T. Martin et al., ASSOCIATION OF INTERMEDIATE UVEITIS WITH HLA-A28 - DEFINITION OF A NEW SYSTEMIC SYNDROME, Graefe's archive for clinical and experimental ophthalmology, 233(5), 1995, pp. 269-274
Background: Endogenous posterior uveitis (PU) can be associated with s
ystemic diseases, and certain forms have strong association with HLA a
ntigens. Much less is known regarding intermediate uveitis (IU). The p
urpose of this study was to determine whether IU is associated with th
e HLA system and whether it can be associated with systemic symptoms.
Methods: In 179 consecutive patients consulting for uveitis, a detaile
d history was obtained and a physical examination performed. HLA typin
g for 71 HLA-A, B, DR and DQ antigens, laboratory tests, and radiograp
hy of the chest, sinuses, and sacroiliac joints were systematically pe
rformed. Results: Thirty-two patients (18%) had IU; 51(28.5%) had PU a
nd constituted our internal control group. Nine of the patients with I
U (28%) had the HLA-A28 antigen, compared with 8.1% of a healthy contr
ol population and 8.6% of the patients with PU (P < 0.001). An associa
ted disease was found in four patients with IU (12.5%) (none was HLA-A
28) and in 45% of the patients with PU (P < 0.01). Some 67% of HLA-A28
patients with IU had arthralgias affecting the kneels), compared with
17% of non-HLA-A28 patients and 18% of patients with PU (P < 0.05 and
P < 0.01 respectively); 55% had gonalgias and hypocomplementemia comp
ared with 9% and 2% respectively (P < 0.01 and P < 0.001). Conclusions
: IU is significantly associated with HLA-A28; patients having this an
tigen may represent a subset of the disease characterized by an increa
sed prevalence of arthralgias and hypocomplementemia.