Objective Hydroxychloroquine (HCQ) is a mainstay of therapy in the treatment of SLE. The effect of HCQ on platelets and vascular health is uncertain. We investigated the relationship between HCQ use and dose with platelet activity, platelet transcriptomics and vascular health in patients with SLE.
Methods Platelet aggregation, platelet mRNA expression and vascular health (sublingual capillary perfused boundary region (PBR), red blood cell filling (RBCF) and brachial artery reactivity testing) were analysed by HCQ use and dose.
Results Among 132 subjects with SLE (age: 39.7±12.9 years, 97% female), 108 were on HCQ. SLE disease activity was similar between subjects on and off HCQ. Platelet aggregation in response to multiple agonists was significantly lower in patients on HCQ. There were inverse relationships between HCQ dose and gene expression pathways of platelet activity. Gene expression of P-selectin (SELP) was inversely correlated with HCQ dose (r=−0.41, p=0.003), which was validated at the protein level. Subjects on HCQ had improved vascular function correlating with HCQ dose as measured by lower PBR (r=−0.52, p=0.007), higher RBCF (r=0.55, p=0.004) and greater brachial artery reactivity (r=0.43, p=0.056).
Conclusion HCQ use was associated with decreased platelet activation and activation-related transcripts and improved vascular health in SLE.
- cardiovascular diseases
- lupus erythematosus
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What is already known about this subject?
Hydroxychloroquine (HCQ) is a mainstay of therapy in patients with SLE.
What does this study add?
Subjects with SLE taking HCQ exhibited reduced platelet aggregation and improved vascular health.
Platelet RNA expression revealed that platelet functional pathways were downregulated in patients on HCQ, and that the expression of these pathways decreased with increasing HCQ dose.
How might this impact on clinical practice or future developments?
HCQ is associated with lower platelet activity and improved vascular health, providing important pleiotropic mechanisms of benefit for HCQ in SLE.
SLE is an autoimmune disease characterised by a wide array of symptoms that can affect virtually all organ systems. The antimalarial medication hydroxychloroquine (HCQ) is the most frequently prescribed long-term medication used to treat this disease, a practice driven by extensive literature supporting its benefits in patients with SLE.1 Notably, HCQ has been associated with several benefits in patients with SLE, including a decrease in the rate of disease flares,2 protection against organ damage,3 improvement in overall survival4 and reduction in the risk of thrombosis.2 5 Although antithrombotic effects have been demonstrated in clinical studies, the underlying mechanisms driving this protective effect are not fully understood. Accordingly, we compared platelet phenotypes and measures of vascular health in patients with SLE who were and were not prescribed HCQ to define the cardiovascular effects of this therapy in SLE.
Subjects with SLE (meeting at least four of the revised American College of Rheumatology (ACR) or Systemic Lupus International Collaborating Clinics criteria)6 7 were recruited into an ongoing NIH-funded study investigating platelet activity, transcriptome and vascular health. Individuals who used aspirin or non-steroidal anti-inflammatory drugs or had a platelet count <100×109/L at the time of blood collection were excluded. Information including medication use, weight and other patient history was recorded at the time of enrolment. Blood was collected for haematology analysis using the Sysmex XN-1000 analyser, platelet aggregation via the Helena AggRAM system, and platelet RNA isolation and storage via magnetic separation using the StemCell kit to deplete CD45+ and GlyA+ cells. Microvascular function was assessed via sublingual sidestream darkfield imaging, and brachial artery reactivity testing was used to evaluate large vessel function. Stored RNA was isolated and analysed by RNA sequencing (Illumina HiSeq 4000 sequencing). FASTQ files from RNA sequencing were processed using the Seq-N-Slide pipeline. Reads were aligned to the hg38 genome using STAR V.2.6.18 and quantified using featureCounts V.184.108.40.206
All downstream analyses were performed in R V.3.6.1. Differential expression analysis was performed via DESeq2 V.1.24. Weighted gene coexpression network analysis (WGCNA) was performed using the WGCNA package enriching for gene sets provided via msigdbr V.7.0.1. Multiple hypothesis correction was done using the Benjamini-Hochberg method. Heatmaps were created using ComplexHeatmap V.2.0.0 and all plotting were done using ggplot2 V.3.2.1. Flow cytometry was performed using a BD Accuri C6 flow cytometer and a Miltenyi Biotec MACSQuant Analyzer. All pairwise comparisons were analysed using non-parametric Wilcoxon tests. Correlational analyses were performed using non-parametric Spearman tests. For all correlational analyses exploring dose response with regard to phenotypic metric, both the correlational values for the entire data set and the Wilcoxon p value for no HCQ versus HCQ were included.
Among 132 subjects with SLE, 108 were on HCQ. The reasons patients were not on HCQ included ocular concerns, gastrointestinal discomfort, rash and patient refusal. The mean age of the entire cohort was 39.7±12.9 and 97% were female. Lupus disease activity at the time of blood draw assessed by the HYBRID SELENA Systemic Lupus Erythematosus Disease Activity Index (SLEDAI), a modification of the original SELENA SLEDAI,10 in which proteinuria UPCR (Urine Protein-Creatinine Ratio) >0.5 g/24 hours is always counted on the renal domain, was 3.58 (range 0–20). Demographics and overall SLE ACR classification criteria and SLEDAI at the time of blood draw did not differ between those on and off HCQ, except for ulcers for the former and alopecia and pyuria for the latter (table 1). Platelet count and size were not different between groups (figure 1A). Since platelet aggregation in response to submaximal agonist concentration is a useful proxy for platelet hyper-reactivity, we assessed platelet aggregation in subjects on and off HCQ. In response to submaximal ADP at multiple concentrations, platelet aggregation was lower in patients on HCQ versus those not prescribed HCQ (figure 1B). There was an inverse relationship between HCQ dosing and platelet aggregation in response to ADP (shown: 1 μM: r=−0.27, p=0.008; figure 1C; online supplemental figure 1A). Since aspirin use was an exclusion criterion, aggregation in response to arachidonic acid (AA) was robust and similar between groups. However, after incubating platelets with aspirin (3 mM) in vitro, platelet aggregation in response to AA was lower in the HCQ group compared with the non-HCQ group (p=0.017; figure 1B).
To investigate potential mechanisms of HCQ relating to decreased platelet aggregation, we evaluated platelet RNA sequencing on samples from 49 patients (41 on HCQ, 8 not on HCQ). Using WGCNA’s eigengene functionality and Gene Ontology (GO) terms from MsigDB, we reduced platelet-specific pathway expression on a per sample basis to a single eigengene. These values were then correlated for each pathway with HCQ use, dose and dose-adjusted for weight. Several pathways were negatively correlated with HCQ dosing, including most significantly platelet dense granule membrane (r=−0.42, p<0.01) and positive regulation of platelet activation (r=−0.37, p=0.01; figure 1D). Positive regulation of platelet activation was inversely related to HCQ, especially when dosing reached levels above the recommended 5 mg/kg (figure 1E).
The gene encoding for P-selectin (SELP) was a major contributor to both of these pathways. The expression of SELP negatively correlated (r=−0.41, p=0.003; figure 1F) with HCQ dose/weight. To validate this finding, P-selectin surface expression in response to thrombin agonist was measured via flow cytometry and reported as a ratio of basal P-selectin expression. Subjects on HCQ had a significantly reduced fold change in P-selectin expression compared with subjects not taking HCQ (p=0.037; figure 1G; online supplemental figure 1B) and this correlated with HCQ dose/weight, although not quite reaching a significance level of p<0.05 (r=−0.29, p=0.066; figure 1G).
Finally, we investigated vascular function in subjects on and off HCQ. Subjects on HCQ had improved microvascular function compared with patients who were not taking HCQ, as demonstrated by an increased proportion of sublingual capillaries filled with red blood cells (p=0.014) and smaller perfused boundary region (PBR, p=0.042). HCQ dosing correlated with both parameters of vascular function (r=−0.52, p=0.007 for PBR, figure 1H; Online supplemental figure 1C; r=0.55, p=0.004, red blood cell fillings, figure 1I; online supplemental figure 1D). Brachial artery reactivity testing also trended positively with HCQ dose/weight (r=0.43, p=0.056; figure 1J; online supplemental figure 1E).
Overall, patients with SLE taking HCQ displayed reduced platelet aggregation and improved metrics of microvascular and large vessel function when compared with those with similar SLE manifestations not on HCQ. Furthermore, these effects appear to be dose-dependent, especially when HCQ was prescribed above the recommended dose of 5 mg/kg. The analysis of platelet transcriptomic data confirmed these results by revealing that platelet activation pathways were negatively correlated with HCQ use, dose and HCQ-adjusted dose/weight.
Given the importance of proper dose per weight to the prescribing of HCQ, we focused results on the correlations between transcriptional expression and the dose/weight ratio. Two pathways that were significantly negatively correlated with HCQ dose/weight were platelet dense granule membrane and positive regulation of platelet activation. These pathways are both related specifically to the composition of the active components in platelets, and the activation of platelets for cell–cell communication and aggregation. P-selectin (SELP) is a major contributor to both of these pathways’ transcriptional profiles. Indeed, P-selectin transcription revealed a negative correlation with dose/weight (r=−0.41, p=0.0031). Consistently, a reduced fold change in P-selectin surface expression was observed in activated platelets from patients on HCQ. P-selectin has been shown to play significant roles in platelet adhesion to endothelial cells and immune cells, and is directly related to platelet activation, coagulation and vascular health.11 The connections between P-selectin and SLE have not been extensively explored. Studies have shown that variations in the SELP gene have been identified to confer higher risk of developing SLE in patients, although through an unknown mechanism.12 Furthermore, recent studies in mouse models of SLE have demonstrated that P-selectin is upregulated in mice with lupus nephritis and treating mice with P-selectin blocking antibodies improved outcome and reduced renal vascular damage and hypoxic injury.13
HCQ as an antithrombotic has been described previously and patients with SLE are noted to have fewer thrombotic events when treated with HCQ.2 5 HCQ has been shown to reduce platelet aggregation in the setting of collagen and ADP-induced aggregation.14 In addition, HCQ has also been shown to affect the rheology of blood by inhibiting red blood cell aggregation.14 To our knowledge, the relationship between platelet transcriptomics and HCQ exposure has never been described, and our findings support previously established clinical effects of HCQ.
Several limitations of this study are acknowledged. A majority of patients were prescribed HCQ, consistent with given current guidelines for the treatment of SLE, but this leads to a significant difference in the number of patients in each cohort. Although gene expression differences between subjects on and off HCQ were less significant than the results seen from dose–response correlations, the sample size of those subjects not on HCQ was limited, therefore reducing our statistical power. Reasons for not taking HCQ included ocular concerns, gastrointestinal discomfort, rash and patient declination. The use of medications that could influence platelet reactivity precluded participation by patients, particularly those with active arthritis. HCQ blood levels were not available. The absence of HCQ levels may overinterpret the presumption of HCQ effects since it is well described that adherence to the drug is a management issue despite continued reinforcement of compliance. While not mitigating having blood levels, we at least attempted to address levels by considering HCQ dose normalised by weight. Moreover, given concerns for retinal toxicity, dosing may often be reduced in stable patients and thus analysis by mg/kg prescribed was also done to see whether HCQ conferred favourable vascular effects even at low prescribed doses.15 Finally, the associations between HCQ and platelet activity were observed in a cross-sectional analysis and an effect on long-term cardiovascular outcomes cannot necessarily be implied.
In aggregate, data from this study demonstrate a dose-dependent association between HCQ and platelet activity, transcriptome and overall vascular health. These results reinforce the antithrombotic properties of HCQ in patients with SLE and potential protective benefit in a disease where premature atherosclerosis is a significant comorbidity.
The authors thank the individuals who agreed to participate in this trial and the staff of the NYU Langone facilities that enabled this work to be done.
MGC and ESL-W contributed equally.
JPB and JSB contributed equally.
Contributors MGC, ESL-W and MG wrote the initial draft of the paper. ESL-W and HEB performed the experiments related to platelet behaviour and isolated the RNA from the platelets. MG and AE collected and curated the clinical data for the patients. MGC performed the bioinformatic processing and analysis for the RNA sequencing. KM, PI, HMB, SK, NS, RC and KR all provided key insights for the overall project and contributed to and edited the manuscript. JPB and JB oversaw the experiments, clinical collection and analytical processes. All authors edited, contributed to and approved the final manuscript.
Funding This work was supported by the National Institutes of Health (grant R01HL139909, JPB and JB; grant T32GM136573, MGC) and National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH (grant P50-AR-07059, JPB and PI).
Competing interests None declared.
Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.
Patient consent for publication Not required.
Ethics approval The study was reviewed and approved by the NYU Langone Data and Safety Monitoring Board.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon reasonable request.
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