Introduction

An outbreak of Coronavirus Disease 2019 (COVID-19) began in December 2019 and has triggered a public health emergency of international concern [1]. The majority of COVID-19 patients have a self-limiting infection and recover, but some suffer severe symptoms and even die [2]. The suddenly deteriorating conditions of some patients are mainly attributed to systematic inflammatory injury caused by the excessive or uncontrolled activation of immune response, known as the cytokine storm, leading to respiratory distress syndrome (ARDS) and multiple organ failure [3].

Insulin-like growth factor 1 (IGF-1) belongs to the IGF family that plays a critical role in diverse biological activities including cell proliferation, metabolism, differentiation, and survival [4]. Cumulative evidence also supports that IGF-1 pathway can regulate the immune response via interaction with various cytokines (e.g., interferons) and immune cells such as T lymphocytes, macrophages, and bone marrow cells [5]. IGF-1 may act as an important switch controlling the amplitude and quality of the immune response [6]. Of note, IGF-1 administration is already an approved therapy for growth failure and may improve symptoms of autoimmune diseases such as type-1 diabetes and multiple sclerosis [7]. However, whether IGF-1 plays a role in COVID-19 prognosis remains unknown.

Therefore, in the current study, we used the UK Biobank resource, with recently released data on COVID-19 tests and updated death records, to investigate the association between pre-diagnostic serum IGF-1 concentrations and mortality among COVID-19 patients.

Methods

Study participants

UK Biobank is a prospective cohort study consisting of approximately half a million participants (aged 37–73 years) recruited across the UK between 2006 and 2010 [8]. Trained nurses collected blood samples from all participants in the assessment centers at baseline and from a subset of approximately 18,000 participants with a repeat assessment between 2012 and 2013. According to the Public Health England database linked to UK Biobank updated on 07 Sep 2020, 1713 patients were diagnosed with COVID-19 among 16,508 participants who had undergone COVID-19 PCR tests. In the current analysis, we also included additional 164 patients who died from COVID-19 according to the National Health Service death records. The patients who had no available data on serum IGF-1 (n = 171) or died from other causes (n = 36) were excluded, leaving 1670 patients in the final analysis. The included participants had no history of ARDS at baseline.

Assessment of IGF-1

Details about serum biomarker measurements and assay performances have been described online (http://biobank.ndph.ox.ac.uk/showcase/showcase/docs/serum_biochemistry.pdf). Briefly, serum concentrations of IGF-1 were measured in UK Biobank’s purpose-built facility using a ‘one step sandwich’ Chemiluminescent Immunoassay method based on DiaSorin Liaison XL Analyzer (Diasorin S.p.A), with a detection range of 1.3–195.0 nmol/L. The average coefficients of variation of IGF-1 derived from internal quality control samples of known high, medium, and low concentrations were 6.18%, 5.29%, and 6.03%, respectively. Moreover, the assay of serum IGF-1 was registered with an external quality assurance (EQA) scheme (RIQAS Immunoassay Speciality 1) to verify accuracy. The EQA results showed that 100% of participated distributions (n = 105) were good or acceptable.

Ascertainment of COVID-19 mortality

Dates and causes of death were obtained from death certificates held by the National Health Service Information Centre (England and Wales) and the National Health Service Central Register Scotland (Scotland) [9]. The outcome of current study was mortality due to COVID-19 (ICD-10 U07) and available death data were updated on 07 Sep 2020.

Ascertainment of covariates

At baseline, participants attended one of 22 assessment centers across England, Scotland, and Wales where they completed a touch-screen, self-completed questionnaire. Ethnicity, smoking status, and alcohol intake were self-reported. Height, body weight, and waist circumference were measured by trained nurses at baseline, and body mass index (BMI) was calculated as weight in kilograms divided by height in meters squared. Townsend deprivation index was derived from residence using data on car and home ownership, unemployment, and household overcrowding. Physical activity was measured as total metabolic equivalent task-minutes per week for all activity including walking, moderate and vigorous activity.

Statistical analysis

Because the date of COVID-19 testing did not represent the time of infection, the survival time for each patient could not be accurately estimated, leading to Cox regression models inapplicable in the current analysis. Therefore, we analyzed the association between IGF-1 and COVID-19 mortality using unconditional logistic regression models. Odds ratios (OR) and 95% confidence intervals (CI) were calculated according to quartiles and continuously per 1-standard deviation (SD) increment in log-transformed IGF-1 concentrations. Model 1 was adjusted for major covariates including age at infection, sex, and ethnicity; Model 2 was further adjusted for Townsend deprivation index, BMI, smoking status, alcohol drinking, physical activity, and prevalent diabetes. We also additionally adjusted for serum glucose, cardiovascular risk factors (triglycerides, cholesterol, high density lipoprotein, low density lipoprotein, diastolic blood pressure, systolic blood pressure, cholesterol lowering and antihypertensive medications), and C-reactive protein (n = 1434). We calculated intraclass correlation coefficients (ICC) to assess the reproducibility between the 2 measurements of IGF-1 available in a subcohort of participants (n = 16,356), and then used the ICC value to recalibrate the ORs per 1-SD increment for regression dilution [10]. We also used a restricted cubic spline with 4 knots to explore the dose–response relationship between IGF-1 levels and COVID-19 mortality in Model 2. A likelihood ratio test was used to compare the model with only the linear term of IGF-1 levels to the model with both the linear and the cubic spline terms. P for nonlinear < 0.05 was considered as nonlinearity, and P for linear < 0.05 as linearity.

Stratified analyses were conducted according to the median age at infection (< 70, ≥ 70 years), sex (male, female), ethnicity (white, non-white), BMI (< 30, ≥ 30 kg/m2), physical activity (≤ median, > median), and smoking status (never, ever) in Model 2. To investigate potential effect modification by these stratification variables, we used a likelihood ratio test comparing the models with and without interaction terms between IGF-1 concentrations and each of the stratification variables.

A sensitivity analysis was performed by excluding participants with baseline cancer or cardiovascular disease. Because IGF-1 is highly related to central obesity, we also did a sensitivity analysis by adjusting for waist circumference instead of body mass index. We used SAS 9.4 for all analyses. All statistical tests were two-sided, and P < 0.05 was considered statistically significant.

Results

Among 1670 COVID-19 patients, 415 deaths occurred due to COVID-19. The median time from baseline blood draw to COVID-19 testing was 11.2 years (interquartile range: 10.5–11.9 years). The distribution of IGF-1 concentrations is shown in Fig. 1, ranging from 4.79 to 58.00 nmol/L, which was similar to the distribution in the whole cohort (data not shown). The mean (SD) value was 21.17 (6.00) in the included COVID-19 patients and 21.40 (5.70) in the rest participants of UK Biobank.

Fig. 1
figure 1

The distributions of original and log-transformed IGF-1 concentrations

Table 1 summarizes the main characteristics of COVID-19 patients according to quartiles of serum IGF-1 concentrations. At baseline, participants with higher IGF-1 had a lower BMI and higher levels of physical activity, and tended to be younger, males, and nonsmokers.

Table 1 Baseline characteristics of COVID-19 patients according to quartiles of serum IGF-1 concentrations

As shown in Table 2, higher IGF-1 concentrations were associated with a reduced risk of COVID-19 mortality in the multivariable models (Model 2: OR comparing quartile 4 versus 1 = 0.59, 95% CI 0.41–0.86, P-trend = 0.01). In the continuous model, per 1-SD increment in log-transformed IGF-1 was associated with a 15% lower risk of mortality (Model 2: ICC corrected OR = 0.85, 95% CI 0.73–0.99). The association remained stable after further adjustment for serum glucose, cardiovascular risk factors, and C-reactive protein. In Fig. 2, restricted cubic spline regression analysis suggested an inverse linear relationship between IGF-1 concentrations and COVID-19 mortality (P for nonlinear = 0.95 and P for linear = 0.049).

Table 2 Association between serum IGF-1 concentrations and COVID-19 mortality
Fig. 2
figure 2

The dose–response relationship between log-transformed IGF-1 concentrations and COVID-19 mortality according to restricted cubic spline regression analysis. The solid line represents estimates of odds ratios and the dashed lines represent 95% confidence intervals

Figure 3 shows the forest plot results of stratified analyses. The inverse association between IGF-1 and COVID-19 mortality was largely consistent across subgroups, except for ethnicity and smoking status. The association appeared to be stronger in non-white participants and nonsmokers (both P-interaction < 0.05).

Fig. 3
figure 3

Forest plots of stratified analysis for the association between serum IGF-1 concentrations and the risk of COVID-19 mortality

Sensitivity analyses showed that the aforementioned association remained basically unchanged by excluding 267 individuals who had baseline cancer or cardiovascular disease (Table 3) or by adjusting for waist circumference instead of body mass index (Table 4).

Table 3 Sensitivity analysis for the association between serum IGF-1 concentrations and COVID-19 mortality after excluding 267 participants with baseline cancer or cardiovascular disease
Table 4 Sensitivity analysis for the association between serum IGF-1 concentrations and COVID-19 mortality with adjustment for waist circumference instead of body mass index

Discussion

To the best of our knowledge, this study was the first to demonstrate an inverse association between pre-diagnostic circulating levels of IGF-1 and COVID-19 mortality risk among COVID-19 patients. Our findings suggest a potential role of IGF-1 in COVID-19 prognosis and have implications for risk stratification and tailored treatment of COVID-19 patients.

Cytokine storm has been recognized as one of the major causes of ARDS and multiple organ failure in COVID-19 patients. Therefore, effectively suppressing the cytokine storm is important to prevent the disease deterioration and reduce COVID-19 mortality. Markedly elevated levels of circulating interleukin-6 (IL-6), IL-2R, IL-10, tumor necrosis factor-α (TNF-α), etc. have been detected in patients with severe COVID-19 [11, 12]. These cytokines are mainly produced by macrophages and lymphocytes which have been implicated in cytokine storm [13]. Several studies in humans and animal models have suggested an anti-inflammatory effect of IGF-1. For example, there is an inverse relationship between circulating IGF-1 and IL-6 levels [14, 15], and IGF-1/IGF binding protein-3 administration to severely burned patients effectively attenuated inflammatory effects and reduced IL-6 levels [16]. Recombinant human IGF-1 infusion into ApoE-deficient mice significantly decreased macrophage infiltration by downregulating IL-6 and TNF-α expression [17]. In addition, recombinant human IGF-1 can mediate autoimmune suppression in mouse models of autoimmune disease by increasing regulatory T cells in affected tissues [7]. These data and our findings shed a light on potential beneficial effects of IGF-1 treatment on COVID-19 patients. However, it remains uncertain whether ethnicity and smoking status modify the role of IGF-1 in immune regulation, and other studies also reported that IGF-1 might exert pro-inflammatory effects [18, 19]. Future studies are necessary to clarify the mechanism of IGF-1 in COVID-19 prognosis and to confirm whether IGF-1 treatment is effective to mitigate the risk of COVID-19 deaths.

Our study has several strengths. First, UK Biobank is a well-designed large cohort and are providing reliable data on COVID-19 diagnosis and related deaths, allowing us to do the analysis in a timely fashion. Second, biochemistry assays of IGF-1 were performed in a single dedicated central laboratory by a standard, reliable method and strict quality control procedures. Third, we were able to adjust for various covariates on demographic and lifestyle factors.

Several potential limitations also need to be acknowledged. First, the observational nature of this study prevents us from inferring causality. However, our sensitivity analyses excluding baseline CVD and cancer supported the robustness of the findings. Second, a single measurement of IGF-1 at baseline may not represent the levels over 10 years. However, the ICC value of 0.78 (95% CI 0.77–0.79) calculated in a subcohort of UK Biobank, together with previous data [20, 21], indicate that IGF-1 levels are generally stable over time. Third, UK biobank enrolled middle and older aged adults only and Caucasians representing the majority of participants, which limited the ability to assess the association among younger people (< 40 years) and other ethnicities. Fourth, due to limited coverage of coronavirus testing in the UK, ascertainment bias cannot be avoided. Fifth, recovery and COVID-19 related deaths have been suggested to be competing risk events [22]. However, there is no available data on recovery status for COVID-19 patients in UK biobank, and therefore the current study did not take recovery as a potential competing risk into account. Finally, UK Biobank is not representative of the UK population. However, valid assessment of exposure-outcome associations may be widely generalizable and does not require a representative sample [23].

Conclusions

The current study indicates that higher serum IGF-1 concentrations are associated with a lower risk of COVID-19 mortality. Further studies are warranted to validate our findings and clarify underlying mechanisms.