
US Bursitis and BMI Predict Joint Issues in Psoriasis
In patients with mild psoriasis and no initial musculoskeletal signs, ultrasound bursitis at entheses was associated with the development of inflammatory symptoms suggestive of psoriatic arthritis (PsA), and those who developed musculoskeletal symptoms had higher BMI and fatigue scores and had a higher risk for transition to PsA.
METHODOLOGY:
This prospective multicentre study included 78 patients with mild psoriasis without musculoskeletal symptoms who were not on systemic treatment; 82% of them had mild disease and 39.7% presented with onychopathy.
Researchers performed ultrasound evaluation of 40 joints and 10 entheses bilaterally at baseline and during follow-up; these were assessed for synovial hypertrophy, power Doppler signal, and entheseal changes including bursitis.
Study outcomes were the diagnosis of PsA and new-onset musculoskeletal symptoms. The median follow-up duration was 76.6 months.
TAKEAWAY:
Among 60 patients who completed the study, 6.6% developed PsA over a mean of 20.2 months according to the CASPAR criteria, corresponding to the annual incidence of approximately 1%.
Overall, 56.6% of patients developed musculoskeletal symptoms and had significantly higher BMI ( P = .013) and abdominal circumference ( P = .022) at baseline.
= .013) and abdominal circumference ( = .022) at baseline. These patients also scored higher on pain (2.14 vs 0.91; P = .047) and fatigue (3.25 vs 1.21; P = .011) components of the baseline Psoriatic Arthritis Impact of Disease questionnaire than those not developed musculoskeletal symptoms.
= .047) and fatigue (3.25 vs 1.21; = .011) components of the baseline Psoriatic Arthritis Impact of Disease questionnaire than those not developed musculoskeletal symptoms. Ultrasound bursitis at entheses was present in 80% of patients who developed inflammatory arthralgia suggestive of PsA ( P = .049).
= .049). The total joint ultrasound score at baseline was significantly higher in patients who developed musculoskeletal symptoms ( P = .037).
IN PRACTICE:
"Around half of the patients with PsO [psoriasis] developed MSK [musculoskeletal] symptoms during the follow-up and they had significantly higher BMI, more joint US [ultrasound] findings and scored higher in pain and fatigue scales at baseline PsAID [Psoriatic Arthritis Impact of Disease] questionnaire, defining a subgroup with potentially higher risk to develop PsA. On the other hand, US bursitis at enthesis was related to the onset of MSK symptoms suggestive of PsA," the authors wrote.
SOURCE:
This study was led by Ana Belén Azuaga, Hospital Clinic, Barcelona, Spain. It was published online on June 04, 2025, in Rheumatology .
LIMITATIONS:
The sample size was relatively small, potentially underestimating the incidence of PsA in patients with psoriasis. The exclusion of patients with musculoskeletal symptoms and those on systemic therapy likely excluded individuals with a higher risk of developing PsA. Additionally, a significant proportion of patients initiated disease-modifying antirheumatic drug therapy during the study, including biologics, which could have affected the development of PsA symptoms.
DISCLOSURES:
This study was supported by research grants from Pfizer and Novartis. Additional support came from the Innovative Medicines Initiative 2 Joint Undertaking. The authors declared having no conflicts of interest.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
11 hours ago
- Yahoo
Doctor: Many prostate cancer screenings involve only a blood test
DETROIT (FOX 2) - When it comes to detecting prostate cancer, it can be a little confusing. Like what does the screening involve and who should get screened, and when? "It's not a death sentence, it's a life sentence," said Dr. Michael Lutz. "It's important to get screened and know if you're at risk." Big picture view Lutz, the president of the Michigan Men's Health Foundation, says there is plenty of living to do after a prostate cancer diagnosis. You have to catch it early. Who's at greatest risk? "We know there are certain men at risk," he said, "Family history, African American, firefighter, fighter pilot - these are going to increase risk." Screening for prostate cancer involves a blood test, the PSA and now Dr. Lutz says the slightly uncomfortable part of the exam, might not be needed. "A lot of men don't want to get screened because of the digital rectal exam rather get a rectal exam - they would rather get bit by cobra," Lutz said. "Get the PSA blood test first. If its low you don't need rectal exam." For those at higher risk, screening can start at 40. Those with average risk it's recommended men start screenings at 50. But the recommendations get murky when it comes to men over the age of 70. Lutz says be your own advocate and ask for the screening no matter your age. "Don't let your chronological age be your determining factor," he said. This weekend, on Father's Day - the Run for the Ribbon is happening at the Detroit Zoo. Everyone is welcome to celebrate survival of prostate cancer. Get more info by tapping in September - get ready for the annual Men's Health Event at Ford Field. Some of the money raised at run for the ribbon will fund the Men's Health Event at Ford Field. That's an incredible event that offers life-changing screenings. The Source This report was based off an interview with Dr, Michael Lutz.


Chicago Tribune
17 hours ago
- Chicago Tribune
Matteson man who survived prostate cancer spreading the word about early detection
Andrin 'AJ' Jones got some scary news when he was diagnosed with prostate cancer, but his experience has pushed him to try to make a difference in other men's lives now that he's a survivor. Jones, a 62-year-old retired Air Force veteran, counts himself lucky that his cancer was caught early enough that it had not spread, so that surgically removing his prostate in 2023 left him healthy. So he wants to spread that good fortune to others by spreading his story about how early testing leads to better outcomes. 'My prognosis was excellent because the biopsy showed the cancer was still contained within the walls of my prostate,' said Jones, who lives in Matteson with his wife, also an Air Force veteran. 'Because of early detection, it had not yet metastasized, the risk level was low to intermediate. I was so thankful for that.' His journey with prostate cancer started in May 2022, when Dr. Lance Wallace, his internist at Specialty Physicians of Illinois, LLC, ordered a full panel of screening labs, including a prostate specific antigen test. That test revealed he had an elevated level of that antigen in his blood. After Wallace saw the test result, he waited a few months to recheck the labs, but they were higher. So he referred Andrin to Dr. James Siegert, a urologist and urological surgeon, also with Specialty Physicians of Illinois, LLC, and practicing with Franciscan Health Olympia Fields, who redid the labs to watch for a trend in elevations. He did the biopsy several months later and found Stage 2 adenocarcinoma. 'Of course I was alarmed at the diagnosis, but at the same time, it was a good reality check to encourage men to not ignore any symptoms,' said Andrin. Andrin said he was given a choice of radiation or surgery and opted for the latter. Siegert said prostate cancer screening was generally recommended for 50- to 60-year-old men at average risk, but for those at increased risk, such as African-American men or those with a family history, the age recommendation drops to 40 to 45. The screening is not usually recommended for men 70 or older. 'Prostate cancer screening is important because it can help detect cancer early, when it's most treatable and potentially curable,' Siegert said. 'Early detection through a PSA blood test may allow patients to avoid more serious complications down the line and preserve their quality of life.' Wallace, Jones' primary care physician, also encouraged early screening. 'Like anything, the earlier you catch it, the less treatment will be involved in treating the cancer, and the chance for success is greater,' Wallace said. Jones said there were a few things that helped him get through the experience, including building a strong relationship with both physicians. 'I'm a person of faith, I trusted God with the situation,' he said. 'I started going for walks in the morning to mentally process things that were going on. 'Along with my wife, family, and church family, that helped me have a good mental perspective,' he said. No matter how difficult the ordeal was he often reminds himself, 'I had cancer — today I don't.' 'Being honest and open with other men about prostate screening' has provided a source of strength for Jones, he said. He still does that on regular walks with his comrades. He also teaches classes on the Bible and is an avid hiker and biker. Siegert said he was struck by Jones' resilience. 'Of the hundreds of men I diagnose and treat for prostate cancer per year, Mr. Jones was unique as throughout his treatment, he maintained a remarkably positive attitude, approaching each step with resilience and hope,' said Siegert. 'Inspired by his experience, he has become a passionate advocate for prostate cancer awareness and early screening, particularly within the African-American and veteran communities, using his voice to encourage others to take charge of their health.'


Medscape
a day ago
- Medscape
IRONMAN: Can PSA Guide Metastatic Prostate Cancer Care?
CHICAGO — Prostate-specific antigen (PSA) levels could help guide treatment decisions for patients with metastatic hormone-sensitive prostate cancer, according to real-world findings from the IRONMAN study. Specifically, an undetectable PSA nadir — defined as PSA level < 0.2 ng/mL — predicted a good prognosis and a PSA level ≥ 0.2 ng/mL predicted poor prognosis among patients receiving androgen deprivation therapy (ADT) or androgen receptor pathway inhibitor (ARPI) therapy for 6-12 months, according to Michael Ong, MD, who presented the findings at the 2025 American Society of Clinical Oncology annual meeting. In other words, this real-world study found that absolute PSA at 6 and 12 months is prognostic in this patient population, said Ong, a medical oncologist at Ottawa Hospital Research Institute, Canada. Patients with a poor prognosis could then be considered for clinical trials offering therapy escalation, whereas those with a better prognosis — particularly those with PSA < 0.1 ng/mL — could be considered for de-escalation, said Ong. Ong explained that prior phase 3 studies have demonstrated that PSA > 0.2 ng/mL is associated with poor prognosis in patients receiving ADT and ARPI. However, data in real-world settings remain limited. Some patients with rapid PSA decline never progress, whereas others develop early resistance despite intensive therapy, he explained. The IRONMAN study set out to answer two main questions: When should PSA cutoffs be interpreted for prognostic significance? And how may PSA cutoffs differ in real-world patients? To this end, Ong and his colleagues included 1219 patients from the prospective IRONMAN cohort with metastatic hormone-sensitive prostate cancer who had received ADT and ARPI therapy, with or without docetaxel, and had PSA data available. PSA was stratified into three groups: ≥ 0.2 ng/mL, 0.10-0.19 ng/mL, and < 0.10 ng/mL. The research team constructed a 12-month landmark population to assess conditional overall survival (OS) and progression-free survival (PFS) at 6 and 12 months across each PSA level. The 12-month analysis was the primary study outcome. Patients were a median age of 70 years, 58% had Gleason score of 8-10, and 75% had de novo metastatic disease. Overall, most (74%) were White and just over half were enrolled from centers outside US or Canada. ARPI agents included abiraterone acetate (44%), apalutamide (21%), enzalutamide (22%), or darolutamide (13%), and 12% of patients received docetaxel in addition to doublet therapy with ADT plus ARPI. PSA levels shifted across the two time points. At 6 months, 52% of patients had a PSA < 0.2 ng/mL, whereas 48% had a PSA level ≥ 0.2 ng/mL. At 12 months, 68% had PSA levels < 0.2 ng/mL and 32% had levels ≥ 0.2 ng/mL. Both the 6- and 12-month landmark analyses showed that PSA ≥ 0.2 ng/mL was associated with worse conditional OS and PFS compared with PSA < 0.2 ng/mL. Ong broke down conditional OS and PFS at 12 months — the primary study outcome —by absolute PSA levels. Absolute PSA 3-year overall survival 3-year progression-free survival OS mortality risk (adjusted hazard ratio) ≥ 0.2 ng/mL 45% 41% 4.85 (3.36-7.01) 0.10-0.19 ng/mL 79% 62% 1.34 (0.82-2.20) < 0.1 ng/mL 84% 80% Reference After adjustment for confounders, PSA ≥ 0.2 ng/mL was associated with an almost fivefold higher risk for death at 12 months (adjusted hazard ratio, 4.85). Ong noted that PSA was prognostic of overall survival regardless of ARPI class or whether patients received doublet or triplet therapy with docetaxel. Invited discussant Rahul Aggarwal, MD, agreed that a PSA nadir between 6 and 12 months 'is strongly prognostic for progression-free and overall survival.' However, Aggarwal cautioned, although 'it is tempting to use PSA nadir to guide treatment decisions in clinical practice,' the approach has not been validated. Plus, other factors and biomarkers may play a role in treatment decisions and help optimize outcomes, including quality of life, treatment and financial toxicity, and the role of the tumor suppressor gene PTEN , added Aggarwal, of the University of California, San Francisco. 'We await randomized trial data to know, in fact, whether we should use this to guide treatment decision-making,' said Aggarwal. Such trials are underway. Ong is co-chair of a phase 3 study assessing survival after treatment escalation for patients with PSA ≥ 0.2 ng/mL after 6-12 months of ADT and ARPI therapy. Another phase 3 study will assess treatment de-escalation in those with PSA ≤ 0.2 ng/mL at 6-12 months after treatment initiation. This study's principal funder was the Movember Foundation; the Prostate Cancer Clinical Trials Consortium was a trial sponsor, plus Amgen, Astellas, AstraZeneca, Bayer, Janssen, Merck, Novartis and Sanofi provided funding support. Ong disclosed relationships with AstraZeneca, Bayer, Bristol-Myers Squibb, EMD Serono, Janssen, Merck, Novartis/AAA, Pfizer, Sanofi, and Ipsen. Aggarwal disclosed relationships with Alessa Therapeutics, Amgen, AstraZeneca, Bayer, BioXcel Therapeutics, Boxer Capital, Curio Science, and others.