- Research article
- Open Access
Adefovir dipivoxil induced hypophosphatemic osteomalacia in chronic hepatitis B: a comparative study of Chinese and foreign case series
BMC Pharmacology and Toxicology volume 19, Article number: 23 (2018)
Adefovir dipivoxil (ADV)-induced renal tubular dysfunction and hypophosphatemic osteomalacia (HO) have been given great consideration in the past few years. However, no standard guidance is available due to a lack of powerful evidence from appropriate long-term prospective case-control studies and variations in the definition of renal adverse events. The aim of this study is to clarify clinical features of ADV-related HO in Chinese chronic hepatitis B patients with long-term ADV treatment in Chinese and non-Chinese comparative case series.
Retrieval of case reports was based on Pubmed, CNKI, Wan Fang and VIP databases using the key words adefovir dipivoxil, hypophosphatemia, osteomalacia and Fanconi syndrome. We divided patients into Chinese (C group) and Foreign (F group) groups according to their nationality. Comparisons involving demographics, clinical manifestations, tests, treatment and prognosis were conducted between the two groups.
Of the patients screened, 120 Chinese patients were identified in the C group, and 32 non-Chinese patients were identified in the F group. The average age of the C group was younger than that of the F group (51.89 years ±10.96 years versus 56.47 years ±11.36 years, t = − 2.084, P = 0.039). No significant difference was found in gender (male to female, 3.29:1 versus 3:1, χ2 = 0.039, P = 0.844). Although there was no significant difference in the duration of ADV therapy before ostalgia onset, the C group tended to develop adverse events earlier, by 2–3 years, while the F group developed adverse events at 4–5 years (Z = − 1.517, P = 0.129). Prognosis was good after adjustment of the ADV dose and supplemental administration of phosphate and calcitriol. Time to resolution of tubular dysfunction was commenced at the first month, and Chinese patients were more prone to recover in the first 3 months than non-Chinese patients (91.3% of patients in the C group versus 56.3% in the F group, Z = − 3.013, P = 0.003).
Sufficient attention is required for middle-aged males before and during exposure to long-term ADV therapy, regardless of nationality. The clinical picture, laboratory and radiograph alterations are important clues for those patients and are usually characterized by polyarthralgia, renal tubular dysfunction and mineralization defects. Implementation of an early renal tubular injury index is recommended for patients with higher risk, which would prevent further renal injury.
Adefovir dipivoxil (ADV) is a nucleotide analogue of adenosine monophosphate, which is effective in viral suppression for both treatment-naive and lamivudine-resistant chronic HBV-infected patients . Chronic hepatitis B virus (HBV) infection affects more than 350 million people worldwide, with 75% living in the Asia-Pacific region . Moreover, chronic HBV infection continues to be a major health problem because it leads to the development of liver cirrhosis and hepatocellular carcinoma and increases the risk of hepatic disease-related death. Various studies have reported that adefovir dipivoxil (ADV) can cause proximal renal tubular complex dysfunction, hypophosphatemic osteomalacia (HO) and even Fanconi syndrome since it was first used in the long-term treatment of chronic hepatitis B in 2002 . However, several pitfalls remain to be explained. First, a unified definition of ADV-related renal dysfunction has not yet been identified. Some studies used serum creatinine or evaluated glomerular filtration rate (eGFR), which mainly reflects glomerular function as an endpoint [4, 5], while some studies only investigated indexes concerning renal tubular absorption [6, 7]. No evidence from case-control studies including Chinese chronic hepatitis B patients have been reported, and sample sizes of previous studies were relatively small [8, 9]. Furthermore, patients not matching the original clinical settings were included. To further determine the clinical features of ADV-induced HO in Chinese chronic hepatitis B patients, we investigated the demographics, clinical spectrum, laboratory tests, treatment and prognosis of ADV-induced HO through a comparison of Chinese and non-Chinese case series.
Comparative series study
PubMed, Chinese National Knowledge Infrastructure (CNKI), the Chinese literature database (Wanfang) and the Chinese Science and Technology Journal Database (VIP)  from October 2002 to October 2015 were searched for case reports and relevant clinical trials. The key words were adefovir dipivoxil, hypophosphatemia, osteomalacia, Fanconi Syndrome, and renal insufficiency. The language was limited to Chinese and English. Search strategies for PubMed are shown below:
#1: Search “adefovir dipivoxil”[All Fields]; #2: Search “Fanconi Syndrome”[Mesh]; #3: Search “osteomalacia”[Mesh]; #4: Search “hypophosphatemia”[All Fields]; #5: Search “renal insufficiency”[All Fields]; #6: Search (#2 OR #3 OR #4 OR #5) AND #1.
Relevant Chinese characters were used as keywords when searching Chinese databases.
All references from articles obtained through the databases were reviewed manually.
Inclusion criteria included three parts as follows: (1) Case reports or clinical studies reporting specific cases and conference abstracts with no formal published articles. (2) Safety-related events restricted to hypophosphatemia, osteomalacia and Fanconi syndrome. (3) Events listed occurred during the use of ADV in mono-therapy or combination therapy in naïve or rescue treatment for HBV infection.
Exclusion criteria included the following: (1) Published data that were recorded repeatedly or were lacking in details (e.g., without exact values for hypophosphatemia). (2) Clinical articles without specific case reports or including patients co-infected with HIV or hepatitis C. (3) Meta-analyses, systemic reviews and conference speeches with lack of details.
Two authors (Nan C and Jian-bo Z) independently screened the titles and abstracts of the collected citations from primary searches. Relevant clinical studies were downloaded for specific case reports, as well as those meeting inclusion criteria. Disagreements between the two authors were resolved by discussion and, if needed, arbitrated by a third author (Kuan-xiao T).
A flow chart of the study selection process and exclusion criteria is shown in Fig. 1. One hundred and thirteen records were identified by the electronic database search. After removing duplicates, 109 articles were screened according to the inclusion/exclusion criteria. The remaining 101 full-text articles were assessed for eligibility. Of these articles, 20 were excluded (see S2 File for a list of reasons for exclusion). The remaining 81 articles were included in the final review. We divided patients into Chinese and Foreign groups according to their nationality (C for the Chinese group and F for the Foreign group). Data such as demographics, history (duration of CHB, hepatitis-related complications and comorbidity) and drug details (antiviral drugs, dose, time of starting and maintaining), clinical manifestation, tests, treatment and prognosis were obtained from published sources. The index of laboratory tests was rated according to the National Cancer Institute Common Toxicity Evaluation Standard (NCICTC) Edition 2.0 . For hypophosphatemia, Grade 1 was defined as 0.60- < 0.80 mmol/L, Grade 2 was defined as 0.30- < 0.60 mmol/L, and Grade 3 was defined as < 0.30 mmol/L. For increased serum creatinine, Grade 1 was defined as ≤132.6 μmol/L (≤1.5 mg/dL), Grade 2 was defined as 132.6 μmol/L- ≤ 176.8 μmol/L (1.5- ≤ 2.0 mg/dL), and Grade 3 was defined as 176.8 μmol/L - ≤ 265.2 μmol/L (2.0- ≤ 3.0 mg/dL). The grade classifications are well accepted .
Normally distributed data were described as the mean ± standard deviation, while a non-normal distribution was described as the median (inter-quartile range). Two independent sample t-tests were used for normally distributed data, while non-parametric tests were used for non-normal data. The count data were analyzed by a Chi-square test or Fisher’s exact test. A Mann-Whitney U test of the two independent samples was used in count data with index variables distributed in one-way orderly, while a Kruskal-Wallis H test and rank correlation analysis were used for ordinal categories with different properties. A two-tailed P-value < 0.05 was considered to be statistically significant.
Demographics (see Table 1)
There were 152 patients eligible for the study, with 120 patients allocated to the C group and 32 non-Chinese patients allocated to the F group. The C group was significantly younger than the F group (51.89 ± 10.96 years versus 56.47 ± 11.36 years, t = − 2.084, P = 0.039). Of all the patients in both groups, the age distribution illustrated a gender difference, with males being predominant in the middle-aged group (62/116, 53.4%) and females being the majority in the older group (18/36, 50%) (Z = − 3.640, P < 0.001). No similar tendency was detected in between-group comparisons, and there was no significant difference between the groups regarding gender (male to female, 3.29:1 versus 3:1, χ2 = 0.039, P = 0.844) and gender proportion among different age groups (males represented 57.6% versus 37.5% (Z = − 0.831, P = 0.406), females represented 46.4% versus 62.5% (Z = − 0.956, P = 0.339)). Asian nationalities accounted for 84.4% in the F group, which were mostly Korean (40.6%) and Japanese (31.3%). The other patients included 2 from France, 2 from Italy and 1 from Spain.
The average duration of ADV therapy was 60 (36–72) months in C group and 57 (38–69) months in the F group (Z = − 0.076, P = 0.939), while the duration of ADV therapy before ostalgia onset was 36 (24–48) months versus 47.5 (28–60) months (Z = − 1.428, P = 0.153). Two to five years of ADV therapy accounted for most patients in both groups (55.7% versus 63.3%, Z = − 0.346, P = 0.729). Although the differences were not significant, the C group tended to develop ostalgia 1–2 years earlier than the F group (Z = − 1.517, P = 0.129). The ADV dosage was administered at 10 mg daily, except for 3 patients given 20 mg daily and 1 patient given 15 mg daily in the C group.
The median duration of CHB was 120 (84–195) months in the C group and 132 (46.5–210) months in the F group (only 5 patients recorded). No significant difference was observed in the proportion of liver cirrhosis (95.8% in the C group versus 83.3% in the F group, P = 0.253), LAM therapy before exposure to ADV (61.29% versus 76.50%, χ2 = 1.739, P = 0.187) or LAM add-on with ADV (38.71% versus 23.50%, χ2 = 0.849, P = 0.357). In addition, there were 6 different comorbid diseases in the C group, including 11 patients with hypertension, 7 with diabetes, and one each with gout, chronic bronchitis, Turner’s syndrome and atopic dermatitis. In the F group, no available details were recorded except that 1 patient had epilepsy and 4 underwent surgery (femoral surgery in 2, kidney transplantation in 1 and subtotal gastrectomy in 1).
All patients presented with persistent ostalgia, occurring originally in the lower limbs (e.g., ankle, knee) and aggravated after load-bearing. Commonly, pain perception progressed gradually from the lower limbs to the thorax, ribs, and upper joints, leading to difficulty in motion, staggering gait and passive position. Moreover, the patients usually complained of fatigue and loss of appetite. Some of them could barely stand up and pursue daily activities. Additionally, it is noted that 14 patients in the C group had non-specific symptoms, such as nocturia and peripheral paresthesia, before the initial onset of ostalgia.
For all patients, body mass index (BMI) was within the normal range (21.21 ± 1.85 kg/m2 in the C group versus 23.44 ± 3.98 kg/m2 in the F group, t = − 1.389, P = 0.192). No significant difference was detected in the tenderness distribution of the two groups (see Fig. 2a). Moreover, Fig. 2b shows the detailed data of the abnormal signs recorded in the C group, which showed that a positive orthopedic special test (PST) had the highest incidence, followed by mobility limitation (ML), reduced muscle strength (RMS), and waddling gait.
Laboratory examination (Table 2)
Bone mineral metabolism
No significant difference was found in the reduction of serum phosphorus between the two groups. A Grade 1 decrease (0.60- < 0.80 mmol/L) was recorded in a total of 32.7% in the C group versus 25.8% in the F group, a Grade 2 (0.30- < 0.60 mmol/L) decrease was recorded in 63.7% versus 67.7%, and a Grade 3 (< 0.30 mmol/L) decrease was recorded in 3.5% versus 6.5% (Z = − 0.880, P = 0.379). In addition, 71.4% versus 81.5% of patients had normal excretion of urine phosphorus (Z = − 0.617, P = 0.657). Moreover, 71.6% versus 63.2% of patients developed hypocalcemia (Z = − 0.720, P = 0.472). Interestingly, 85.7% versus 88.9 and 78.8% versus 83.3% of patients had a normal level of 25-(OH) D3 (Z = − 0.249, P = 0.804) [13,14,15,16,17] and PTH (Z = − 0.289, P = 0.772), respectively. The C group had more information regarding bone biochemical metabolism, and 5.3, 93.8 and 76.9% of patients had increased levels of osteocalcin, Type I tropocollagen amino terminal extension of the peptide (PINP), and special series I type collagen peptide carboxyl end β (β-CTX), respectively, which reflected activation of both osteoblasts and osteoclasts. Though the F group had a higher mean value of alkaline phosphatase (AKP), 81.8% versus 100% of patients had drastically increased AKP. It is not difficult to conclude that patients with ADV-induced HO have hypophosphatemia, hypocalcemia, and increased levels of alkaline phosphatase (AKP), which is essentially different from osteoporosis in bone and mineral metabolism, with the latter including over-activated bone reabsorption. Interestingly, most patients had a normal level of 25(OH)VitD3 in both groups.
No significant difference was found in the level blood uric acid, serum creatinine, plasma glucose and serum PH. Hypouricemia was seen in 90.8% of patients in the C group and 100% in the F group (Z = − 1.089, P = 0.276). The C group was more prone to experiencing hypokalemia, with an average serum potassium of 3.48 ± 0.40 mmol/L versus 3.75 ± 0.42 mmol/L (t = − 2.01, P = 0.048). Of note, 88.4% versus 78.9% of patients had increased serum creatinine in Grade 1 (Z = − 1.090, P = 0.276). Interestingly, positive urine glucose was detected in both groups, even in those without diabetes. Both groups had markedly elevated urinary β2-microglobulin (β2-MG). Though no significant differences were noted, the C group had a lower rate of N-acetyl beta D glucose anhydride enzyme (NAG) increase (87.5% versus 100%) and proteinuria over 0.5 g per 24 h (82.4% versus 100%). Furthermore, the C group also had less tendency to develop acidosis despite a median serum PH value (40% versus 83.3%) at the lower limit of the normal range.
A significant inverse correlation between age and serum creatinine was found in the C (γ = − 0.820, P = 0.005) and F group (γ = − 0.840, P = 0.006). This correlation was not seen in age and serum phosphorus or in serum creatinine and serum phosphorus. For 20 patients with severe proteinuria, no correlation was observed with serum creatinine. Hypophosphatemia, hypouricemia, hypocalcemia, and proximal renal tubular dysfunction were characterized by an increased excretion of urine phosphorus, calcium, β2-MG, NAG, severe proteinuria and renal tubular acidosis, which are commonly present in ADV-related HO. No correlation was found between hypophosphatemia and age or serum creatinine. In contrast to conventional wisdom, serum creatinine did not show a positive trend with age and was insensitive for the detection of early pathological alterations.
No significant difference was found in the results of bone mineral density by dual energy X-ray absorptiometry (DEXA), with 65.2% in the C group versus 62.5% in the F group, which had a T score below − 2.5 standard deviation (SD), as well as a distribution of abnormality in the 99mTc-MDP whole body bone scintigraphy. There were increased multiple foci with radiotracer symmetrically distributed in the area of the lower joints (ankles, knees, sacroiliac joints, and hips), upper joints (shoulders), thorax (ribs), back (spines), and skull. In addition, 4 patients in the C group were diagnosed with neurogenic damage through an electromyogram.
No comparison was conducted in this situation since there was a significant difference in sample size. Twenty patients in the C group had a renal biopsy, of whom 18 displayed proximal tubular epithelium atrophy and dramatic vacuolization of epithelial cells with a fading of the brush border and 9 had simultaneous glomeruli lesions. The other two patients were diagnosed with IgA nephropathy by electron microscopy. Renal biopsy was reported in only two patients in the F group. One patient had significant renal tubular lesions, while the other had lesions limited to the glomeruli. Three patients had bone biopsies in the F group, and the biopsies mainly showed local osteoid accumulation and a lack of mineralization. One patient had a muscle biopsy in the C and F groups, and no significant abnormality was found in response to myasthenia. Multiple myeloma was excluded for one patient having bone marrow cytology in the C group.
Misdiagnosis and diagnosis
Twenty-seven patients in the C group (Fig. 3) reported misdiagnosis. Osteoporosis (10/27, 18.0%), ankylosing spondylitis (9/27, 16.0%), lumbar disc herniation (6/27, 12.0%), osteoarthritis (4/27, 10.0%) and bone tumors (4/27, 10.0%) were more frequent. For the F group, only 3 patients had misdiagnoses, including osteoporosis, ankylosing spondylitis and Paget’s disease.
All of the patients were diagnosed with hypophosphatemia and developed hypophosphatemic osteomalacia except for 10 patients in the C group who only reported hypophosphatemia. General damage of proximal renal tubular function, namely, Fanconi syndrome, was recorded in 57 patients in the C group versus 16 in the F group.
Treatment and prognosis
Treatment (Table 3)
There was a significant difference in the proportion of ADV dosage adjustment; 89% of patients in the C group versus 67.9% in the F group had treatment discontinuation (χ2 = 5.652, P = 0.017), while 4.4% versus 28.6% had reduced ADV dosage or a prolonged dosage interval (χ2 = 13.802, P < 0.001). Furthermore, 56% versus 36.7% of patients replaced ADV with entecavir after ADV discontinuation (χ2 = 3.542, P = 0.06).
Bone mineral metabolism regulation
There was no significant difference in the proportion of phosphate (58.2% versus 71.4%, χ2 = 1.570, P = 0.210) or vitamin D3 (57.1% versus 42.9%, χ2 = 1.758, P = 0.185) supplementation between the two groups. The C group was more prone to supplement with calcium than the F group (51.6% versus 10.7%, χ2 = 14.726, P < 0.001).
Prognosis (Table 4)
Time of symptom remission
Significant differences were found in the median time of pain remission (1.5 (1, 2) months in the C group versus 3 (2, 6) months in the F group, Z = − 2.951, P = 0.003), with the C group being more likely to recover in the first 3 months (91.3% of patients in the C group versus 56.3% in the F group, Z = − 3.013, P = 0.001).
Recovery of serology
Though no significant difference was observed in the median time of resolution of serum phosphorus (2 (1, 3) months in the C group versus 3.5 (1.75, 6) months in the F group, Z = − 1.157, P = 0.115), the C group tended to recover in the first three months (81.5% of patients versus 50%, Z = − 1.649, P = 0.099).
Here, we reported a Chinese woman with generalized bone pain for 8 months without antecedent trauma. The study was approved by the ethics committee of Qilu Hospital of Shandong University, and the study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki. The individual in this manuscript had given written informed consent to publish the case details.
The patient was a 43-year-old woman with chronic hepatitis B for more than eight years. ADV was administered from diagnosis until the occurrence of pain initiating from the foot joints eight months ago. No remarkable history of hypertension or renal insufficiency was noted. She experienced progressive bone pain extending from the lower limbs to the lower back and ribs in the next two months. Laboratory tests showed a serum phosphorus level of 0.62 mmol/L, a calcium level of 2.21 mmol/L, and an AKP of 160 U/L. Urine testing revealed proteinuria and glucosuria. Electrolytes from the urinalysis showed a calcium level of 19.84 mmol/24 h, a potassium level of 74.48 mmol/24 h, and a phosphate level of 35.77 mmol/24 h. Impaired renal tubular reabsorption was noted as a drastic increase of urine micro-albumin (75.8 mg/L) and β2-microglobulin (11.8 mg/L). Bone biochemical metabolism tests showed a decreased level of 25-OH vitamin D with no further abnormalities. DEXA detected a decreased femur neck mineral density (BMD) with a mean Z-score of − 3.0 standard deviations. The whole-body 99mTc-MDP diphosphonate bone scintigraphy (Fig. 4) showed increased symmetrical uptake in the ankles, knees, hips, sacroiliac joints and multiple ribs and increased diffuse uptake in the limbs, pelvis, spine, sternum and skull. A clinical diagnosis of ADV-induced HO with secondary Fanconi syndrome was suspected. ADV was discontinued and supplementation with oral phosphate, calcium, and vitamin D was started. The patient’s symptoms improved after two weeks, and the serum phosphorus increased to 0.63 mmol/L. Systemic pain was adequately relieved one month after discharge. Two months later, all of the symptoms disappeared, and the serum phosphorus returned to normal (no test data available).
To the best of our knowledge, this is the first study to investigate the differences among the demographics, clinical manifestation, tests, treatment and prognosis in ADV-related HO between Chinese and non-Chinese CHB patients. Several studies have shown that males older than 50 years are at an increased risk of developing HO [5, 12]. Consistently, middle-aged males were highly vulnerable to HO in our study. Moreover, it seems that being a middle-aged male may be a predictor of HO regardless of nationality. Chinese patients were prone to developing HO earlier, which might due to the difference in sample size. Potential gender-specific association of HO with ADV need to be elucidated in further studies for females. The elderly seemed to be more predisposed to HO. Such considerable age difference in genders regarding the incidence of HO may partly be explained by the variance in bone structure and strength, body fat deposition, sex hormone levels, and the risk of falls between men and women . Intriguingly, the F group is predisposed compared to Asian nationals, probably due to the high incidence of hepatitis B in Asians, race differences and personal genetic susceptibility [19, 20].
Hypophosphatemia mostly occurs one year after ADV therapy in a time- and dosage-dependent manner [12, 21]. As shown in our study, the median course before onset of HO was 3–4 years, with Chinese patients predisposed earlier occurrence, indicating a preexistence of underlying hypophosphatemia. The symptoms of patients varied from mild, such as fatigue, muscle weakness and paresthesia, to severe skeletal pain, disabling myopathy, walking difficulty, and even fractures. However, for some patients, ostalgia never occurred, which might due to differences in duration of CHB, the severity of hypophosphatemia and personal tolerance. Non-specific malnutrition causing muscle atrophy is commonly present in CHB patients with decreased muscle strength, which in turn decreases bone mineral density .
Hypophosphatemic osteomalacia (HO) is one of the serious adverse events of ADV, which is mainly related to proximal renal tubular dysfunction. The underlying mechanisms have not been well-explained. ADV is excreted from the kidney in its original form; human organic anion transporter 1 (hOAT1) in the basolateral membrane of the proximal renal tubules  and multidrug resistance–associated protein type 2 (MRP2) in the apical membrane  control basolateral uptake and luminal excretion, respectively. The polymorphism of genes encoding these two drug transporters may play a role in individual susceptibility , leading to generalized dysfunction of proximal renal tubular reabsorption after exposure to ADV. Moreover, ADV has a low-level activity against mitochondrial DNA polymerase-γ when inhibiting HBV-DNA polymerase simultaneously, ultimately leading to mitochondrial dysfunction, impaired oxidative phosphorylation, and tissue injury . Nonetheless, differences in general health and personal tolerance might result in different clinical phenotypes of mitochondrial toxicity , leading to differences in the clinical spectrum.
Moreover, it must be outlined that renal abnormalities are frequently observed in patients without any oral antihepatitis B virus treatment. In a cross-section study, Amet et al.  found that the prevalence of renal dysfunction in CHB patients was approximately 64.6% and emphasized the necessity for regular monitoring of renal function. Several studies [5, 12, 29, 30] showed middle-aged male patients, especially those with cirrhosis, were more vulnerable, because low-grade renal abnormalities are frequently found in such patients with a history of CHB. Our study showed that over 80% of patients in both groups developed renal tubular dysfunction with elevated β2-MG and NAG. Furthermore, severe proteinuria frequently occurred in the patients, even if serum creatinine was still normal or near normal. The underlying mechanisms are unknown. One study reported that the expression of hepatitis B virus in kidney tissues through an immune-complex mechanism  results in direct pathological lesion and chronic immunologic injury. Interestingly, in contrast to common sense, serum creatinine is not positively correlated with age in such patients. However, it should be noted that the extent to which ADV contributed to the observed renal abnormalities was confounded by the concomitant use of nephrotoxic medications, including valproic acid in epilepsy , and co-morbid conditions such as diabetes, hypertension and non-alcoholic fatty disease .
A small number of patients in both groups were exposed to LAM therapy before ADV or had ADV treatment after LAM intolerance. Whether LAM increases renal toxicity remained undetermined until recently. Recent studies showed that LAM was not a risk factor for renal impairment in either the univariate or multivariate analysis . Additional studies are necessary to elucidate the renal safety of LAM.
Metabolic disturbances of bone are common complications in patients with chronic liver disease, mainly osteoporosis . Our study showed that more than 80% of patients had cirrhosis, over 70% had osteopenia, and over 60% had moderate hypophosphatemia. Though osteoporosis accounted for a large portion of misdiagnoses, a total of 142 (93.4%) patients were diagnosed with osteomalacia. Multiple factors, such as vitamin D deficiency, low levels of osteocalcin, PTH, insulin growth factor-1(IGF-1), hypogonadism, behavioral factors such as low body mass index (BMI), malnutrition , and a sedentary lifestyle with physical inactivity  are frequently observed in these patients, especially those with cirrhosis. There is no doubt that long-term administration of antiviral therapy in such patients would further increase the risk of bone loss resulting from decreased remodeling of bone in the absence of adequate phosphorus and calcium, leading to softening and distortion of the skeleton. Unexpectedly, over 85% of patients maintained a normal level of 25-(OH) D3 in our study , which may be explained by the heterogeneity of the subjects in different reports and by differences in the statistical methods used.
According to our present study, routine renal function tests based on serum creatinine are not sensitive enough to detect early abnormalities of renal structure and function . Previous studies have demonstrated biomarkers such as fractional excretion of filtered phosphate (FEPO4) , retinol-binding protein (RBP) and N-acetylglucosamine (NAG)  may be used for early renal tubular injury detection during long-term ADV treatment. No complete data can be found in the application of the above indices in our study, which implicates that tests reflecting early kidney injury are still not yet widely implemented in the daily clinical setting. In addition, significant differences found in serum potassium and AKP may due to differences in the sample size and methods used. ADV-related nephrotoxicity manifests as a proximal renal tubular dysfunction and is primarily featured by the onset of gradual decreases in serum phosphorus, usually mild to moderate in severity, and can be accompanied by changes in serum potassium, bicarbonate, uric acid, glycosuria, and proteinuria. Though lacking predictor analysis, we still emphasize the importance of monitoring serum phosphorus, calcium, AKP, urine electrolytes, serum uric acid, urine routine testing, and biomarkers of renal tubular injury (NAG, β2-MG, FEPO4) during long-term ADV therapy. Special care is needed, especially for differential diagnoses, since oeteomalacia and osteoporosis commonly co-exist in such patients, and both are characterized by reduced bone mineral density, diffuse bone pain and susceptibility to fracture. Radiologically, pseudofractures are seen most commonly in stress-bearing bones of osteomalacia patients in 99mTc-MDP whole body bone scintigraphy. 99mTc-MDP whole body bone scintigraphy would be preferable to diagnose osteomalacia primarily characterized by mineralization defects, despite the ability of DEXA to diagnose osteoporosis.
Treatment of ADV-induced HO is still not well established. Modification of risk factors involving smoking, alcohol and malnutrition is of prime importance. Some studies suggest that changes of the antiviral drug are more favorable than a phosphate regimen for the purpose of bone protection, preferring dosing-interval adjustment [41, 42]. In this respect, our study showed that Chinese patients were more prone to ADV withdrawal, while non-Chinese patients were prone to dosage adjustment. However, comprehensive consideration, including the potential risk for viral breakthrough, aggravation of liver function, therapy cost and tolerance, is essential before adjustment. For most mildly affected patients, dosage interval adjustment or termination is sufficient without further phosphate supplementation, while for severe cases, phosphate supplementation is indispensable. Our study indicated that both groups adopted phosphate supplementation, in combination with vitamin D3 supplementation, whereas Chinese patients more commonly had calcium supplementation. Several patients were treated with drugs that regulate bone metabolism, such as calcitonin. It is important to note that calcitonin is not optimal, since it can reduce renal tubular phosphate reabsorption and inhibit osteoclast activity even though it has obvious analgesic functions . Other drugs affecting proximal renal tubular reabsorption, such as valproic , should also be adjusted. Individual differences in bone remodeling period, duration of CHB, and comorbidity (e.g., osteoporosis) may result in different times to remission. Our study showed that the resolution of proximal renal tubular dysfunction started in the first month, and most patients did not resolve completely until three months of treatment, with Chinese patients being prone to resolve earlier. We consider such variable responses to therapy to be a result of race differences and bias in reports. On the whole, ADV-induced abnormalities are reversible after appropriate drug modification, and remission is predictable at the first month of therapy.
In addition, differences in group samples and the absence of multivariable analysis limit the power of our study. A large clinical prospective case-control study is required to further elucidate the risk factors and assist clinical implementation.
There are limitations in this study. First, this is a retrospective study, and it was hard to collect all of the required lab parameters. Second, multivariate analysis is a useful way to show figures more clearly, but considering the loss of effective information, it is impossible to analyze in that way. Third, the smaller population in the F group compared to the Chinese group leads to a deviation error in the conclusions. Further investigation with more detailed information is in process and will be published in the future.
To date, there are no common definition for adequate vitamin D status measured as 25(OH)D serum concentrations, and the range of 25-(OH) D3 varies from article to article. National Institute of Health, Office of Dietary Supplements, considered 25(OH) D levels < 12 ng/ml as 25-(OH) D3 deficiency, and 12- < 20 ng/ml as insufficient and > 20 ng/ml sufficient. However, some researchers and clinicians defined 25-(OH) D3 deficiency as < 20 ng/ml . Besides, explanations of the normal ranges for 25-(OH) D3 in adults and children from ARUP laboratories (one of the major reference laboratories in the USA) are present in http://ltd.aruplab.com/Tests/Pdf/203. In the current study, we collected the information from various case reports and other clinical reports, which is closed to NIH Office of Dietary supplements definition. Moreover, the level of 25-(OH) D3 is a composition of endogenous synthesis of 25-(OH) D3 as well as absorption of exogenous 25-(OH) D3, and variation between different races and even different countries because of diet, geological and other factors might also contribute to the difference for the normal range of 25-(OH) D3.
In conclusion, middle-aged male patients have a higher risk of HO during long-term ADV treatment, especially those with cirrhosis, and Chinese patients are more prone to develop HO earlier than foreign patients. Sufficient attention is needed for older females, regardless of nationality. The clinical picture and laboratory and radiograph alterations are the most important factors in the diagnosis for those suspected of HO and are characterized by polyarthralgia, renal tubular dysfunction, and mineralization defects. Routine tests are not appropriate. Monitoring early indicators reflecting proximal renal tubular function before and during exposure to ADV is paramount, because renal abnormalities are still revisable after prophylactic or therapeutic intervention. Prognosis is good after adjustment of ADV therapy, and phosphate as well as calcium supplementation might be necessary otherwise.
Our results show that attention should be paid to middle-aged males before and during exposure to long-term ADV therapy in both the Chinese patients and selected non-Chinese patients included in our study. Clues such as clinical picture and laboratory and radiograph alterations are necessary for suspected patients, and they are characterized by polyarthralgia, renal tubular dysfunction and mineralization defects. Implementation of an early renal tubular injury index is beneficial for higher-risk patients to avoid further renal injuries.
Body mass index
Chronic viral hepatitis B
Chinese National Knowledge Infrastructure
Dual energy X-ray absorptiometry
Evaluated glomerular filtration rate
Insulin growth factor-1
Multidrug resistance–associated protein type 2
N-acetyl beta D glucose anhydride enzyme
Positive orthopedic special test
Reduced muscle strength
Chinese Science and Technology Journal Database
Collagen peptide carboxyl endβ
Lim SG, Marcellin P, Tassopoulos N, Hadziyannis S, Chang TT, Tong M, Sievert W, Hu P, Arterburn S, Brosgart CL, et al. Clinical trial: effects of adefovir dipivoxil therapy in Asian and Caucasian patients with chronic hepatitis B. Aliment Pharmacol Ther. 2007;26(10):1419–28.
Lavanchy D. Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures. J Viral Hepat. 2004;11(2):97–107.
Segovia MC, Chacra W, Gordon SC. Adefovir dipivoxil in chronic hepatitis B: history and current uses. Expert Opin Pharmacother. 2012;13(2):245–54.
Ha NB, Ha NB, Garcia RT, Trinh HN, Vu AA, Nguyen HA, Nguyen KK, Levitt BS, Nguyen MH. Renal dysfunction in chronic hepatitis B patients treated with adefovir dipivoxil. Hepatology. 2009;50(3):727–34.
Kim YJ, Cho HC, Sinn DH, Gwak GY, Choi MS, Koh KC, Paik SW, Yoo BC, Lee JH. Frequency and risk factors of renal impairment during long-term adefovir dipivoxil treatment in chronic hepatitis B patients. J Gastroenterol Hepatol. 2012;27(2):306–12.
Gara N, Zhao X, Collins MT, Chong WH, Kleiner DE, Jake Liang T, Ghany MG, Hoofnagle JH. Renal tubular dysfunction during long-term adefovir or tenofovir therapy in chronic hepatitis B. Aliment Pharmacol Ther. 2012;35(11):1317–25.
Shimizu M, Furusyo N, Ikezaki H, Ogawa E, Hayashi T, Ihara T, Harada Y, Toyoda K, Murata M, Hayashi J. Predictors of kidney tubular dysfunction induced by adefovir treatment for chronic hepatitis B. World J Gastroenterol. 2015;21(7):2116–23.
Shimizu Y, Hiraoka A, Yamago H, Shiraishi A, Imai Y, Tatsukawa H, Tanihira T, Miyata H, Ninomiya T, Tokumoto Y, et al. Hypophosphatemia in patients with hepatitis B virus infection undergoing long-term adefovir dipivoxil therapy. Hepatol Res. 2014;44(11):1081–7.
Xu LJ, Jiang Y, Liao RX, Zhang HB, Mao JF, Chi Y, Li M, Wang O, Liu XQ, Liu ZY, et al. Low-dose adefovir dipivoxil may induce Fanconi syndrome: clinical characteristics and long-term follow-up for Chinese patients. Antivir Ther. 2015;20(6):603–11.
Yang S, Du A, Zhang Y, Shen L. Meta-analysis of personality of child abuse in China. West Indian Med J. 2015; https://doi.org/10.7727/wimj.2015.135.
Cancer therapy evaluation program, common toxicity criteria. Version 2.0. CTD, NCI, NIH, DHHS, March 1998, revised March 23, 1998; published date: April 30, 1999; http://clep.cancer.gov/forms/ctcv20_4-30-992.pdf.
Tanaka M, Suzuki F, Seko Y, Hara T, Kawamura Y, Sezaki H, Hosaka T, Akuta N, Kobayashi M, Suzuki Y, et al. Renal dysfunction and hypophosphatemia during long-term lamivudine plus adefovir dipivoxil therapy in patients with chronic hepatitis B. J Gastroenterol. 2014;49(3):470–80.
Gifre L, Peris P, Monegal A, Martinez de Osaba MJ, Alvarez L, Guanabens N. Osteomalacia revisited : a report on 28 cases. Clin Rheumatol. 2011;30(5):639–45.
Wang BF, Wang Y, Wang BY, Sun FR, Zhang D, Chen YS. Osteomalacia and Fanconi's syndrome caused by long-term low-dose adefovir dipivoxil. J Clin Pharm Ther. 2015;40(3):345–8.
Law ST, Li KK, Ho YY. Nephrotoxicity, including acquired Fanconi's syndrome, caused by adefovir dipivoxil - is there a safe dose? J Clin Pharm Ther. 2012;37(2):128–31.
Kawate H, Taketomi A, Watanabe T, Nomura M, Kato M, Sakamoto R, Ikegami T, Soejima Y, Maehara Y, Takayanagi R. Hypophosphatemic osteomalacia as a long-term complication after liver transplantation. Transplantation. 2011;91(1):e6–8.
Wu C, Zhang H, Qian Y, Wang L, Gu X, Dai Z. Hypophosphatemic osteomalacia and renal Fanconi syndrome induced by low-dose adefovir dipivoxil: a case report and literature review suggesting ethnic predisposition. J Clin Pharm Ther. 2013;38(4):321–6.
Li M, Xu Y, Xu M, Ma L, Wang T, Liu Y, Dai M, Chen Y, Lu J, Liu J, et al. Association between nonalcoholic fatty liver disease (NAFLD) and osteoporotic fracture in middle-aged and elderly Chinese. J Clin Endocrinol Metab. 2012;97(6):2033–8.
Chen YC, Su YC, Li CY, Wu CP, Lee MS. A nationwide cohort study suggests chronic hepatitis B virus infection increases the risk of end-stage renal disease among patients in Taiwan. Kidney Int. 2015;87(5):1030–8.
Chen YC, Su YC, Li CY, Hung SK. 13-year nationwide cohort study of chronic kidney disease risk among treatment-naive patients with chronic hepatitis B in Taiwan. BMC Nephrol. 2015;16:110.
Wei Z, He JW, Fu WZ, Zhang ZL. Osteomalacia induced by long-term low-dose adefovir dipivoxil: clinical characteristics and genetic predictors. Bone. 2016;93:97–103.
Yadav A, Carey EJ. Osteoporosis in chronic liver disease. Nutr Clin Pract. 2013;28(1):52–64.
Ho ES, Lin DC, Mendel DB, Cihlar T. Cytotoxicity of antiviral nucleotides adefovir and cidofovir is induced by the expression of human renal organic anion transporter 1. J Am Soc Nephrol. 2000;11(3):383–93.
Schaub TP, Kartenbeck J, Konig J, Spring H, Dorsam J, Staehler G, Storkel S, Thon WF, Keppler D. Expression of the MRP2 gene-encoded conjugate export pump in human kidney proximal tubules and in renal cell carcinoma. J Am Soc Nephrol. 1999;10(6):1159–69.
Vigano M, Facchetti F, Dongiovanni P, Valenti L, Soffredini R, Fargion S, Colombo M, Lampertico P. Drug transporter gene polymorphism predicts renal tubular toxicity in patients with chronic hepatitis B on long-term adefovir and lamivudine comnination. Dig Liver Dis. 2010;42:S8.
Qi X, Wang J, Chen L, Huang Y, Qin Y, Mao R, Zhang J. Impact of nucleos(t)ide analogue combination therapy on the estimated glomerular filtration rate in patients with chronic hepatitis B. Medicine (Baltimore). 2015;94(15):e646.
Hulgan T, Haas DW, Haines JL, Ritchie MD, Robbins GK, Shafer RW, Clifford DB, Kallianpur AR, Summar M, Canter JA. Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study. AIDS. 2005;19(13):1341–9.
Amet S, Bronowicki JP, Thabut D, Zoulim F, Bourliere M, Mathurin P, de Ledinghen V, Benhamou Y, Larrey DG, Janus N, et al. Prevalence of renal abnormalities in chronic HBV infection: the HARPE study. Liver Int. 2015;35(1):148–55.
Hartono JL, Aung MO, Dan YY, Gowans M, Lim K, Lee YM, Lee GH, Low HC, Tan PS, Thwin MA, et al. Resolution of adefovir-related nephrotoxicity by adefovir dose-reduction in patients with chronic hepatitis B. Aliment Pharmacol Ther. 2013;37(7):710–9.
Tamori A, Enomoto M, Kobayashi S, Iwai S, Morikawa H, Sakaguchi H, Habu D, Shiomi S, Imanishi Y, Kawada N. Add-on combination therapy with adefovir dipivoxil induces renal impairment in patients with lamivudine-refractory hepatitis B virus. J Viral Hepat. 2010;17(2):123–9.
Bhimma R, Coovadia HM. Hepatitis B virus-associated nephropathy. Am J Nephrol. 2004;24(2):198–211.
Hall AM, Bass P, Unwin RJ. Drug-induced renal Fanconi syndrome. QJM. 2014;107(4):261–9.
Guo J, Shao M, Lu F, Jiang J, Xia X. Role of Sirt1 Plays in Nucleus Pulposus Cells and Intervertebral Disc Degeneration. Spine (Phila Pa 1976). 2017;42(13): E757–66.
Lucaci C, Acalovschi M. Hormonal and cytokine implications in the pathophysiology of osteoporosis occurring in chronic liver diseases. Maedica (Buchar). 2012;7(4):358–63.
Santos LA, Romeiro FG. Diagnosis and Management of Cirrhosis-Related Osteoporosis. Biomed Res Int. 2016;2016:1423462.
Gatta A, Verardo A, Di Pascoli M, Giannini S, Bolognesi M. Hepatic osteodystrophy. Clin Cases Miner Bone Metab. 2014;11(3):185–91.
Hao Y, Ma X, Shen Y, Ni J, Luo Y, Xiao Y, Bao Y, Jia W. Associations of serum 25-hydroxyvitamin D3 levels with visceral adipose tissue in Chinese men with normal glucose tolerance. PLoS One. 2014;9(1):e86773.
Jia HY, Ding F, Chen JY, Lian JS, Zhang YM, Zeng LY, Xiang DR, Yu L, Hu JH, Yu GD, et al. Early kidney injury during long-term adefovir dipivoxil therapy for chronic hepatitis B. World J Gastroenterol. 2015;21(12):3657–62.
Assadi F. Hypophosphatemia: an evidence-based problem-solving approach to clinical cases. Iran J Kidney Dis. 2010;4(3):195–201.
Hall AM, Hendry BM, Nitsch D, Connolly JO. Tenofovir-associated kidney toxicity in HIV-infected patients: a review of the evidence. Am J Kidney Dis. 2011;57(5):773–80.
Kim du H, Sung DH, Min YK. Hypophosphatemic osteomalacia induced by low-dose adefovir therapy: focus on manifestations in the skeletal system and literature review. J Bone Miner Metab. 2013;31(2):240–6.
Shiffman ML, Pol S, Rostaing L, Schiff E, Thabut D, Zeuzem S, Zong J, Frederick D, Rousseau F. Efficacy and pharmacokinetics of adefovir dipivoxil liquid suspension in patients with chronic hepatitis B and renal impairment. J Clin Pharmacol. 2011;51(9):1293–301.
Azria M. Possible mechanisms of the analgesic action of calcitonin. Bone. 2002;30(5 Suppl):80S–3S.
Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357(3):266–81.
We would like to thank the patient for letting us share her medical history. We also would like to thank our colleagues, including Mei Cheng, Zhenxia Han, Qian Cai, and Chunli Fu, for the careful diagnosis, treatment and nursing care during the case.
Special Research Fund of Clinical Medicine of the Chinese Medical Association (13060990484), the Natural Science Foundation of Shandong Province (ZR2015HM074), Key Research and Development Plan of Shandong Province (2016GSF201014), and the Joint Scientific Research Fund of Shandong University (11671315).
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This study was approved by Qilu Hospital Shandong University. As this was a retrospective study with no direct patient identifiers revealed, individual consent was waived.
Consent for publication
The authors declare that the paper has not been submitted and/or is not currently under consideration elsewhere.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Chen, N., Zhang, Jb., Zhang, Q. et al. Adefovir dipivoxil induced hypophosphatemic osteomalacia in chronic hepatitis B: a comparative study of Chinese and foreign case series. BMC Pharmacol Toxicol 19, 23 (2018). https://doi.org/10.1186/s40360-018-0212-7
- Adefovir dipivoxil
- Renal insufficiency
- Fanconi syndrome