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A comparative assessment of some biochemical markers in occupational lead exposure. Bhagwat V R 1 , Patil A J 2 and Bhagwat K V 3 1. Prof & HOD (Biochemistry), SBH Govt. Medical College, DHULE. 2. Associate Professor (Biochemistry) KIMSU,KARAD. 3. Asstt Professor, Humanity Dept, SSVP’s College of Engineering, DHULE (Maharashtra)

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A comparative assessment of some biochemical markers

in occupational lead exposure.

Bhagwat V R1, Patil A J2 and Bhagwat K V3

1. Prof & HOD (Biochemistry), SBH Govt. Medical College, DHULE.2. Associate Professor (Biochemistry) KIMSU,KARAD. 3. Asstt Professor, Humanity Dept, SSVP’s College of Engineering, DHULE (Maharashtra)

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Introduction

Lead, an industrially useful metal with wide applications.

Industrialization use ………… Pollution.

Biologically Pb has no role, useless, unwanted mineral for living organisms.

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Industrial use of LEAD

Occupations such as Lead battery manufacturing, silver jewelry making, painting have inherent dangers of lead toxicity.

Occupational exposure at small scale units in developing countries unregulated.

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LEA

D

Silv

er Je

welry

Lead is used as alloy in making all types of Silver Jewelry. And for marking designs on silver rings.

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Lead

(

Pb)

Metarubricytosis and slight basophilic stippling of erythrocytes in lead toxicosis. The remaining erythrocytes appear hypochromic because lead inhibits the synthesis of hemoglobin (Wright-Leishman stain).

Lead toxicity most organ systems. Major Hematological, Nervous etc

Moderate to clinically significant toxicity is very common in small scale industrial units.

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Lead lines

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Lead interference

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Enzyme inhibition by LeadLead inhibits 3 enzymes in Hb

biosynthesis1. δ-Amino Levulinic acid

dehydratase (ALAD) (Step 2)

2. Coproporpyrinogen oxidase. (Step 6)

3. Ferrochelatase (step 8)

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Erythropiesis and lead

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Purpose of the study:To assess the lead toxicity in SSI workers and to evaluate biochemical markers suitable for screening occupational exposure in developing country like India.

Aims & Objecti

ves

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Mate

rial a

nd

Meth

od

s

Setting & Design: Industrial, Rural, Case control study.

Subjects: Employees of SSI units of,› Battery manufacturing & recycling.› Silver jewelry making.› Spray painting. Size & selection: 30 from each category,

Random, non-stratified.

Controls: 30 healthy subjects from rural areas,

clinically normal, age matched (non-exposed) Samples:

Random blood, urine samples with proper preservatives. Processing (Pre analytical treatment)

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Methods of sample analysis

Lead (Pb) by Atomic absorption spectrophotometry (Perkin Elmer A300; Abs λ 283.3 nm).

Zinc Protoporphyrin (ZPP): by Hematoflurometry (Wayne NA NSSLS – C42A; 1996). Ex 415 nm, Em 595 nm)

δ-amino levulinic acid (ALA) by colorimetric method (Wada et al Br J Industr Med 1969; 26: 240-43).

Porphobilinogen (PBG) by colorimetric method, Ehrlich’s reaction (Mauzeroall & Granick, JBC 1956; 435-46).

Cost-Effective index: Cost-Benefit analysisStatistical methods: Mean, SD, Student t test.

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Scheme of ALA analysis

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Marker(units)

BMWn=30

SJMn=30

SPn=30

NECn =35

1 BPb(μg/dl)

53.65 ± 16.98(25.8 – 78.0)

48.56 7.39*(30.2 - 64.7)

22.32 8.87*(7.5 - 45.7)

12.52 ± 4.08(2.8 – 22.0)

2 UPb(μg/dl)

20.04 ± 15.20(5.2 – 62.8)

9.39 6.52

(2.0 - 30.7)11.22 7.15**

(1.5 - 30.2)6.97 ± 3.59(1 – 13.2)

3 ZPP(μg/dl)

122.6 ± 201.5(10 – 972)

9.55 3.21

(1.0 - 11)15.67 4.24*(8.12 - 23.12)

8.25 ± 7.79(1 – 35)

4 ALA(mg/dl)

38.10 ± 17.52(9.3 – 74.9)

25.13 9.52*(9.38- 50)

11.82 3.53***

(7.05 - 21.17)9.62 ± 5.45(2.5 – 17.5)

5 PBG(mg/dl)

13.95 ± 5.23(7.0 - 24.7)

12.06 4.81***

(7.05 - 24.7)10.45 3.33

(1.0 - 57)10.10 ± 2.87(3.5 – 15.8)

Table I Biochemical markers in the occupation groups.

(Figures are mean + SD. Those in parenthesis are range of values).BMW = Battery Manufacture workers; SJM = Silver Jewelry makers; SP = Spray painters; NEC = Non exposed controls, BPb = Blood lead; UPb = Urine lead; ZPP = Erythrocyte zinc protoporphyrin; ALA = Urinary δ-Amino levulinic acid; PBG = Urinary porphobilinogen.Figures in red are highest values & those in blue are the lowest one.

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Biochemical markers in lead exposure

0

20

40

60

80

100

120

140

BPb UPb eZPP uALA uPBGMarkers

va

lue

s

BMW SJM SP NEC

BMW = Battery workers, SJM = Silver Jewelry makers, SP = Spray painters, NEC = Controls.BPb = Blood lead, UPb =Urinary lead, eZPP = Erythrocyte zinc protoporphyrin,

uALA = Urinary δ-amino levulinic acid, uPBG = Urinary Porphobilinogen.

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Lead levels in Subjects

BPb, 53.63

BPb, 48.56

BPb, 22.32

BPb, 12.52

UPb, 20.04

UPb, 9.39

UPb, 11.22

UPb, 6.97

0 10 20 30 40 50 60 70 80

BMW

SJM

SP

NEC

Microgram /dl

BMW = Battery workers, SJM = Silver Jewelry makers, SP = Spray painters, NEC = Controls.BPb = Blood lead, UPb =Urinary lead, eZPP = Erythrocyte zinc protoporphyrin,

uALA = Urinary δ-amino levulinic acid, uPBG = Urinary Porphobilinogen.

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Table IIComparison of biochemical markers for screening

occupational Pb exposure.

ZPP PBG ALA

Precision (%) CV Intra assay Inter assay

4.92.3

4.23.2

2.81.5

Sensitivity Non-linear Poor Linear ~40 mg/L

SpecificityPoor

( Chr Fe defy anemia, Porphyria, febrile state)

Moderate( Porphyria)

High(Amino acetone ns)

Correlation vs PbB 0.3789 0.1648 0.5798

Normal Range 1–16 μg/dl 7–13 mg/L 4–15 mg/L

95% CI 5.5 - 11.0 9.1 - 11.1 7.7 - 11.5

Level at PbB = 20 μg/dl 21.32 10.97 14.67

Level at PbB = 50 μg/dl 132.6 12.58 34.19

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Table IIIComparison of biochemical markers for screening

occupational Pb exposure.

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ZPP PBG ALAAssay design (steps) Simplest (1) Simple (4) Multi step (8)Time/test < 3 mins ~ 8 mins ~ 20 minsSamples used WB (R) Urine (R) Urine (R)Storage, Stability <4.°C, 5 w pH 8-9, dark,

<4°C, 2wpH 3-4, dark,

<4°C, 2 wInterference in assay

Bilirubin, Riboflavin,several drugs >5

Ehrlich’ +ve substances

Amino acetone(NR 0 – 1 mg/L)

Specificity Poor Moderate HighTest type Invasive Non-Invasive Non-InvasiveCost/test (2004) 35.11 16.98 35.53Cost effective index 3.3 2.4 7.1Rating for screening *** ** *****

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ConclusionZPP is not a suitable marker for

screening of occupational lead exposure due to poor specificity which makes it unfit for screening low level toxicity at earlier stages. Urinary ALA is ideal & convenient marker as it has higher sensitivity & specificity apart from being an cost effective non-invasive investigation.

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