The age again in the eye of the COVID-19 storm: evidence-based decision making

One hundred fifty million contagions, more than 3 million deaths and little more than 1 year of COVID-19 have changed our lives and our health management systems forever. Ageing is known to be one of the significant determinants for COVID-19 severity. Two main reasons underlie this: immunosenescence and age correlation with main COVID-19 comorbidities such as hypertension or dyslipidaemia. This study has two aims. The first is to obtain cut-off points for laboratory parameters that can help us in clinical decision-making. The second one is to analyse the effect of pandemic lockdown on epidemiological, clinical, and laboratory parameters concerning the severity of the COVID-19. For these purposes, 257 of SARSCoV2 inpatients during pandemic confinement were included in this study. Moreover, 584 case records from a previously analysed series, were compared with the present study data. Concerning the characteristics of lockdown series, mild cases accounted for 14.4, 54.1% were moderate and 31.5%, severe. There were 32.5% of home contagions, 26.3% community transmissions, 22.5% nursing home contagions, and 8.8% corresponding to frontline worker contagions regarding epidemiological features. Age > 60 and male sex are hereby confirmed as severity determinants. Equally, higher severity was significantly associated with higher IL6, CRP, ferritin, LDH, and leukocyte counts, and a lower percentage of lymphocyte, CD4 and CD8 count. Comparing this cohort with a previous 584-cases series, mild cases were less than those analysed in the first moment of the pandemic and dyslipidaemia became more frequent than before. IL-6, CRP and LDH values above 69 pg/mL, 97 mg/L and 328 U/L respectively, as well as a CD4 T-cell count below 535 cells/μL, were the best cut-offs predicting severity since these parameters offered reliable areas under the curve. Age and sex together with selected laboratory parameters on admission can help us predict COVID-19 severity and, therefore, make clinical and resource management decisions. Demographic features associated with lockdown might affect the homogeneity of the data and the robustness of the results.

69 pg/mL, 97 mg/L and 328 U/L respectively, as well as a CD4 T-cell count below 535 cells/μL, were the best cutoffs predicting severity since these parameters offered reliable areas under the curve. Conclusion: Age and sex together with selected laboratory parameters on admission can help us predict COVID-19 severity and, therefore, make clinical and resource management decisions. Demographic features associated with lockdown might affect the homogeneity of the data and the robustness of the results.
Keywords: Severe acute respiratory syndrome coronavirus 2, COVID-19, Immunosenescence, Lockdown, Immunity, Renin-angiotensin-aldosterone system inhibitors, Cut-off points, Lymphocytes, Area under the curve Background SARS-CoV-2 infection became widespread [1], being possibly the worst trouble worldwide, as its effects have altered virtually any feature in our lives. Health, economy and individual freedom are seriously threatened all around the world. Almost 16 months after the first diagnosed case, several waves and strains have hit global health. The virus has infected 152.974.685 people and killed 3.204.478 with an overall case-fatality rate of 2.09% [2]. Identifying risk or severity factors for COVID-19 will help clinicians and clinical managers to make decisions about the best therapy [3], and the kind and amount of resources necessary to face new waves [4]. Severity factors might be related to health-based restrictions and should be considered before making public health decisions [5,6].
Since the early days of the pandemic, enormous efforts have been made to identify epidemiological and clinical factors that can predict the severity of the disease [7][8][9][10][11][12][13][14][15]. These efforts have firmly established age as one of the crucial elements along with comorbidities closely associated with age, most notably hypertension, diabetes, and obesity [16][17][18][19][20][21][22][23]. Independently, the male sex has also been described to be related to a severe evolution [16, 18-20, 22, 23]. Likewise, the analytical parameters related to an exacerbated inflammatory state and an exhausted adaptive immune system have been described in association with the most severe forms [16,[24][25][26]. Despite the similarity in the overall description of the parameters associated with the severity of COVID-19 disease, there are notable differences in the risk factors and the analytical parameter values, among the articles published [27]. The causes for these differences can rely on the geographical origin of the study populations, the different study designs and the severity criteria adopted. Additionally, some elements, which are not usually reflected in the scientific literature, might influence the pandemic landscape. One of these elements would be the effect of the pandemic lockdown restrictions, with the meaning of "stay-at-home orders" in the patient baseline characteristics. These differences may be especially relevant in defining cut-off points for analytical parameters that could be extrapolated to different populations and different pandemic moments. The objective of this study is twofold. First, to obtain cut-off points for laboratory parameters that can help us in clinical decision-making. Secondly, to evaluate the effect that confinement may have on the patient demographic and clinical characteristics. This study aims to analyse the effect of pandemic lockdown on epidemiological, clinical, and laboratory parameters concerning the severity of the COVID-19; for this purpose, we have compared the baseline demographic and clinical characteristics as related to the severity of COVID-19 inpatients infected before complete lockdown, with those of patients admitted to hospital during close lockdown period.
Descriptive baseline characteristics of the population (valid n, frequencies, percentages, mean, median, standard deviation and interquartile range) are shown in Table 1. Categorical variables stratified by severity are shown in Table 2.
Males accounted for 58% of cases. Ages in our cohort ranged from 18 to 97 years, with a median of 68 years (IQR 54-90). Concerning comorbidities, 16.9% had obesity, 15.8% were smoker or ex-smokers, 49.2% had hypertension, 32.1% of them were treated with ACEIs (angiotensin converting enzyme inhibitors) and 33% with ARBs (angiotensin receptor blockers). 41.6% had dyslipidaemia and 27.6% suffered diabetes mellitus. The presence of immunodeficiency was most often secondary to other processes, such as a transplantation or chemotherapy treatment; it accounted for 19% cases (n = 45) as seen in Table 1.
Age above 60 (p = 0.046), male gender (p = 0.049) and institution or community transmission (p < 0.001) arose as severity determinants in our series (Table 2). Neither hypertension nor the use of renin-angiotensin system blockers (RAABs) was significantly associated with severity. Mild cases accounted for 10.1% of patients with age ranged between 60 and 75 years, and 17.1% of patients over 75, whereas only 5.6% of home nursing cases were mild.
Most comorbidities were age-related, such as hypertension, dyslipidaemia, diabetes and primary immunodeficiency. Smoking status was both age and sex-related (Table 3) (Fig. 1).
On admission, the median of laboratory parameters, IL6, CRP, ferritin, D-dimer and lactate dehydrogenase (LDH) were above reference ranges; but both, percentage and median lymphocyte counts were under reference ranges (Table 1). Higher severity was significantly associated with higher IL6, CRP, ferritin, LDH, and leukocyte counts, and lower percentage and lymphocyte counts (Table 4). Results from 76 cases with data of lymphocyte subpopulations on admission showed that higher severity was significantly associated with lower CD4 and CD8 counts ( Table 4).
Comparison of the two series: patients recruited on the very first days of pandemic vs. close confinement Our group has previously published data on the risk factors and laboratory parameters of a multicentre series of patients admitted by COVID-19 during the first weeks of the pandemic [16]. A comparison of data corresponding to the close confinement (phase 2 from now on) with the previous series (phase 1 from now on) was performed.
Even with the same inclusion criteria, along with current data and the previous compilation, there were significantly less mild inpatients in phase 2 in comparison with phase 1 (p < 0.001). Age was significantly higher (p = 0.027) within the second period. More cases were reported to have dyslipidaemia (p < 0.001), a history of secondary immunodeficiency (p < 0.001) and fewer patients were on treatment with angiotensin II receptor blockers (p = 0.002) (Supplementary Tables 1 and 2).
Laboratory parameters such as IL-6, CRP and ferritin, although increased, were significantly lower during confinement than in the early months of the pandemic (p = 0.028, < 0.001 and < 0.001 respectively). In contrast, lymphopenia and declining CD8+ cell counts were more evident in the second phase but did not reach significance (Supplementary Table 2).
Severity distribution within male inpatients was almost identical within the two series, but mild female cases decreased as moderate ones grew (p < 0.001, Fig. 2). Severity was significantly higher for all age groups during confinement, especially within the 60 to 75 years old group. Cases above 75 years were predominantly severe both at the beginning of the pandemic and during confinement. Mild inpatients were older in May (p = 0.01) than in March and so were (p = 0.028) severe ones (Fig. 3).
Normolipidemic cases were less frequently mild to become moderate in May (p < 0.001) as compared to March (Fig. 4).
Regarding raw data stratified by severity, some laboratory parameters such as IL-6, CRP, ferritin and LDH, although high, showed values significantly lower than those in phase one. IL6, CRP and ferritin upon arrival were lower in May moderate cohort and CRP as well in mild inpatients. LDH was lower in May mild group as compared to that of March. In the same line, the lowering of CD8 cell count was more evident in phase two but did not reach the significance. All the other parameters compared yielded similar results in the first and second cohorts (data not shown).

Diagnostic accuracy of laboratory parameters
To look for cut-off points in laboratory parameters at admission that would allow us to predict the severity of COVID-19 disease, data from the two series of patients were pooled. Kurtosis and asymmetry were calculated for both cohorts and both fell apart > 10% for every parameter but age, lymphocyte count and LDH. In terms of diagnostic accuracy, only IL-6, CRP, LDH levels and lymphocyte CD4+ count offered a reliable area under the curve. The optimal cut-off and the diagnostic statistics for each parameter are shown in Table 5. Moreover, two extreme thresholds were determined in the merged cohort. A threshold with a likelihood ratio positive (LR+ ) appropriate for predicting severe COVID-19 and a point with a likelihood ratio negative (LR-) suitable for discarding severe COVID-19 was calculated. Extreme cut-offs for each parameter are shown in Table 5. When assessing diagnostic accuracy, CD19 count had an unacceptable AUC of 0.59 (95% CI: 0.47-0.71).

Discussion
This study raises the question of whether the decision values for both clinical and laboratory parameters associated with severe COVID-19 might change, depending on external or environmental factors such as lockdown.
Even working with the same population, selection criteria, and observers, a certain degree of data heterogeneity arises and searching for prognostic risk factors or laboratory cut-off values becomes troublesome. Noise factors should be therefore discarded to simplify and improve triage algorithms. Regarding severity of SARS-CoV-2 infection, different risk factors or comorbidities and laboratory parameters have been reported to date, but none of them is consistent across published studies [27]. Our group has previously described the relationship among demographic, clinical and laboratory parameters with COVID-19 severity in a retrospective study including 584 patients infected for SARS-CoV-2, just before the alarm state declaration and the close confinement in our country in March 2020 [16]. In the present work, with the same case selection and severity criteria, we describe the relationship between clinical risk factors and laboratory parameters at admission in a group of 257 patients admitted to Spanish hospitals during confinement in May 2020.
Concerning clinical risk factors found at the first moment (age, male sex, hypertension, diabetes, hyperlipidaemia, ARBs intake) only age and male sex remain relevant in this second moment. The epidemiological background, which was not recorded in the first phase, was a risk factor for severest COVID-19. Laboratory parameters such as leukocytes, neutrophils, IL-6, CRP, ferritin, D-dimer, and LDH increased with the severity conversely to the decrease in lymphocyte percentage.
However, as comparing both cohorts, severity, and the presence of comorbidities such as dyslipidaemia and secondary immunodeficiency (SID) was significantly higher Abbreviations: ACEI a Angiotensin-converting enzyme inhibitors, ARB b Angiotensin II receptor blockers in patients hospitalized during confinement while the use of ARBs was significantly lower. Strikingly, IL-6, CRP and ferritin, whose elevations were associated with greater severity in both phases, were lower in this second phase than in the first one. There is no straightforward explanation for this finding. One of the major differences that could be a decisive factor is that cases included in the first series were infected just before strict containment measures were enacted in Europe. Meanwhile, cases included in the second series were admitted during close confinement. We may guess that during strict confinement, the epidemiological background would have been oscillating to institutional contagions. In the second phase, the epidemiological background was recorded, and it is worth noticing that 25% of the cases were institutionalized in nursing homes. A higher number of institutionalized cases would mainly impact data because of their older age and a higher rate of second-stage patients' preexisting morbidities. In turn, the relative weight of the age-associated factors might be even higher in this series. Therefore, the relative weight of other factors, such as those associated with the viral infection, might be lower. Additionally, medical prescribing habits for such as the use of RAASBs might have been influenced either by institutionalization or by the highly changing huge number of variable-quality scientific reports at the beginning of pandemics.
A remarkable effort has been made to identify clinical and laboratory factors that can help us predict the  [17,18]. Regarding laboratory data upon admission, in line with our findings, several studies reveal a significant increase in IL-6 [17,[27][28][29], CRP [17,[27][28][29], Ddimer [17,18,27,28], ferritin [17,29], LDH [17,18], leukocytes [17,28,29], neutrophils [27][28][29], and a decrease of lymphocytes [17,18,[27][28][29][30], a decrease of T lymphocytes CD4+ [27,29,30] and CD8+ [18,27,29,30], related to the severity. However, in some of these papers [17,28] the authors warn about heterogeneity across different studies selected for meta-analysis, pointing out as possible causes the origin of the data, the sample size and the month of publication. In our current work, some previously identified factors associated with severity along the first period lost their significant relationships while age and gender were consolidated as severity factors. In addition to remark, age remains a determinant of the main comorbidities initially identified as risk factors. Furthermore, significant quantitative differences within laboratory values have been detected as comparing both periods, pointing out a temporal bias. Particular attention has been paid as well to clarify the role of RAASBs in SARS-CoV-2 infection and the severity of COVID-19 disease. Several meta-analyses have addressed this central issue, but no consensus is met to date. An overall protective effect of RAASBs use is described, this would be mainly attributable to the use of ACEIs (OR:0.652; 95% CI: 0.478-0.891), but not similar effect is observed with concomitant ACEIs plus ARBs (OR:0.867; 95% IC:0.638-1.179) or ARBs alone intakes (OR:0.810; 95% IC:0.629-1.044) [31]. In another meta-analysis where the relationship of the use of RAASBs with the probability of COVID-19 is stated, geographical differences are evidenced, detecting that the use of RAASBs is generally associated with a better prognosis only in studies carried out in Asian countries (OR.0.37; 95% CI: 0.16-0.89) whereas, in those carried out in North America, it is commonly associated with an even more significant increase in ICU admissions (OR: 1.75; 95% CI: 1.37-2.23) and in those carried out in Europe it is related with a higher death probability (OR: 1.68; 95% CI: 1.05-2.70). The authors note that ACEIs would be mainly protective and conversely, ARBs would be associated with an increased risk of death [32]. In a different sense are the findings of the meta-analyses of Megaly et al. [33] and Chan et al. [34]. In the first one, the use of RAASBs is associated with a lower risk of death (OR: 0.57; 95% CI: 0.32-0.98) [33]. In the latter, the use of RAASBs is not globally associated with an increased risk of infection (ACEIs OR: 0.95; 95% CI: 0.86-1.05), (ARBs OR: 1.05; 95% CI: 0.97-1.14) [34]. However, ARBs increase the risk of infection in young subjects, while ACEIs do not increase the susceptibility to infection, not the severity or mortality from COVID-19 [34]. In the phase 1 of our study, a protective effect promoted by ACE inhibitors' intake was described, while the use of ARBs was associated with increased severity [16]. However, our current study does not find any effect of the use of RAAS inhibitors, neither protection nor higher risk. Due to the widespread use of this drug and the apparent beneficial effects concerning COVID-19 disease of ACEIs compared with the deleterious effect of ARBs, more controlled studies are necessary to delve into this major concern.
In order to search for cut-off points of laboratory parameters at the time of admission, which would help us predict the evolution of the patients, data from both series were merged. In terms of diagnostic accuracy, only IL-6, LDH, CRP and CD4 + lymphocyte counts offered an acceptable area under the curve (Table 5).
IL-6 levels are used in the context of COVID-19 disease for patient follow-up and clinical decision-making. Several levels of IL-6 have been proposed in different studies to predict severity progression. In the metaanalysis by Elshazli et al. a cut-off point of 22.9 pg/mL obtained an AUC of 0.63 (95% CI 0.616-0.648) (Sensitivity 71.4%, Specificity 71.4%) [28]. A similar cut-off point, 34.9 pg/mL, showed an AUC of 0.760 and an OR of 12.750 (95% CI 2.2-75.3) to predict ICU admission [3]. A 64 pg/mL cut-off point for IL-6 is also part of a model to predict patients who will need high-flow O2  input (hazard ratio 18) [4]. A higher cut-off, 163.4 pg/ mL, has been proposed for predicting death with a 91.7% sensitivity and 57.6% specificity [39]. In our study a value of 69.08 pg/mL has been found as a predictor of severity (AUC 0.70, 95% CI:0.64-0.76) pg/mL (Sensitivity: 51.2%; Specificity: 79.8%) ( Table 5). Concerning the extreme thresholds, the value 175 pg/mL had an LR+ of 5.2 for diagnosing severe disease and a value of 5.56 pg/ mL had an LR-of 0.19 for discarding severe COVID-19. An elevated neutrophil count, lymphopenia, and an elevated neutrophil/Lymphocyte ratio are characteristic of severe COVID-19 [23,28,40]. Lymphopenia is also part of the infection pathogenesis and is both a cause and a consequence of the severity [41]. Ji et al. have proposed a cut-off point of 1*10 3 lymphocytes/μL for the diagnosis of severe disease (HR 3.7, 95% CI 1.8-7.8) [20]. Tahtasakal et al. have proposed a cut-off point of 1.04*10 3 cells/ μL for the diagnosis of severe disease (AUC 0.678) [23]. In a meta-analysis with 6320 patients, a cut-off point of 0.98*10 3 cells/μL (AUC 0.867, 95% CI 0.861-0.873) is proposed (sensitivity 81.2%, specificity 87.5%), as a marker of severe COVID-19 [28]. In our study, the AUC of this parameter was low 0.61 (95% CI:0.57-0.65) and the best cut-off was 0.725 cells*10 3 /μL (Sensitivity: 39.9%; Specificity: 77.7%) ( Table 5). Regarding extreme thresholds, the value 0.365 cells*10 3 /μL had an LR+ of 5.34 for diagnosing severe disease. No lymphocyte count value had a reliable LR-under 0.5 for discarding severe COVID-19. In summary, both the low AUC and the absence of extreme values with adequate LR-mean that no reliable lymphocyte count values were found to help predict evolution in our study.
Finally, age has been ratified as a crucial factor in COVID-19 severity in our series. Age correlates with endothelial damage and coagulation dysfunction, immunosenescence, inflammaging, including the effects of chronic cytomegalovirus infection, increased prevalence of COVID-19-associated comorbidities, and low levels of vitamin D [43]. Immunosenescence refers to age-related changes in the immune system [44]. Older individuals are more susceptible to infections due to immunological changes associated with the ageing process [45]. These progressive changes affect both innate and adaptive immunity. They include a decrease in naive lymphocytes, the contraction of lymphocyte repertoire, increased memory lymphocytes, fibrotic changes in lymph node architecture, and dysregulation in cytokine production [46]. The low-grade chronic inflammatory state that accompanies ageing, called inflammaging, may predispose older adults to severe COVID-19 by impairing the immune response to SARS-CoV-2. Inflammaging is characterized by high levels of acute-phase proteins and proinflammatory cytokines [47]. It has been suggested that individuals with more severe SARS-CoV-2 infection may have a cytokine storm syndrome characterized by increased levels of cytokines and chemokines [45]. Cytokine storm in elderly with severe SARS-CoV-19 is associated with age-related pathophysiological processes, including senescent cell inflammatory phenotype, excess oxygen radical production, immunosenescence, and lack of vitamin D [48]. Endothelial damage is a critical point that allows us to identify patients prone to develop severe COVID-19. Endothelial barrier mechanisms are independently compromised by diabetes, obesity, age [49] and hypertension, that are known to determine bad COVID-19 prognosis. The hypothesis that attributes the severity of COVID-19 evolution to age-related changes is partly speculative, but supported by different experimental studies. Thus, Rydyznski et al., studying the specific humoral and cellular response to SARS-Cov-2, point out that age correlates with a more severe specific antigen immune response. Older individuals present an uncoordinated humoral and cellular response to SARS-CoV-2. This coordination is notably affected in those over 65 years of age. T lymphocytes' shortage is associated with age and worse COVID-19 prognosis [50]. Baas et al. performing genomic analysis of the response to SARS-CoV-1 in a murine model, point out that older individuals present an exacerbated immune response and that the expression of the genes of TNF-α, IL-6, CCL2, CCL3, CXCL10 and INF-γ exhibit a biphasic pattern that correlates with the peak of viral replication and with the flow of lymphocytes to the areas of more severe histopathological damage in the lungs [51]. Sims et al. characterize the cytokine storm that accompanies severe COVID-19 and find a panel of markers, such as IL-6, PTX3, IL-1RA, CTSL1, IL-18 and RAGE that would reflect vascular endothelial disruption [52]. An unbalanced production of pro-inflammatory cytokines has been described in immunosenescence in healthy individuals. Thus, Shurin et al. demonstrate that INF-γ-inducible chemokines (MIG and IP-10) increase with age [53]. Concerning the above, Tincati et al. analysing the phenotype of cytokines and chemokines that characterizes the worsening of COVID-19 in the second week of the disease, point out that this critical point in the evolution of the disease is associated to higher levels of CXCL8/IL-8, CXCL-9/MIG and CXCL10/IP-10, and that the presence of circulating neutrophils is associated to these levels [54]. Likewise, Xiong et al., employing the transcriptomic analysis of the characteristics of bronchoalveolar lavage and peripheral blood mononuclear cells of individuals with COVID-19 pneumonia, point out the association between the pathogenesis of the disease and the excessive release of cytokines such as CCL2/MCP-1, CXCL10/IP-10, CCL3/MIP-1A and CCL4/MIP-1B [55]. Moreover, IP-10 (CXCL10) [56,57] and MCP-1 [56] have been proposed as biomarkers related to the risk of death in COVID-19 [56] and severity [57]. In the autopsies of the patients who died due to COVID-19, besides the mononuclear inflammatory infiltration, the diffuse alveolar damage and the formation of hyaline membranes, the particular presence of vascular affectation with epithelial damage points to a probable direct cytopathic role of the virus stands out [58]. A hypothesis could be built, where the changes associated with ageing, such as epithelial dysfunction and changes in basal levels of cytokines and chemokines (standing out CXCL-10/IP-10 and CCL2/MCP-1) would enhance an exaggerated response triggered by the direct cytopathic action of the virus on endothelium. The specific response against SARS-CoV-2, when uncoordinated due to ageing, would contribute to a worse evolution.

Conclusions
Some reliable and informative parameter cut-offs could help clinical coping with COVID-19 but lockdown data can rise heterogeneity and should be therefore cautiously managed.
The relationship between the use of RAABs and COVID-19 severity although widely commented, is not conclusively established. Controversial results should guarantee future controlled studies.
Age plays a pivotal role in COVID-19 severity, but not other age-related comorbidities. The hypothesis can be drawn of ageing related changes (epithelial dysfunction and basal levels of cytokines and chemokines) enhancing an exacerbated response to the direct cytopathic action of SARS-CoV2 on vascular endothelium. A specific but uncoordinated immune response against SARS-CoV-2 would determine a bad COVID-19 prognosis.

Study design and participants
A retrospective multicentre analysis was performed on a consecutive set of SARS-CoV-2 infected inpatients, microbiologically confirmed by positive polymerase chain reaction (CRP) test, admitted to the 13 hospitals, during May 2020. Cases were tracked for a five-week follow-up period from admission to discharge. A minimum sample size of 20 patients was considered for every hospital. A total of 260 individuals over 18 years old, from 13 Spanish hospitals were recruited. After data quality assessment, 257 patients were included in the analyses. Cases were stratified into three severity groups, when recorded for inclusion in this study according to the following criteria, adapted from the technical document published by the World Health Organization [59].
Mild: whenever clinical symptoms were mild with no abnormal radiological findings. Moderate: cases with confirmed pneumonia that was not considered severe Severe: when at least one of the following criteria was met: acute respiratory distress, shock, admission to the intensive care unit (ICU), the process was so considered by the physician in charge. Any death was as well classified as severe.
This retrospective observational study was conducted according to national regulations, institutional policies and in the tenets of the Helsinki Declaration. It was approved by the local institutional Ethics Committee of any involved hospitals.
Data from 584 case records from the previously analysed series [16], were compared with data from the 257 cases in the present study and both were pooled to explore cut-off values.

Data collection
Any data analysed were extracted from electronic medical records. The collection form included demographic, epidemiological and clinical data: age, sex, history of diabetes mellitus (DM), dyslipidaemia, hypertension (HTA), renin-angiotensin-aldosterone system blockers (RAASBs) and statins intake, the smoking status, obesity, time from onset to diagnosis, laboratory data on admission, and COVID-19 severity using the criteria previously defined.
Additionally, data from a former study conducted by our group the pre-confinement phase [16] were compared to those in the current study and merged for cutoff analyses. Inclusion and severity criteria were the same for both cohorts.

Statistical analysis
Demographic and clinical characteristics of patients were expressed as their mean and standard deviation (SD); when not adjusting to a normal distribution, the median was used to represent non-parametric data for continuous variables and frequency distributions represented categorical variables.
Kolmogorov-Smirnov test was performed on each continuous variable to contrast normality. To analyse the overall differences between the three groups: mild, moderate, and severe type, the ANOVA was tested on variables with normal distribution and n > 30 (% and CD4 lymphocyte count, % of CD8 lymphocytes, % of NK and C3 concentration). The Kruskal-Wallis test was used to analyse the relationship with severity for non-parametric variables. To contrast the "Ho" of independence within categorical variables, Chi-square and Fisher's exact test were used.
A comparison of data collected during the lockdown period with our published data collected outside the lockdown [16] was performed as independent samples' Wilcoxon test for medians.
Pooling data from the two series searching for predictive cut-off values: We have previously published the association of laboratory parameters with severity from a cohort of COVID-19 hospitalized patients before complete lockdown. We merged the data from this cohort with those obtained during our country home confinement. To determine the diagnostic validity of each laboratory parameter, sensitivity, specificity, the receiver operating curve (ROC), the area under the curve (AUC) and the optimal cut-off (Youden index) were calculated. The maximum value of the Youden index can be used as a criterion for selecting the optimal cut-off value when a diagnostic test is expressed as a numerical value [60]. Moreover, to maximize the specificity (to rule in severe COVID-19) and the sensitivity (to rule out severe COVID-19), likelihood ratio positive and negative were calculated. A diagnostic test will be more beneficial to the extent that its positive likelihood ratio (+LR) is of greater magnitude since it allows confirming with certainty the presence of disease, and its -LR has a low value since it rules out the disease [61].