Vitamin D status and viral response to therapy in hepatitis C infected children

Abstract

AIM: To study the frequency of vitamin D deficiency in patients with hepatitis C virus (HCV) infection and to evaluate the role of vitamin D supplementation in improving antiviral therapy.

METHODS: Sixty-six children aged from 7-14 years (mean ± SD, 11.17 ± 2.293) diagnosed with HCV infection were matched to 28 healthy controls. Serum levels of 25 (OH) D3, calcium, phosphorus, alkaline phosphatase and plasma level of parathormone were measured. Quantitative PCR for HCV was performed Bone density was determined by dual energy X-ray absorptiometry. All cases received conventional therapy, and only 33 patients received vitamin D supplementation.

RESULTS: Children with HCV showed significantly increased levels of HCV RNA (P < 0.001), parathormone (P < 0.01) and decreased vitamin D levels (P < 0.05) (33.3% deficient and 43.3% insufficient) compared with controls. Abnormal bone status (Z score -1.98 ± 0.75) was found in ribs, L-spine, pelvis and total body. Cases treated with vitamin D showed significant higher early (P < 0.04) and sustained (P < 0.05) virological response. There was a high frequency of vitamin D deficiency among the Egyptian HCV children, with significant decrease in bone density. The vitamin D level should be assessed before the start of antiviral treatment with the correction of any detected deficiency.

CONCLUSION: Adding vitamin D to conventional Peg/RBV therapy significantly improved the virological response and helped to prevent the risk of emerging bone fragility.

Core tip: Does vitamin D supplementation improves the viral response in hepatitis C infection? Previous studies raised the possibility that disease progression is associated with higher levels of vitamin D, and thus vitamin D supplementation does not have a role in chronic hepatitis C patients. This study aimed to investigate the frequency of vitamin D deficiency among Egyptian hepatitis C virus-infected children, with assessment of bone status by measuring calcium, parathormone and alkaline phosphatase levels, and bone mineral density and to evaluate the role of vitamin D supplementation in improving the viral response of these patients.

INTRODUCTION

Hepatitis C virus (HCV) infection remains an evolving cause of morbidity and mortality worldwide. Despite limited epidemiological data, a higher prevalence is found in Eastern Europe and in the Middle East[1]. Egypt has the highest prevalence of HCV infection; about 9% country wide and up to 50% in certain rural areas[2].

Vitamin Dis a potent immunomodulator that improves insulin sensitivity, suppresses proinflammatory cytokines, increases anti-inflammatory cytokines, and improves CD4 T cell hyper-responsiveness[3]. Recently, specific vitamin D receptors (VDRs) were observed to be expressed in liver cells and this expression of VDRs is reduced in chronic Hepatitis C patients. In addition, an inverse relationship between the liver VDR expression and inflammation severity was observed[4,5].

Abnormal bone metabolism, vitamin D axis, calcium (Ca) and parathormone (PTH) dysfunction have been reported in cholestatic children[6] with the disturbance in vitamin D metabolism, gonads, or chronic inflammation[7]. The role of chronic HCV infection in osteoporosis is supported with the decreased fracture risk in HCV children with successful antiviral treatment[8]. However, other studies demonstrated osteosclerosis in HCV infection[9].

The relation between vitamin D and the antiviral therapy response remains unclear, with previous studies raising the possibility of inconsistent results and failure of the reference methodology[10].

The present study aimed to investigate the frequency of vitamin D deficiency among Egyptian HCV infected children, and to assess bone status by measuring calcium, parathormone, alkaline phosphatase and bone mineral density. We also evaluated the role of vitamin D supplementation in improving the virological response of these patients.

MATERIALS AND METHODS

This prospective study included 66 cases (43 male and 23 female) aged from 7-14 years with HCV infection. They were admitted to the Gastroenterology and Hepatology unit at Assiut Children University Hospital from June 2010 to December 2012. The diagnosis of HCV was based on the quantitation of HCV RNA by quantitative real-time polymerase chain reaction[11].

Exclusion criteria

Patients with chronic liver disease other than HCV, patients with immunodeficiency, malignancy, decompensated liver cirrhosis, and patients on vitamin D or calcium therapy in the previous 3 mo were excluded.

Another 28 apparently healthy volunteer children drawn from Assiut Children University Hospital, of matched age and sex, were recruited as controls. The medical ethical committee of the Faculty of Medicine, Assuit University approved the study, and informed written consent was obtained from the parents or legal guardians.

A full history was taken and a thorough clinical examination was performed for all members of both study groups. All cases were subjected to the following investigations: (1) serum liver enzymes (AST and ALT), Ca, phosphorus, alkaline phosphatase, 25 (OH) D 3 and PTH levels; (2) PCR for HCV RNA; and (3) bone mineral density (BMD) as measured by the dual energy X-ray absorptiometry method (Hologic Model Delphi, CT, United States). BMD (g/cm² and Z-score) of the ribs, arms, head, lumbar spine, pelvis, legs and total body were measured. The BMD values were compared with those of the healthy controls. Osteoporosis was considered with a Z-score of -2 standard deviations (SDs) and osteopenia between -1.0 and 2.0 SDs in relation to the patient’s age, as suggested by the World Health Organization[12].

The patients were classified randomly by a simple randomization method into two groups: Group A received PEG-alpha-2b interferon (60 μg/kg per week) SC and ribavirin (15 mg/kg per day) orally for 48 wk together with vitamin D3 2000 IU/d orally. Group B received the same therapy without vitamin D supplementation. Vitamin D insufficiency, deficiency and sufficiency were defined according to 25OHD levels as > 75 nmol/L, from 75-30 nmol/L, and < 30 nmol/L, respectively[13].

Follow up for all patients was performed at 12 and 24 wk from the beginning of the therapy and at 24 wk after cessation of therapy by measuring PCR for HCV RNA and liver functions. All complications and side effects during the course of treatment were recorded. Six cases (two from group A and four from group B) were excluded from the study after 12 wk of treatment because of a lack of response. Non-responders were defined as those who failed to clear HCV RNA from serum after 24 wk of therapy.

Discontinuation of therapy occurred if HCV RNA level after 12 wk < 2 log unit compared to baseline or neutropenia < 500/cm, platelets < 5000 mm³ and Hb < 8 gm/dL. Sustained virological response (SVR) was considered when an undetectable HCV-RNA was found at 24 wk after therapy.

Sample collection and laboratory investigations

Venous blood samples were collected from patients under standardized conditions. Samples were centrifuged (3000 × g for 10 min); serum and plasma samples were divided and stored in aliquots at -20 °C until analysis. Serum calcium, phosphorus and alkaline phosphatase were measured by conventional methods using a COBAS INTEGRA 400 autoanalyzer. Serum 25-OH Vitamin D measurement was performed by Immundiagnostik AG kit (Bensheim; Germany; Ref.K2110), using an enzyme immunoassay technique, based on competition of 25 (OH) D present in the sample with 20(OH) D tracer for the binding pocket of vitamin D binding protein. Assay of plasma levels of parathyroid hormone using MAGLUMI Intact PTH (Shenzhen; China) Ref. 13330211001M (Sandwich immunoluminometric assay) Quantitative PCR for HCV was performed using an AB Applied Biosystems 7500 Fast Real-Time PCR System.

Statistical analysis

Statistical analysis was carried out using SPSS (version 16, SPSS Inc., Chicago, IL, United States). Quantitative data were expressed as mean ± SD and categorical data were presented in the form of frequency and percent (%), as appropriate. Student’s t-test was used for parametric data and non-parametric χ² was used for independent variables when comparing the two groups. Multiple groups were compared using the one-way ANOVA test. Linear correlations were performed by Pearson’s test. For all tests, a difference was considered significant if the probability (P) was < 0.05.

RESULTS

Positive family history of HCV was significantly different between group A and B (P < 0.05) (Table 1).

Table 1.

Demographic and clinical data for the studied groups and control

	A	B	Total	Control	P value
	(n = 31)	(n = 29)	(n = 60)	(n = 28)
Age (yr)	11.1 ± 2.178	11.043 ± 2.882	11.17 ± 2.293	9.35 ± 3.24	0.445
Duration of illness (yr)	3.4 ± 1.984	3.123 ± 1.688	3.262 ± 1.832	-	0.563
BMI (kg/m2)	20.81 ± 4.29	20.28 ± 3.13	20.54 ± 3.73	21.21 ± 2.34	0.588
Male/female	23/8 (74.1%/25.8%)	20/9 (68.9%/31.1%)	43/17 (71.6%/28.3 %)	17/13 (60.7%/46.4%)	0.284
Blood transfusion, n (%)	16 (51.6)	16 (55.1)	32 (53.3)	-	0.602
Positive family history of HCV	8 (25.8)	1 (3.4)	9 (15.0)	-	0.051
Jaundice, n (%)	19 (61.2)	13 (44.8)	32 (53.3)	-	0.098
Fever, n (%)	9 (29.0)	9 (31.0)	18 (30.0)	-	0.611
History of bleeding, n (%)	17 (54.8)	16 (55.1)	33 (55.0)	-	0.501

¹Significance total vs control. No significant difference between group A and B. Data are presented as the mean ± SD or number (%) as appropriate. BMI: Body mass index.

Complications during the course of treatment were detected in 10 cases, with mild symptoms in the form of fever, nausea, itching, headache, anemia < 9 gm/dL, neutropenia < 5000/cm³ or thrombocytopenia < 100000 mm³, where the antiviral dose were reduced to half the dose.

Significant decrease in serum vitamin D levels (P < 0.05) and significant increases in plasma PTH (P < 0.01) and HCV RNA (P < 0.001) were detected in the studied cases compared with the controls, despite no significant differences being found regarding liver enzymes, albumin, Phosphorus and ALP between the two groups (Table 2).

Table 2.

Mean ± SD values of laboratory parameters in the studied groups and control

	Group A	Group B	Total	Control (n = 28)	P value
	(n = 31)	(n = 29)	(n = 60)
ALT (IU/L)	75.46 ± 18.18	87.96 ± 14.11	81.71 ± 18.25	21.35 ± 6.21	0.148
AST (IU/L)	75.5 ± 24.95	104 ± 11.204	89.75 ± 23.41	35.74 ± 4.92	0.24
Calcium (mg/dL)	6.733 ± 1.52	6.657 ± 1.24	6.69 ± 1.38	8.2 ± 0.91	0.83
Phosphorus (mg/dL)	4.24 ± 0.42	4.21 ± 0.39	4.25 ± 0.41	3.1 ± 0.65	0.68
Alkaline phos (IU/L)	140.97 ± 10.98	99.12 ± 24.94	120.05 ± 27.66	78.48 ± 21.10	0.20
HCV RNA (IU/mL)	1393290 ± 52580	967371 ± 56534	1180334 ± 79910	10.21 ± 0.74	0.0011
Vitamin D (nmol/L)	65.26 ± 22.71	57.9 ± 16.17	61.58 ± 17.05	98.31 ± 3.50	0.051
PTH (pg/mL)	179.10 ± 10.25	188.03 ± 14.96	186.56 ± 25.67	65.71 ± 12.05	0.011

¹Significance total vs control. No significant difference between group A and B. AST: Aspartate transaminase; ALT: Alanine transaminase; PTH: Parathormone.

Table 3 represents the mean values of Bone density parameters in the studied groups with HCV infection. There were significant differences in Z- score regarding ribs (P < 0.04), pelvis (P < 0.04), L-spine (P < 0.05) and total BMD (P < 0.03) between the two groups (Table 3).

Table 3.

Mean ± SD values of bone density parameters in the studied groups with hepatitis C virus infection

	A (n = 31)	B (n = 29)	Total (n = 60)	Z- score	P value
Head	1.226 ± 0.394	1.12 ± 0.383	1.173 ± 0.389	-0.16 ± 0.42	0.297
Arm	1.063 ± 1.223	0.89 ± 0.277	0.976 ± 0.883	-0.916 ± 1.2	0.453
Leg	0.912 ± 0.225	0.969 ± 0.38	0.94 ± 0.311	-1.13 ± 1.34	0.482
Rib	0.688 ± 0.248	0.869 ± 0.411	0.778 ± 0.349	-1.31 ± 0.78	0.0431
Pelvis	0.839 ± 0.187	0.92 ± 0.238	0.879 ± 0.216	-2.8 ± 1.53	0.051
L Spine	0.77 ± 0.207	0.901 ± 0.294	0.835 ± 0.261	-2.43 ± 1.7	0.0511
Total	0.834 ± 0.281	0.913 ± 0.381	0.874 ± 0.334	-1.98 ± 0.75	0.0361

¹Significance between total BMD of HCV patients vs control. BMD: Bone mineral density (g/cm²). HCV: Hepatitis C virus.

Vitamin D sufficiency was present in 23.3%, insufficiency in 43.3% and deficiency in 33.3% of cases. There were significant decreases in serum calcium levels in the deficient group vs the sufficient group. Serum vitamin D showed a statistically significant difference between the sufficient, insufficient and deficient groups compared with the control. PCR for HCV RNA was significantly different in the sufficient and insufficient versus the deficient groups and also compared with control (Table 4).

Table 4.

Mean ± SD values of laboratory parameters in relation to Vitamin D status in the studied groups

	Vitamin D status			Control (n = 28)	Suff vs Insuff	Suff vs Def	Insuff vsDef	Total P value
	Sufficient (n = 14)	Insufficient (n = 26)	Deficient (n = 20)
ALT (IU/L)	97.643 ± 18.06	75.654 ± 15.954	78.45 ± 17.824	21.35 ± 6.21	0.327	0.475	0.885	0.610
AST (IU/L)	97.786 ± 24.215	94.923 ± 13.151	77.4 ± 13.363	35.74 ± 4.92	0.934	0.453	0.551	0.772
Calcium (mg/dL)	7.993 ± 1.183	7.023 ± 1.396	6.13 ± 1.185	8.2 ± 0.91	0.769	0.031	0.090	0.077
Phosphorus (mg/dL)	3.31 ± 0.25	4.21 ± 0.31	4.24 ± 0.61	3.1 ± 0.65	0.354	0.412	0.614	0.456
Alkaline phosphatase (IU/L)	82.92 ± 15.62	109.34 ± 13.08	159.96 ± 14.64	78.48 ± 21.10	0.493	0.068	0.233	0.192
HCV RNA(IU/mL)	1300824 ± 664010	1417943 ± 137873	787100 ± 65915	10.21 ± 0.74	0.705	0.031	0.0221	0.0432
Vitamin D (nmol/L)	84.21 ± 17.821	49.23 ± 15.07	22.6 ± 3.858	98.31 ± 3.50	0.0001	0.001	0.0001	0.0012
PTH (pg/mL)	128.53 ± 20.37	164.05 ± 12.63	179.46 ± 19.24	65.71 ± 12.05	0.181	0.322	0.607	0.296

¹Significance between groups vs control;

²Significance total vs control. AST: Aspartate transaminase; ALT: Alanine transaminase; PTH: Parathormone; Suff: sufficient; Insuff: Insufficient; Def: Deficient.

There were significant difference in ribs (P < 0.04), pelvis (P < 0.05), L spine (P < 0.05) and head (P < 0.005) in BMD between the sufficient and deficient groups (Table 5).

Table 5.

Mean ± SD values of bone mineral density in relation to Vitamin D status in the studied groups

	Vitamin D status			Suff vs Insuff	Suff vs Def	Insuff vs Def	Total
	Sufficient (n = 14)	Insufficient (n = 26)	Deficient (n = 20)				P value
Head	0.921 ± 0.343	1.237 ± 0.415	1.267 ± 0.317	0.0201	0.0051	0.790	0.0182
Arm	1.03 ± 0.901	0.879 ± 0.259	1.065 ± 1.325	0.428	0.931	0.487	0.759
Leg	0.873 ± 0.28	1.001 ± 0.321	0.978 ± 0.291	0.341	0.428	0.798	0.067
Rib	0.856 ± 0.34	0.749 ± 0.358	0.662 ± 0.353	0.365	0.0431	0.910	0.637
Pelvis	0.996 ± 0.234	0.895 ± 0.219	0.748 ± 0.107	0.990	0.051	0.469	0.738
L- Spine	0.959 ± 0.115	0.838 ± 0.24	0.716 ± 0.258	0.808	0.0591	0.766	0.892
Total	0.918 ± 0.444	0.897 ± 0.11	0.812 ± 0.28	0.863	0.398	0.340	0.596
Z score	1.121 ± 0.577	0.927 ± 0.25	-1.875 ± 0.441	0.619	0.0421	0.431	0.493

¹Significance between groups;

²Significance total vs control. BMD: Bone mineral density (g/cm²). Suff: Sufficient; Insuff: Insufficient; Def: Deficient.

At 12 wk, there were no significance in the early virological response (EVR) between the two groups, where 10/31 patients (32.3%) from group A and 6/29 (20.6%) from group B were HCV-RNA negative. At 24 wk, there were significant differences in virological response (P value < 0.04),where 24/31 patients (77.4%) from group A and 17/29 (58.6%) from group B were negative for HCV-RNA. A significant difference in SVR was detected at 24 wk after treatment, between group A and B (P < 0.05). 22/31 patients (70.9%) from group A and 15/29 (51.7%) from group B were HCV-RNA negative.

DISCUSSION

Egypt has the highest worldwide prevalence of HCV infection, about 9% countrywide and up to 50% in rural areas[2]. This goes with our results where 15% of patients had positive family history of HCV, with a significant higher proportion in group A than in group B.

The baseline of PCR HCV RNA (> 400000 IU/mL) was significantly higher compared with the controls in this study, with no significance between group A and B. Assy et al[13] showed that patients supplemented with vitamin D had a significantly higher baseline of HCV RNA (60%) than those treated without vitamin D (40%). While Abu-Mouch et al[14], found that the baseline of HCV RNA with high viral load (> 800000 IU/mL) in patients treated with vitamin D (50%) showed higher significant results than those without vitamin D treatment (42%).

In this study, vitamin D sufficiency was present in 23.3%, insufficiency in 43.3% and deficiency in 33.3% of cases with no significant difference between the two groups. This agrees with the results of previous studies[13,14], which found no significant difference regarding the baseline vitamin D between cases supplemented with vitamin D and those without. Highleyman[15] stated the importance of vitamin D in the immune response against HCV infection: 84% of adult patients with HCV infection have low vitamin D levels and 1/3 of patients had severe deficiency.

Mandorfer et al[16] also found sufficient levels of vitamin D in 1/5 of their participants and 57% were insufficient and 23% were deficient. Ladero et al[17], found vitamin D insufficiency in 40% and deficiency in 36% of adult patients.

Vitamin D status may differ across different geographical locations and environments[13]. Consequently, its influence on disease pathogenesis is likely to vary from one location to the other. Vitamin. D deficiency could be related to lack of exposure to sunlight, although Africa is sunny, and/or to the lack of vitamin D in the diet[13].

Vitamin D is an important modulator of inflammatory responses and fibrosis in HCV infection by inhibiting TNF-α, which regulates the immune response and inhibits the fibrosis process by suppressing TGF-β, which affects fibrosis progression[18]. Ladero et al[17], concluded that vitamin D deficiency is more common in Spanish patients with HCV infection, but it is neither related to biochemical and virological variations, nor to fibrosis stage or IL 28B polymorphisms.

On the contrary, other studies[19], raised the possibility that the disease progression is associated with higher levels of vitamin D, and thus vitamin D supplementation does not have a role in chronic hepatitis C patients. Terrier et al[20], showed that were no associations between serum 25 OH D3 levels and viral response to therapy or the severity of immunodeficiency in HCV patients.

The present study observed significantly higher plasma PTH levels in HCV patients compared with controls. This may be related to the functioning feedback mechanisms of low serum calcium and 25(OH)D levels. Malabanan et al[21] stated that when the 25(OH)D concentration reaches < 50 nmol/L (20 ng/mL), the PTH concentration increases.

In the present study, plasma PTH levels were negatively associated with BMD and the Z-score of the total body (Figure 1). The increased PTH levels found in our patients may lead to increased bone resorption and decreased BMD. The decrease in sensitivity of the PTH effect on bone resorption[22] or the anabolism of the osteoblasts to PTH could be an explanation[23]. Similarly, Choudhary et al[24] found a negative correlation between PTH and BMD in viral cirrhosis. By contrast, other studies[25,26] revealed normal or low PTH levels in HCV infection. This discrepancy could be explained by the increased prevalence of 25(OH)D deficiency or insufficiency in Egyptian children with HCV infection.

Figure 1.

Correlation between plasma parathormone levels and the Z-score of the total body.

In partial agreement with other studies[27], we observed that the peripheral skeleton was less influenced than the axial skeleton in our HCV patients. The accelerated growth in the peripheral skeleton in children could explain this, while during puberty, it occurs in the axial skeleton[27]. In addition, most of our patients had been diagnosed before puberty. Therefore, the highest bone mass was obtained during the disease process, which affects the bone status in these patients. The protective role of puberty on bone tends to be opposite to temporary bone loss, which seems to be a complication of the disease[28].

Regarding bone density in the present study, the Z score was significantly decreased and showed significant difference between the two groups. This is agrees with the results of El Karmouty et al[29], who revealed that BMD, T score and Z score were significantly lower in children with HBV and HCV than HAV infection. The severity of osteoporosis increases with the severity of liver disease. However, no significant correlation could be detected between serum Ca, Phosphorus, vitamin D and the degree of bone loss, which is higher in osteoporosis than in osteomalacia[29]. Kryskiewicz et al[6] observed some risk factors of bone tissue pathology, which included hepatocyte dysfunction, disorders of vitamin D, Ca and Phosphorus metabolism, immunosuppressive therapy and malnutrition. Theoretically disturbance in the endocrine Ca - PTH- vitamin D axis seems to play a role in the pathogenesis of osteo metabolic disturbances.

López-Larramona et al[30] stated that the origin of hepatocyte osteodystrophy is unclear; it may be multifactorial and its etiology and severity vary in accordance with the underlying liver disease. Bone loss occurs as a result of increased bone turnover and/or remodeling in balance, the latter being caused by reduced formation, and increased resorption or a combination of both. Vitamin D metabolism in severe HCV infection and deficiency may cause hyperparathyroidism, increase bone turnover and accelerate the loss of BMD. This regulation of the RANKL/OPG system is activated by cytokines involved in the pathogenesis of chronic liver disease (IL 1, 11, 6, TNF-α1). Previous studies[24,31] found that patients with chronic liver disease have low BMD in 93% of cases. Other factors, including decreased physical activity, decreased body mass, deficiency of vitamin D and low IGF level were considered.

Yurci et al[32] stated that all anti osteoporotic agents in hepatic osteodystrophy seems to be safe and effective. Oral bisphosphonate (anti resorptive drug) was the most effective in preventing both cortical and trabecular bone loss in patients with chronic viral hepatitis, but only limited data are available.

By contrast, Yenice et al[25], stated that hepatitis B and C infection do not pose a risk factor for osteoporosis and bone loss, and that the diagnosis of BMD should be based on multiple parameters. It should be kept in mind that the key osteomalacia is rare and requires bone biopsy. The differences observed between reports may be related to the study design, different methods used for measuring BMD and selection of patients.

Regarding the use of vitamin D in this study, cases in group A showed significantly higher rates of EVR, a greater response after 24 wk and higher SVRs than group B (Figure 2). This agrees with a previous study[14] that found that patients treated with vitamin D in addition to conventional antiviral therapy had significantly higher responses at 4 wk than those treated without vitamin D (44% vs 17%), at 12 wk (94% vs 43%), and at 24 wk after stoppage of therapy (86% vs 42%) with a small relapse rate (8%). Previous studies[13,14] concluded that the addition of vitamin D to the therapy in HCV patients increases the rate of rapid and early SVR. Therefore, assessment of vitamin D levels before combined therapy and correction during the course of therapy may be needed.

Figure 2.

Early and sustained viral response of hepatitis C virus RNA in group A and B. PTH: Parathormone.

Bitetto et al[33] concluded that unfavorable responses to antiviral therapy are predicted in vitamin D deficient patients with RHC. Supplementing vitamin D improves the possibility of achieving an SVR after antiviral treatment. In addition, low levels of vitamin D are associated with significant poor rate of EVR and SVR in co-infection of HIV[16], and this decreased vitamin D is limited to fibrosis and low SVR in interferon-based therapy[34]. The exact mechanism of vitamin D supplementation action on EVR, RVR and SVR is unclear. It may reflect the fact that 1, 25 dihydroxy vitamin D appears to be an immunomodulator via regulation of T cell function through its effect on T cell antigen[35]. T helper cell type I action is intensified when vitamin D is insufficient or when VDR signals are weak[36]. Vitamin D increases the expression of VDR proteins and inhibits viral replication[37].

Gal-Tanamy et al[38], stated that the interferon sparing effect of vitamin D improves the antiviral treatment in patients with HCV infection. 25(OH) D3 is a novel antiviral agent and a better therapeutic option to reduce the enzyme activity in patients with HCV[39].

In conclusion, there was a high frequency of Vitamin D deficiency among the Egyptian HCV children studied, with significant decrease in bone density. Vitamin D levels should be assessed before the start of antiviral treatment, with correction of any detected deficiency. Adding vitamin D to conventional Peg/RBV therapy significantly improved viral response and helped to prevent the risk of emerging bone fragility.

ACKNOWLEDGMENTS

We acknowledge the great support to all staff members and nursing team in the GIT Outpatient Clinic of the Pediatric Department at the Assiut Children University Hospital, Egypt for their help and cooperation in this work.

COMMENTS

Background

Hepatitis C virus (HCV) infection remains an evolving cause of morbidity and mortality worldwide. Despite limited epidemiological data, a higher prevalence is found in Eastern Europe and the Middle East. Abnormal bone metabolism, vitamin D axis, calcium and parathormone dysfunction have been reported in cholestatic children. The relation between vitamin D and antiviral therapy response remains unclear, with previous studies raising the possibility of inconsistent results.

Research frontiers

To investigate the frequency of vitamin D deficiency among Egyptian HCV-infected children, with assessment of bone status by measuring calcium, parathormone and alkaline phosphatase levels, and bone mineral density. We also to evaluated the role of vitamin D supplementation in improving the viral response of these patients.

Innovations and breakthroughs

Previous studies raised the possibility that disease progression is associated with higher levels of vitamin D, and thus vitamin D supplementation does not have a role in chronic hepatitis C patients. In this study, cases supplemented with vitamin D showed a significantly higher percentage of early virological response (EVR), higher response after 24 wk and a higher sustained virological response (SVR) than those without supplementation.

Applications

The addition of vitamin D to the therapy in HCV patients increases the rate of rapid and early SVR. Cases supplemented with vitamin D showed a significantly higher percentage of EVR, higher response after 24 wk and a higher SVR than those without supplementation.

Terminology

The addition of vitamin D to the therapy in HCV patients increases the rate of rapid and early SVR. Assessment of Vitamin D levels before combined therapy and correction during the course of therapy is required.

Peer review

The study investigated the effect of vitamin D in the response to antiviral treatment in chronic infected pediatric patients with HCV. There are several works published in the literature exploring this issue, however the relation between vitamin D status and the antiviral response to therapy remains unclear.