Disease Markers

Volume 35 (2013), Issue 5, Pages 505–511

http://dx.doi.org/10.1155/2013/265051

Research Article

Procalcitonin Levels in Patients with Complete and Incomplete Kawasaki Disease

Hwa Jin Cho, Young Earl Choi, Eun Song Song, Young Kuk Cho, and Jae Sook Ma

Department of Pediatrics, Chonnam National University Hospital, Chonnam National University Medical School, 8 Hakdong, Dong-gu, Gwangju 501-757, Republic of Korea

Received 15 July 2013; Revised 10 September 2013; Accepted 16 September 2013

Academic Editor: Natacha Turck

Copyright © 2013 Hwa Jin Cho et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Incomplete Kawasaki disease (iKD) is considered to be a less complete form of Kawasaki disease (cKD), and several differences in the laboratory presentations of iKD and cKD have been noted. We investigated serum procalcitonin levels in patients with iKD, cKD, and other febrile diseases (a control group). Seventy-seven patients with cKD, 24 with iKD, and 41 controls admitted to our hospital from November 2009 to November 2011 were enrolled in the present study. We obtained four measurements of serum procalcitonin levels and those of other inflammatory markers from each patient. Samples were taken for analysis on the day of diagnosis (thus before treatment commenced; D0) and 2 (D2), 14 (D14), and 56 days (D56) after intravenous immunoglobulin infusion. We obtained control group data at D0. The mean D0 serum procalcitonin levels of cKD patients ( ng/mL) and controls ( ng/mL) were significantly higher than those of iKD patients ( ng/mL) ( and , resp.). No significant difference in mean procalcitonin level was evident among groups at any subsequent time. In conclusion, the serum procalcitonin level of patients with acute-stage cKD was significantly higher than that of iKD patients.

1. Introduction

Kawasaki disease (KD) is a form of systemic vasculitis, the etiology of which is unknown. No definitive diagnostic laboratory test exists [1, 2]. Diagnosis is based on clinical signs raising suspicion of the disease, including fever of over 5 days in duration and at least four of the following five symptoms: bilateral bulbar conjunctival infection, changes in the oral mucosa, changes in the peripheral extremities, polymorphous rash, and cervical adenopathy more than 1.5 cm in diameter [3].

Complete KD (cKD) is diagnosed if all diagnostic criteria are fulfilled, whereas incomplete KD (iKD), which occurs in 15–20% of KD patients, is diagnosed when not all clinical features are present provided that several suspicious features are evident, laboratory findings suggest the presence of KD, and alternative diagnoses have been excluded [4]. Because only some (thus not all) clinical symptoms typical of cKD are apparent, iKD diagnosis can be delayed [5, 6], and such delay is a risk factor for development of coronary artery lesions [7, 8].

Although iKD is considered to be an incomplete form of cKD, because iKD and cKD patient demographic and laboratory findings are similar [9, 10], several differences in clinical and laboratory presentations have been described. Relatively more children with iCD are found at the extremes of the childhood age spectrum (≤1 year of age, or 5–9 years old), and low levels of both serum alanine aminotransferase (ALT) and gamma-glutamyltransferase and low proportions of hyponatremia and pyuria have been reported in children with iKD [11, 12].

Procalcitonin is a peptide precursor of calcitonin, the level of which increases in response to proinflammatory stimuli, especially those of bacterial origin. Procalcitonin levels >5 ng/mL are closely associated with the presence of severe infection, usually bacteremia [13]. Various procalcitonin levels have been reported in patients with KD. Okada et al. [14] found that patients with KD had serum procalcitonin levels significantly higher than normal and bacterial infections occurred more frequently in KD patients compared to those with autoimmune diseases or viral infections, or healthy children. The cited authors also found that four patients who developed coronary aneurysms had elevated procalcitonin levels. In contrast, Chakrabartty and Apong reported that all 38 KD patients studied had low procalcitonin levels (<0.5 ng/mL) but elevated C-reactive protein (CRP) concentrations and erythrocyte sedimentation rates (ESRs) [15]. To date, no report examining possible differences in procalcitonin levels between patients with cKD and iKD has appeared. We therefore measured the serum concentrations of procalcitonin in such patients and compared these levels with those of patients with other febrile illnesses.

2. Materials and Methods

2.1. Patients

We enrolled child patients admitted to Chonnam National University Hospital from November 2009 to November 2011. Informed written consent was obtained from the parents of all patients. A total of 101 patients diagnosed with KD were enrolled. Of these, 77 were diagnosed with cKD and 24 with iKD. cKD was diagnosed if all diagnostic criteria were fulfilled [3]. iKD was diagnosed if fewer than three diagnostic criteria were met (although the presence of fever was required); the laboratory findings were typical of KD patients; and no alternative diagnosis was apparent [3]. We also enrolled 41 patients (controls) with other febrile diseases. These patients had experienced more than 3 days of fever, ranged in age from 3 months to 7 years, and had elevated CRP (>2.0 mg/dL) levels. We excluded potential controls with known congenital heart disease or clinically recognizable myocarditis.

2.2. Two-Dimensional Echocardiography

We performed two-dimensional echocardiography on four occasions on each KD patient: on the day of diagnosis (prior to treatment; D0) and 2 (D2), 14 (D14), and 56 days (D56) after intravenous immunoglobulin (IVIG) infusion. We checked all scans for the presence of pericardial effusion, coronary artery lesions, and mitral regurgitation, and we assessed left ventricular function including the ejection fraction (EF). Both the electrocardiographic rhythm and the heart rate were monitored during each examination. The size of each coronary artery was converted to a -score to compare dilatation among individuals. A coronary artery lesion was regarded as present if the -scores were ≥2.5 for both the proximal right coronary artery and the left anterior descending artery [16].

2.3. Peripheral Venous Blood Examination

Peripheral venous blood was drawn to measure serum procalcitonin levels in cKD and iKD patients and controls. We also obtained complete blood cell counts and ESRs and measured the levels of CRP, total protein, albumin, sodium, blood urea nitrogen (BUN), creatinine, aspartate aminotransferase (AST), ALT, creatine kinase (CK), CK-MB, myoglobin, troponin-I, and N-terminal pro-brain natriuretic peptide (NT-proBNP). We measured serum procalcitonin levels on four occasions in each KD patient: at D0, D2, D14, and D56. Control data were collected only during the acute stage of disease (D0). We compared the D0 values of the cKD, iKD, and control groups and those from cKD and iKD patients gathered at later times. Serum NT-proBNP was analyzed using an electrochemiluminescence immunoassay (Elecsys ProBNP Sandwich Immunoassay; Roche Diagnostics, Basel, Switzerland). Serum procalcitonin levels were quantitated by immunoassay (Elecsys BRAHMS PCT Procalcitonin, Roche). The lower and maximum limits of detection were 0.02 and 100 ng/mL, respectively.

2.4. Statistical Analysis

The chi-squared test was used to assess the statistical significance of differences in the values of independent variables, and analysis of variance (ANOVA), followed by application of Tukey’s post hoc test, was employed to compare data among the three groups. Two-way repeated-measures ANOVA followed by use of Tukey’s post hoc test was employed for intragroup analysis. Continuous variables were expressed as means ± standard deviations. A probability of <0.05 was considered to indicate statistical significance. The software package SPSS (version 20.0; SPSS, Chicago, IL) was used for all data analysis.

2.5. Ethics Statement

The present study was approved by the Institutional Review Board of Chonnam National University Hospital (Protocol no. I-2009-09-103). All data were treated confidentially.

3. Results

3.1. Patients’ Characteristics

Patient demographics are shown in Table 1. Seventy-seven cKD patients were enrolled; the male-to-female ratio was 2.08. Mean patient age was years (range, 5 months to 6.8 years) and the mean body weight  kg. Twenty-four iKD patients were enrolled, and the male-to-female ratio was 1.7. Mean patient age was years (range, 3 months to 10 years) and the mean body weight  kg. The proportion of patients at the age extremes (<1 year or ≥5 years) in the iKD group (, 58.3%) was higher than in the cKD group (, 35.0%) ().

Table 1: Demographic characteristics of patients with complete Kawasaki disease (cKD), incomplete KD (iKD), and other infectious diseases (controls).

Complete KD

Incomplete KD

Control

P value

Age (years; mean ± SD)

0.451

Gender (M/F)
52/25
15/9
28/13
0.662

Duration of fever (days; mean ± SD)

0.815

Duration of fever prior to admission (days; mean ± SD)

0.581

KD: Kawasaki disease.

All KD patients (those with either cKD or iKD) were treated with 2 g/kg intravenous immunoglobulin (IVIG) given as a single infusion. All patients were prescribed 30–50 mg/kg oral aspirin during the acute inflammatory stage, and the dose was tapered to 3–5 mg/kg after the acute stage had passed. Twelve patients with cKD and one with iKD who failed to respond to initial IVIG therapy received a second dose of IVIG. Two cKD patients who did not respond to this second dose of IVIG were given infliximab. Eight cKD and six iKD patients yielded positive bacterial blood cultures.

Forty-one patients were enrolled as controls; the male-to-female ratio was 2.15. The mean age was years (range, 11 months to 8.0 years) and the mean body weight  kg. Neither gender nor duration of fever differed significantly among the three groups. The clinical diagnoses of controls were as follows: pneumonia (), bacteremia (), acute tonsillitis (), cervical lymphadenitis (), acute bronchiolitis (), acute gastroenteritis (), acute epiglottitis (), bacterial keratoconjunctivitis (), acute otitis media (), and acute cellulitis (). Only two control patients yielded positive bacterial blood cultures.

3.2. Clinical Presentations in Patients with Kawasaki Disease

At admission, of the 77 patients with cKD, 74 (96%) had bilateral bulbar conjunctival infections, 71 (92%) a polymorphous rash, 73 (94%) changes in the oral mucosa, 61 (79%) cervical adenopathy with lymph nodes greater than 1.5 cm in diameter, and 50 (64%) changes in the peripheral extremities. Among 24 patients with iKD, 21 (87%) had bilateral bulbar conjunctival infections, 15 (62%) rash, 18 (75%) changes in the oral mucosa, 7 (29%) cervical adenopathy, and 7 (29%) changes in the peripheral extremities. All clinical features except bilateral bulbar conjunctival infection were significantly more prevalent in cKD than in iKD patients (Table 2).

Table 2: Clinical features and echocardiographic findings in patients with complete and incomplete Kawasaki disease (KD).

Complete KD

Incomplete KD

P value

Classic clinical presentations

    Bilateral bulbar conjunctival infection
74 (96.0%)
21 (87.0%)
0.178

    Polymorphous rash
71 (92.0%)
15 (62.0%)
0.007

    Changes in oral mucosa
73 (94.0%)
18 (75.0%)
0.032

    Cervical adenopathy
61 (79.0%)
7 (29.0%)
<0.001

    Changes in the peripheral extremities
50 (64.0%)
7 (29.0%)
0.002

    Resistance to first IVIG
12 (16.0%)
1 (4.0%)
0.020

Echocardiography

    Coronary artery dilatation
4 (5.2%)
0
0.045

    Increased perivascular echogenicity
12 (15.6%)
4 (16.6%)
0.696

    Vascular irregularity
12 (15.6%)
2 (8.3%)
0.464

    Mitral regurgitation
7 (9.1%)
2 (8.3%)
0.807

    Pericardial effusion
1 (1.2%)
1 (4.2%)
0.486

Data are represented as numbers (percentages).

3.3. Two-Dimensional Echocardiographic Findings in Patients with Kawasaki Disease

The basic echocardiographic findings are summarized in Table 2. The EFs (derived using the cubed method) in the cKD group were % (D0), % (D2), % (D14), and % (D56). The EFs in the iKD group were % (D0), % (D2), % (D14), and % (D56). No significant between-group difference was evident. The number of patients with dilatation of the coronary artery was significantly greater in cKD than in iKD patients (four [5.2%] versus nil).

3.4. Laboratory Findings at the Time of Diagnosis and Changes over Time

Laboratory data obtained at the time of diagnosis are shown in Table 2. Peripheral blood from all 101 KD patients was drawn on D0, D2, D14, and D56 and from the 41 controls on D0 and D2.

On D0, the WBC () and platelet count (), the ESR (), and the NT proBNP level () were significantly higher in KD patients than controls. CRP () and troponin I () levels were significantly higher in the cKD group than controls. The hematocrit was significantly lower in the iKD group than controls (). The potassium concentration was significantly higher in the iKD group than in either the cKD or control groups (). The laboratory data from all three groups at diagnosis (D0) are shown in Table 3.

Table 3: Laboratory findings at diagnosis in patients with Kawasaki disease (KD) and controls.

Complete KD

Incomplete KD

Control

White blood cell count (/mm³)

Neutrophil proportion (%)

Eosinophil proportion (%)

Hemoglobin (g/dL)

Hematocrit (%)

Platelets (10³/mm³)

Erythrocyte sedimentation rate (mm/h)

C-reactive protein (mg/dL)

Aspartate aminotransferase (U/L)

Alanine aminotransferase (U/L)

Total protein (g/dL)

Albumin (g/dL)

Sodium (mEq/L)

Potassium (mEq/L)

Chloride (mEq/L)

Creatine kinase (IU/L)

Creatine kinase-MB (ng/mL)

Myoglobin (ng/mL)

Troponin I (ng/mL)

N-terminal pro BNP (pg/mL)

KD: Kawasaki disease. Data are shown as means ± SD. , complete Kawasaki versus incomplete Kawasaki disease; , complete Kawasaki disease versus control; , incomplete Kawasaki disease versus control.

On D2, the total protein level was significantly higher in the cKD group than in iKD patients or controls (). To explore the significance of this finding, we sought to correlate total protein levels with the total IVIG dose, body weight, and body surface area. No correlation was evident, and further work in this area is required. On D14, both platelet () and albumin levels () were significantly higher in cKD than in iKD patients. No significant difference in any of the WBC, the ESR, or CRP and NT proBNP levels was evident between cKD and iKD patients at any later time.

cKD and iKD patients experienced significant reductions in the WBC and CRP level at D2, D14, and D56, compared to the D0 findings. The NT-proBNP levels of cKD patients at D2 and D14 were significantly lower than those at D0 (Figure 1).

(a)

(b)

(c)

(d)

Figure 1: Laboratory data from patients with complete Kawasaki disease (KD), incomplete KD, and other febrile illnesses (controls), collected on the day of diagnosis and 2, 14, and 56 days after intravenous immunoglobulin (IVIG) treatment. (a) White blood cell count, (b) C-reactive protein level, (c) erythrocyte sedimentation rate, and (d) N-terminal pro-brain natriuretic protein (NT-proBNP) level. versus day of diagnosis in children with complete KD, versus day of diagnosis in children with incomplete KD. ; a statistically significant difference was evident between the complete KD group and controls. ; a statistically significant difference was evident between the incomplete KD group and controls.

3.5. Serum Procalcitonin Levels at the Time of Diagnosis and Changes over Time

Of the 101 KD patients and 41 controls, we measured serum procalcitonin levels of 85 patients (cKD: 64, iKD: 21) and 34 controls at D0. The mean D0 serum procalcitonin levels in cKD patients ( ng/mL) and controls ( ng/mL) were significantly higher than those of iKD patients ( ng/mL) ( and , resp.) (Figure 2).

Figure 2: Differences in procalcitonin levels among patients with complete Kawasaki disease (KD), incomplete KD, and other febrile illnesses (controls), on the day of diagnosis and 2, 14, and 56 days after intravenous immunoglobulin (IVIG) treatment. versus day of diagnosis in children with complete KD, versus day of diagnosis in children with incomplete KD. ; a statistically significant difference was evident between the complete and incomplete KD groups. ; a statistically significant difference was evident between the control and incomplete KD groups.

We measured D2 serum procalcitonin levels in 82 patients (cKD: 65, iKD: 17) and 15 controls (after resolution of fever); D14 levels in 85 patients (cKD: 66, iKD: 19); and D56 levels in 22 patients (cKD: 18, iKD: 4). The mean control procalcitonin level ( ng/mL) at D2 was significantly higher than that of the iKD group ( ng/mL) (). However, no significant difference in mean serum procalcitonin level was evident between cKD and iKD patients at any later time.

cKD patients showed significant reductions in procalcitonin levels at D14 () and D56 () compared to D0. Likewise, iKD patients experienced significant reductions at D2 () and D14 () (Figure 2). No significant difference was evident between the four cKD patients with coronary artery dilatation ( mm) and those without dilatation ( mm). Also, no significant correlation was evident between procalcitonin level and the presence of a coronary artery lesion at any later time. However, a lack of statistical power may have precluded identification of such a correlation; very few patients had coronary artery dilatation.

4. Discussion

In the present study, we have shown the utility of measuring serum procalcitonin levels in patients with cKD, iKD, and other febrile illnesses, at different stages of disease. KD patients had significantly higher WBC and platelet counts and ESR than did those with other febrile illnesses. Also, during the acute stage of disease, cKD patients and those with other febrile illnesses had significantly higher levels of serum procalcitonin than did iKD patients.

Procalcitonin has been suggested to be an acute-phase reactant, because synthesis thereof is thought to be induced by IL-6 or TNF-, and procalcitonin levels increase after development of inflammation [13, 17]. Although CRP is a sensitive marker of inflammation, CRP levels rise and then become normalized, only at later stages of disease. Also, CRP levels cannot be used to predict the presence of infection [18]. Several studies have reported high procalcitonin levels in the absence of infection in patients with Behcet’s disease, KD, and active Wegener’s granulomatosis [14, 19–21]. Okada et al. [14] suggested that procalcitonin level could serve as a novel marker for clinical diagnosis of KD. The serum concentration of procalcitonin was significantly higher in 25 acute KD patients ( ng/mL) and 17 with bacterial infections ( ng/mL) than in patients with autoimmune diseases (,  ng/mL) or viral infections (,  ng/mL), or healthy children (, ). The cited authors concluded that the serum procalcitonin level may be of clinical utility when determining the severity of KD and might assist in the differential diagnosis of patients with inflammatory diseases. It was also found that four patients who developed coronary aneurysms exhibited higher procalcitonin levels ( ng/mL) [14]. Procalcitonin levels are not elevated in patients with inflammatory (including autoimmune) diseases, but the levels of other acute phase reactants including CRP, IL-6 and/or neopterin may indeed be higher than normal [22, 23].

In contrast, Chakrabartty and Apong reported that KD patients expressed low levels of procalcitonin [15]. The cited authors sought a marker assisting in differentiation of KD from sepsis so that KD patients would not be unnecessarily prescribed antibiotics. Procalcitonin levels were low (<0.5 ng/mL) in all of 38 admitted KD patients, but all had high ESRs and CRP levels [15].

In our present study, we considered that procalcitonin was an acute-phase reactant and compared the levels thereof in patients with both types of KD and controls with other febrile illnesses. During the acute stage of disease, procalcitonin levels were significantly higher in patients with cKD and other febrile illnesses than in iKD patients, decreased in both types of KD patients to D14 after IVIG treatment, and remained steady thereafter. No statistically significant correlation between the presence of coronary artery disease and procalcitonin level was evident although, as explained above, our analysis may have lacked adequate statistical power. The observed differences in procalcitonin levels may be explained by the fact that cKD patients exhibit more advanced inflammatory reactions than do iKD patients. This pathophysiologic feature of KD requires further study. In the present work, we found that serum procalcitonin levels were relatively low in both cKD ( ng/mL) and iKD ( ng/mL) patients compared with the level ( ng/mL) reported by Okada et al. [14]. One possible explanation is that the cited authors worked with only 25 patients; we studied 101. Also, a relatively small proportion (4%) of our patients had coronary artery lesions, compared to 25% of patients in the cited study. Chakrabartty and Apong reported low procalcitonin levels (<0.5 ng/mL) in their 38 KD patients [15].

Several well-known laboratory findings support the diagnosis of either iKD or cKD. Most KD patients have an elevated CRP level or ESR [24], and an elevated NT-proBNP level at the acute stage of KD appears to be a reliable indicator of the presence of either cKD or iKD [25, 26]. A recent large-scale study by Manlhiot et al. [12] showed that cKD () and iKD () patients yielded similar laboratory findings in terms of WBC, ESR and albumin, AST, and CRP levels but not ALT levels. The level of ALT in cKD patients (median: 27 U/L, range: 4–328 U/L) was higher than in patients with iKD (median: 22 U/L, range: 2–154 U/L; ) [12]. Perrin et al. [27] reported that the serum levels of both ALT and gamma-glutamyltransferase were significantly higher in 39 patients with cKD ( U/L,  U/L, resp.) than in 20 patients with iKD ( U/L,  U/L, resp.). However, none of CRP or ESR and blood cell count (including WBC) differed significantly between cKD and iKD patients at admission.

In our present study, WBC and platelet count and the ESR were significantly higher in KD patients compared to those with other febrile illnesses, at the time of diagnosis. Also, in the subacute stage, WBC and platelet counts, the ESR, and the CRP level were significantly higher in KD patients than controls. The total protein level was significantly higher in the cKD than in the iKD or control groups and was not correlated with any of IVIG dose, body weight, or body surface area. This finding requires further study. However, none of the WBC, the ESR, or the levels of CRP and NT-proBNP differed significantly between cKD and iKD patients. None of the levels of total protein, albumin, AST, ALT, sodium, or chloride differed significantly among the two KD groups and controls. Only serum potassium level (in the iKD group) was significantly higher than in the cKD group and controls.

One limitation of the present study is that some follow-up data are missing probably because parents refused to permit blood to be drawn as recovering children appeared to be healthy.

In conclusion, this is the first report of serial procalcitonin measurements in patients with both types of KD and controls. The mean D0 serum procalcitonin levels of cKD and controls were significantly higher than those of iKD patients during the acute stage of disease. In contrast, the levels of other inflammatory markers including the WBC, the ESR, and CRP level did not significantly differ between patients with cKD and iKD. Further exploration of differences in procalcitonin levels between cKD and iKD patients is needed to better understand the incomplete presentation of iKD.

Conflict of Interests

The authors have no conflict of interest to disclose.

Acknowledgment

This study was supported by a Grant (CRI 10-027-1) of the Chonnam National University hospital Research Institute of Clinical Medicine.

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