Evaluation of proximal tubule functions in children with COVID-19:a prospective analytical study

atma Devrim · Elif B?ncüoF?lu · Elif K?ymet · ?ahika ?ahinkaya · Ela Cem · Mine Düzg?l · Aybüke Akaslan Kara ·Kamile ?tiken Ar?kan · Asl? Kantar · Ebru ?Ylmaz · Nida Din?el · Nuri Bayram · ?lker Devrim

Keywords Coronavirus disease 2019 (COVID-19) · Proteinuria · Proximal tubular dysfunction · Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) · Tubular reabsorption of phosphate

tInroduction

Except for multisystemic inf lammatory syndrome associated in children (MIS-C) associated with coronavirus disease 2019 (COVID-19), the clinical course and outcome of COVID-19 are signif icantly better in pediatric patients than in adults [ 1, 2]. The studies conducted in China and Italy indicated that children are mildly aff ected, accounting for approximately 5% of cases and less than 1% of hospital admissions [ 1, 3]. Despite the fact that the majority of clinical presentations are due to pulmonary involvement,extra-pulmonary manifestations, such as gastrointestinal,cardiovascular, hematological, musculoskeletal, and endocrinological, as well as the renal system, may occur [ 4].

COVID-19-related renal impairments have been studied primarily in adult patients. Proteinuria and hematuria were the most frequently reported clinical f indings in one study of 701 adults with COVID-19, occurring in 43.9%and 26.7% of patients, respectively and followed by elevated blood urea nitrogen, elevated serum creatinine, and low glomerular f iltration rates [ 5]. The primary route of the entry of severe acute respiratory syndrome coronavirus 2 (SARSCoV-2) into cells is via angiotensin-converting enzyme 2(ACE2) receptor. These receptors are predominantly found in the lung, but also in the heart, gastrointestinal organs,and kidneys [ 6]. SARS-CoV-2 has a detrimental eff ect on the kidney, manifesting clinically as an increase in proteinuria, hematuria, and serum creatinine. The virus particles are more prevalent in the glomeruli and proximal tubule cells of the kidney [ 7]. The involvement of proximal tubule cells is particularly signif icant because ACE2 proteins on the surface of proximal tubule cell allow for the entry of SARS-CoV-2 viruses [ 6]. The proximal tubules of the kidney are where albumin, low molecular weight proteins,glucose, amino acids, phosphate, bicarbonate, and uric acid are absorbed effi ciently. Proteinuria, hypophosphatemia(decreased tubular phosphorus reabsorption in the presence of a normal or low serum phosphorus level), hyperuricosuria, neutral aminoaciduria, and normoglycemic glycosuria are all symptoms of proximal tubular dysfunction (PTD) [ 8].

There are few studies focusing on renal eff ects of COVID-19 infection and PTD in children with COVID-19 infection[ 9— 11]. The purpose of this study was to assess the proximal tubule’s functions in hospitalized children with conf irmed acute COVID-19.

Methods

This prospective descriptive study was conducted at the University of Health Sciences Dr. Beh?et Uz Children’s Hospital in ?zmir, Turkey, from October 11 through January 31,2021. The study included children aged 1 month to 17 years who were admitted to the pediatric infectious diseases ward with conf irmed COVID-19. The diagnosis of COVID-19 was conf irmed by the quantitative real-time polymerase chain reaction (RT-PCR) positivity. The RT-PCR protocol followed the WHO’s recommendation [ 12]. SARS-CoV-2 samples were recommended for only symptomatic patients in our national and hospital-based protocols. COVID-19 severity was determined using clinical features, laboratory testing, and chest X-ray imaging and included asymptomatic infection, mild, moderate, severe, and critical cases [ 13].Urine samples were collected prior to the any medication or intravenous f luid administration.

Inclusion criteria

Patients with acute COVID-19 infections by RT-PCR, as well as children aged 1 month to 17 years, were included in the study.

Exclusion criteria

Patients with a history of renal disease, those who were followed up in a pediatric intensive care unit, and those who had missing data, such as serum creatinine and routine urinalysis, were all excluded from the study. Patients on hydroxychloroquine-containing drugs before admission,as well as those with other chronic diseases, were excluded.Patients who had a history of high phosphate intake also were excluded. The patients' urine samples were taken before any medication or intravenous f luid administration and any patients who did not fulf ill the criteria were excluded. Children diagnosed with MIS-C were not included in the study.During the hospitalization, blood and urine samples were collected for basic biochemical parameters and urine analysis, including urine electrolytes, protein, glucose, and microalbumin. The patient’s demographic features, such as age,gender, initial serum creatinine levels and electrolytes, uric acid, glucose, and routine urinalysis with microscopy also were recorded. In addition, estimated glomerular f iltration rate (eGFR), tubular reabsorption of phosphate (TRP), maximum renal tubular phosphate threshold (TmP), renal tubular phosphate loss (TmP/eGFR), presence of normoglycemic glucosuria, hyperuricosuria were calculated for all patients according to the criteria below.

Def initions

(1) TRP: renal tubular phosphate involvement was used to assess tubular reabsorption. Because 85 and 95% of the phosphate is reabsorbed from the proximal tubule, TRP rate below 85% was indicated as tubular phosphate leakage [ 14]. This rate was calculated as “100 × {1 - [(urinary phosphate × serum creatinine)/(urinary creatinine × serum phosphate)]}”. Serum creatinine and phosphate levels were expressed as mg/dL [ 14]; (2) TmP: [serum phosphate - (urinary phosphate × serum creatinine)]/urinary creatinine [ 15]; (3) TmP/eGFR: the values of TmP/eGFR ＜ 2.8 mg/dL indicated the renal tubular phosphate loss [ 15]; (4) normal serum creatinine was def ined as 0.2—0.4 mg/dL (18—35 micromol/L) for infants,0.3—0.7 mg/dL (27—62 micromol/L) for children, 0.5—1 mg/dL (44—88 micromol/L) for adolescents [ 16]; (5) eGFR was determined using the modif ied Schwartz criteria [ 17]; (6)normoglycemic glucosuria is def ined as increased urine glucose excretion in the presence of normal serum glucose levels. The presence of glucose positivity in the urine with a dipstick was intended to be signif icant; (7) hyperuricosuria: after the age of three, the result obtained using the formula "uric acid (mg/dL) × serum creatinine (mg/dL)/urine creatinine (mg/dL)", which also uses glomerular f iltration rate, is greater than 0.56 mg/dL, indicating hyperuricosuria[ 18]; (8) urinary uric acid/creatinine ratio: it was evaluated and described as normal according to the previous study performed on Turkish children [ 19]; (9) hypouricemia: a blood uric acid level of less than 2 mg/kg is considered as hypouricemia [ 20]; (10) proteinuria: the upper limit of normal for the spot urine protein-to-creatinine ratio changes by age as following; ＜ 0.5 mg protein/mg creatinine at age 6—24 months (infants and toddlers); ＜ 0.2 mg protein/mg creatinine at age 24 months to 18 years (children and young adults). The spot urine protein-to-creatinine ratio that is indicative of nephrotic range proteinuria is ＞ 3 mg protein/mg creatinine [ 21]; (11) diagnosis of proximal tubular dysfunction: the presence of at least two of the following four abnormalities [ 22]; including the presence of increased renal tubular phosphate loss, normoglycemic glycosuria,hyperuricosuria, and proteinuria, was used to diagnose proximal tubular dysfunction.

Statistical analysis

SPSS statistical software (version 22; SPSS, Chicago, IL,USA) was used for the statistical analysis. The Student’s

t

test was used to compare continuous parametric variables,the Mann—Whitney

U

test was used to compare continuous nonparametric variables, and

χ

2 or Fisher’s exact tests were used when appropriate. A two-tailed

P

value of ＜ 0.05 was considered to be statistically signif icant.

Ethical consent

This study was approved by the local Ethical Committee of Dr. Behcet Uz Children's Training and Research Hospital with the registration number 452 (approval number: 166;date: 09.24.2020).

Results

The demographics of the study population

A total of 115 hospitalized patients who met the study’s criteria were included in the study. Seventy-three (63.5%)of the patients were male, and 42 (47.9%) were female. The median age of patients was 10 years (range: 1 months to 17 years). Regarding the age distribution, 18 (15.7%) of the patients were under 1-year-old and 68 (59.1%) were 12 years and older. The median body weight of the patients was 39.0 kg (range: 3.9—115 kg), and the median height was 145 cm (range: 54—186 cm). Fifteen (13.0%) patients had body mass index (BMI) ≥ 25. Eight (6.9%) patients were overweight (BMI = 25—29.9), and seven (6.0%) patients were obese (BMI ≥ 30).

Fever (51, 44.3%) and cough (48, 41.7%) were the most common symptoms, followed by headache (29, 25.2%),myalgia (25, 21.7%), sore throat (19, 16.5%), diarrhea (18,15.6%), chest pain (16, 14.0%), anosmia (15, 13.2%), vomiting (9, 7.8%), nasal discharge (8, 6.9%), rash (2, 1.7%).

The baseline characteristics of the laboratory tests

The average serum creatinine level was 0.6 ± 0.1 mg/dL(range: 0.4—1.00 mg/dL) with 38 (33.0%) patients having high creatinine levels (Table 1). The mean serumphosphate level was 4.5 ± 0.8 mg/dL. Hypophosphatemia was found in 10 (8.7%) patients of the whole group. The mean eGFR was 85.98 ± 18.38 (range: 44.6—131.4).

Table 1 Baseline characteristics of the 115 patients with serum biochemical parameters and urinalysis

estimated glomerular f iltration rate, standard deviation

Variables Mean ± SD Minimum—maximum Serum creatinine (mg/dL) 0.6 ± 0.1 0.4—1.0 Serum calcium (mg/dL) 9.3 ± 0.6 7.3—10.5 Serum phosphate (mg/dL) 4.5 ± 0.8 1.0—6.6 Serum sodium (mmol/L) 138.4 ± 2.4 129—142 Serum potassium (mmol/L) 4.4 ± 0.5 3.3—6.1 Serum chloride (mmol/L) 105.6 ± 3.1 95—114 Serum glucose (mg/dL) 102.9 ± 21.0 73—227 Serum urea (mg/dL) 10.7 ± 6.9 2.0—63.0 Serum uric acid (mg/dL) 4.1 ± 1.4 1.0—9.8 Serum protein (g/dL) 7.0 ± 0.8 4.1—8.3 Serum albumin (g/L) 4.3 ± 0.5 2.4—5.0 eGFR (mL/min/1.73 m 2 ) 85.98 ± 18.38 44.6—131.4 Urinary protein/urinary creatinine ratio, median 0.1740 0.03—2.62

Evaluation of diagnostic criteria for proximal tubular injury

The median urinary protein/urinary creatinine ratio was 0.17 (range: 0.03—2.62) indicating 39 (33.9%) patients had proteinuria. The mean age in the patients with proteinuria was 87.54 ± 68.98 months (range: 1 month to 17 years) and the mean age of those without proteinuria was 118.57 ± 68.71 months (range: 2 months to 17 years).Mean age was signif icantly lower in the proteinuria group(

P

= 0.024). In the patients without proteinuria, 15.8%(

n

= 12) of the patients had microalbuminuria (Table 2).Tubular phosphate leakage measured by TRP was present in 27 (23.5%) patients. TMP/eGFR values also revealed abnormal renal tubular phosphate loss (＜ 2.8 mg/dL) in 10 (8.7%) patients and normal range in 105 (91.3%)patients. Hypophosphatemia was found in 10 (8.7%)patients of the whole group. Two (1.73%) patients had normoglycemic glycosuria. Hyperuricosuria was present at 28.6% (

n

= 33) of the population. The median age in the patients with hyperuricosuria was 4 years (range: 1 month to 16 years), while that of patients without hyperuricosuria was 12.5 years (range: 2 months to 17 years). The median age was signif icantly lower in the patients with hyperuricosuria (

P

＜ 0.001). The percentage of patients with hypouricemia was 4.3% (

n

= 5).

Table 2 The distribution of the patients with COVID-19 infections for the diagnostic criteria for proximal tubule dysfunction

- coronavirus disease 2019, proximal tubular dysfunction . *The cells, showed the 24 (20.8%) patients with PTD depending on two positivity of diagnostic criteria. “+” positive, “—” negative

Diagnostic criteria for proximal tubule dysfunction Hyperuricosuria Proteinuria Renal tubular phosphorus loss Normoglycemic glycosuria Number of cases— — — — 59— — + — 2— + — — 16* — + + — 4* — + + + 1+ — — — 14* + — + — 1* + + — — 15* + + — + 1* + + + — 2 115

Evaluation of patients for proximal tubule dysfunction

As shown in Table 2, 7 (6.0%) patients had both proteinuria and increased renal tubular phosphate loss measured by TmP/eGFR, 18 (15.6%) patients had both proteinuria and hyperuricosuria, and 3 (2.6%) patients had both increased renal tubular phosphate loss and hyperuricosuria. There were 24 (20.9%) patients with proximal tubular pathology based on the presence of two diagnostic criteria positivity(Table 2). Four (3.5%) patients had at least three positive diagnostic criteria (Table 2). The probability of occurrence of PTD was 0.209 (95% conf idence interval 0.134—0.283).

The percentage of male patients was 58.3% (

n

= 14) in the PTD group and was 64.8% (

n

= 59) in the patients with normal proximal tubule function. No signif icant diff erence was present between these two groups (

P

＞ 0.05). The median age was 6 years (range: 1 month to 17 years) in the patients with PTD and was 10 years (range: 2 months to 17 years) in the patients without PTD. The median age was signif icantly lower in the patients with PTD (

P

= 0.028). A binary logistic regression model that specif ied presence/absence of PTD as a function of age (months) was not statistically signif icant,[

χ

2 = F(1, 115) = 79.1,

P

＞ 0.05], indicating that age could not be used to distinguish between presence or absence of PTD.

Discussion

In this prospective study, PTD was evaluated in children with COVID-19. About a third of the patients had higher serum creatinine levels or proteinuria. In addition, abnormal renal tubular phosphorus loss measured by TMP/eGFR was found in 10 (8.7%) patients, and hyperuricosuria was found in 28.6%. As a result, overall PTD was found in one of f ive patients in our study.

The kidney has been identif ied as a specif ic target for SARS-CoV-2 infection in several investigations [ 23— 26].The postmortem examination of the kidney revealed the accumulation of SARS-CoV-2 antigens in the renal epithelial cells [ 23]. Despite the published articles, limited studies have focused on COVID-19’s eff ect on proximal tubule functions [ 7, 22, 27]. Detection of viral particles of SARS-CoV-2 in the proximal tubular epithelium and podocytes associated with foot process eff acement, vacuolation,and detachment of podocytes from the glomerular basement membrane indicated the involvement of the proximal tubules by SARS-CoV-2 [ 26]. Another renal impairment was SARS-CoV-2-related acute kidney injury and was generally reported in the critically ill patients [ 28, 29]. In our patient's group, no acute kidney injury related to SARS-CoV-2 was observed. This result is primarily related to the study group’s characteristics. We focused on children who did not require intensive care unit admission and were thus less likely to be aff ected by COVID-19 infections.

Werion et al. reported that 70—80% of the patients with COVID-19 had low-molecular-weight proteinuria and that 46% and 19% of the patients had an inappropriate urinary loss of uric acid and phosphate, respectively [ 7]. In another study 75% of the COVID-19 patients had at least two of the four criteria for PTD [ 22]. Patients requiring pediatric critical care units were more likely to show signs of renal involvement, such as proximal tubule injury, according to recent studies [ 22]. Despite the fact that the present study used similar diagnostic criteria, the rate of PTD was 20.8%,which was lower than the previous study. The higher rates of PTD in the previous study could have been attributed to a smaller sample size and to more patients being followed up in the critical care unit, which may be diff erent from our study [ 22]. The administration of considerably more nephrotoxic medications to patients in the intensive care unit may be associated with a higher rate of PTD as a result of having concomitant diseases. For this reason, in our study patients receiving any nephrotoxic drugs and patients with comorbid diseases were excluded to provide homogeneity of the study group and to prevent any possible confounding with patients in the intensive care units. As a result, it is possible that PTD will be found in a signif icant number of children with COVID-19 and that enrolling patients in intensive care units will almost certainly raise the proportion with PTD.

According to our f indings, proximal tubule dysfunction is found not only in adults but also in children with COVID-19.Children were reported to have fewer symptoms than adults,and the attributable mortality in the children was considerably lower than adults [ 1]. Although the pathogenesis of age-related diff erences of severity was not clearly understood, the variety of ACE2 and transmembrane protease,serine-subtype-2 (TMPRSS2) was one of the important candidates for pathogenesis [ 30]. One of the most popular hypotheses is that ACE and TMPRSS2 expression and affi nity increase with age, while the opposing hypothesis is that ACE2 has anti-inf lammatory properties [ 31— 34]. Proximal tubular cells have been found to express high levels of ACE2 and TMPRSS2, making them a promising target for SARSCoV-2 at the early stage [ 35]. Apart from renal cells, ACE2 is found in the parietal epithelium of Bowman’s capsule,collecting ducts, a thick ascending limb of Helen, podocytes,proximal cell brush border, and mesangial cells, implying that SARS-CoV-2 targets various sites [ 36]. As previously stated, the greater affi nity of SARS-spike CoV-2’s protein for ACE was linked to disease severity [ 37]. This notion was supported by the fact that the proportion of children with PTD was lower than that of adults in investigations. On the other hand, the signif icantly younger age in the patients with PTD supported the ACE-related hypothesis and revealed unknown complicated mechanisms and interactions in addition to SARS-CoV-2 and ACE receptors on the proximal tubule cells.

Normoglycemic glycosuria was one of the PTD was def ining criteria. Werion et al. reported that although other elements of PTD were present in the patient cohort with diff erent rates, no normoglycemic glucosuria was recorded[ 7]. While, Korman et al. reported that normoglycemic glucosuria was present in 11 (28%) of the patients and that the majority of these patients came from intensive care units [ 22]. Only two (1.73%) patients in our study exhibited normoglycemic glucosuria, indicating that the children had a low rate compared to most adult studies.There were numerous causes for the diff erence in PTD and COVID-19 infections between adults and children in the literature. Besides the better prognosis of the COVID-19 infections, the comparatively low burden of chronic diseases and concomitant medications, the low rate of intensive care, and the mechanical ventilation requirement in children are key explanations for the diff erence.

Our study had several limitations, including a small number of measurements for some markers, lack of renal biopsy,and failure to detect SARS-CoV-2 at the proximal tubule cells, as well as the study’s single-center methodology. The current study’s f indings, on the other hand, may be more credible because the study included more unvarying groups by the excluding patients in intensive care units, who may have more possible confounding factors. A better marker,such as low molecular weight proteins including beta-2 microglobulin and retinol-binding protein, might be more helpful; however, we were unable to conduct these tests.To our knowledge, this is one of the f irst comprehensive studies focusing on the eff ect of SARS-CoV-2 infections on the proximal tubule functions in children with COVID-19 infections. Our f indings could help to design a screening test.In addition, the longer follow-up of the patients for recovery of PTD was missing, which would be planned in the future.In conclusion, our f indings suggested that 20.8% of the children with COVID-19 infections had proximal tubular dysfunction. Proximal tubular dysfunction has been documented not only in adults but also in children. Children with COVID-19 infections should be followed up for recovery of proximal tubule dysfunction. More research for the evaluation of renal eff ects of SARS-CoV-2 on pediatric patients is needed.

Author contributions

DF involved in protocol development and manuscript writing. BE, KE, ?S, CE, DM involved in data collection. KAA,AK? and KA involved in data collection, and microbiological investigations. YE and DN involved in protocol development and data collection. BN involved in protocol development, data collection. DI involved in data analysis and manuscript writing and will act as guarantor for the paper. All the authors approved the f inal version of the manuscript.

Funding

None.

Data availability

The data and materials are available from the authors on reasonable request.

Declarations

Ethical approval

This study was approved by the local Ethical Committee of Dr. Behcet Uz Children's Training and Research Hospital with the registration number 452 (approval number: 166; date:09.24.2020). Written consent for publication of the case details together with imaging or videos were obtained from participants (or their parent or legal guardian in the case of children under 16).

Conflict of interest

Ilker Devrim had educational grant from BD and Ilker Devrim has educational webinars for BD and Pf izer. However, all other authors including ?lker Devrim have no conf licts of interest about this manuscript.