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Difficulties making a fist in patients presenting with recent-onset arthralgia of small joints without clinically detectable arthritis is considered a risk factor for progression to inflammatory arthritis (IA) and rheumatoid arthritis (RA). This is also reflected by this sign being incorporated in the European League Against Rheumatism (EULAR) definition of arthralgia suspicious for progression to RA.1 However, to date, there is barely scientific evidence for its predictive value and little comprehension on the underlying mechanism in recent-onset arthralgia. We studied if difficulties making a fist is indeed predictive for the development of IA and RA, and whether this sign is associated with subclinical inflammation.
Patients presenting with recent-onset (<1 year) arthralgia of the small joints were consecutively included in the Leiden clinically suspect arthralgia (CSA) cohort.2 At baseline, the ability to completely close the fist (actively close the fist with all fingertips touching the palm) and fist strength (measured by a patient squeezing the assessor’s fingers) were determined (figure 1). It was determined by trained research nurses in all patients, and for reliability purposes also by rheumatologists in a subset of patients. Contrast-enhanced 1.5T MRI of the wrist and second to fifth metacarpophalangeal (MCP) joints was performed and scored for synovitis, bone marrow oedema, tenosynovitis and MCP extensor peritendinitis. Patients were followed on the development of clinically apparent IA, determined by rheumatologists (median follow-up 16 months (IQR 4–25)). A detailed description of the cohort, MRI protocol and statistics are presented supplementary. Cox regression was performed with IA and RA (1987-criteria or 2010-criteria positivity) as primary and secondary outcome, respectively; time-to-event was time from the first presentation until IA development. Associations between difficulties making a fist and subclinical inflammation in the same hand at baseline were assessed with logistic regression.
Flowchart and baseline characteristics are presented as supplementary material. From 606 CSA patients, 86 (14%) had incomplete fist closure and 233 (38%) had decreased fist strength. In univariable Cox regression, the HR of incomplete fist closure was 2.22 (95% CI 1.36 to 3.64) and of decreased fist strength 1.33 (0.87–2.05). In multivariable analyses, corrected for age, gender, C-reactive protein (CRP) status and anti-citrullinated protein antibody (ACPA) status, both signs were independently associated with IA development; incomplete fist closure HR 2.33 (1.38–3.93) and decreased strength HR 1.62 (1.04–2.54). Similar findings were obtained with RA development as outcome (online supplementary file 1).
Supplemental material
To better understand the underlying pathology, as clinical arthritis was absent and therefore not the explanation, we evaluated whether fist problems were related to subclinical inflammation. Incomplete fist closure was associated with MCP flexor tenosynovitis and wrist flexor and extensor tenosynovitis in univariable analysis, and MCP flexor tenosynovitis in multivariable analysis (OR 3.79 (2.04–7.04), figure 1). Decreased fist strength was associated with MCP and wrist flexor tenosynovitis in univariable analysis, and wrist flexor tenosynovitis in multivariable analysis (OR 2.79 (1.52–5.12), figure 1).
Finally, the two tests were assessed by different observers in a subset of patients. Agreement was substantial for fist closure (n=324, Cohen’s kappa 0.61), but only fair for fist strength (n=318, Cohen’s kappa 0.28; online supplementary file 1).
Difficulties making a fist in recent-onset arthralgia in the absence of clinically apparent arthritis is considered a sign of imminent RA. This is the first study providing scientific support for the predictive value of this sign; incomplete fist closure, in particular, had better reliability and higher predictive value.
Intuitively, assessment of fist strength (normal/decreased) by physicians who get pinched may be more subject to interobserver variation than visual evaluation if the fist is completely closed, this was illustrated by lower values of agreement. The lower reliability may also have contributed to lower HRs for fist strength.
The association between fist problems and tenosynovitis is plausible as tenosynovitis can hamper tendon gliding within its sheath, limiting tendon excursion and the ability to distribute muscle strength to the fingers. It is reasonable that fist closure was especially associated with MCP flexor tenosynovitis and fist strength with wrist flexor tenosynovitis as these respective tendons are important for these movements.
Thus, difficulties making a fist in CSA is a sign of underlying flexor tenosynovitis. Incomplete fist closure, in particular, is predictive for RA development. In contrast to MRI, fist closure is simple to assess, also by physicians with little experience in joint examination. Therefore, fist closure, a component of the EULAR definition of arthralgia suspicious for progression to RA,1 is a feasible and valuable sign for use in daily clinical practice. However, as predictive values are dependent on prevalence, the value of this test in different patient populations (eg, primary care) needs further investigation.
Acknowledgments
The authors thank G Kracht, photographer at the Department of Radiology of the Leiden University Medical Center, for making and processing the pictures.
Footnotes
EN and AHMvdH-vM are joint senior authors.
Handling editor Josef S Smolen
Contributors FW, FJvdG, EN and AHMvdH-vM developed the study concept and design. FW and XMEM contributed to the data acquisition. FW performed data analyses. FW, EN and AHMvdH-vM wrote the first version of the manuscript. All authors critically reviewed the paper and approved the final manuscript.
Funding This work was supported by the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (Starting grant, agreement No. 714312) and the Dutch Arthritis Society.
Competing interests None declared.
Patient consent for publication Obtained.
Ethics approval Ethical approval is provided by a Local Medical Ethics Committee, named ‘Commissie Medische Ethiek’.
Provenance and peer review Not commissioned; externally peer reviewed.