
Lower Blood Pressure Targets for Type 2 Diabetes
This transcript has been edited for clarity.
Today I am going to discuss a recent paper on intensive blood pressure control in people with type 2 diabetes. This was a big study. It included over 12,000 participants who were older than age 50, and had type 2 diabetes and an increased risk for cardiovascular disease; either they'd had a prior cardiovascular event, had two or more risk factors, or had a reduced estimated glomerular filtration rate (eGFR).
The study was performed in China and it was really done to determine, potentially once and for all, what the target should be in treating patients with type 2 diabetes. The ACCORD trial tried to answer this question, but it didn't show overall improvement in outcomes with blood pressure reduction, although when they did subset analysis, they did show benefit in certain groups. It still didn't have that definitive feel, and I think this study does.
They were looking only at systolic blood pressures, and they wanted to target a systolic blood pressure of less than 120 mm Hg in the intensively treated group; in the standardly treated group, the blood pressure target was a systolic of less than 140 mm Hg. The primary endpoint was nonfatal stroke, nonfatal MI, treatment or hospitalization for heart failure, or death from cardiovascular disease causes.
In this study, 45% were women. The average age was 63.8 years. Body mass index was 26.7 and 25% smoked. The baseline blood pressure was 140/76 mm Hg and the mean blood pressure over approximately 4 years of follow-up was 121.6 mm Hg in the intensively treated group vs 133.2 mm Hg in the standard treatment group.
You basically began to see a difference between the two in terms of the primary endpoint after about a year, so you started to see this split. At the end of the study, there was a very significant difference in terms of the primary endpoint between the two groups.
I want to point out that, in my brain, those blood pressure targets that were reached are actually fairly standard. The intensively treated group was about 120 mm Hg, and that's compared with the standard treatment group, which was around 130 mm Hg.
I must say that, in my own practice, given all the changes that we've seen over the years in blood pressure targets, the results from this study have actually motivated me to lower my systolic target, at least in terms of how I treat patients in clinic, because I think they may get further benefit.
That then begs the question of how did they measure blood pressures in this study? I get patients who have what's called white coat hypertension. They come into my office, their blood pressure is higher, and then I have them test at home and it's better.
In this study, they tried to take away some of that interference. They had patients come into clinic having had no exercise, no coffee, and no cigarettes for at least 30 minutes before their appointment. The patients had 5 minutes of seated rest, and then they had three blood pressure measurements, each done 1 minute apart. There was no talking or joking around. They just sat there and had their blood pressures measured in the appropriate way.
The average systolic blood pressure was used of those three readings to determine whether treatment was changed. They followed pretty standard treatment regimens for hypertension, which are the ones we use in our ADA guidelines for the management of hypertension.
People in the intensive group ended up on one or two additional medications compared with those in the standard group. The overall rate of severe adverse events was equivalent in both groups, but there was more symptomatic hypotension and hyperkalemia in the intensively treated group.
As I said, this has actually changed how I'm treating my patients. The difference between 120 mm Hg and 133 mm Hg isn't that big in my brain, and yet there does seem to be a difference in terms of outcomes, primarily cardiovascular outcomes, as the primary endpoint.
I think that, if a patient can tolerate a lower blood pressure without symptomatic hypotension, I am going to be treating them down to a lower target. I think this was a well-done study that actually will probably inform practice and guidelines in the future because I think it helps inform us of what is potentially the best target for our patients.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


The Verge
32 minutes ago
- The Verge
Here's what's inside Meta's experimental new AR glasses
Meta has revealed more information about Aria Gen 2, its experimental smart glasses designed to serve as a test platform for research about augmented reality, AI, and robotics. The glasses pack several improvements into their lightweight frame that could one day translate into consumer products, including an improved eye-tracking system that can track gaze per eye, detect blinks, and estimate the center of pupils. 'These advanced signals enable a deeper understanding of the wearer's visual attention and intentions, unlocking new possibilities for human-computer interaction,' Meta writes. Meta initially announced Aria Gen 2 in February, saying they will 'pave the way for future innovations that will shape the next computing platform.' They build upon Meta's first iteration of the glasses in 2020, which were similarly available for researchers only. Along with an improved eye-tracking system, Aria Gen 2 comes with four computer vision cameras that Meta says enable 3D hand and object tracking. Meta says researchers can use this information to enable highly precise tasks like 'dexterous robot hand manipulation.' The glasses also have a photoplethysmography sensor built into the nosepad, which allows the device to estimate a wearer's heart rate, along with a contact microphone that Meta says provides better audio in loud environments. There's a new ambient light sensor as well, allowing the glasses to differentiate between indoor and outdoor lighting. The Aria Gen 2 glasses include folding arms for the first time, weigh around 75 grams, and come in eight different sizes. Meta plans on opening applications for researchers to work with Aria Gen 2 later this year. The initiative builds on the successful development of Meta's Ray-Ban smart glasses, a form factor it aims to expand with its Orion augmented-reality glasses, a rumored partnership with Oakley, and a high-end pair of 'Hypernova' glasses with a built-in screen.

Associated Press
37 minutes ago
- Associated Press
What is Fusarium graminearum, the fungus US authorities say was smuggled in from China?
NEW YORK (AP) — Federal prosecutors charged two Chinese researchers on Tuesday with smuggling a crop-killing fungus into the U.S. last summer — charges that come amid heightened political tensions between the two countries and as the Trump administration moves to revoke visas from visiting Chinese students. Yunqing Jian and Zunyong Liu are charged with conspiracy, smuggling, making false statements and visa fraud for allegedly bringing the fungus Fusarium graminearum into the U.S. Jian, 33, was booked in a Detroit federal court. Liu, 34, is thought to be in China. According to the FBI, Liu had small baggies of the fungus stashed in his backpack when he flew to the U.S. last year and, after claiming ignorance about the plant material inside them, said he was planning to use it for research at a University of Michigan lab where Jian worked and where Liu previously worked. What is Fusarium head blight? Fusarium graminearum causes a disease called Fusarium head blight that can wipe out cereal crops such as wheat, barley and maize and rice — it inflicts $1 billion in losses annually on U.S. wheat and barley crops, according to the U.S. Department of Agriculture. It isn't the only fungus to cause Fusarium head blight, but it's the most common culprit in the U.S. The fungus infects plants early in the growing season, shriveling wheat grains and blanching crop heads a whitish-tan color. It also causes a toxin to accumulate in wheat kernels that can make them unsafe for people and livestock to eat. Nicknamed 'vomitoxin' because it's most known for causing livestock to throw up, it can also cause diarrhea, abdominal pain, headache and fever in animals and people. Wheat and other grain crops are screened for various toxins, including Fusarium graminearum, before they can be used to feed animals and humans. Farmers have to throw out any infected grains, which can cause devastating losses. 'It's one of the many problems that farmers have to deal with that risks their livelihood,' said David Geiser, a Fusarium expert at Penn State. What are the accusations? Although Jian and Liu are accused of smuggling Fusarium graminearum into the country, the fungus is already prevalent in the U.S. — particularly in the east and Upper Midwest — and scientists have been studying it for decades. Researchers often bring foreign plants, animals and even strains of fungi to the U.S. to study them, but they must file certain permits before moving anything across state or national borders. Studying the genes of a foreign fungus strain, for example, can help scientists learn how it tolerates heat, resists pesticides or mutates. 'We look at variations among individuals just like we do humans,' said Nicole Gauthier, a plant pathologist at the University of Kentucky who studies Fusarium. That said, it's unclear why the Chinese researchers might have wanted to bring that strain of Fusarium graminearum into the U.S. and why they didn't fill out the proper paperwork to do so. ___ The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.


Bloomberg
an hour ago
- Bloomberg
Live Q&A: Inside China's Race to Dominate the AI-Fueled Humanoid Robotics Industry
After years of American companies like Boston Dynamics and Elon Musk's Tesla leading the development of humanoid robots, Chinese startups are now making rapid advancements using AI. What's the current tech landscape like and what's next? Join Bloomberg's reporters on June 3 at 9:30 p.m. ET / June 4 at 9:30 a.m. HKT for a live discussion. This conversation will be recorded and be made available to listen and share. Bloomberg digital subscribers and Terminal clients are invited to sign in and ask our team questions while it's live.