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Non-invasive IGFBP1, IGFBP2 biomarkers as predictors and outcomes of usual interstitial pneumonia (UIP) therapeutic response



Usual interstitial pneumonia (UIP) is a fatal disease that is associated with poor prognosis and survival. Several growth factors such as IGFs (insulin-like growth factors) and IGFBPs (insulin-like growth factor binding proteins) seem to take part to this pathogenesis.

Pirfenidone is an immunosuppressant drug that is thought to have anti-inflammatory and anti-fibrotic effects both in vitro and in vivo.


To assess IGFBP1 and IGFBP2 as non-invasive biomarkers for prediction and outcomes of UIP clinical activity and therapeutic response to the anti-fibrotic pirfenidone.


Serum levels of IGFBP1 and IGFBP2 were significantly higher in the UIP group than in the healthy subjects (p ≤ 0.005). After 6 months therapy, UIP patients were divided into 2 groups according to improvement in MRC dyspnea grading into clinically improved and non-improved groups. 6MWT and SPaO2 were significantly improved in the clinically improved group compared to the non-improved one with no differences as regards other parameters (p < 0.0001). Both IGFBP1 and IGFBP2 were significantly decreased in serum while only IGFBP2 was decreased in BAL of all UIP after completing 12 months therapy.


IGFBP1 and IGFBP2 were increased in active UIP patients and reduced after 12 months anti-fibrosing therapy. IGFBPs may be promising biomarkers and predictors of response to therapy in UIP.


Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrosing interstitial pneumonia with inevitable loss of lung function. Internationally recognized guidelines recommend the multidisciplinary evaluation of clinical, radiologic, and pathologic disease features in the diagnosis and management of ILD [1]. Radiological usual interstitial pneumonia (UIP) is characterized on high-resolution computed tomography (HRCT) by the presence of reticular opacities, often associated with traction bronchiectasis, typically in a basal, subpleural, and patchy distribution [2].

Histopathologic UIP consists of a combination of fibrotic areas with scarring and honeycomb change alternate with areas of less affected or even normal lung parenchyma [3]. The patchy interstitial fibrosis, collagen deposition, and architectural distortion characteristic of the UIP pathologic pattern, evident by surgical pathology or at the macroscale by HRCT, are generally associated with poor prognosis and survival [4].

The insulin-like growth factor (IGF) system comprises the two primary ligands, namely IGF1 and IGF2; six high-affinity fully characterized IGF-binding proteins (IGFBP1–IGFBP6); and the IGF receptors. IGF1 and IGF2 are anabolic peptides with extensive structural and functional homology with insulin. IGF1 and IGF2 affect local and systemic responses through autocrine, paracrine, and endocrine mechanisms [5].

During human fetal lung development, IGF1 and 2 transcripts are localized to cells of mesenchymal origin (pleura, interlobular septa, perivascular fibroblasts) while immunocytochemistry identifies IGF peptides in association with airway epithelium. These findings suggest that IGFs act locally in the lung in an autocrine or paracrine manner [6].

Regulation of IGF activity in the lung depends on the expression of the IGFs and IGF receptors and the modulation of IGF activity by specific IGF-binding proteins (IGFBPs). IGFBP2 is a member of a family of six insulin-like growth factor binding proteins, which has recently been identified in IPF [5].

Many clinical trials with anti-fibrotic drugs for IPF were available in the last decade, including bosentan, imatinib, and interferon (IFN)-1b. Pirfenidone, an orally administered pyridine, demonstrated combined anti-inflammatory, anti-oxidant, and anti-fibrotic actions both in vitro and in animal models of pulmonary fibrosis, consisting in the regulation of the expression of TGF-β and inhibition of fibroblast and collagen synthesis [7].

The revision of the 2011 guidelines released a conditional recommendation for the use of nintedanib and pirfenidone for the treatment of IPF. In many countries, pirfenidone and nintedanib are approved with reimbursement for the treatment of patients with mild-to-moderate disease, who therefore present with well-defined impairments of lung function [8].

Aim of the study

We aimed to assess IGFBP1 and IGFBP2 as non-invasive biomarkers for prediction and outcomes of UIP clinical activity and therapeutic response to the anti-fibrotic pirfenidone.


Study data were collected within the period from March 2016 to February 2018. According to the 2011 joint statement by the American Thoracic Society (ATS), European Respiratory Society (ERS), Latin American Thoracic Association (ALAT), and Japanese Respiratory Society (JRS) [9], the diagnosis of IPF can be secured by the presence of a UIP pattern on high-resolution computed tomography (HRCT).

Inclusion criteria

Patients with IPF and aged 40–80 years with diagnostic criteria conforming to the current guideline based on ATS/ERS guidelines and the dose of pirfenidone ≥ 1800 mg daily were included in this analysis [9].

Exclusion criteria

Patients who had other causes of UIP except IPF (such as collagen vascular diseases and history of exposure to drugs, radiation, and asbestosis) and incomplete data collection were excluded.


Prior to initiating pirfenidone therapy, all patients were subjected to the following:

  1. 1.

    Thorough history taking and careful clinical examination including age, sex, body mass index (BMI), smoking habits, and associated co-morbidity.

  2. 2.

    Laboratory tests including complete blood count (CBC), and renal and liver panels were performed before administration of the compound during the period of diagnosis, as well as 6 and 12 months post-treatment initiation.

  3. 3.

    Pulmonary function testing using computerized spirometry with a SensorMedics Vmax 229 (SensorMedics, Yorba Linda, CA, USA).

  4. 4.

    Chest X-ray and HRCT (high-resolution CT) chest.

  5. 5.

    Arterial blood gasses.

  6. 6.

    O2 saturation by pulse oximetry in follow-up of the patients and 12 months after medication.

  7. 7.

    6MWT (6 min walking test) for all patients before and 12 months after medication.

  8. 8.

    Bronchoscopy and bronchoalveolar lavage (BAL): for all patients before and 12 months after medication.

  9. 9.

    Measure IGFBP1 and IGFBP2 in blood and BAL by ELISA for all patients before and 12 months after medication.

Pirfenidone treatment

Pirfenidone is available as 267 mg capsules. Initial dosing is one capsule three times daily with meals on days 1 through 7. On days 8 through 14, the dose is advanced to two capsules three times daily with meals. The daily dose should be titrated to the full dosage of nine capsules per day (2403 mg/day) or three capsules three times a day with meals onward starting on day 15. Consider temporary dosage reduction, treatment interruption, or discontinuation for management of adverse reactions. For those patients who have treatment interruption of 14 or more days, therapy should be reinitiated by undergoing the initial 2-week titration regimen to the maintenance dosage [10].

Patients were informed for known adverse events of pirfenidone and were instructed to avoid exposure to sunlight and alcohol consumption.

Dyspnea was assessed using the MRC dyspnea scale at presentation and after completed pirfenidone therapy.

Statistical analysis

Analysis using SPSS version 12 was performed with respect to the main study aim. Descriptive characteristics for participants are expressed as means and standard deviation (SD) for continuous variables, and number and percent for categorical variables. We used the independent sample test to show the significant difference between the continuous variables and chi-square test for the categorical variables. The level of significance was accepted at p ≤ 0.05.


Subject demographic and functional characteristics

This study was carried out on 23 UIP patients (16 males and 7 females, with a mean age of 65.09 ± 6.01 years) and 25 healthy patients (15 males and 10 females, with a mean age of 62.87 ± 3.99 years) with no significant statistical difference between both groups as regards age, sex, or smoking habits.

Serum growth factors before start therapy

There were significant increases in serum IGFBP1 and IGFBP2 of the UIP group compared to the healthy one (p ≤ 0.005) (Table 1).

Table 1 Demographic parameters and biomarkers of the UIP group versus control group

The UIP patients were divided into 2 groups according to clinical improvement in MRC dyspnea scale into improved or non-improved after completing the pirfenidone course. Comparing both groups, there were significant improvements in 6MWT and SPaO2 in the clinically improved group compared to the non-improved one with no differences as regards other parameters (Table 2).

Table 2 Comparison between the clinically improved and clinically non-improved groups as regards IGFBP1 and IGFBP2 in serum and BAL, 6MWT, and SPaO2

Serum and BALF growth factors after completing 12 months therapy

On comparing all the UIP patients before and after completing their pirfenidone course, there were significant decreases in serum levels of both IGFBP1and IGFBP2 with significant improvement in the SPaO2 and 6MWT after 12 months therapy. By contrast, there was no significant difference between the groups regarding the BALF levels of IGFBP1 (Table 3, Fig. 1).

Table 3 Comparison between UIP patient before and after treatment as regards IGFBP1 and IGFBP2 in both serum and BAL, 6MWT, and SPaO2
Fig. 1

Mean and SD of biomarkers before and after treatment

Relationship between growth factors and other parameters

Moreover, our study showed a direct relationship between circulating levels of IGFBP2 and BALF levels, while we did not find any correlation between IGFBP1 in serum and BALF or between both growth factors and any other biomarkers assessed in our study (Table 4).

Table 4 Correlation between some biomarkers and dyspnea score in UIP group before treatment

Of great interest, there was an inverse relationship between MRC dyspnea score and 6MWT and also with SPaO2 in UIP patients after completing 12 months treatment (Tables 4 and 5).

Table 5 Relation between some biomarkers and dyspnea score in UIP group after treatment


Biomarkers are highly needed in IPF as tools for differential diagnostic, predictor of the progression of the disease and treatment response. Specifically in IPF, early diagnosis is important to reduce as much as possible the disease progression [11].

A key initiating event hypothesized in the pathobiology of IPF is alveolar epithelial dysfunction leading to innate immune cell activation, dysregulated epithelial-mesenchymal communication, myofibroblast differentiation and proliferation, and excessive extracellular matrix deposition [12].

Many biomarkers have been studied in BALF and in serum as potential diagnostic or prognostic tools. However, the predictors’ value of these new biomarkers still needs further studies.

IGFBP1 and IGFBP2 are members of a highly conserved family of six insulin-like growth factor (IGF) binding proteins; IGFBPs are described to be involved in cell proliferation and differentiation [13]. Therefore, we focused on measuring both biomarkers in serum and BALF of UIP patients. To the best of our knowledge, we are the first to study both IGFBP1 and IGFBP2 levels in both serum and BAL of patients who suffer from usual interstitial pneumonia (UIP) and to compare their results.

Although previous studies such as Chadelat et al. [14] and Mouhieddine et al. [15] were focused on IGFBP2 in fibrosis which showed an increase of IGFBP2 in the bronchoalveolar lavage and in the lung tissue of patients with interstitial lung disease (ILD) in vivo and in vitro, none of these studies focused on the usual interstitial pneumonia pattern.

Our study showed for the first time that UIP featured a marked increase in serum IGFBP1 and IGFBP2 and in BALF. Even the serum levels remained higher than those measured in healthy subjects. In addition, IGFBP1 and IGFBP2 were attenuated in those patients completing the 12-month therapy with anti-fibrotic treatment. Those results were in concordance with that reported by Guiot et al. [16] who showed a marked increase in serum IGFBP1 and IGFBP2, with decreased IGFBP2 levels in those patients receiving anti-fibrotic treatment.

Of great interest, the present study also found that IGFBP2 levels showed significant decrease in both serum and BALF of UIP patients after completing the 12-month therapy, thus supporting the idea that IGFBP2 can bind to the lung extracellular matrix [17] and it can favor the IGF activity by increasing its local availability, which results in an increase of cellular response to IGF [13]. Alternatively, we cannot rule out the fact that high IGFBP2 in IPF may actually reflect a protective feedback mechanism to limit the disease progression by neutralizing IGFs [18].

As regards the clinical effect of the anti-fibrotic therapy and its effect on the quality of life of the UIP patients and its relations to the measured IGFBP1 and IGFBP2 in both serum and BALF, we found a marked improvement in MRC dyspnea scale with significant improvement in 6MWT and SPaO2 and decrease in both IGFBP1 and IGFBP2 serum levels of UIP patients after completing the 12-month therapy with pirfenidone that may increase the awareness of using those biomarkers as predictors for the disease progression as well as monitoring anti-fibrotic therapy. It also supports the idea that IGFBP2 may play a role in the fibrotic process in the lung. As our patients were not treated with corticoids, we can here discard any possible impact of corticosteroids on IGFBP levels.


Our findings suggest that IGFBP1 and IGFBP2 biomarkers may have the potential to predict the progression of patients with UIP and could also be used to monitor the response to anti-fibrotic therapy. Further, longitudinal studies are needed to evaluate their usefulness as biomarkers in UIP.


One of the limitations of our study is the reduced number of UIP patients who agree to complete the study to the end. As we have chosen IGFBP1 and IGFBP2 biomarkers’ detection in serum and BALF of UIP patients according to our thinking and their potential usefulness, the lack of longitudinal studies for those biomarkers constitutes another limitation of this study.

We believe that further longitudinal multicenter studies are highly needed to evaluate the clinical impact of those biomarkers in a single or multivariate analysis as diagnostic, prognostic, and monitoring tools.

Availability of data and materials

All data of the patients is available on computerized patient file in the Recording Department of King Fahd Hospital, Almadina Almonoura, Kingdom of Saudi Arabia.



Insulin-like growth factor binding protein 1


Usual interstitial pneumonia


Insulin-like growth factors


Insulin-like growth factor binding proteins


High-resolution computed tomography


Six minute walking test


Bronchoalveolar fluid


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Thanks to all the co-authors for their help, support, and collaboration to the redaction of this review.


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HM: responsible for data collection and writing the manuscript. AF: responsible for writing the manuscript. SE: responsible for data collection and writing the manuscript. ZM: responsible for data collection and statistical analysis. All authors have read and approved the manuscript.

Corresponding author

Correspondence to M. Habeb.

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King Fahd Hospital-Medina, Kingdom of Saudi Arabia. Number (59) at May 2018. The written consent form of the patients was taken and was available when needed.

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Habeb, M., Embarak, S., Fathy, A. et al. Non-invasive IGFBP1, IGFBP2 biomarkers as predictors and outcomes of usual interstitial pneumonia (UIP) therapeutic response. Egypt J Bronchol 15, 6 (2021).

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  • IGFBP1
  • IGFBP2
  • UIP
  • Anti-fibrotic pirfenidone