NIR fluorescent probe could help diagnose osteoarthritis early
A near-infrared (NIR) fluorescent probe may make it easier to diagnose and monitor osteoarthritis, a painful joint disease that is often detected late in development after painful symptoms occur.
A near-infrared (NIR) fluorescent probe may make it easier to diagnose and monitor osteoarthritis, a painful joint disease that is often detected late in development after painful symptoms occur. Earlier diagnosis might lead to better management and patient outcomes. A new study by researchers at Tufts University Medical Center (TUMC; Boston, MA) reports that a NIR fluorescent probe tracked the development of osteoarthritis in male mice, brightening as the disease progressed.
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In this case, the probe was a harmless fluorescent molecule that detected the activity leading to cartilage loss in the joint, the key characteristic of osteoarthritis. The lab and mouse study, led by researchers from TUSM and the Sackler School of Graduate Biomedical Sciences at Tufts, is the first to demonstrate that NIR fluorescence—a specific type of light invisible to the human eye but possible to see with optical imaging—can be used to detect osteoarthritis changes over time. The new approach might also help analyze the effectiveness of osteoarthritis drugs, leading to improved treatments.
"Patients are frequently in pain by the time osteoarthritis is diagnosed. The imaging tests most frequently used, x-rays, don't indicate the level of pain or allow us to directly see the amount of cartilage loss, which is a challenge for physicians and patients," says co-first author Averi A. Leahy, B.A., an MD/Ph.D. student in the medical scientist training program at TUSM and the Sackler School.
"The fluorescent probe made it easy to see the activities that lead to cartilage breakdown in the initial and moderate stages of osteoarthritis, which is needed for early detection and adequate monitoring of the disease. To measure the probe's signal, we used an optical imaging system, to noninvasively look inside the knee,” says co-first author Shadi A. Esfahani, MD, MPH, postdoctoral fellow in the division of nuclear medicine and molecular imaging at Massachusetts General Hospital, and in the department of radiology at Harvard Medical School.
The right knees of 54 mice were affected by injury-induced osteoarthritis and served as the experimental group (the mice received pain medication). The healthy, left knees of the mice served as the control group.
Over a two-month period, the researchers took images of each knee every two weeks to determine if the fluorescent probe emitted a signal. Strikingly, the signal became brighter in the injured right knee, at every examined time point, through the early to moderate stages of osteoarthritis. The probe emitted a lower signal in the healthy left knee, and did not increase significantly over time.
The corresponding and senior author is Li Zeng, Ph.D., associate professor in the department of integrative physiology and pathobiology at TUSM, and member of the cellular, molecular, and developmental biology program faculty at the Sackler School. Leahy is one of her students. The work was done in collaboration with Umar Mahmood, MD, Ph.D., director of the Center for Translational Nuclear Medicine and Molecular Imaging, co-director of Nuclear Medicine and Molecular Imaging, both at Massachusetts General Hospital; and associate professor in the department of radiology at Harvard Medical School.
Zeng reports that the next step is to monitor the fluorescent probe over a longer period of time to determine whether the same results are produced during the late stages of osteoarthritis. She also hopes to use the probe to help develop treatments for animals, as some dogs are prone to osteoarthritis.
The Zeng laboratory at Tufts studies the mechanisms of tissue formation and degradation to develop effective strategies to treat arthritis. Her team uses tissue engineering techniques to examine approaches that can be used to generate stronger, more stable cartilage tissue that is resistant to inflammation commonly caused by osteoarthritis.
Previous research had identified that an increase in enzymes called matrix metalloproteinases (MMP) contributes to the cartilage degradation that occurs with osteoarthritis. The fluorescent probe was introduced into the knee joint and measured MMP activity.
Full findings appear in the journal Arthritis & Rheumatology; for more information, please visit http://dx.doi.org/10.1002/art.38957.
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