Role of lupus retinopathy in systemic lupus erythematosus

Systemic lupus erythematosus (SLE) is a chronic, autoimmune, connective tissue disorder affecting multiple organ systems often with a relapsing and remitting clinical course. SLE is often called a “woman’s disease” because 90 % of affected individuals are females [1]. Manifestations of SLE are protean and any organ or system of the body including the eye can be affected due to the inflammatory response to the circulating immune complexes [1].

Ocular manifestations are a marker for overall systemic disease activity and can occur in up 1/3rd of all SLE patients. The incidence of retinal involvement in SLE is 7–26 % [2] and is the second most common ocular manifestation after keratoconjunctivitis sicca [3]. It is one of the most common vision-threatening complications of systemic lupus erythematosus with an incidence of up to 29 % in patients with active systemic disease [3]. The presence of active SLE retinal vasculopathy is an extremely accurate guide to the presence of systemic disease activity, occult or overt. Additionally, life-table survival estimates have shown decreased survival in patients with SLE retinopathy, compared to SLE patients without retinopathy [3]. Retinal lesions in SLE patients, therefore, are of critical importance, both visually and prognostically [4].

The control of systemic SLE is the mainstay of treatment for lupus retinopathy which can be achieved by systemic corticosteroids and immunosuppression [3]. Initial treatment is usually with oral corticosteroids (prednisolone 1 mg/kg/day), but may be preceded by intravenous methylprednisolone (500 mg–1 g daily for 3 days). This is then supplemented with, or replaced by, other immunosuppressive agents as part of a steroid-sparing strategy or for resistant disease [3]. Periocular steroid injections may have a role in unilateral/asymmetric disease; however, they should be used cautiously and avoided in patients with necrotising scleritis [2]. In the presence of significant vaso-occlusive disease with the presence of antiphospholipid antibody, anti-coagulation and the addition of low-dose acetylsalicylic acid may be beneficial [5]. Proliferative retinopathy usually requires treatment with laser photocoagulation akin to the treatment of proliferative diabetic retinopathy [6].

A prospective study was conducted among the established cases of SLE referred to the eye department from the various departments of Tribhuvan University Teaching Hospital between 2008 and 2010. After dilated fundus evaluation, presence or absence of lupus retinopathy was identified and grading was done. Mild lupus retinopathy consists of cotton–wool spots, perivascular hard exudates, retinal hemorrhages, and vascular tortuosity [7]. Moderate lupus retinopathy has focal or generalized arteriolar constriction and venous tortuosity. At the severe end of the spectrum, there is occlusion of retinal arterioles and consequent retinal infarction, termed vaso-occlusive retinopathy [8] causing artery/vein occlusions, vitreous hemorrhage, retinal ischemia, and neovascularisation [8‐11].

The patients were divided into two groups according to the presence or absence of lupus retinopathy, and a comparison of clinical and laboratory findings between two groups was done. Patients were followed up for 2 years.

A total of 91 SLE patients (182 eyes) were examined to evaluate the presence of lupus retinopathy.

Retinopathy is one of the important manifestations of SLE, which develops with an incidence of 7–26 % [4] of SLE patients, although the frequency of the findings varies depending on the patient population being studied and systemic disease activity [12]. According to Ushiyama et al. [13], the incidence of lupus retinopathy is 10 % (7/69) which is similar to our incidence of lupus retinopathy {12.1 % (11/91)}. Our study reveals incidence of lupus retinopathy in admitted patients to be 27.3 % which correlated with the other literature where lupus retinopathy in the admitted patients could be as high as 29 % [14].

Ushiyama et al. [13] reported the mean age at onset of SLE in the patients with and without retinopathy to be 34.2 and 31.9 years, respectively, and all of them were females. This is comparable with our study where the mean ages at onset of SLE in our patients were 30.4 and 31.9 years, respectively, of them, 10 were females and 1 male. Sex hormones are known to affect the clinical course of SLE; estrogen enhances the disease and testosterone suppresses it [15, 16] and 90 % of women are of child-bearing age [17].

Retinopathy in SLE is suggestive of high disease activity during the course of SLE, and hence, is a marker of poor prognosis for survival, that is SLE patients with retinopathy have overall worse prognosis and decreased survival, compared to SLE patients without retinopathy [3]. Interestingly, the severe form of vaso-occlusive retinopathy is associated with similar changes in the central nervous system vasculature [8, 18, 19].

We found that the renal dysfunction in SLE without retinopathy was 59.3 %, but in patients with retinopathy was 100 %. Although it is unclear whether lupus retinopathy is directly associated with renal disease, retinopathy may develop in severe SLE which also involves the kidney or CNS, or both. It has a major impact on morbidity and mortality.

Several studies report that retinal vascular disease in SLE patient parallels systemic disease activity [14, 20] and that the effective treatment of the systemic disease, along with simultaneous control of any associated systemic hypertension, results also in concurrent decrease in the retinal lesions, especially the disappearance of cotton–wool spots [9, 14].

The serologic hallmark of SLE is the presence of ANAs in highly sensitive and useful screening tool. Anti-dsDNA antibody is SLE specific and correlates with disease activity [21]. The antiphospholipid antibody is thrombogenic and is associated with both CNS and ocular vaso-occlusive phenomena [18] that can manifest as visual disturbances, transient monocular blindness, and chorioretinopathy in patients with SLE [22]. A higher incidence of antiphospholipid antibodies in SLE patients with retinal vascular disease, compared to those without (77 vs. 29 %), has been reported [23] and in our study also the incidence was 18.1 versus 4.4 %.

The ocular fundus is the only part of the human body where we can directly observe small vessels without injuring the tissue. And lupus retinopathy reflects systemic vascular damage, so ocular fundus examination should be regularly done. Finally, the eyes may be the harbinger of a potentially severe systemic flare-up of SLE, so careful monitoring is needed. A symbiotic relationship among rheumatologist, physicians, dermatologist, and ophthalmologist may be formed to better understand the disease status and plan the treatment strategy of the patients with SLE.