Sage Journals: Discover world-class research

Abstract

This study aimed to examine the hemostatic abnormalities in patients with systemic sclerosis (SSc) and the relationship between these abnormalities and thrombotic events (THEs), focusing on the difference in diffuse cutaneous SSc (dcSSc) and limited cutaneous SSc (lcSSc). The plasma levels of ADAMTS-13 (a disintegrin-like and metalloproteinase with thrombospondin type 1 motifs 13), von Willebrand factor (VWF), VWF propeptide (VWFpp), d-dimer, and soluble fibrin (SF) were measured in 233 patients with SSc. The relationship between their levels and organ involvement, including THEs and interstitial lung disease (ILD), was evaluated. The plasma levels of VWF and VWFpp were significantly elevated and ADAMTS-13 activity was significantly decreased in patients with SSc compared to healthy participants. The VWFpp in dcSSc was significantly higher than in lcSSc. Twelve patients with SSc were complicated with acute THE, and 25 patients with SSc were complicated with past THE. The plasma levels of d-dimer and SF were significantly elevated in patients with SSc having THE. The plasma levels of VWF and VWFpp were significantly elevated in patients with SSc having ILD. The plasma levels of d-dimer were elevated in patients with SSc having other connective tissue diseases (CTDs). The plasma levels of ADAMTS-13 were significantly decreased and VWF, VWFpp, and SF were increased in patients with a d-dimer level of ≥1 μg/mL. Systemic sclerosis carries a high risk of THE, especially in patients with other CTDs. Plasma hemostasis-related markers are closely related to ILD and THE. These markers are important as markers of organ involvement as well as THE.

Keywords

systemic sclerosis VWF VWFpp ADAMTS-13 soluble fibrin

Introduction

Connective tissue diseases (CTDs), especially systemic lupus erythematosus (SLE),¹ are well known to be accompanied by a high-risk disease of developing various thrombotic events (THEs), including deep vein thrombosis (DVT), pulmonary embolism (PE), cerebral thrombosis, acute coronary syndrome, and thrombotic microangiopathy (TMA).² While the reported frequency of THEs is low in non-SLE CTD patients, including those with systemic sclerosis (SSc),³ the risk of THEs in patients with SSc is still higher than in non-SSc individuals.^{4
–6} Indeed, cardiovascular disease accounts for 20% to 30% of all SSc deaths.⁷ Various biomarkers of inflammation, thrombophilia, and organ dysfunction have been identified in patients with SSc.^{8

–12} It is also known that around half of patients with SSc having renal crisis develop TMA.¹³

ADAMTS-13, a disintegrin-like and metalloproteinase with thrombospondin type 1 motifs 13, cleaves unusual large multimers of von Willebrand factor (VWF) to inhibit the pathological activation of platelets. Thrombotic thrombocytopenic purpura, caused by a severe deficiency of ADAMTS-13,¹⁴ is a major complication in CTD and causes around 20% of TMA in patients with CTD.¹⁵ The serum levels of the vascular endothelial cell injury markers VWF, VWF propeptide (VWFpp),¹⁶ and thrombomodulin (TM),¹⁷ are elevated in patients with TMA or disseminated intravascular coagulation.

As we reported previously, the plasma levels of VWF and VWFpp are elevated in patients with SSc and antiphospholipid antibody syndrome (APS),¹⁸ suggesting the presence of vascular endothelial cell injury. In the present study, we measured the plasma levels of ADAMTS-13, VWF, VWFpp, and several other hemostatic biomarkers in 233 patients with SSc and evaluated the relationship between these hemostatic biomarkers and several manifestations of SSc, including the spread of skin involvement, THE, interstitial lung disease (ILD), and complication of other CTDs.

Materials and Methods

The patients who consulted the clinics of dermatology or hematology at Mie University Hospital from January 1, 1994, to December 31, 2016, were enrolled in the present study. We diagnosed SSc according to the 2013 Classification Criteria for Systemic Sclerosis (American College of Rheumatology/European League Against Rheumatism [ACR/EULAR])¹⁹ and classified patients as having limited cutaneous SSc (lcSSc) and diffuse cutaneous SSc (dcSSc) based on the definition of LeRoy and Medsger.²⁰ Systemic lupus erythematosus was diagnosed by the 1997 update of the 1982 American College of Rheumatology Revised Criteria for Classification of Systemic Lupus Erythematosus.²¹ Dermatomyositis and polymyositis were diagnosed based on the criteria of Bohan and Peter.^22,23 Sjögren syndrome was diagnosed based on the 2012 American College of Rheumatology Classification Criteria for Sjögren Syndrome.²⁴ Rheumatoid arthritis was diagnosed based on the 2010 Rheumatoid Arthritis Classification Criteria: ACR/EULAR.²⁵ As controls, healthy volunteers matched for age and sex were randomly selected.

Thrombosis was diagnosed based on the clinical manifestations and was confirmed by appropriate clinical and radiological examinations. The presence of PE and DVT was diagnosed by a whole-leg compression ultrasound examination and/or contrast computed tomography (CT). Cerebral and other organ thromboses were diagnosed by CT or magnetic resonance imaging. Thrombotic events diagnosed within 3 days after the onset were classified as acute THE. Thrombosis that developed more than a month before was classified as past THE. The presence of ILD was defined by the radiology reports: the presence of any ground-glass appearance, fibrotic interstitial changes, or honeycombing. ILD was then confirmed by high-resolution CT.^26,27

The plasma samples were prepared as reported previously.⁸ In brief, plasma was separated using a 0.38% sodium citrate preparation with 3000g centrifugation at 4°C for 15 minutes. The plasma was stored at −80°C until use. The ADAMTS-13 activity was measured by Kokame method using a FRETS-VWF73 peptide (Peptide Institute, Inc, Osaka, Japan).²⁸ The plasma levels of VWF and VWFpp were measured by a VWF & Propeptide assay kit (GTI Diagnostics, Waukesha, Wisconsin).²⁹ The plasma levels of soluble fibrin (SF) and d-dimer were measured by 2 latex agglutination methods using IATRO-SF and LPIA-ACE d-Dimer II (LSI Medience Corporation, Tokyo, Japan), respectively. The plasma level of TM was measured by a chemiluminescent enzyme immunoassay using STACIA CLEIA TM (LSI Medience Corporation). The tricuspid regurgitation pressure gradient (TRPG) was measured using cardiac ultrasound.

The study protocol was approved by the human ethics review committee of Mie University School of Medicine (approval number: 2629), and informed consent was obtained from all the patients. This study was carried out in accordance with the principles of the Declaration of Helsinki.

Statistical Analyses

The results were expressed as the median (25th-75th percentiles). Differences between groups were analyzed using the Mann-Whitney U test. P values of <.05 were considered to indicate a statistically significant difference. The significance of a frequency was examined by the χ² test. All statistical analyses were performed using the SPSS Statistics software program (version 22; IBM, New York, New York).

Results

The laboratory data of 233 patients with SSc were serially investigated, including 173 patients with lcSSc (mean age, 64.5 [11.7] years) and 60 patients with dcSSc (mean age, 68.0 [11.3] years),¹⁹ as shown in Table 1. All of THEs that developed in lcSSc and dcSSc are shown in Table 2. In patients with SSc, the plasma levels of ADAMTS-13 were significantly decreased and the plasma levels of VWF and VWFpp were significantly elevated compared to those of healthy controls (P < .001; Figure 1A–C).

Table 1.

Patients.

	n		n			n
All SSc: N = 233	lcSSc	173	lcSSc without other CTD or RA	113
			lcSSc with other CTD or/and RA	60	RA	16
					SS	12
					SLE	8
					PM	8
					RA and SS	5
					SLE and RA	4
					DM	3
					SLE and SS	3
					SLE and PM	1
	dcSSc	60	dcSSc without other CTD or RA	39
			dcSSc with other CTD or/and RA	21	RA	8
					SLE	4
					SS	3
					PM	2
					DM	1
					SLE and RA	1
					SLE and SS	1
					RA and SS	1

Abbreviations: CTD, connective tissue disease; dcSSc, diffuse cutaneous SSc; DM, dermatomyositis; lcSSc, limited cutaneous SSc; PM, polymyositis; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; SS, Sjögren syndrome; SSc, systemic sclerosis.

Table 2.

All THEs Developed in LcSSc and DcSSc.

	n			n
lcSSc (N = 173)	With acute THE	10 (5.8%)	DVT or/and PE	6
			Portal vein thrombosis	1
			Splenic vein thrombosis	1
			MI	1
			CI	1
	With past THE	19 (11%)	CI	12
			DVT or/and PE	4
			MI	3
	Without THE	144 (83.2%)
dcSSc (N = 60)	With acute THE	2 (3.3%)	TTP	2
	With past THE	6 (10%)	MI	3
	With past THE	6 (10%)	CI	3
	Without THE	52 (86.7%)

Abbreviations: CI, cerebral infarction; dcSSc, diffuse cutaneous SSc; DVT, deep vein thrombosis; lcSSc, limited cutaneous SSc; ; MI, myocardial infarction; PE, pulmonary thrombosis; THE, thrombotic event; TTP, thrombotic thrombocytopenic purpura.

Figure 1.

A, Plasma ADAMTS-13 activity in systemic sclerosis (SSc) and healthy volunteers. B, Plasma von Willebrand factor (VWF) levels in SSc and healthy volunteers. C, Plasma von Willebrand factor propeptide (VWFpp) levels in SSc and healthy volunteers. ***P < .001 (Mann-Whitney U test).

Between patients with lcSSc and dcSSc, no significant difference was detected in values of ADAMTS-13, VWF, D-dimer, SF, TM/estimated glomerular filtration rate (eGFR), or TRPG. However, the plasma levels of VWFpp and eGFR were significantly higher in patients with dcSSc than in those with lcSSc (P < .05). There were no significant differences in the risk of acute THE or past THE between lcSSc and dcSSc (Table 3).

Table 3.

A Comparison Between LcSSc and DcSSc.^a

		SSc: N = 233 (F/M, 211/22)		P Value
		lcSSc (n = 173)	dcSSc (n = 60)	P Value
Age, years, mean (SD)		64.5 (11.7)	68.0 (11.3)	.76
F/M		158/15	53/7	.61
SSc	SSc without other CTD	113	39	.90
SSc	SSc with other CTD	60	21	.90
THE in this study	Acute THE	10	2	.74
	Past THE	19	6	1.0
	Total	29	8	.68
ILD		25	25	<.001
ADAMTS-13 (%)		80.66 (60.76, 97.91)	87.29 (66.98, 98.87)	.10
VWF, U/dL		140 (95, 162)	138 (114, 199)	.33
VWFpp, U/dL		114 (85, 157)	128 (111, 159)	.049
d-dimer, μg/mL		0.52 (0.32, 1.39)	0.53 (0.35, 1.43)	.83
Soluble fibrin, μg/mL		1.00 (0.30, 3.00)	0.40 (0.30, 2.60)	.13
TM/eGFR, mL/minute/1.73 m²		0.1843 (0.1337, 0.2370)	0.1596 (0.1013, 0.2227)	.097
eGFR, mL/minute/1.73 m²		72.2 (60.3, 83.5)	81.2 (66.6, 90.2)	.016
TRPG, mm Hg		20 (17, 26)	21 (18, 23)	.26

Abbreviations: CTD, connective tissue disease; dcSSc, diffuse cutaneous SSc; eGFR, estimated glomerular filtration rate; F, female; ILD, Interstitial lung disease; lcSSc, limited cutaneous SSc; M, male; SD, standard deviation; SSc, systemic sclerosis; THE, thrombotic event; TM, thrombomodulin; TRPG, tricuspid regurgitation pressure gradient; VWF, von Willebrand factor; VWFpp, von Willebrand factor propeptide.

^aThe data are presented as the median (Q1, Q3).

The plasma levels of d-dimer and SF in patients with SSc with THE were significantly higher than those in patients without THE (P < .001 and P < .01, respectively). The C-reactive protein (CRP), lactate dehydrogenase (LDH), prothrombin time (PT), and activated partial thromboplastin time (APTT) also showed significant difference between patients having SSc with and without THE (Table 4).

Table 4.

A Comparison Between Patients Having SSc With and Without THE.^a

	SSc: N = 233 (F/M, 211/22)		P Value
	Without THE: n = 196	With THE: n = 37	P Value
lcSSc/dcSSc	144/52	21/16	.49
ILD	40	10	.39
Age, years	65.0 (58.0, 73.0)	67.0 (60.5, 76.0)	.17
ADAMTS-13, %	85.49 (63.76, 99.15)	78.32 (37.50, 95.38)	.17
VWF, U/dL	136 (96, 165)	144 (128, 164)	.43
VWFpp, U/dL	118 (87, 156)	145 (98, 195)	.077
d-dimer, μg/mL	0.50 (0.31, 1.07)	2.39 (0.73, 6.69)	<.001
Soluble fibrin, μg/mL	0.70 (0.30, 3.00)	3.75 (0.30, 21.80)	.0040
TM/eGFR, ng/mL²/min/1.73 m²	0.1770 (0.1222, 0.2338)	0.1877 (0.1402, 0.2331)	.86
eGFR, mL/min/1.73 m²	75.4 (63.7, 87.2)	68.5 (57.7, 78.5)	.072
TRPG, mm Hg	20 (17, 25)	21 (20, 25)	.55
PT, seconds	11.5 (10.8, 12.1)	11.8 (11.1, 13.4)	.015
APTT, seconds	29.4 (27.0, 31.6)	30.1 (28.3, 35.6)	.039
CRP, mg/dL	0.080 (0.030, 0.38)	0.18 (0.040, 1.76)	.047
LDH, IU/L	201 (178, 235)	235(206, 320)	.0020
IgG, mg/dL	1256 (1095, 1555)	1291 (1008, 1651)	.95

Abbreviations: APTT, activated partial thromboplastin time; CRP, C-reactive protein; dcSSc, diffuse cutaneous SSc; eGFR, estimated glomerular filtration rate; F, female; IgG, immunoglobulin G; ILD, Interstitial lung disease; lcSSc, limited cutaneous SSc; LDH, Lactate dehydrogenase; M, male; PT, prothrombin time; SSc, systemic sclerosis; THE, thrombotic event; TM, thrombomodulin; TRPG, tricuspid regurgitation pressure gradient; VWF, von Willebrand factor; VWFpp, von Willebrand factor propeptide.

^aThe data are presented as the median (Q1, Q3).

The prevalence of ILD in patients with dcSSc was significantly higher than in those with lcSSc, in concordance with previous findings (P < .001; Table 3). Surprisingly, the plasma levels of VWF and VWFpp were significantly higher in the patients with SSc with ILD than in those without ILD (P < .05). In patients with SSc having other CTDs, the plasma levels of VWF and VWFpp in patients with SSc with ILD were significantly high than in those without ILD (P < .05; Table 5).

Table 5.

A Comparison Between Patients Having SSc With and Without ILD.^a

		Without ILD	With ILD	P Value
All SSc	ADAMTS-13, %	83.11 (62.08, 99.65)	86.24 (61.25, 97.34)	.52
	VWF, U/dL	132 (94, 162)	154 (132, 208)	.013
	VWFpp, U/dL	114 (84, 157)	133 (109, 171)	.028
	D-dimer, μg/mL	0.51 (0.31, 1.18)	1.20 (0.36, 2.63)	.052
	Soluble Fibrin, μg/mL	0.90 (0.30, 3.00)	0.50 (0.30, 3.00)	.63
	TM/eGFR, ng/mL²/min/1.73 m²	0.1817 (0.1192, 0.2327)	0.1600 (0.1412, 0.2801)	.98
	eGFR, mL/min/1.73 m²	75.6 (64.4, 88.2)	70.3 (61.1, 79.2)	.050
	TRPG, mm Hg	21 (17, 25)	20 (17, 22)	.57
SSc without other CTD	ADAMTS-13, %	85.41 (62.58, 102.92)	86.24 (46.34, 97.42)	1.0
	VWF, U/dL	135 (90, 162)	151 (118, 163)	.23
	VWFpp, U/dL	114 (83, 157)	117 (107, 147)	.56
	d-dimer, μg/mL	0.50 (0.29, 1.05)	0.76 (0.34, 1.97)	.14
	Soluble fibrin, μg/mL	0.90 (0.30, 3.00)	0.85 (0.30, 3.50)	.79
	TM/eGFR, ng/mL²/min/1.73 m²	0.1822 (0.1169, 0.2407)	0.1603 (0.1380, 0.2839)	.83
	eGFR (mL/min/1.73 m²	76.3 (65.0, 87.8)	71.1 (62.6, 79.6)	.15
	TRPG, mm Hg	21 (17, 25)	19 (15, 26)	.47
SSc with other CTD	ADAMTS-13, %	82.78 (55.23, 90.18)	84.78 (68.92, 97.28)	.28
	VWF, U/dL	129 (93, 160)	166 (136, 190)	.015
	VWFpp, U/dL	112 (84, 157)	152 (125, 192)	.018
	d-dimer, μg/mL	0.62 (0.43, 1.51)	1.23 (0.41 - 3.17)	.32
	Soluble fibrin, μg/mL	0.90 (0.30, 3.00)	0.50 (0.30, 5.08)	.72
	TM/eGFR, ng/mL²/min/1.73 m²	0.1808 (0.1266, 0.2192)	0.1490 (0.09376, 0.2638)	.91
	eGFR, mL/min/1.73 m²	74.8 (60.1, 89.0)	68.8 (57.5, 79.9)	.23
	TRPG, mm Hg	20 (18, 22)	21 (19, 22)	.76

Abbreviations: CTD, connective tissue disease; eGFR, estimated glomerular filtration rate; ILD, Interstitial lung disease; SSc, systemic sclerosis; TM, thrombomodulin; TRPG, tricuspid regurgitation pressure gradient; VWF, von Willebrand factor; VWFpp, von Willebrand factor propeptide.

^aThe data are presented as the median (Q1, Q3).

The plasma d-dimer level of patients having SSc with other CTDs was significantly higher than that of patients having SSc without other CTDs (P < .05; Table 6). The plasma level of ADAMTS-13 was significantly lower in patients with SSc having a high d-dimer level (≥1 μg/mL) than in those with a low d-dimer level (<1 μg/mL). Interestingly, patients with a high d-dimer level (≥1 μg/mL) showed higher VWF, VWFpp, SF, LDH, and CRP levels as well as daily and total corticosteroid doses and duration than patients with a low d-dimer level (<1 μg/mL). In contrast, the TM/eGFR, eGFR, TRPG, age, PT, APTT, and immunoglobulin G titer showed no significant difference between the low and high d-dimer groups (Table 7).

Table 6.

A Comparison Between Patients Having SSc With and Without Other CTD.^a

	SSc Without Other CTD: n = 152	SSc With Other CTD: n = 81	P Value
ADAMTS-13, %	85.57 (62.58, 101.23)	82.57 (59.27, 92.68)	.28
VWF, U/dL	136 (99, 162)	140 (101, 194)	.21
VWFpp, U/dL	114 (87, 157)	131 (100, 171)	.081
d-dimer, μg/mL	0.50 (0.31, 1.16)	0.91 (0.41, 1.94)	.026
Soluble fibrin, μg/mL	0.90 (0.30, 3.00)	0.70 (0.30, 3.00)	.92
TM/eGFR, ng//mL²/min/1.73 m²	0.1813 (0.1202, 0.2425)	0.1757 (0.1272, 0.2215)	.79
eGFR, mL/min/1.73 m²	75.7 (64.4, 86.5)	73.0 (60.3, 86.7)	.43
TRPG, mm Hg	21 (16, 26)	20 (18, 22)	.87

Abbreviations: CTD, connective tissue disease; eGFR, estimated glomerular filtration rate; SSc, systemic sclerosis; TM, thrombomodulin; TRPG, tricuspid regurgitation pressure gradient; VWF, von Willebrand factor; VWFpp, von Willebrand factor propeptide.

^aThe data are presented as the median (Q1, Q3).

Table 7.

A Comparison Between Patients Having SSc With Low and High D-Dimer Level.^a

	d-Dimer <1 μg/mL	d-Dimer ≥1 μg/mL	P Value
lcSSc/dcSSc	83/30	54/17	.73
THE (acute or past)	8	24	<.001
Acute THE	0	10	<.001
Past THE	8	14	.038
ILD	17	21	.024
Age, years	66.0 (57.0, 73.0)	69.0 (60.0, 76.0)	.13
ADAMTS-13, %	87.58 (70.03, 102.09)	48.50 (37.50, 79.39)	.0010
VWF, U/dL	127 (85, 156)	147 (132, 197)	.012
VWFpp, U/dL	113 (85, 142)	156 (126, 188)	.0020
Soluble fibrin, μg/mL	0.40 (0.30, 2.20)	4.45 (1.43, 9.13)	<.001
TM/eGFR, ng/mL²/min/1.73 m²	0.1675 (0.1154, 0.2251)	0.1828 (0.1481, 0.2579)	.56
eGFR, mL/min/1.73 m²	77.5 (63.7, 87.0)	70.5 (63.2, 86.0)	.33
TRPG, mm Hg	21 (18, 25)	21 (19, 28)	.65
PT, seconds	11.6 (11.0, 12.3)	11.6 (10.9, 12.4)	.80
APTT, seconds	29.7 (27.6, 32.3)	29.8 (27.6, 33.3)	.82
CRP, mg/dL	0.060 (0.030, 0.17)	0.59 (0.12, 3.28)	<.001
LDH, IU/L	197 (179, 230)	220 (180, 291)	.0090
IgG, mg/dL	1239 (1037, 1498)	1323 (1029, 1693)	.65
Dose of steroid	0 (0, 5)	5 (0, 10)	.0010
, prednisolone mg	0 (0, 5)	5 (0, 10)	.0010
Duration of steroid, years	0.11 (0, 8.1)	5.6 (0, 11.8)	.0030
Total dose of steroid	1288 (0, 16620)	13500 (0, 28560)	.0010
, prednisolone mg	1288 (0, 16620)	13500 (0, 28560)	.0010

Abbreviations: APTT, activated partial thromboplastin time; CRP, C-reactive protein; dcSSc, diffuse cutaneous SSc; eGFR, estimated glomerular filtration rate; IgG, immunoglobulin G; ILD, Interstitial lung disease; lcSSc, limited cutaneous SSc; LDH, Lactate dehydrogenase; PT, prothrombin time; SSc, systemic sclerosis; THE, thrombotic event; TM, thrombomodulin; TRPG, tricuspid regurgitation pressure gradient; VWF, von Willebrand factor; VWFpp, von Willebrand factor propeptide.

^aThe data are presented as the median (Q1, Q3).

Discussion

Systemic sclerosis induces systemic inflammation followed by severe vascular lesions of small arteries, smooth muscle involvement of digestive systems, and collagen deposition in skin, lung, and various internal organs. Clinically, typical skin lesions, including digital ulcers, nail fold capillary thrombosis, and digital pitting scars, are suggestive of the presence of ischemic vascular changes and hemostatic and/or coagulation abnormalities. In general, these changes are more apparent in dcSSc than in lcSSc.

However, in contrast to arterial vascular changes, the venous abnormalities associated with SSc have not been fully investigated. The incidence of venous thromboembolism (VTE) per 1000 person-years was reported to be 6.56 in patients with SSc, and the multivariable hazard ratio for VTE among patients with SSc was 3.47 in comparison to non-SSc patients.⁴ Interestingly, the present study noted the development of acute THE in 5.8% of patients with lcSSc and 3.3% of patients with dcSSc and past THE in 11.0% of patients with lcSSc and 10.0% of patients with dcSSc. This suggests a high risk of THE in SSc. Surprisingly, the prevalence of THE showed no marked difference between patients with lcSSc and dcSSc. This implies the presence of other factors related to THE in patients with SSc. The overlap of other CTDs is common in patients with SSc, and CTDs other than SSc, especially SLE, induce the development of various THEs more often than does SSc.^3,30 The present study revealed an increase in the THE risk by the overlap of CTDs complicating hemostatic abnormalities.

Patients with SSc showed lower plasma levels of ADAMTS-13 and higher plasma levels of VWF and VWFpp than healthy participants, suggesting that high coagulability exists in patients with SSc. The plasma levels of d-dimer and SF were high in patients with THE, suggesting that SSc may be a causative condition for THE. Soluble fibrin has a shorter half-life than d-dimer, and d-dimer is a more sensitive marker for clinical diagnosis for THE.³¹ Thus, the increased d-dimer levels in SSc suggest a thrombotic state.³² A d-dimer level of ≥1 μg/mL has been proposed as a hallmark for a prethrombotic state.³³ In the present study, plasma levels of ADAMTS-13 were lower and plasma levels of VWF and VWFpp were higher in patients with SSc having high D-dimer levels (≥1 μg/mL) than in those with low d-dimer levels (<1 μg/mL). These findings suggest that a decreased ADAMTS-13 level and elevated VWF and VWFpp levels indicate the presence of hypercoagulability in patients with SSc. Changes in the VWF and VWFpp levels might result from vascular endothelial cell injury.¹⁶ The plasma levels of d-dimer in patients having SSc with other CTDs were higher than in patients having SSc without CTDs, possibly due to the presence of CTDs such as SLE or APS.⁸

The plasma levels of VWFpp were significantly elevated in patients with dcSSc, suggesting the greater vascular endothelial cell injury in patients with dcSSc than in patients with lcSSc. The prevalence of ILD is known to be higher in patients with dcSSc than in patients with lcSSc. However, the pathogenesis of ILD has not been fully clarified. Surprisingly, the plasma levels of VWF and VWFpp were significantly higher in the patients with SSc with ILD than in those without ILD in the present study, suggesting a close relationship between ILD and vascular endothelial cell injury. Interestingly, very strong expression of VWF messenger RNA and the presence of immunoreactive VWF in the endothelial cells of murine small and microvessels of the lungs have been reported.³⁴ The present results suggest the involvement of VWF and VWFpp in pulmonary endothelial cells in the pathogenesis of ILD in patients with SSc.

In conclusion, SSc carries a high risk of THE, especially in patients with other CTDs. Plasma hemostasis-related markers are closely related to ILD and THE. These markers are important as markers of organ involvement as well as THE.

Footnotes

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported in part by a Grant-in-Aid from the Ministry of Health, Labor and Welfare and Research on intractable diseases of Japan for systemic sclerosis.

References

Ünlü

Zuily

Erkan

. The clinical significance of antiphospholipid antibodies in systemic lupus erythematosus. Eur J Rheumatol. 2016;3(2):75–84.

Wada

Matsumoto

Yamashita

. Natural history of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Semin Thromb Hemost. 2014;40(8):866–873.

Romero-Díaz

García-Sosa

Sánchez-Guerrero

. Thrombosis in systemic lupus erythematosus and other autoimmune diseases of recent onset. J Rheumatol. 2009;36(1):68–75.

Schoenfeld

Choi

Sayre

Aviña-Zubieta

. Risk of pulmonary embolism and deep venous thrombosis in systemic sclerosis: a general population-based study. Arthritis Care Res (Hoboken). 2016;68(2):246–253.

Man

Zhu

Zhang

. The risk of cardiovascular disease in systemic sclerosis: a population-based cohort study. Ann Rheum Dis. 2013;72(7):1188–1193.

Ngian

Sahhar

Proudman

Stevens

Wicks

Van Doornum

. Prevalence of coronary heart disease and cardiovascular risk factors in a national cross-sectional cohort study of systemic sclerosis. Ann Rheum Dis. 2012;71(12):1980–1983.

Mok

Lau

. The burden and measurement of cardiovascular disease in SSc. Nat Rev Rheumatol. 2010;6(7):430–434.

Ihn

Sato

Fujimoto

Takehara

Tamaki

. Increased serum levels of soluble vascular cell adhesion molecule-1 and E-selectin in patients with systemic sclerosis. Br J Rheumatol. 1998;37(11):1188–1192.

Andersen

Caidahl

Kazzam

. Correlation between increased nitric oxide production and markers of endothelial activation in systemic sclerosis: findings with the soluble adhesion molecules E-selectin, intercellular adhesion molecule 1, and vascular cell adhesion molecule 1. Arthritis Rheum. 2000;43(5):1085–1093.

10.

Cerinic

Valentini

Sorano

. Blood coagulation, fibrinolysis, and markers of endothelial dysfunction in systemic sclerosis. Semin Arthritis Rheum. 2003;32(5):285–295.

11.

Denton

Bickerstaff

Shiwen

. Serial circulating adhesion molecule levels reflect disease severity in systemic sclerosis. Br J Rheumatol. 1995;34(11):1048–1054.

12.

Hettema

Zhang

Stienstra

Smit

Bootsma

Kallenberg

. No effects of bosentan on microvasculature in patients with limited cutaneous systemic sclerosis. Clin Rheumatol. 2009;28(7):825–833.

13.

Penn

Howie

Kingdon

. Scleroderma renal crisis: patients characteristics and long-term outcomes. QJM. 2007;100(8):485–494.

14.

Scully

. Thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome microangiopathy in pregnancy. Semin Thromb Hemost. 2016;42(7):774–779.

15.

Fujimura

Matsumoto

. Registry of 919 patients with thrombotic microangiopathies across Japan: database of Nara Medical University during 1998-2000. Intern Med. 2010;49(1):7–15.

16.

Habe

Wada

Ito-Habe

. Plasma ADAMTS13, von Willebrand factor (VWF) and VWF propeptide profiles in patients with DIC and related diseases. Thromb Res. 2012;129(5):598–602.

17.

Mori

Wada

Okugawa

. Increased plasma thrombomodulin as a vascular endothelial cell marker in patients with thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Clin Appl Thromb Hemost. 2001;7(1):5–9.

18.

Habe

Wada

Matsumoto

. Plasma ADAMTS13, von Willebrand factor (VWF) and VWF propeptide profiles in patients with connective tissue diseases and antiphospholipid syndrome. Clin Appl Thromb Hemost. 2017;23(6):622–630.

19.

www.rheumatology.org/Portals/0/Files/2013%20ACR%20EULAR%20SSc%20Classification%20Criteria_Complete20%20article.pdf.

20.

LeRoy

Black

Fleischmajer

. Scleroderma(systemic sclerosis): classification, subsets and pathogenesis. J Rheumatol. 1988;15(2):202–205.

21.

www.rheumatology.org/Portals/0/Files/1997%20Update%20of%201982%20Revised.pdf.

22.

Bohan

Peter

. Polymyositis and dermatomyositis (first of two parts). N Engl J Med. 1975;292(7):344–347.

23.

Bohan

Peter

. Polymyositis and dermatomyositis (second of two parts). N Engl J Med. 1975;292(8):403–407.

24.

www.rheumatology.org/Portals/0/Files/2012%20ACR%20Sjogrens%20Classification%20Criteria%20v.pdf.

25.

www.rheumatology.org/Portals/0/Files/2010_revised_criteria_classification_ra.pdf.

26.

Steele

Hudson

Baron

; Canadian Scleroderma Research Group. Clinical decision rule to predict the presence of interstitial lung disease in systemic sclerosis. Arthritis Care Res (Hoboken). 2012;64(4):519–524.

27.

Hinchcliff

Fischer

Schiopu

Steen

; PHAROS Investigators. Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma (PHAROS): baseline characteristics and description of study population. J Rheumatol. 2011;38(10):2172–2179.

28.

Kokame

Nobe

Kokubo

Okayama

Miyata

. FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay. Br J Haematol. 2005;129(1):93–100.

29.

Ito-Habe

Wada

Matsumoto

. Elevated von Willebrand factor propeptide for the diagnosis of thrombotic microangiopathy and for predicting a poor outcome. Int J Hematol. 2011;93(1):47–52.

30.

Lee

Pope

. A meta-analysis of the risk of venous thromboembolism in inflammatory rheumatic diseases. Arthritis Res Ther. 2014;16(5):435.

31.

Yamaguchi

Wada

Miyazaki

. Fibrin-related markers for diagnosing acute-, subclinical-, and pre-venous thromboembolism in patients with major orthopedic surgery. Int J Hematol. 2016;103(5):560–566.

32.

Hasegawa

Wada

Miyazaki

. The evaluation of fibrin-related markers for diagnosing or predicting acute or subclinical venous thromboembolism in patients undergoing major orthopedic surgery. Clin Appl Thromb Hemost. 2017.

33.

Yamamoto

de Waard

Fearns

Loskutoff

. Tissue distribution and regulation of murine von Willebrand factor gene expression in vivo. Blood. 1998;92(8):2791–2801.

34.

Wada

Kobayashi

Abe

. Elevated levels of soluble fibrin or D-dimer indicate high risk of thrombosis. J Thromb Haemost. 2006;4(6):1253–1258.

The Plasma Levels of ADAMTS-13,von Willebrand Factor,VWFpp,and Fibrin-Related Markers in Patients With Systemic Sclerosis Having Thrombosis

Abstract

Keywords

Introduction

Materials and Methods

Statistical Analyses

Results

Discussion

Footnotes

Declaration of Conflicting Interests

Funding

References