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Research article · 2020 · Full text

International Journal of Advanced Biochemistry Research

Prealbumin variation in neonatal bacterial infections

Coly NFSylla ThiamAli SambaI BassA NdiayeIY SoumahF DiedhiouF CisséO BoyeM DjitéD DoupaDiagne Gueye NDRGueye PmAgne FD

Volume 4(2) · Pages 04–07 · DOI: 10.33545/26174693.2020.v4.i2a.47 ↗

Research areasNeonatal Health and BiochemistryInflammatory Biomarkers in Disease Prognosis

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Abstract

Author-written

This is a prospective cross-sectional study carried out at the department of pediatric of the Diamniadio children's hospital in 2016. This includes subjects aged between 0 and 28 days admitted for neonatal infection according to clinical and anamnestic criteria. Prealbumin assay was carried out using the immuno-turbidimetry technique with the A15 automate of Biosystems®. In 50 newborns, bacterial neonatal infection was confirmed in 24% of the population. Prealbumin concentration of newborns with isolated germs (179.08±108.87 mg / L) is lower compared to the group where no germ was isolated (199.41±108.87 mg / L) but without significant difference. However, Gram-negative infection was responsible for a greater decrease in prealbumin. It is therefore important to include the dosage of prealbumin in the monitoring of neonatal bacterial infections to prevent complications.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Prealbumin, also known as transthyretin (TTR), is a plasma protein used as a biochemical marker to reflect a patient's nutritional status. View evidence ↗

      Why it matters

      Prealbumin, also known as transthyretin (TTR), is a plasma protein used as a biochemical marker to reflect a patient's nutritional status.

      In the paper's own words

      “Prealbumin also called transthyretin (TTR) is known as a biochemical marker that reflects the nutritional status of patients.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Prealbumin levels typically drop quickly during acute events like surgery, trauma, and bacterial infections as the body prioritizes inflammatory proteins. View evidence ↗

      Why it matters

      Prealbumin levels typically drop quickly during acute events like surgery, trauma, and bacterial infections as the body prioritizes inflammatory proteins.

      In the paper's own words

      “It is quickly lowered during acute attacks such as those resulting from trauma, surgery, and especially bacterial infections [5] in favor of many inflammatory proteins.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Managing bacterial infections in newborns is challenging because clinical signs and existing laboratory markers are often non-specific. View evidence ↗

      Why it matters

      Managing bacterial infections in newborns is challenging because clinical signs and existing laboratory markers are often non-specific.

      In the paper's own words

      “However, the management of neonatal bacterial infections remains a major problem due to the non-specificity of clinical signs and diagnostic laboratory markers.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. What they did

    • The researchers conducted a prospective cross-sectional study in 2016 at the Diamniadio Children's Hospital. View evidence ↗

      What they did

      The researchers conducted a prospective cross-sectional study in 2016 at the Diamniadio Children's Hospital.

      In the paper's own words

      “This is a prospective cross-sectional study carried out in newborns of consenting parents admitted to the pediatric department of the Diamniadio Children's Hospital for neonatal infection in 2016.”

      Page 2

      Found in: Type of study

      Read it in the full textOpen PDF at page 2 ↗
    • The study included newborns aged 0 to 28 days who were hospitalized for suspected neonatal infection based on clinical and anamnestic criteria. View evidence ↗

      What they did

      The study included newborns aged 0 to 28 days who were hospitalized for suspected neonatal infection based on clinical and anamnestic criteria.

      In the paper's own words

      “Patients aged between 0 and 28 days, hospitalized in the neonatology unit of the pediatric department for a suspected neonatal infection according to clinical-anamnestic criteria were included in this study.”

      Page 2

      Found in:  Study population

      Read it in the full textOpen PDF at page 2 ↗
    • Prealbumin levels in serum were measured using the immuno-turbidimetry technique on a Biosystems® A15 auto analyzer. View evidence ↗

      What they did

      Prealbumin levels in serum were measured using the immuno-turbidimetry technique on a Biosystems® A15 auto analyzer.

      In the paper's own words

      “The A15 auto analyzer by Biosystems® was used. The prealbumin assay was made from serum using the immuno-turbidimetry technique with the reagent from Biosystems®.”

      Page 2

      Found in:  Determination of prealbumin

      Read it in the full textOpen PDF at page 2 ↗
    • The study population consisted of 50 newborns, with bacterial infection confirmed in 24% of them. View evidence ↗

      What they did

      The study population consisted of 50 newborns, with bacterial infection confirmed in 24% of them.

      In the paper's own words

      “In 50 newborns, bacterial neonatal infection was confirmed in 24% of the population.”

      Page 1

      Found in: Conclusion

      Read it in the full textOpen PDF at page 1 ↗
  3. What they found

    • A significant majority of the patients (70%, n=35) had normal prealbumin levels, while 15% (n=15) had abnormal levels (p=0.010). View evidence ↗

      What they found

      A significant majority of the patients (70%, n=35) had normal prealbumin levels, while 15% (n=15) had abnormal levels (p=0.010).

      In the paper's own words

      “70% of patients had normal prealbumin (n = 35) versus 15% with abnormal prealbumin (n = 15). With a p-value = 0.010.”

      Page 2

      Found in: Discussion

      Read it in the full textOpen PDF at page 2 ↗
    • No significant difference in prealbumin levels was found between males (200.88±86.05 mg/L) and females (187.71±90.22 mg/L), with a p-value of 0.83. View evidence ↗

      What they found

      No significant difference in prealbumin levels was found between males (200.88±86.05 mg/L) and females (187.71±90.22 mg/L), with a p-value of 0.83.

      In the paper's own words

      “The mean level of prealbumin in female patients was 187.71 with a standard deviation ±90.221 while the mean level of prealbumin in male patients was 200.88 with a standard deviation ±165.36”

      Page 2

      “Also regarding sex, the difference was not significant with a p-value equal to 0.83 between an average prealbumin equal to 200.88±86.05 mg / L in males and 187, 71±90.22 mg / L for female subjects”

      Page 3

      Found in: Fig 1: Variation of the mean prealbumin according to sex

      Read it in the full textOpen PDF at page 2 ↗
    • Prealbumin concentrations were lower in newborns infected with Gram-negative bacilli (including enterobacteria and non-fermentative bacteria) compared to those infected with cocci, although the difference was not significant. View evidence ↗

      What they found

      Prealbumin concentrations were lower in newborns infected with Gram-negative bacilli (including enterobacteria and non-fermentative bacteria) compared to those infected with cocci, although the difference was not significant.

      In the paper's own words

      “Subjects infected with Gram negative bacilli had lower prealbumin concentrations (Table III).”

      Page 3

      “Prealbumin was lower for subjects infected with bacilli, non-fermentative bacteria and enterobacteria, compared to cocci, but without a significant difference.”

      Page 3

      Found in: Discussion

      Read it in the full textOpen PDF at page 3 ↗
  4. What it means

    • The authors conclude that confirmed bacterial infections and specifically Gram-negative bacilli are associated with lower prealbumin concentrations, likely due to the virulence of the bacteria. View evidence ↗

      What it means

      The authors conclude that confirmed bacterial infections and specifically Gram-negative bacilli are associated with lower prealbumin concentrations, likely due to the virulence of the bacteria.

      In the paper's own words

      “The group with a confirmed bacterial neonatal infection had a lower average prealbumin concentration whereas neonates infected with Gram-negative bacilli had lower TTR concentrations, probably related to their virulence.”

      Page 3

      Found in: Conclusion

      Read it in the full textOpen PDF at page 3 ↗
    • The authors recommend including prealbumin dosage in the monitoring of neonatal bacterial infections to help prevent complications. View evidence ↗

      What it means

      The authors recommend including prealbumin dosage in the monitoring of neonatal bacterial infections to help prevent complications.

      In the paper's own words

      “It is therefore important to include the dosage of prealbumin in the monitoring of neonatal bacterial infections to prevent complications.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗

Visual summary

2 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (neonatal blood plasma and Gram-negative bacilli bacteria). It explains the idea and does not show study data.↗ Enlarge
Prealbumin Response to Infection
AI-generated conceptual illustration (neonatal blood plasma and Gram-negative bacilli bacteria). It explains the idea and does not show study data.

AI-generated conceptual illustration (neonatal blood plasma and Gram-negative bacilli bacteria). It explains the idea and does not show study data.

Open full-size image ↗

Prealbumin Response to Infection

AI-generated conceptual illustration (neonatal blood plasma and Gram-negative bacilli bacteria). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Pre-albumin (mg / L): Enterobacteriaceae vs Non-fermentation vs Staphylococci vs Streptococci
Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Pre-albumin (mg / L): Enterobacteriaceae vs Non-fermentation vs Staphylococci vs Streptococci

Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Distribution of the population according to theTable 1Page 2Variation of prealbumin depending on the type ofTable 2Page 2Variation of the mean prealbumin according to sexFigure 1Page 2Variation of the mean prealbumin according to the typeTable 3Page 3
FULL TEXT Original article · reflowed for reading

Introduction

Prealbumin also called transthyretin (TTR) is known as a biochemical marker that reflects the nutritional status of patients. It is a plasma protein mainly synthesized by the liver. Its half-life ranges from 2 to 4 days [1] . Small amounts of TTR are also synthesized by the choroid plexus [2] , pancreas and retina, but they probably do not affect serum protein concentration [3] . As per its characteristics, it is a protein marker of interest in the biological diagnosis of early malnutrition [4] . It is quickly lowered during acute attacks such as those resulting from trauma, surgery, and especially bacterial infections [5] in favor of many inflammatory proteins. The interaction between nutritional status and infections has been studied extensively [6,7] . In intensive care units, the combination of low concentrations of TTR and albumin can help identify patients at high risk of developing sepsis [8] . In newborns, the levels of transthyretin may be affected by several factors such as gestational age, inflammation, infection, and surgery [9] . Though all pathologies can be accompanied by malnutrition, extreme ages are mostly affected due to physiological peculiarities, especially in newborns. Malnutrition is often unknown in hospitals and more specifically in pediatrics [10] . When combined with other markers, variation in prealbumin concentration can help understand the severity of a disease [2] and the change in the nutritional status of a patient, which may result in the increasing of the length of hospitalization [11] . Early recognition of malnutrition is necessary in the prevention of sepsis, morbidity, as well as mortality [11] from a possible related disease. Thus, TTR may have the potential to detect and reflect various types of clinical circumstances as a biomarker [12] such as in systemic inflammatory response syndrome (SIRS) where its synthesis is reduced in favor of acute phase proteins [13] . In this study, our objective was to assess concentrations of the plasma prealbumin and to analyze whether these plasma concentrations can predict neonatal infection.

Type of study

This is a prospective cross-sectional study carried out in newborns of consenting parents admitted to the pediatric department of the Diamniadio Children's Hospital for neonatal infection in 2016.

 Study population

Patients aged between 0 and 28 days, hospitalized in the neonatology unit of the pediatric department for a suspected neonatal infection according to clinical-anamnestic criteria were included in this study.

 Sampling

Samples are taken at the hospitalization Unit by qualified personnel on a dry tube and on a blood culture bag.

 Determination of prealbumin

The A15 auto analyzer by Biosystems® was used. The prealbumin assay was made from serum using the immunoturbidimetry technique with the reagent from Biosystems®. An internal quality control was carried out to validate the results.

 Principle

The presence of prealbumin in the sample precipitates in the presence of anti-human prealbumin antibodies. The light s attering generated by the antigen-antibody complexes was proportional to the prealbumin concentration and can be quantified by turbidimetry.

 Statistical analysis

Statistical analysis was performed using SPSS version 20 software. The statistical analysis methods used are Fisher's F tests and KHI-DEUX test. A p> 0.05 is considered significant. where bacterial infection was confirmed with isolation of a germ had a lower prealbumin concentration (179.08±80.44 mg / L) than those in group II (199.41±108, 87) where infection was not confirmed but without significant difference.

Results

Results

Fig 1: Variation of the mean prealbumin according to sex

The mean level of prealbumin in female patients was 187.71 with a standard deviation ±90.221 while the mean level of prealbumin in male patients was 200.88 with a standard deviation ±165.36 (figure 1). Prealbumin was lower for subjects infected with bacilli, non-fermentative bacteria and enterobacteria, compared to cocci, but without a significant difference.

Figure 1. Variation of the mean prealbumin according to sex
Variation of the mean prealbumin according to sex↗ Enlarge
Figure 1
Variation of the mean prealbumin according to sex

Variation of the mean prealbumin according to sex

Open full-size image ↗
Original paper figureSource PDF · page 2 ↗

Discussion

In our population consisting of 50 newborns, 70% had normal prealbumin values (Table I) with a significant difference (p = 0.01). In newborns, real malnutrition was rare [14] . At birth, plasma TTR concentrations were approximately two-thirds of those measured in healthy mothers, and then increase linearly as the infant grows [5] .

Based on the type of infection, particularly in the case of early neonatal infection (INNP) which occurs between D0 and D7 and late neonatal infection (INNT) which occurs between D8 and D28, no significant difference was observed (Table II). However, subjects with an NNRT had higher prealbumin values. This comparison also corresponds to the study of the variation of prealbumin as a function of age, which was therefore not significant.

The result was contradictory with the one of Johnson [15] who demonstrated that prealbumin varied with age. Jono's multicenter study [12] also demonstrated variation with age for both sexes. This contradiction may be related to the size and age difference between our populations and theirs. Also regarding sex, the difference was not significant with a pvalue equal to 0.83 between an average prealbumin equal to 200.88±86.05 mg / L in males and 187, 71±90.22 mg / L for female subjects (Figure 1). According to Ingenbleek [16] , the difference based on sex was apparent because of androgenic hormones on anabolic processes. Similarly, Aliyazıcıoğlu [17] noted a difference according to gender for a determination of prealbumin in the umbilical cord. As per his findings, the levels of gonadotropins in the umbilical cord were significantly higher in men than in women. This explains the differences found in relation to our results. Moreover, the evaluation of prealbumin based on the isolation of germs allowed us to obtain an average of 179.08±108.87 mg / L for group I and of 199.41±108.87 mg / L for group II (Table IV). The average of the prealbumin concentration of the group where a germ was isolated was lower compared to the group where no germ was isolated but without significance with a p-value equal to 0.33 well above 0.05. However, no difference was observed that may depend on the type of germs isolated. Subjects infected with Gram negative bacilli had lower prealbumin concentrations (Table III). This is because bacteria in this group can express pathogenicity factors that allow them to overcome various obstacles in the body's specific and non-specific defenses. They can then directly access the targeted tissues or allow toxins to diffuse therein, which could lead to temporary or permanent cellular alterations [18] . Nonfermenting Pseudomonas aeruginosa for example, is very pathogenic in subjects with impaired means of defense.

As evidenced by the study by Cynober et al. [19] which reported that burns with sepsis had very low serum TTR levels compared to those who did not. He concluded that low serum TTR levels seemed to predict fatal outcomes for patients. Bernstein's study [13] also demonstrated among hospitalized patients that the TTR was lower in patients with Systemic Inflammatory Response Syndrome with an increased white blood cell count of over 12,000 / µl, and procalcitonin (PCT) of more than 2.0 pg / ml.

Conclusion

Our results highlighted normal values for most of our targeted population. The group with a confirmed bacterial neonatal infection had a lower average prealbumin concentration whereas neonates infected with Gramnegative bacilli had lower TTR concentrations, probably related to their virulence.

Figures and tables from the paper

Table 1. Distribution of the population according to the
Normal prealbuminNumberPercentage
NO1530%
YES3570%
Total50100%

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Distribution of the population according to the↗ Enlarge
Table 1
Distribution of the population according to the

Distribution of the population according to the

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Original paper tableSource PDF · page 2 ↗
Table 2. Variation of prealbumin depending on the type of
Type of infectionNumberPrealbumin (mg/L)p-value
INNP38186,43±80,620,26
INNT12219,08±105,93
Group I12179,08±80,440,33
Group II38199,41±108,87

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Variation of prealbumin depending on the type of↗ Enlarge
Table 2
Variation of prealbumin depending on the type of

Variation of prealbumin depending on the type of

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Original paper tableSource PDF · page 2 ↗
Table 3. Variation of the mean prealbumin according to the type
Isolated germsnumbersPre-albumin (mg / L)p-value
Enterobacteriaceae3145,67
Non-fermentation2129,500,8
Staphylococci6176,33
Streptococci3214,00

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Variation of the mean prealbumin according to the type↗ Enlarge
Table 3
Variation of the mean prealbumin according to the type

Variation of the mean prealbumin according to the type

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Original paper tableSource PDF · page 3 ↗

References

19 in the original paper
  1. Yang HT, Yim H, Cho YS et al. Serum Transthyretin Level is associated with clinical severity rather than nutrition status in Massively Burned Patients. Journal of Parenteral and Enteral Nutrition. 2014; 38(89):966-72.
  2. Ambrosius W, Slawomir M, Kazmierski R et al. Predictive value of serum transthyretin for outcome in acute ischemic stroke. PLoS ONE. 2017; 12(6):e0179806.
  3. International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). Clinical indications for plasma protein assays: transthyretin (prealbumin) in inflammation and malnutrition. Clin Chem Lab Med. 2007; 45(3):419-426.
  4. Aussel C, Ziegler F. Évaluation de l'état nutritionnel. Revue Francophone des Laboratoires - septembre/octobre, 2014 -N°465, cahier 1.
  5. Ingenbleek Y, Bernstein LH. Plasma Transthyretin as a Biomarker of Lean Body Mass and Catabolic States. Adv Nutr. 2015; 6:572-80.
  6. Chevalier Ph, Delpeuch E et Maire B. Le complexe malnutrition-infection: premier problème de santé publique chez les populations défavorisées. Méd Mal Infect. 1996; 26:366-70.
  7. Scrimshaw NS, Taylor CE, Gordon JE. Interactions entre l'état nutritionnel et les infections. Genève; OMS, 1971, n°57.
  8. Devakonda A, George L, Raoofet S. Transthyretin as a marker to predict outcome in critically ill patients. Clinical Biochemistry. 2008; (41):1126-1130.
  9. Nash P, MSN NNP-BC. Transthyretin (aka Prealbumin): Why Is It Part of TPN Labs? Neonatal Network. 2009; 28(n°5):339-341.
  10. Joosten KFM, Hulst JM. Nutritional screening tools for hospitalized children: Methodological considerations. Clin Nutr. Févr. 2014; 33(1):1-5.
  11. Cunningham LL, Madsen MJ, Van Sickels JE. Using Prealbumin as an Inflammatory Marker for Patients with Deep Space Infections of Odontogenic Origin. J Oral Maxillofac Surg. 2006; 64:375-378.
  12. Jono H, SU Y, Obayashi K et al. Sources of variation of transthyretin in healthy subjects in East and Southeast Asia: Clinical and experimental evidence for the effect of alcohol on transthyretin metabolism. Clinica Chimica Acta. 2016; 458:5-11.
  13. Bernstein LH, Transthyretin and the Systemic Inflammatory Response. Current Nutrition & Food Science. 2009; 5:71-74.
  14. Picaud JC. Dénutrition périnatale: prise en charge nutritionnelle spécifique du nouveau-né. Nutrition clinique et métabolisme, Numéro hors-série Archives de pédiatrie. 2005; 19(vol. 12, n° 4):1238-243.
  15. Johnson AM, MerlinI G, Sheldon J et al. Clinical indications for plasma protein assays: transthyretin (prealbumin) in inflammation and malnutrition. Clin Chem Lab Med. 2007; 45(3):419-426.
  16. Ingenbleek Y, Young VR. Significance of Transthyretin in Protein Metabolism. Clin Chem Lab Med. 2002; 40(12):1281-1291.
  17. Aliyazıcıoğlu Y, Değer O, Caner Karahan S et al. Reference values of cord blood transferrin, ceruloplasmin, alpha-1 antitrypsin, prealbumin, and alpha-2 macroglobulin concentrations in healthy term newborns. The Turkish Journal of Pediatrics. 2007; 49:52-54.
  18. Sansonetti P. Déterminants de virulence chez les bacilles à Gram négatif. Medecine Sciences. 1987; 3:68-74.
  19. Cynober L, Prugnaud O, Lioret N et al. Serum transthyretin levels in patients with burn injury. Surgery. 1991; 109:640-644.

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