Swaminathan S, Goldblatt F, Dugar M, Gordon T P, Roberts-Thomson P J
Department of Immunology, Allergy and Arthritis, Flinders Medical Centre, Adelaide, South Australia, Australia.
Intern Med J. 2008 Dec;38(12):897-903. doi: 10.1111/j.1445-5994.2008.01636.x. Epub 2008 Apr 14.
The presence of sicca symptoms is a frequent finding in patients with systemic sclerosis (SSc). The aim of this study was to examine the prevalence of sicca symptoms in a South Australian cohort of SSc patients and correlate this to a number of parameters, including autoantibody status, use of anticholinergic medication, age and the presence of functional anti-muscarinic-3 receptor (M3R)-blocking antibodies.
A screening questionnaire was sent out to all patients on the South Australian Scleroderma Register from the years 1998-2006 to determine the prevalence of sicca symptoms. A subset of patients on the register had ocular sicca symptoms tested by use of Schirmer's strips to validate the accuracy of the questionnaire. Eight patients were tested for anti-M3R-blocking antibodies using a functional physiological assay.
One hundred and ninety-three SSc patients took part in this study. Sicca symptoms were present in 59% of patients with the limited form of SSc, compared with 49% of patients with the diffuse form and 40% of patients with the overlap syndrome. The use of anticholinergic medication or thyroxine was associated with higher sicca scores in SSc patients. SS-A and SS-B autoantibodies (seen in Sjögren's syndrome) were detected in eight patients in this study. The detection of anti-M3R-blocking antibodies correlated well to presence of sicca.
This study confirmed that sicca symptoms are found in a high proportion of patients with SSc, especially those with the limited variant. Further testing of larger numbers of SSc patients with sicca for anti-M3R-blocking antibodies will be needed before more definitive conclusions can be drawn. Physicians should be made aware that sicca symptoms are a frequent cause of morbidity for SSc patients*.
干燥症状在系统性硬化症(SSc)患者中很常见。本研究的目的是调查南澳大利亚一组SSc患者中干燥症状的患病率,并将其与一些参数相关联,包括自身抗体状态、抗胆碱能药物的使用、年龄以及功能性抗毒蕈碱3受体(M3R)阻断抗体的存在情况。
向1998年至2006年南澳大利亚硬皮病登记册上的所有患者发送一份筛查问卷,以确定干燥症状的患病率。登记册上的一部分患者通过使用施默试验条测试眼部干燥症状,以验证问卷的准确性。使用功能性生理试验对8名患者进行抗M3R阻断抗体检测。
193名SSc患者参与了本研究。局限性SSc患者中有59%出现干燥症状,弥漫性SSc患者中这一比例为49%,重叠综合征患者中为40%。抗胆碱能药物或甲状腺素的使用与SSc患者较高的干燥评分相关。本研究中有8名患者检测到SS-A和SS-B自身抗体(见于干燥综合征)。抗M3R阻断抗体的检测与干燥症状的存在密切相关。
本研究证实,SSc患者中很大一部分存在干燥症状,尤其是局限性变异型患者。在得出更明确的结论之前,需要对更多有干燥症状的SSc患者进行抗M3R阻断抗体的进一步检测。应让医生意识到干燥症状是SSc患者发病的常见原因。