Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption

Sae Bit Yu; Yena Lee; Arum Oh; Han-Wook Yoo; Jin-Ho Choi

doi:10.6065/apem.1938142.071

Ann Pediatr Endocrinol Metab > Volume 25(2); 2020 > Article

Yu, Lee, Oh, Yoo, and Choi: Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption

Original Article

Annals of Pediatric Endocrinology & Metabolism 2020;25(2): 112-117.

Published online: June 30, 2020

DOI: https://doi.org/10.6065/apem.1938142.071

Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption

Sae Bit Yu, MD, Yena Lee, MD, Arum Oh, MD, Han-Wook Yoo, MD, PhD, Jin-Ho Choi, MD

Department of Pediatrics, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea

Address for correspondence: Jin-Ho Choi, MD Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea
Tel: +82-2-3010-3991
Tel: +82-2-473-3725 E-mail: jhc@amc.seoul.kr

Received August 28, 2019 Revised October 29, 2019 Accepted October 31, 2019

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

Oral supplementation of vitamin D can be inefficient in patients with vitamin D deficiency caused by intestinal malabsorption. This study investigated the efficacy and safety of parenteral vitamin D supplementation in infants and children with vitamin D deficiency caused by intestinal malabsorption.

Methods

This study included 11 patients with vitamin D deficiency who were unresponsive to oral vitamin D or were unable to try oral vitamin D therapy due to underlying conditions. All patients were treated with weekly intramuscular injection of cholecalciferol 50,000 IU. Radiological findings and biochemical parameters including serum calcium, phosphorus, alkaline phosphatase, 25-hydroxyvitamin D<sub>3</sub> (25(OH)D<sub>3</sub>), and parathyroid hormone levels were reviewed retrospectively.

Results

Underlying diseases included small bowel atresia (n=3), necrotizing enterocolitis (n=3), congenital megacolon (n=2), chronic intestinal pseudoobstruction (n=1), congenital mesenteric band (n=1), and Crohn disease (n=1). Three patients exhibited rickets on X-ray findings. The mean duration of treatment was 4.8±2.9 weeks. The alkaline phosphatase levels were decreased from 710±650 IU/L to 442±284 IU/L (P=0.143). The 25(OH)D₃ level was increased from 6.0±3.4 ng/mL to 50.4±28.8 ng/mL (P=0.008) after 3 months. Two patients with rickets showed improved radiologic findings after parenteral treatment.

Conclusions

Parenteral vitamin D therapy was effective and safe in patients with vitamin D deficiency caused by intestinal malabsorption. Long-term follow-up is needed to establish the efficacy of parenteral vitamin D therapy in a large number of patients.

Keywords: Malabsorption, Rickets, Vitamin D, Vitamin D deficiency

Introduction

Vitamin D is an important nutrient for absorption of intestinal calcium and phosphorus [1], cellular proliferation and differentiation, muscle function, and immunity [2,3]. Vitamin D deficiency can cause rickets in growing children and osteomalacia in adults.4) Deficiency in this vitamin is defined as serum 25-hydroxyvitamin D₃ (25(OH)D₃) level < 12 ng/mL, while vitamin D insufficiency is 25(OH)D3 level of 12–20 ng/mL [5].

Children with vitamin D deficiency should be treated to prevent hypocalcemia and bone deformity. Several treatment regimens have been proposed to treat vitamin D deficiency in infants and children [5-8]. One clinical trial suggested that 2,000 IU of oral ergocalciferol (vitamin D₂) daily, 50,000 IU of vitamin D₂ weekly, or 2,000 IU of cholecalciferol (vitamin D₃) daily demonstrated the same outcomes in treatment of vitamin D deficiency among infants and toddlers without any complications [7]. Another study reported that intramuscular injection of 10,000 IU/kg of cholecalciferol is a safe and effective therapy for infants and toddlers with vitamin D-deficient rickets [9]. Recent guidelines have recommended 2,000 IU of vitamin D3 daily or 50,000 IU weekly for 3 months followed by a maintenance amount of 400 IU/day in children younger than 1 year of age. For children older than 1 year, 3,000–6,000 IU of vitamin D3 daily or 150,000 IU weekly are recommended [5].

Intestinal absorption of vitamin D occurs primarily in the jejunum and ileum [10]. Vitamin D deficiency is recognized as the most prevalent nutrient deficiency in patients with intestinal failure [11]. Enteral supplementation of vitamin D was inefficient in patients with vitamin D deficiency caused by intestinal malabsorption, such as cystic fibrosis, short bowel syndrome, inflammatory bowel disease, and intestinal accessory organ dysfunction [11,12]. In these cases, parenteral supplementation of vitamin D is a promising alternative strategy [10]. Therefore, this study was performed to investigate the efficacy and safety of parenteral vitamin D supplementation in infants and children with vitamin D deficiency caused by intestinal malabsorption.

Materials and methods

1. Subjects

This study included 11 patients (8 males and 3 females) with vitamin D deficiency caused by intestinal malabsorption who were unresponsive to oral vitamin D supplementation or were unable to try oral vitamin D therapy due to other underlying conditions. Vitamin D deficiency was defined as 25(OH)D₃ level <12 ng/mL [5].

2. Methods

Parenteral vitamin D3 (cholecalciferol) was administered intramuscularly at a dosage of 50,000 IU/wk. Parenteral vitamin D₃ was switched to oral vitamin D₃ at a dosage of 400 IU/day when the serum 25(OH)D₃ level rose above 30 ng/mL. Clinical and radiological features, laboratory findings, and duration of vitamin D3 supplementation were reviewed retrospectively. Laboratory investigations included serum calcium, phosphorus, alkaline phosphatase (ALP), 25(OH)D₃, and parathyroid hormone (PTH) levels. Height and weight were expressed as a z-score for age- and sex-matched Korean youth according to the 2017 Korean National Growth Chart [13].

3. Statistical analysis

Data were analyzed using IBM SPSS Statistics ver. 21.0 (IBM Co., Armonk, NY, USA). All data are expressed as mean±standard deviation values. The Wilcoxon signed rank test was used to compare the baseline and current growth profiles based on z-score. Repeated measures analysis of variance was conducted to compare the biochemical parameters at baseline and at 3 months and 6 months following treatment. A P-value <0.05 was considered statistically significant.

Results

1. Baseline characteristics before parenteral vitamin D treatment

The baseline characteristics of the subjects are summarized in Table 1. Among the 11 patients, 6 (55%) were preterm infants (gestational age<37 weeks), and 5 (45%) were extremely low birth weight (birth weight<1,000 g). Four patients (36%) underwent ileostomy due to congenital megacolon (n=2), chronic intestinal pseudo-obstruction (n=1), or congenital mesenteric band (n=1). Six patients (55%) with small bowel atresia (n=3) or necrotizing enterocolitis (n=3) underwent small bowel resection, resulting in short bowel syndrome. The remaining 1 patient (9%) was diagnosed with Crohn disease at the age of 5 months. This patient underwent ileostomy and was recurrently admitted for nutritional support due to uncontrolled disease. The median age at the time of the diagnosis of any underlying diseases was 20 days (range, 1–170 days).

Oral cholecalciferol at 2,000 IU/day was administered to 8 patients (73%) before parenteral vitamin D₃. The median duration of oral vitamin D₃ therapy prior to parenteral vitamin D₃ was 2.5 months (range, 20 days to 16 months). The other 3 patients were not able to eat anything including medication because of their underlying condition such as feeding intolerance and bowel adhesion after surgery. The mean 25(OH) D3 level before and after oral vitamin D₃ therapy was 9.8±7.6 ng/mL and 6.0±3.4 ng/mL, respectively (P=0.263). The mean ALP level increased from 605±303 IU/L (range, 333–1,082 IU/L) to 710±650 IU/L (range, 237–2,353 IU/L) after oral vitamin D3 replacement; however, there was no statistical significance (P=1.00). All patients received nutritional support via parenteral nutrition.

2. Effect of parenteral vitamin D treatment

The median age at the start of parenteral vitamin D₃ supplementation was 3.9 months (range, 1–45 months). The height and weight standard deviation scores (SDSs) before parenteral vitamin D₃ treatment were -3.6±5.3 and -5.4±4.5, respectively. The serum calcium, phosphorus, and ALP levels were 9.2±0.5 mg/dL, 4.8±1.9 mg/dL, and 710±650 IU/L (range, 237–2,353 IU/L), respectively. Five patients (45%) showed elevated ALP level. Initial serum 25(OH)D₃ and PTH levels before parenteral vitamin D treatment were 6.0±3.4 ng/mL and 145±186 pg/mL (range, 11.3–508 pg/mL), respectively. Five patients (45%) had elevated serum PTH level at baseline (reference range, 10–65 pg/mL) (Table 2). Three of those (27.2%) (subjects 1, 8, and 9) with elevated serum PTH showed X-ray findings of rickets, such as flaring of the distal end of the radius, ulna, and phalanges and bowing of both femurs. Three patients (subjects 1, 7, and 8) had a history of fracture of forearm or lower leg.

All patients were treated with 50,000 IU of parenteral vitamin D₃ weekly. The duration of treatment was 4.8±2.9 weeks (range, 1–9 weeks). Serum calcium, phosphorus, and ALP levels were not significantly changed during parenteral vitamin D₃ therapy (Fig. 1). The mean ALP level decreased from 710±650 IU/L (range, 237–2,353 IU/L) to 442±284 IU/L (range, 236–1,080 IU/L), but there was no statistical significance (P=0.143). The 25(OH)D₃ level was increased from 6.0±3.4 ng/mL to 50.4±28.8 ng/mL after 3 months of treatment (P=0.008) and to 55.7±32.8 ng/mL at 6 months (Table 3). The intact PTH level decreased from 119±155 pg/mL (range, 11.3–508 pg/mL; median, 94 pg/mL) to 37±26 pg/mL (range, 10.8–47.6 pg/mL; median, 27.6 pg/mL) (P=0.209). However, PTH level normalized after parenteral vitamin D3 treatment in 5 patients with high PTH level (P=0.043).

Six patients maintained normal 25(OH)D₃ level with 400 IU/day of oral vitamin D₃ therapy after parenteral vitamin D3 therapy for a mean duration of 5.0±2.8 weeks (range, 2–9 weeks). In subject 7, who had Crohn disease, the serum 25(OH) D₃ level was >30 ng/mL after 1 month of parenteral vitamin D₃ therapy. However, parenteral vitamin D3 therapy was continued because of the patient's poor general condition and preference for parenteral therapy. Two patients (subjects 6 and 8) were treated with oral cholecalciferol 2,000 IU/day due to low serum 25(OH)D₃ level, osteopenia, or high ALP level. Subject 1 was diagnosed with necrotizing enterocolitis, and subject 9 had small bowel atresia; neither required further treatment with vitamin D₃.

Among the 3 patients with rickets (subjects 1, 8, and 9), 2 (1 and 9) showed improved radiologic findings following parenteral treatment. The remaining patient (8) with short bowel syndrome due to necrotizing enterocolitis exhibited slight improvement in the flaring of the distal end of the radius, ulna, and phalanges after treatment, but osteopenia was still visible upon X-ray on the last day of follow-up.

The median current age on the last day of follow-up was 55 months (range, 7.5–112 months). Height and weight SDSs increased from -3.6±5.3 to -2.7±2.1 (P=0.026) and from -5.4±4.5 to -2.6±1.8 (P=0.013), respectively. There were no adverse effects of high-dose parenteral therapy, such as hypercalcemia, hyperphosphatemia, or hungry bone syndrome.

Discussion

This study demonstrated that parenteral vitamin D₃ treatment was safe and effective in infants and children with vitamin D deficiency caused by intestinal malabsorption. Oral vitamin D₃ treatment was inefficient, and a high dose of parenteral vitamin D₃ was required in patients with intestinal failure.

In the present study, all patients were treated with 50,000 IU of parenteral vitamin D3 weekly [6]. However, various treatment regimens have been proposed to treat vitamin D deficiency in children, including daily or weekly dosing for varied periods. Several studies were conducted to investigate the efficacy of a single, large dose of oral or intramuscular vitamin D, which was called "stoss therapy," for better convenience and compliance with therapy (Table 4) [9,14-16]. One retrospective cohort study of 61 children with rickets revealed that a single intramuscular injection of 600,000 IU vitamin D₃ and a weekly oral dosage of 60,000 IU vitamin D₃ for 10 weeks were equally effective and safe [16]. Tannous et al. [15] reported that 100,000 IU of oral cholecalciferol weekly for 4 weeks is as safe and effective as 5,000 IU oral cholecalciferol daily for 80 days in children older than 2 years. In contrast, Mittal et al. [14] showed that hypercalciuria and hypercalcemia have been more often described in children receiving stoss therapy. Recent guidelines do not recommend stoss therapy as first-line management of vitamin D deficiency; however, stoss therapy might be more practical for those who are noncompliant with daily dosing and those with intestinal malabsorption [5]. Previously, 10%–20% of patients with intestinal failure were reported to require daily oral vitamin D₃ at a dosage of 5,000–6,000 IU. Additionally, a smaller number of patients still do not respond to a high amount of vitamin D₃ [11]. Grenade et al. [11] reported that a loading dosage of 20,000–40,000 IU of vitamin D₃ once a week, with a daily maintenance dosage of 4,000–6,000 IU/day on the remaining 6 days, has shown efficiency in improving the vitamin D level of 3 patients with intestinal failure. A prospective study with 40 infants and toddlers in Qatar reported that parenteral injection of a megadose (10,000 IU/kg) of vitamin D3 for 3 months normalized all the laboratory findings and radiological manifestations [9].

Preterm infants have an increased risk of low 25(OH)D₃ level compared with full-term infants [17-19], but the association between gestational age and vitamin D status remains uncertain. The increased prevalence of vitamin D deficiency in preterm infants might be correlated with a lack of sunlight exposure during prolonged hospitalization along with difficulty in adequate enteral feeding [20]. Furthermore, preterm infants are at high risk of necrotizing enterocolitis, which can lead to short bowel syndrome and intestinal malabsorption [21].

As vitamin D has an important role in absorption of calcium and phosphorus, only 10%–15% of dietary calcium and 50%–60% of dietary phosphorus are absorbed in patients with vitamin D deficiency [22]. Poor absorption of calcium causes hypocalcemia [8]. However, no patients in the present study showed hypocalcemia. Low serum ionized calcium level stimulates PTH secretion, causing phosphorus loss in the urine [10]. As high PTH level affect bone metabolism by increasing bone turnover, decreased serum PTH level during treatment suggests efficacy of vitamin D therapy [23]. All patients with high PTH level demonstrated normalized PTH level after 6 months of parenteral vitamin D₃ treatment.

There were some limitations to this study. This investigation was a retrospective study and included a small number of patients at a single medical center. The duration of treatment varied among patients. Therefore, long-term follow-up is needed to establish a precise protocol about the duration and doses of parenteral vitamin D₃ treatment.

In conclusion, parenteral vitamin D treatment was safe and effective to prevent rickets in infants and children with vitamin D deficiency caused by intestinal malabsorption. Long-term follow-up is required to monitor the efficacy and safety of parenteral vitamin D therapy in a large cohort of patients.

Notes

Ethical statement

This study was approved by the Institutional Review Board at Asan Medical Center in Seoul, Korea (2019-1042).

Conflicts of interest

No potential conflict of interest relevant to this article was reported.

ACKNOWLEDGMENTS

This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2017R1D1A1B03029638).

Fig. 1.

Laboratory data obtained from patients being treated with parenteral vitamin D₃. 25(OH)D₃, 25-hydroxyvitamin D₃.

Table 1.

Demographic findings and underlying diseases of patients with vitamin D deficiency

No.	Sex	Gestational age (wk)	Birth weight (kg)	Underlying disease	Surgery	Age at diagnosis of underlying disease (day)	Age at start of parenteral vitamin D treatment (mo)	Weight SDS before treatment	Height SDS before treatment	Current age (mo)	Weight SDS at current age	Height SDS at current age
1	M	26⁺⁵	0.49	Necrotizing enterocolitis	Small bowel resection	42	1.8	-11.2	-12.72	55	-4.97	-2.66
2	F	36⁺⁶	3.66	Congenital megacolon	Ileostomy	5	2.3	-1.07	0.16	57	-0.56	-1.59
3	F	37⁺⁶	3.68	Congenital mesenteric band	Ileostomy	2	5.3	-0.49	-0.92	7.5	0.37	0.74
4	M	39⁺⁵	3.52	Congenital megacolon	Ileostomy	5	4.7	-5.44	-2.32	12	-5.24	0.95
5	M	25⁺⁵	0.41	Necrotizing enterocolitis	Small bowel resection	8	1	-12.4	-13.2	60	-3.68	-3.23
6	M	37⁺⁵	3.3	Small bowel atresia	Small bowel resection	1	45	-0.79	-0.61	112	-1.8	-1.05
7	M	37⁺⁶	2.8	Crohn disease	Ileostomy	170	31	-2.54	-3.95	56	-2.14	-3.81
8	M	24	0.6	Necrotizing enterocolitis	Small bowel resection	40	1	-10.67	-11.15	34	-2.58	-3.53
9	M	26⁺²	0.69	Small bowel atresia	Small bowel resection	30	4	-5.94	-7.15	21	-3.26	-5.61
10	M	27⁺⁴	0.58	Small bowel atresia	Small bowel resection	54	5.7	-9.2	-11.02	32	-4.14	-4.38
11	F	38⁺⁴	2.94	Chronic intestinal pseudo-obstruction	Ileostomy	20	7	-3.23	-1.42	58	-0.92	-0.8

SDS, standard deviation score.

Table 2.

Baseline laboratory findings and X-rays in patients with vitamin D deficiency

No.	Calcium (mg/dL)	Phosphorous (mg/dL)	Alkaline phosphatase (IU/L)	25-Hydroxyvitamin D₃ (ng/dL)	Parathyroid hormone (pg/mL)	Rickets
1	8.6	5.8	450	4.9	235	Yes
2	9.4	6.5	251	4.9	11.3	No
3	9.1	4.9	344	3.5	52.8	No
4	9.9	4.4	396	2.7	18.3	No
5	9.6	4.5	549	3.2	NA	No
6	8.4	3.8	537	3.2	72.1	No
7	8.9	4.4	269	11.6	10.4	No
8	9.8	2.8	2353	5.8	150	Yes
9	9.4	3	1330	10.6	508	Yes
10	9.5	9.5	1103	4.4	117	No
11	8.7	3.6	237	11.3	13.6	No
Mean±SD	9.2±0.5	4.8±1.9	710±649	6.0±3.4	145±186

NA, not assessed; SD, standard deviation.

Table 3.

25-Hydroxyvitamin D₃ levels (ng/dL) during treatment of parenteral vitamin D₃

No.	Baseline	At 1 month	At 3 months	At 6 months
1	4.9	52.2	23	55.2
2	4.9	3.5	29.3	37.2
3	3.5	17.8	36.5	NA
4	2.7	20.4	67.8	NA
5	3.2	63.9	91.1	121
6	3.2	NA	12.9	18.3
7	11.6	34	58.4	69.8
8	5.8	25.5	45.2	48.9
9	10.6	36.2	107	72.1
10	4.4	17.3	48.6	NA
11	11.3	NA	34.1	23.6
Mean±SD	6.0±3.4	30.1±18.8	50.4±28.8	55.7±32.8

NA, not assessed; SD, standard deviation.

Table 4.

Previous studies with stoss therapy

Variable	Mittal et al. [14] (RCT)	Tannous et al. [15] (RCT)	Mondal et al. [16] (RCT)	Soliman et al. [9] (prospective study)	Grenade et al. [11] (case report)
Number	76	151	61	40	3
Age	0.5–5 Years	2–16 Years	0.5–5 Years	7–23 Months	2.3–6.8 Years
Durationx	12 Weeks	4 Weeks	10 Weeks	3 Months	3 Months
Dose	300,000 IU or 600,000 IU oral vitamin D₃ single dose	100,000 IU weekly oral vitamin D₃	Group 1: 600,000 IU as a single intramuscular dose	10,000 IU/kg intramuscular single dose (maximum 150,000 IU)	20,000–36,000 IU of vitamin D weekly followed by 4,000 IU on the remaining 6 days of the week
Dose	300,000 IU or 600,000 IU oral vitamin D₃ single dose	100,000 IU weekly oral vitamin D₃	Group 2: 60,000 IU orally once a week	10,000 IU/kg intramuscular single dose (maximum 150,000 IU)
Underlying disease	Nutritional rickets	25(OH)D₃ <20 ng/mL	Nutritional rickets	Vitamin D-deficient rickets	Vitamin D deficiency with intestinal failure
Efficacy	Not effective	Effective	Effective (both group)	Effective	Effective
Side effect	Hypercalcemia in 5 patients	None	None	None	None

RCT, randomized controlled trial; 25(OH)D₃, 25-hydroxyvitamin D₃.

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