Dear editor
I read with great interest the article by Cui et al1 entitled “The impact of disease activity and psychological status on quality of life for Chinese patients with primary Sjögren’s syndrome”, in which the authors revealed that primary Sjögren’s syndrome (pSS) could significantly impair the quality of life (QoL) of the patients, and measuring QoL might be an important part of the comprehensive management of the disease.1 This case–control study was undoubtfully well designed and conducted by quantifying the symptoms and disease activity using various scales and indices.1 A recent study also showed that patients with pSS showed decreased QoL with mood disorders.2
However, I would like to point out that the parameters for symptoms and signs of dry eye disease (DED) were not included in the analyses, although autoimmune destruction of the lacrimal gland and ocular surface damage is one of the key features of pSS.3 DED may also have association with psychiatric disorders including depression, anxiety, and stress.4 Le et al5 also demonstrated that dry eye symptoms might have adverse impact on QoL and mental health of the patients. These findings suggest that dry eye symptoms in patients with pSS might also have impact on psychological status and QoL.
Although the severity of DED could be reflected by disease activity of pSS, studies showed the lack of correlation between dry eye symptoms and signs.3,4 In pSS, serious ocular surface damage can paradoxically lead to lack of ocular discomfort due to damage to corneal nerves.3 Therefore, I believe further studies including both dry eye signs including tear film break-up time, Schirmer score, and ocular staining score and dry eye symptoms including ocular discomfort, pain, dryness, and grittiness in the analyses would be helpful for the determination of QoL in pSS.
Acknowledgments
This study was supported by 2017 Research Grant from Kangwon National University.
Footnotes
Disclosure
The author reports no conflicts of interest in this communication.
References
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