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Lymphocyte propionyl-CoA carboxylase and its activation by biotin are sensitive indicators of marginal biotin deficiency in humans ^1,2,3

¹ From the Departments of Biochemistry and Molecular Biology (SLS, AB, MMM, DMM, and NIM) and of Pediatrics (DMM), University of Arkansas for Medical Sciences, Little Rock, AR, and the General Clinical Research Center of the University of Arkansas for Medical Sciences, John L McClellan Veterans Hospital, Little Rock, AR (AW and DMM)

² Supported by grants no. RO1DDK36823 from the National Institutes of Health and GCRC M01RR14288 from the University of Arkansas for Medical Sciences General Clinical Research Center.

³ Reprints not available. Address correspondence to DM Mock, Department of Biochemistry and Molecular Biology #516, University of Arkansas for Medical Sciences, 4301 West Markham, Little Rock, AR 72205. E-mail: mockdonaldm{at}uams.edu.

	ABSTRACT

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Background: Marginal biotin deficiency may be a human teratogen. A biotin status indicator that is not dependent on renal function may be useful in studies of biotin status during pregnancy. A previous study of experimental biotin deficiency suggested that propionyl-coenzyme A carboxylase (PCC) activity in peripheral blood lymphocytes (PBLs) is a sensitive indicator of biotin status.

Objective: We examined the utility of measuring PCC activity and the activation of PCC by biotin in detecting marginal biotin deficiency.

Design: Marginal biotin deficiency was induced in 7 adults (3 women) by egg-white feeding for 28 d. Blood and urine were obtained on days 0, 14, and 28 (depletion phase) and 44 and 65 (repletion phase). PBLs were incubated with (activated) or without (control) biotin before PCC assay. The activation coefficient of PCC is the ratio of PCC activity in activated PBLs to that in control PBLs. The significance of differences for all measurements was tested by repeated-measures analysis of variance with Fisher's post hoc test and Bonferroni correction.

Results: Changes in the urinary excretion of biotin and of 3-hydroxyisovaleric acid confirmed that marginal biotin deficiency was successfully induced. By day 14, PCC activity had decreased (P < 0.0001) to below the lower limit of normal in all subjects. By day 28, the activation coefficient of PCC had increased significantly (P = 0.003) and was above the upper limit of normal in 6 of 7 subjects.

Conclusion: PCC activity is the most sensitive indicator of biotin status tested to date. In future pregnancy studies, the use of lymphocyte PCC activity data should prove valuable in the assessment of biotin status.

Key Words: Biotin • biotin deficiency • humans • lymphocytes • propionyl-CoA carboxylase • activation coefficient

	INTRODUCTION

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Clinical studies from our group and others have shown that marginal biotin deficiency is common in certain circumstances, including pregnancy and long-term anticonvulsant therapy (1-4). Because maternal marginal biotin deficiency is clearly teratogenic in several animal species (5), recent reviews expressed concern that maternal marginal biotin deficiency may also be teratogenic in humans (5). Even more recently, we reported evidence of marginal biotin deficiency in adult female smokers (6), an observation that expands on teratogenic concerns and also raises the possibility that smoking and marginal biotin deficiency may have synergistic deleterious effects on the developing fetus. However, concerns about teratogenesis related to biotin deficiency must be evaluated in light of the following caveat: most of the current conclusions about biotin status in pregnancy are based on urinary indicators of biotin status (2, 3), and renal function is affected by pregnancy per se. Accordingly, an indicator of biotin status that is largely independent of renal function would be useful, particularly in testing conclusions from previous studies.

We recently published an initial evaluation of a blood-based indicator of biotin status (7). That study of 11 subjects who were made biotin-deficient by egg-white feeding found that propionyl-coenzyme A carboxylase (PCC) activity in peripheral blood lymphocytes (PBLs) is an early and sensitive indicator of marginal biotin deficiency (7). In the current study, we sought to confirm or refute those findings in a new cohort of subjects and to examine the specificity of the PCC activity findings in these subjects. We also sought to test the validity of an additional blood-based indicator of biotin status—the biotin activation coefficient (AC) of PCC in PBLs.

	SUBJECTS AND METHODS

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Subjects, study design, and diet
Inclusion criteria included good health without a history of renal disease severe enough to be likely to lead to chronic impairment of renal function. Exclusion criteria included smoking and consumption of either dietary supplements known to contain biotin or certain medications (eg, certain anticonvulsants known to accelerate biotin catabolism; 4).

Eight healthy adult volunteers (3 women) completed the study. One man admitted that he did not comply with the study protocol; his data are excluded. The 7 remaining subjects ranged in age from 19 to 43 y. Their body mass index (BMI; in kg/m²) ranged from 22.2 to 28.4. Their racial-ethnic distribution was white (n = 3), Asian (n = 2), Hispanic (n = 1), and African American (n = 1).

Written informed consent was obtained from all subjects. The study was approved by the institutional review board of the University of Arkansas for Medical Sciences (UAMS).

Details of the experimental induction of biotin deficiency were published previously (8). In the current study, to normalize biotin status at the start of the depletion phase (day 0), subjects completed a biotin-loading and -washout phase before the initiation of egg-white feeding. Subjects were housed as inpatients in the UAMS General Clinical Research Center (GCRC) from day 0 to day 28 and were provided a dietitian-monitored eucaloric diet. Subjects consumed an egg-white drink with each meal. As described in a previous report from this study (9), the egg white contained sufficient avidin to bind 7 times the subjects' controlled daily dietary intake of biotin (9). Energy intake, biotin intake, and egg-white drink consumption were monitored daily by the GCRC research dietitian. On day 28, subjects were discharged from the GCRC, and thereafter they consumed a self-selected mixed general diet. During this repletion phase, the biotin status of the subjects was monitored for 38 d.

Despite the rigorous control of the GCRC environment, one subject admitted to noncompliance with the dietary regimen; this subject both consumed foods obtained from outside the GCRC and failed to consume most of the egg-white beverage as instructed. As expected, this subject's urinary excretion of biotin and 3-hydroxyisovaleric acid (3HIA) confirmed that marginal biotin deficiency was not induced. That subject's data were excluded from statistical analyses.

Blood and urine sample collection
Blood was collected in syringes (to which a stock solution of heparin was added to result in a concentrationof 15 U heparin/mL whole blood to prevent coagulation) on days 0, 14, and 28 during the depletion phase of the study and on days 44 and 65 during the repletion phase. PBLs were separated from whole blood by density gradient centrifugation and stored as previously described (7). Urine collections were obtained for the 24-h period just before blood collections and processed as described previously (7).

Urinary biotin and 3-hydroxyisovaleric acid
Urinary biotin was quantitated first by HPLC separation and then by an avidin-binding assay performed as described previously (10). Urinary 3HIA was quantitated by gas chromatography–mass spectroscopy as described previously (9).

Measurement of lymphocyte propionyl-CoA carboxylase activity and the activation coefficient of propionyl-CoA carboxylase
The ¹⁴CO₂ incorporation assay for measurement of PCC activity in PBLs was completed in triplicate for each blood sample as described previously (7, 11). Activity was normalized by protein concentration of the PBL preparation as determined by bicinchoninic acid protein assay as previously described (7). For the AC of PCC, the suspended PBLs, prepared as described above, were incubated at 25 °C for 30 min with (activated) or without (control) 10 nmol biotin/L before the protein and PCC assays. ACs were the ratio of PCC of activated PBLs to PCC of control PBLs.

Statistical analysis
For definitions of normal ranges for urinary biotin, 3HIA, and PCC acvitity in PBLs, the upper and lower limits were chosen as the 10th and 90th percentiles, because the distributions were not normal. For urinary excretion of biotin, the normal range was based on 54 subjects from several previous studies and included the day 0 values of the 3 egg white–feeding studies (2, 3, 6, 9, 12-15). For urinary excretion of 3HIA, the normal range was based on 68 subjects and included the day 0 values from the same studies (2, 3, 6, 9, 15). For PCC activity, the normal range was based on 18 subjects and included the day 0 values in the current study and the same values from 1 previous egg white–feeding study (7). For the AC of PCC, the normal range was based on the day 0 values in the 7 subjects in the current study.

The significance of changes in urinary biotin, urinary 3HIA, PCC activity, and the AC of PCC during the depletion phase (day 0 to day 28) was tested by one-way analysis of variance (ANOVA) with repeated measures. The significance of changes in each variable during the repletion phase (day 28 to day 65) was tested by one-way ANOVA with repeated measures. When ANOVA significance was P < 0.05, Fisher's post hoc test was used to ascertain the significance of differences between time points. The P values given are the least significant of the Fisher's comparison P values after Bonferroni correction for multiple comparisons. For all analyses, STATVIEW software (version 5.01; SAS Institute, Cary, NC) was used.

	RESULTS

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Induction of marginal biotin deficiency
Urinary excretion rates for biotin and for 3HIA were previously validated as indicators of marginal biotin deficiency (9, 15). Increased excretion of 3HIA reflects decreased hepatic activity of the biotin-dependent enzyme methylcrotonoyl-CoA carboxylase (16-20). As intended, none of the overt signs or symptoms of biotin deficiency developed in these subjects during the study. However, on the basis of urinary biotin and 3HIA, marginal biotin deficiency was successfully induced in these 7 subjects (Figure 1). By day 28, urinary biotin excretion had decreased significantly (P = 0.0002) and was below the lower limit of normal in all 7 subjects (Figure 1A). With repletion by consumption of a mixed general diet, biotin excretion rates increased significantly from day 28 to day 65 (P = 0.011) and were above the lower limit of normal in 3 of 7 subjects. By day 28, urinary 3HIA excretion had increased significantly (P = 0.0003) and was above the upper limit of normal in 6 of 7 subjects (Figure 1B). With repletion, 3HIA excretion decreased significantly from day 28 to day 65 (P < 0.0001) and was normal in 5 of 7 subjects.

View larger version (58K): [in this window] [in a new window]   FIGURE 1.. Evidence of the induction of biotin deficiency. The urinary excretion of biotin and 3-hydroxyisovaleric acid shows the successful induction of marginal biotin deficiency in 7 subjects fed the study diet. Each different symbol (eg, x, +, , ...) indicates data for one of the subjects. The analytic variability for a single subject at a single timepoint is approximately the same size as the symbols (data not presented). The shaded rectangle denotes the normal range. Significance during both depletion and repletion phases was tested by repeated-measures one-way ANOVA. *Significantly different from day 0 value, P < 0.002. **Significantly different from day 28 value, P < 0.008.

Figure 2

View larger version (55K): [in this window] [in a new window]   FIGURE 2.. Effects of biotin depletion and repletion on lymphocyte propionyl-coenzyme A (CoA) carboxylase activity. Each different symbol (eg, x, +, , ...) indicates data for one of the subjects. Individual representations, analytic variability, normal range, and statistical analysis are as in Figure 1. *Significantly different from day 0 value, P < 0.0002. **Significantly different from day 28 value, P < 0.0002.

Figure 3

View larger version (38K): [in this window] [in a new window]   FIGURE 3.. Effects of biotin depletion and repletion on the activation coefficient of propionyl-coenzyme A (CoA) carboxylase (PCC) in lymphocytes. Each different symbol (eg, x, +, , ...) indicates data for one of the subjects. The activation coefficient is defined as the ratio of the PCC activity in viable lymphocytes incubated with biotin to the PCC activity in lymphocytes without biotin. Individual representations, analytic variability, and statistical analysis are as in Figure 1. The shaded rectangle represents the range of the activity coefficient on day 0 in the 7 subjects. *Significantly different from the day 0 value, P < 0.004. **Significantly different from the day 28 value, P < 0.002.

	DISCUSSION

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

However, confidence in this conclusion is limited by our arbitrary choice of conditions for incubation of the PBLs with biotin. The generally accepted mechanism for activation is the intracellular accumulation of apoenzyme during deficiency. The apoenzymes are thought to be activated when the deficient vitamin is provided in vitro. For this study, we propose that apopropionyl-CoA carboxylase chains accumulate in PBLs and are biotinylated by holocarboxylase synthetase when biotin is transported into the PBLs during in vitro incubation with biotin. The observed activation also implies that adequate amounts of apopropionyl-CoA carboxylase ß chain and holocarboxylase synthetase are present intracellularly. We did not conduct optimization experiments for time, temperature, or extracellular concentration of biotin because the PBLs available under our institutional review board limitations were insufficient. Furthermore, Baez-Saldana et al (21) recently reported the effects of in vivo biotin supplementation on carboxylase activities. Persons with and without type 2 diabetes who were not biotin deficient were supplemented with 5 mg biotin 3 times/d for 28 d. Activities of the biotin-dependent enzymes PCC, pyruvate carboxylase, and acetyl-CoA carboxylase in PBLs increased 3-fold. This observation indicates that the activity of biotin-dependent carboxylases could increase substantially more with chronic in vivo supplementation than we observed in the current study. Accordingly, there is a distinct possibility that the transport into the lymphocytes was not optimal in restoring biotin status and that sufficient time and temperature were not allowed for maximal carboxylation of the accumulated apopropionyl-CoA carboxylase. With an optimized in vitro biotin incubation, we speculate that the AC of PCC may gave increased sooner or to a greater extent. Nevertheless, the incubation of concentration for biotin was 20 times the physiologic concentration, and the absolute magnitudes of the AC of PCC activity we observed were similar to the ACs observed by others for other vitamins (22), which suggests that adequate biotin was transported and incorporated.

Comparison of the PBL PCC data with 3HIA excretion data provides preliminary evidence that PBL PCC activity is a better indicator of marginal biotin deficiency than is 3HIA excretion. On the basis of PBL PCC activity, 7 of 7 subjects were marginally biotin deficient by day 14. In contrast, 1 subject never excreted abnormal amounts of 3HIA. This observation is consistent with our previous studies of 3HIA in which marginal biotin deficiency was not induced (data not shown). In those studies (9, 15), 10% of subjects did not show an increase in 3HIA excretion. We speculate that the 3HIA pathway for the metabolic disposition of intracellular accumulation of 3-methylcrotonyl-CoA is not active in those particular persons. We also speculate that the direct quantitation of PCC activity may prove to be both more sensitive and more specific for detecting marginal biotin deficiency than is urinary excretion of 3HIA.

Available data indicate that the lower expression of the genes for the and ß chains of PCC contributes little if at anything to the dramatic reduction in PCC activity. In a previously published study in these same 7 subjects (8), we observed that the mRNA in PBLs for the chain of PCC decreased to 75% of the day 0 value by day 28 (P = 0.027), and that for the ß chain of PCC decreased to 86% of the day 0 value (P = 0.067). Thus, a decrease in gene expression could explain at most only one-fourth of the decrease in PCC activity.

A related study of biotin deficiency in our pregnant mouse model (23) provides additional data consistent with the proposed mechanisms for a decrease in PCC activity and an increase in AC of PCC. In this study, mouse dams and fetuses were rendered biotin-deficient by egg-white feeding. We found that a decrease in carboxylase activity was mediated by a decrease in the abundance of the biotinylated carboxylases rather than by a decrease in the expression of their mRNA. The abundance of biotinylated carboxylases decreased in both maternal (to 48% of control) and fetal (to 6% of control) liver in parallel with a decrease in PCC activity. In contrast, mRNA for the chain of PCC did not change significantly. Moreover, the metabolically less active dam exhibited a smaller decrease than did the metabolically more active fetus.

This study is limited in 2 additional ways. First, the number of persons who successfully completed this rigorous inpatient study is small; thus, extrapolation to larger populations must be cautious. Nevertheless, the results of the current study concerning the utility of PCC activity in PBLs are entirely consistent with the results of a previous study in 11 subjects (7). Second, the normal range for the AC for PCC in PBLs was ascertained in only 7 subjects; no other reports of this index have been published. Although this finding represents a careful initial observation, inferences concerning diagnostic sensitivity must be made with caution.

The in vitro increase in vitamin-dependent enzyme activity with vitamin incubation is frequently used as a measure of the status of several water-soluble vitamins, including thiamine, riboflavin, and vitamins B-6 and B-12 (22, 24-26). These activation coefficients are generally accepted as valid measures of vitamin status (27, 28); however, the functional implications of identified deficiencies remain controversial in most cases. The turnover of biotin in lymphoid tissue, as judged by [¹⁴C]biotin degradation (29), is slower than that in liver. Thus, the decrease in PCC activity and the increase in the AC of PCC in lymphocytes may lag behind biotin depletion in more metabolically active tissues such as hepatocytes, and the deleterious effects of deficiency may even precede these early indicators.

Previous studies using urinary excretion of 3HIA as the primary indicator of biotin status indicated that marginal biotin deficiency occurs commonly during normal human gestation. Despite the limitations discussed above, we conclude that the study presented here provides evidence that PCC activity in PBLs will be useful in future studies that attempt to further assess biotin status in normal human gestation. An important subsequent step would be the assessment of the functional implications of the identified biotin deficiency.

	ACKNOWLEDGMENTS

 
We thank Cecil Bogy for serving as Study Coordinator, and we thank David Hachey (Vanderbilt University) for measurements of urinary 3-hydroisovaleric acid.

SLS, AB, MMM, and NIM performed various laboratory measurements. AW served as study dietitian. SLS performed statistical analyses, drafted the manuscript, and prepared the figures. DMM served as Principal Investigator and is responsible for the final version of the manuscript, statistics, figures, and figure legends. None of the authors had any personal or financial conflict of interest.

	REFERENCES

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 

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