses of KAPIDEX
- Persistent heartburn two or more days a week, despite treatment and diet changes, could be acid reflux disease (ARD). Prescription KAPIDEX capsules are used in adults to treat heartburn related to ARD, to heal acid-related damage to the lining of the esophagus (called erosive esophagitis or EE), and to stop EE from coming back. Individual results may vary. Most damage (erosions) heals in 4–8 weeks.
Talk to your doctor or healthcare professional. Please see full Prescribing Information for KAPIDEX.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
KAPIDEX™ is a trademark of Takeda Pharmaceuticals North America, Inc., and is used under license by Takeda Pharmaceuticals America, Inc.
LPD-00767

