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Response to: ‘High risk of systemic lupus erythematosus development in patients with ITP: antiphospholipid syndrome is also a concern?’ by Inanc et al
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  1. James Cheng-Chung Wei1,2,3,
  2. Fang Xiao Zhu4,
  3. Jing-Yang Huang1,5
  1. 1Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan
  2. 2Department of Allergy, Immunology & Rheumatology, Chung Shan Medical University Hospital, Taichung, Taiwan
  3. 3Graduate Institute of Integrated Medicine, China Medical University, Taichung, Taiwan
  4. 4Department of Rheumatology and Immunology, The Second Affiliated Hospital of Guilin Medical University, Guilin, Guangxi, China
  5. 5Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan
  1. Correspondence to Dr Fang Xiao Zhu; 1123551518{at}qq.com

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We thank Inanc et al1 for their comments on our article entitled ‘Risk of systemic lupus erythematosus (SLE) in patients with idiopathic thrombocytopenic purpura (ITP): a population-based cohort study’. In our article, we concluded that ITP is strongly associated with incidental SLE.2

We agree with Inanc et al1 that antiphospholipid syndrome (APS) is an important effect modifier in ITP and SLE. We also acknowledge that Inanc et al1 addressed the difference of APS (2.77% in the ITP group vs 0.02% in the non-ITP controls) in table 1 of our article.2 Actually, ITP, APS and SLE sometimes overlapped in clinical practice. As in table 1, there are more baseline comorbidities in the ITP group, including thrombotic event, cardiovascular disease and ITP. Hence, we did propensity score to match these differences rather than exclude these comorbidities in patient selection as in figure 1. The reason for this is that once you exclude these effect modifiers, then you cannot study their effects. Thus, we prefer matching and stratified analysis on important effect modifiers, rather than exclusion.3

Table 1

The crude and age and sex adjusted incidence rate of SLE in general individuals, ITP, Hashimoto’s disease, Graves’ disease and AIHA population

As Inanc et al1 mentioned, many claim-based or patient-reported databases have concerns of validity and uncertainty. Unfortunately, the National Taiwan Insurance Research Database (NHIRD) did not provide laboratory data, such as antinuclear antibody (ANA) and APS profiles. Although this is a limitation, the NHIRD had been validated and appreciated in many high impact publications.4 5 In our study, we had tried to minimise this information bias by adding sensitivity tests and also stratifies analysis on important confounders, such as thrombosis cardiovascular disease and some infections and life style-related diseases to reduce the bias from comorbidities, including APS. These had been discussed in-depth in Discussion section of our article.

We agree that APS clinical features and laboratory profiles and ANA are important baseline evaluation for every patient with ITP. It is also indeed our study purpose and conclusion. Furthermore, even though baseline ANA and aPL were negative, we suggest that patients with ITP should still be monitored yearly for clinical and serological lupus or APS. We hope this clinical application will improve the quality of our daily practice.

References

Footnotes

  • Handling editor Josef S Smolen

  • Funding The present study was supported by the Programme of Scientific and Technology Project (Guilin Science Research and Technology Development; grant no. 2016012706–2).

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Commissioned; internally peer reviewed.

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