Prevalence and Mortality due to COVID-19 in HIV Co-Infected Population: A Systematic Review and Meta-Analysis

Abstract

Introduction

The coronavirus disease 2019 (COVID-19) was defined as a species of beta coronavirus causing atypical respiratory disease in humans. The COVID-19 pandemic has resulted in an unprecedented health and economic crisis worldwide. Little is known about the specifics of its influence on people living with human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS) (PLWHA). In this study, we aim to investigate the prevalence and mortality in PLWHA co-infected with COVID-19.

Methods

The databases PUBMED, EMBASE, BioRxiv, and medRxiv were searched up to 9 March 2021 to explore the prevalence and mortality rate of COVID-19 in PLWHA. Cohort studies and case series meeting the inclusion criteria were included in this review.

Results

We identified 14 eligible studies, 9 of which were cohort and 5 were case series. A total of 203,761 patients with COVID-19 were identified (7718 PLWHA vs. 196,043 non-PLWHA). Meta-analyses estimated the prevalence and mortality rate of COVID-19 in PLWHA was 0.774% [95% confidence interval (CI) 0.00393–0.01517] and 8.814% (95% CI 0.05766–0.13245) respectively. COVID-19 co-infected PLWHA do not seem to be associated with higher mortality, as compared to non-PLWHA [relative risk (RR) 0.96 (95% CI 0.88–1.06)]. The presence of comorbidities such as diabetes mellitus, RR 5.2 (95% CI 4.25–6.36), hypertension and chronic cardiac disease, RR 4.2 (95% CI 1.09–16.10), and chronic kidney disease, RR 8.43 (95% CI 5.49–12.93) were associated with an increased mortality in COVID-19 co-infected PLWHA.

Conclusion

The estimated prevalence and mortality rate of COVID-19 in PLWHA were 0.774% and 8.814%, respectively. Since most of the included studies used unmatched populations, comparisons between PLWHA and non-PLWHA should be interpreted with caution. Further investigations are needed for a more comprehensive understanding of the relationship between cluster of differentiation 4 cell count, HIV viral load, antiretroviral therapy, and COVID-19 related prognosis in PLWHA.

Supplementary Information

The online version contains supplementary material available at 10.1007/s40121-021-00447-1.

Key Summary Points

Why carry out this study?

The coronavirus disease 2019 (COVID-19) pandemic has become a major public health crisis globally. The correlation between human immunodeficiency virus (HIV) and COVID-19 remains unclear.

People living with HIV/acquired immunodeficiency syndrome (AIDS) (PLWHA) are generally thought to be at a higher risk for developing a severe course and outcome of COVID-19 infection due to immunodeficiency. Therefore, there is an underlying interest to investigate the impact of COVID-19 on this population.

What was learned from the study?

This study defined a total of 203,761 patients with COVID-19 (7718 PLWHA vs. 196,043 non-PLWHA). Meta-analyses showed estimated prevalence and mortality rate of COVID-19 in PLWHA was 0.774% and 8.814%, respectively.

This study indicated increased mortality among COVID-19 co-infected PLWHA having co-morbid conditions such as diabetes mellitus, chronic kidney disease, hypertensionand chronic cardiac disease.

No statistical significance was observed in mortality between PLWHA and non-PLWHA.

Further studies are needed to address the role of cluster of differentiation 4 cells, HIV viral load, and antiretroviral therapy in COVID-19 co-infection.

Digital Features

This article is published with digital features, including a summary slide, to facilitate understanding of the article. To view digital features for this article go to https://doi.org/10.6084/m9.figshare.14381498.

Introduction

Since coronavirus disease 2019 (COVID-19) emerged in China in late 2019, it has proven to be an urgent threat to global health. As of 21 March 2021, COVID-19 has affected 215 countries and territories, resulting in more than 100 million identified cases and 27 million confirmed deaths [1]. Global statistics from 2019 show approximately 38 million people chronically infected with human immunodeficiency virus (HIV) [2]; therefore, there has been a deep interest to explore the impact of COVID-19 infection among people living with HIV/acquired immunodeficiency syndrome (AIDS) (PLWHA). However, the prevalence and prognosis, as well as other clinical characteristics of COVID-19 co-infected PLWHA, have not been studied extensively. A recent cohort study by Had et al. of 404 HIV patients showed no statistical significance in mortality due to COVID-19 co-infection when compared to a matched control population [3]. Conversely, two cohort studies conducted by Boulle et al. [4] (3978 HIV patients) and Huang et al. [5] (6001 HIV patients) indicated that HIV was associated with higher mortality as compared to controls. However, the prevalence and prognosis of COVID-19 and the role of other characteristics [e.g., age, comorbidities, HIV viral load, cluster of differentiation 4 (CD4) cell count, and antiretroviral therapy (ART)] during infection in this population is not clear. Hence, a systematic review and meta-analysis will help to summarize the results.

Methods

Protocol and Registration

This meta-analysis was conducted in accordance with the statement of the preferred reporting items for systematic reviews and meta-analysis (PRISMA) [6]. The registration number for the international prospective register of systematic review (PROSPERO) is CRD42021231640. The primary outcome for this systematic review and meta-analysis is the prevalence and mortality rate of COVID-19 in PLWHA. Additional outcomes included mortality comparison in PLWHA and non-PLWHA due to COVID-19 co-infection, as well as the roles of comorbidity, CD4 cells, ART, and HIV viral load in COVID-19-related outcomes in PLWHA. Subgroup analyses were conducted based on the study population and country.

Eligibility Criteria

We included preprints to capture emerging evidence. Studies reporting the following data were considered for inclusion: (1) investigated clinical outcomes of COVID-19 co-infection in PLWHA, including prevalence, mortality, need for intensive care support, comorbidity, duration of hospitalization, and recovery; (2) laboratory findings: inflammation biomarkers during hospitalization, HIV viral load, and count of CD4 cells prior to the co-infection; and (3) validated diagnostic criteria of COVID-19 and accurate study dates.

Exclusion criteria were as follows: (1) studies without available data for synthesis; and (2) single case reports, case series with a reported number of participants less than 15, review editorials, and conference abstracts. There were no restrictions regarding age, sex, or duration of the study.

Detailed studies with large populations and multi-center involvement were preferred for this review as these reduced deviations and met requirements for studies conducted in the same region/country and having a population overlap.

Electronic Search

A systematic search was independently performed by two authors through electronic databases, including PUBMED, EMBASE, BioRxiv, and medRxiv, which were searched up to 9 March 2021 with the publication language restricted to English. Studies were retrieved by utilizing medical subject headings (MeSH) and MeSH-derived topical terms. Our search term for PUBMED was ((“COVID-19” OR “2019 novel coronavirus disease” OR “COVID19” OR “COVID-19 pandemic” OR “SARS-CoV-2 infection” OR “COVID-19 virus disease” OR “2019 novel coronavirus infection” OR “2019-nCoV infection” OR “coronavirus disease 2019” OR “coronavirus disease-19” OR “2019-nCoV disease” OR “COVID-19 virus infection”) AND (“HIV” OR “Human Immunodeficiency Virus*” OR “Human T Cell Lymphotropic Virus Type III” OR “Human T-Cell Leukemia Virus Type III” OR “LAV-HTLV-III” OR “Lymphadenopathy-Associated Virus*” OR “Human T Lymphotropic Virus Type III” OR “AIDS Virus*” OR “Acquired Immun* Deficiency Syndrome Virus” OR “HTLV-III”)).

Study Selection

Articles that were considered to be potentially relevant to the topic were obtained in full text. Two independent reviewers (Shivank, S. and Shantanu, S.) performed the search, two independent reviewers screened the titles, abstracts, and full texts (C.N.C. and M.F.C.), and disputes were resolved by consensus or consultation with the supervisors (M.L. and S.F.T.).

Data Collection Process

The following information was extracted from each included study: (1) first author’s name, year of publication; (2) location; (3) study design; (4) comparison or control; (5) sample size; (6) patient characteristics: median age; (7) ART; (8) confirmation method for COVID-19; and (9) outcome: mortality. Data were extracted by three authors (C.N.C, S.F.T, and N.L.) and validated by a fourth author (Shantanu. S.).

Risk of Bias of Individual Studies

The quality assessment for the case series was conducted in accordance with the Joanna Briggs Institute (JBI) checklist for case series [7]. The JBI checklist for case series rates the quality of selection, measurement, and comparability of studies, giving a score ranging from 0 to 10. For cohort studies, biases were assessed with the Newcastle–Ottawa scale, which included ratings of selection bias, comparability issues, and outcome reporting bias [8]. Two reviewers (C.N.C. and N.L.) assessed the risk of bias for each study independently. Any disagreement was resolved by consultation with the supervisors (M.L. and S.F.T.).

Statistical Methods

We calculated prevalence estimates using the variance of the ‘logit of accuracy indices’, since the weightage of inverse variance in meta-analysis is sub-optimum while dealing with data having non-normal distribution and low prevalence [9]. For dichotomous outcomes, we calculated the relative risk (RR) with 95% confidence interval (CI). We assessed for statistical heterogeneity by visual inspection of the forest plot and calculation of the Higgin's I² statistic [10]. According to the Cochrane Handbook for Meta-analysis, when meta-analysis was possible because of acceptable clinical and methodological heterogeneity, we reported the fixed-effects model summary estimate for I² < 25% and the random-effects model summary estimate for I² > 25% [11]. We expected the existence of heterogeneity (I² > 25%), due to concerns of study design, the number in the population, and varied statistical approaches in studies. Therefore, meta-analyses were performed based on a randomized effect model in this review. Meta-analyses and forest plots were performed in R (v.4.0.2; R Foundation for Statistical Computing, Vienna, Austria), using the meta-package [12].

Compliance with Ethics Guidelines

This article is based on previously conducted studies and does not contain any studies of human participants or animals performed by any of the authors.

Results

Study Selection

The primary outcome of interest for this review was the prevalence of COVID-19 in PLWHA and the mortality rate in those who were co-infected with COVID-19. A total of 3,344 articles were retrieved from electronic databases up to 9 March 2021. After the removal of irrelevancy and duplicates, 83 articles were taken for full-text screening, and, finally, 14 studies providing outcomes of interest were included for review [4, 5, 13–24]. Of these included studies 13 were peer-reviewed, while 1 case series was unpublished [19]. A PRISMA flow chart for the literature search is shown in Fig. 1.

Fig. 1.

PRISMA flowchart of literature search and study selection

Study Characteristics

A total of 203,761 patients with COVID-19 were identified (7,718 PLWHA vs. 196,043 non-PLWHA). To assess the prevalence of COVID-19 in PLWHA, a total of 757,103 patients were included. Table 1 outlines the characteristics and data extracted from the included studies. Nine studies were of cohort design [4, 5, 13, 15, 17, 18, 20–22] and the other five were case series [14, 16, 19, 23, 24]. Only one cohort study used matched population design while comparing PLWHA and non-PLWHA[21]. Seven of the studies were conducted in Europe (England, UK [18], Italy [14, 20], Spain [13], France [17]), Germany [24], and Central/East European countries [19]. The others were from Asia (China [5]), Africa (Western Cape [4]), North America (United States [16, 21–23]), and South America (Chile [15]), respectively. Four of the cohort studies used a mass database(provincial/national) for population recruitment [4, 5, 18, 22], another two had a multi-center involvement [13, 15], and three studies had a single-center involvement [17, 20, 21]. Four out of the five case series were of a multi-center design [14, 16, 19, 24]. For analysis of COVID-19 prevalence in PLWHA, we identified six studies with a population total of 757,103 patients. For analysis of mortality due to COVID-19 in PLWHA, 14 studies were included, with a total of 5626 patients. For comparison of mortality due to COVID-19 between PLWHA and non-PLWHA, six studies with a total number of 5,090 PLWHA and 195,812 non-PLWHA patients were included. Additionally, four studies provided data of comorbidities among PLWHA and non-PLWHA, which enabled us to perform a comparison for the risk of COVID-19 co-infection based on various comorbidities in the two groups. Only two of the included studies reported data of CD4 count and HIV viral load before/during hospitalization between COVID-19-infected and non-COVID-19-infected PLWHA [5, 20]. However, since the reported data of these two items were not standardized, this resulted in the infeasibility of determining the role of either of the two crucial factors in the risk of COVID-19 co-infection in this population. Also, due to insufficient data reported in studies, we failed to assess socio-demographic disparities (e.g., age, sex, ethnicity) of COVID-19 co-infection in PLWHA.

Table 1.

Characteristics of trials included in the systematic review and meta-analyses

Source	Study design	Country/region	Data source	Identified case of COVID-19 (n)	Median age (IQR)	Diagnostic methods for COVID-19	CD4 cells/HIV VL	Patient on ART (%)	Most reported comorbidities	Mortality patient (%)
Boulle [4]	Provincial-based cohort study	Western Cape province, South Africa	Using data from the WCPHDC of public sector, patients aged ≥ 20 years with documented sex and not known to have died before 1 March 2020 and follow-up through 9 June 2020	3978 PLWHA vs. 18,330 non-PLWHA	41 years in PLWHA vs. 40.6 years in non-PLWHA	SARS-CoV-2 PCR test	7.6% with VL > 1000 copies/ml or CD4 cell count < 200 cells/ml, 34.7% with VL unknown in past 15 months	Not reported in detail	DM; HTN; CKD; Chronic pulmonary disease / asthma	115 (3%) PLWHA vs. 510 (2.8%) non-PLWHA
Geretti [18]	Prospective cohort study	England, UK	Using the ISARIC WHO CCP-UK database, people aged ≥ 18 years and admitted to participating hospital(207atthetime) with either laboratory-confirmed or highly likely COVID-19 infection	122 PLWHA vs. 47,470 non-PLWHA	56 years in PLWHA vs. 74 years in non-PLWHA	Either laboratory confirmed or highly likely infection	Not reported	25 (83%) on ART deceased vs. 87 (94%) on ART alive	Chronic cardiac disease; Chronic pulmonary disease; CKD; DM; Obesity; Chronic neurological disorder; Dementia; Liver disease; Cancer; Chronic hematological disease; Rheumatological disease; Malnutrition	30 (24.5%) PLWHA vs. 13,969 (29.4%) non-PLWHA
Huang [5]	Cohort	Wuhan City, China	Using systems of NNIDRS and CRIMS, PLWHA included with confirmed, clinically diagnosed, suspected, and asymptomatic cases	35 PLWHA vs. 50,333non-PLWHA	37 years in PLWHA	SARS-CoV-2 PCR test, suspected, clinically diagnosed	CD4 count: 200–499 cells/ml; 66% VL < 20 copies/ml	32 (91.4%) on ART	Not reported	2 (5.7%) PLWHA vs. 3869 (7.7%) non-PLWHA
Biagio [14]	Multi-center Case series	Italy	Using data from Infectious Diseases Departments participating in the CISAI study group, PLWHA referred to the centers with a diagnosis of COVID-19	69 PLWHA	53 years	SARS-CoV-2 PCR test	Not reported	Not reported in detail	HTN; DM; CVD;	7 patients deceased
Amo [13]	Multi-center Cohort	Spain	PLWHA referred to 60 Spain hospitals with COVID-19 diagnosis between 1 February and 15 April 2020 and data from the 2019 National HIV Hospital Survey	236 PLWHA	55.8 years	SARS-CoV-2 PCR test	Not reported	100% on ART	Not reported	20 patients deceased
Maggiolo [20]	Single center, prospective cohort	Italy	Not reported	55 PLWHA	54 (49–48) years	SARS-CoV-2 PCR test	CD4 count:904 (557–1110) cells/μl; 98% VL < 50 copies/ml	100% on ART	CVD; HTN; Cancer; DM	4 patients deceased
Etienne [17]	Single center, prospective cohort	Paris, France	Consecutive PLWHA taken in care in the department and having developed COVID-19 clinical symptoms and/or hospi- talized for COVID-19 in the hospital	54 PLWHA	54 (47–60) years	Not reported	CD4 count: 583 (474–773) cells/μl; 96.2% VL < 40 copies/ml	100% on ART	DM; HTN; CKD; Respiratory disease; Cirrhosis; Cancer; CVD	1 patient deceased
Meyerowitz [23]	Single center Case series	Massachusetts, USA	PLWHA with confirmed COVID-19 infection hospitalized in a local hospital	36 PLWHA	53.4 years	SARS-CoV-2 nasopharyngeal swab PCR	CD4 count: 691 cells/μl; No report in VL	35 (97.2%) on ART	DM, HTN, NASH, HLD, COPD	2 patients deceased
Collins[16]	Multi-center Case series	Georgia, USA	PLWHA with confirmed COVID-19 infection in three of the local centers	20 PLWHA	57 (48–62) years	SARS-CoV-2 PCR test	CD4 count:425 (262–815) cells/μl; 90% VL < 200 copies/ml	19 (95%) on ART	HTN, DM, Chronic lung disease, CKD	3 patients deceased
Härter [24]	Multi-center Case series	Germany	PLWHA with confirmed COVID-19 infection in German HIV centers	33 PLWHA	48 years	SARS-CoV-2 PCR test	CD4 count: > 350 cells/μl; 94% virally suppressed	100% on ART	DM; HTN; COPD; CVD; CKD; Hepatitis B infection	3 patients deceased
Kase [19]	Case series	12 countries in central and eastern Europe	PLWHA with confirmed COVID-19 infection in ECEE Network Group	34 PLWHA	42.7 years	SARS-CoV-2 PCR test	CD4 count:558 (312–719) cells/μl;53% VL < 50 copies/ml	15 (44.1%) on ART	CVD; Chronic lung disease; DM; Obesity; Hepatitis C infection; Hepatitis B infection	3 patients deceased
Nagarakanti [21]	Single center, retrospective cohort, matched designed	New Jersey, USA	PLWHA with confirmed COVID-19 infection in a local medical center	23 PLWHA vs. 254 non-PLWHA	59 (51–67) years in PLWHA vs 62 (50–74) years in non-PLWHA	SARS-CoV-2 PCR test	Not reported	15 (65.2%) on ART	HTN; DM; CKD; CAD; COPD	In hospital deceased: 3 (13%) PLWHA vs. 6 (2.4%) non-PLWHA
Tesoriero [22]	Multi-center, cohort	New York, USA	The NYS HIV surveillance registry, ECLRS, and SHIN-NY	2988 PLWHA vs. 375,260 non-PLWHA	54 years in PLWHA vs. 63 years in non-PLWHA	SARS-CoV-2 PCR test	Not reported	Not reported	Not reported	In hospital deceased: 207(23.1%) PLWHA vs 14,522(23.6%) non-PLWHA
Ceballos [15]	Multi-center, prospective cohort	Chile	PLWHA with confirmed COVID-19 infection hospitalized in 23 hospitals in Chile	36 PLWHA vs. 4360 non-PLWHA	44 (26–85) years in PLWHA; unavailable in non-PLWHA	SARS-CoV-2 PCR test	CD4 count:202 (168–446) cells/μl; 55% VL < 50 copies/ml	30 (83%) on ART	DM; HTN; Obesity; COPD; Asthma; CKD; Chronic liver disease; CVD; Cancer;	5(13.9%) PLWHA vs 4,360(23.8%) non-PLWHA

-PLWHA People living with immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS), IQR Interquartile range, WCPHDC Western Cape Provincial Health Data Center, ISARIC International severe acute respiratory and emerging infections consortium, WHO CCP-UK World Health Organization–clinical characterization protocol–United Kingdom, VL viral load, ART antiretroviral therapy, PCR polymerase chain reaction, NNIDRS national notifiable infectious disease report system, CRIMS China national HIV/AIDS comprehensive response information management, CISAI Coordinamento italiano per lo studiodell’infezione da HIV e Allergie, ECLRS Electronic clinical laboratory reporting system, SHIN-NY State health information network for New York, NYS New York State, ECEE Central and Eastern Europe, DM diabetes mellitus, HTN hypertension, NASH nonalcoholic steatohepatitis, HLD hyperlipidemia, COPD chronic obstructive pulmonary disease, CKD chronic kidney disease, CAD coronary artery disease, CVD cardiovascular diseases

Risk of Bias Within Studies

The risk of bias assessment of the included studies and reasons for judgment are presented in Tables 2 and 3. Overall, cohorts and case series were assessed to have a moderate risk of bias. The average score among cohort studies was 6 points out of 9 (varying between 5 and 9 points individually). Under-reporting of the non-exposed group, retrospective design, and inadequate follow-up contribute to various disadvantages of the cohort studies. The average score among case series was 6 points out of 10 (varying between 3 and 9 points of inter-agreement with risk of bias domains). The disadvantages of case-series studies were inadequate reporting of participant recruitment, their demographic presentation, and a short duration of follow-up.

Table 2.

The methodological quality score of included studies based on Newcastle–Ottawa quality assessment score

Source	Selection				Comparability	Outcome			Total score
	Representativeness of the exposed group	Selection of the non-exposed group	Ascertainment of exposure	Demonstration that outcome of interest was not present at start of study	Comparability of study on the basis of the design or analysis	Assessment of outcome	Was follow-up long enough for outcomes to occur?	Adequacy of follow-up of the groups	Out of 9
Boulle [4]	1	1	1	1	2	1	0	0	7
Geretti [18]	1	1	1	0	2	1	1	0	7
Huang [5]	1	1	1	0	1	1	1	0	6
Amo [13]	1	0	1	0	2	1	0	0	5
Maggiolo [20]	1	1	1	0	1	1	0	0	5
Etienne [17]	1	0	1	0	1	1	1	0	5
Nagarakanti [21]	1	1	1	0	1	1	0	0	5
Tesoriero [22]	1	1	1	0	2	1	0	0	6
Ceballos [15]	1	1	1	1	2	1	0	0	7

Table 3.

Quality appraisal of included case series employing Joanna Briggs Institute Case Series Checklist

	Meyerowitz [23]	Collins [16]	Harter [24]	Kase [19]	Biagio [14]
Were there clear criteria for inclusion in the case series?	Y	Y	Y	Y	Y
Was the condition measured in a standard, reliable way for all participants included in the case series?	Y	Y	Y	N	Y
Were valid methods used for identification of the condition for all participants included in the case series?	Y	Y	N	N	Y
Did the case series have consecutive inclusion of participants?	Y	Y	Y	N	Y
Did the case series have complete inclusion of participants?	?	Y	Y	N	?
Was there clear reporting of the demographics of the participants in the study?	Y	Y	Y	N	N
Was there clear reporting of clinical information of the participants?	Y	Y	Y	Y	?
Were the outcomes or follow-up results of cases clearly reported?	N	N	N	N	N
Was there clear reporting of the presenting site(s)/clinic(s) demographic information?	N	Y	N	N	N
Was statistical analysis appropriate?	Y	Y	Y	Y	Y
Score (Y or N/A = 1, N or? = 0)	7	9	7	3	5

Results of Meta-Analyses

Primary Outcome

Findings of prevalence and mortality rate for COVID-19 infected PLWHA were of interest. Pooled results from six of the included studies showed the prevalence of co-infection with COVID-19 in PLWHA was 0.774% (95% CI 0.00393–0.01517) (Fig. 2). For the mortality rate of COVID-19 in PLWHA, pooled results from 14 included studies showed a rate of 8.814% (95% CI 0.05766–0.13245) (Fig. 3). Subgroup analyses categorized by country can be found in the Supplementary Material.

Fig. 2.

Prevalence of COVID-19 in PLWHA

Fig. 3.

The COVID-19 mortality rate in PLWHA and non-PLWHA

Additional Outcomes

Additional outcomes include: (1) the risk of mortality in PLWHA due to COVID-19 infection compared to non-PLWHA; (2) the risk of COVID-19 co-infection grouped by various comorbidities between PLWHA and non-PLWHA; (3) comparison comorbidity in the risk of COVID-19 mortality in PLWHA; and (4) the role of CD4 count, HIV viral load, and ART in COVID-19 co-infection in PLWHA. Six studies reported outcomes of mortality in both populations. The pooled data indicated that, compared to non-PLWHA, a COVID-19 course in PLWHA having an estimated RR 0.96 (95% CI 0.88–1.06, I² = 0%; Fig. 4) was not associated with higher mortality across all settings. Five studies were included in the subgroup analysis of hospitalized patients, which indicated that there is no evidence that HIV was associated with higher mortality due to COVID-19, RR 0.94 (95% CI 0.85–1.04, I² = 0%, Fig. 4).

Fig. 4.

Comparison mortality between PLWHA and non-PLWHA due to COVID-19

Data of comorbidities were available from four cohort studies, which reported chronic kidney disease, chronic respiratory disease, diabetes mellitus, and hypertension and chronic cardiac disease in both PLWHA and non-PLWHA. Pooled results showed that none of the comorbidities were associated with a higher risk of infection with COVID-19 when PLWHA and non-PLWHA were compared: for chronic kidney disease, RR 1.18 (95% CI 0.80–1.76, I² = 55%; Fig. 5); for chronic respiratory disease, RR 0.72 (95% CI 0.63–0.82, I² = 0%; Fig. 5); for diabetes mellitus, RR 1.07 (95% CI 0.41–2.76, I² = 95%; Fig. 5); and for hypertension and chronic cardiac disease, RR 0.76 (95% CI 0.57–1.02, I² = 58%; Fig. 5).

Fig. 5.

Comparison of comorbidity in the risk of COVID-19 co-infection between PLWHA and non-PLWHA

An analysis grouped by comorbidities was performed in PLWHA. Three studies were included in the analysis. The result indicated that chronic kidney disease, RR 8.43 (95% CI 5.49–12.93, I² = 0%; Fig. 6), diabetes mellitus, RR 5.20 (95% CI 4.25–6.36, I² = 0%; Fig. 6), hypertension and chronic cardiac disease, RR 4.20 (95% CI 1.09–16.10, I² = 84%; Fig. 6) have a strong association with increased mortality due to COVID-19 in PLWHA.

Fig. 6.

Comparison comorbidity in the risk of COVID-19 mortality in PLWHA

The classification of HIV viral load, CD4 count, and ART was not standardized, hence we failed to estimate their impact in COVID-19 co-infected PLWHA.

Discussion

Several studies have reported the prevalence of COVID-19 among PLWHA, with an estimated rate ranging from 0.8 to 9.7% [25–27]. However, their conclusions were based on single studies and only a few systematic reviews and meta-analyses have estimated the odds comprehensively and quantitatively. A recent, unpublished systematic review and meta-analysis indicated that the prevalence and mortality rate of PLWHA hospitalized for COVID-19 was 1.22% and 12.35%, respectively [28]. Unfortunately, as only 573 PLWHA were included in the pooled analysis and seven out of nine included studies were conducted in New York City, the strength of the evidence presented in the unpublished review is possibly limited for reflecting the generalized population. As increased evidence has since been published, our review and meta-analysis uses a large sample size from multiple diverse regions. Our findings suggested that the prevalence and mortality rate of COVID-19 in PLWHA was 0.774% and 8.814%, respectively. The estimated prevalence rate is lower than the existing reports, possibly due to varying sample sizes across studies and the epidemiological characteristic difference between regions (Supplementary Material). Distinct examples of this are an included study, conducted in Wuhan, China, which estimated 0.583% COVID-19 prevalence out of 5966 PLWHA [5], and an excluded conference report, the Veterans Aging Cohort Study conducted in the USA, which estimated a 9.7% prevalence for COVID-19 out of 30,891 PLWHA [25]. True prevalence could be higher, as HIV remains disproportionately concentrated in low-income regions which also have the highest HIV-related morbidity and mortality [29, 30]. PLWHA in these regions might have poor disease management, which consequently results in an increased risk of contracting COVID-19 due to being immunocompromised. These patients might not be identified as COVID-19 co-infected due to inadequate detection capacity or the limitations of local governments.

There is also a growing interest regarding the characteristics and prognosis of COVID-19 between PLWHA and non-PLWHA. Some evidence from multiple European HIV/AIDS organizations acknowledged that there is not sufficient evidence showing a varying disease course or higher COVID-19 infection rates in PLWHA compared to non-PLWHA [31]. Consistent with these conclusions, a recently published systematic review and meta-analysis conducted by Sarkar et al. indicated no significant impact in COVID-19 mortality between PLWHA and non-PLWHA [RR 0.99 (95% CI 0.82–1.19)] [32]. However, this finding was in contrast to another study conducted by Mellor et al. [33], which suggested that PLWHA had a higher risk of COVID-19 mortality compared to the general population [HR 1.95 (95% CI 1.62–2.34)]. It is a much-debated topic whether HIV plays a pivotal role in COVID-19 prognosis, as the evidence has been derived from cohort studies that were performed in unmatched populations. The number of PLWHA having COVID-19 co-infection was relatively low in such cases (Table 1). On the other hand, both of the above-mentioned meta-analyses are suspected to have included studies having overlapping populations and periods between each other, which might have led to inappropriate interpretation [34]. Sarkar’s review used data collected from four studies conducted in the same region (New York City) and one study of a multi-center design [3]. In Mellor’s review, two of the included studies were conducted at national level in the UK [18, 35].

Despite having an unmatched population, our study showed insufficient evidence for a higher risk of COVID-19 mortality in PLWHA when compared to non-PLWHA across all settings (Fig. 4). This leads to a puzzling question: Why are PLWHA not at higher risk for developing a severe course and outcome of COVID-19 infection compared to the general population even though they might be immunosuppressed? A pharmacologic hypothesis might explain why this might be the case. PLWHA have usually prescribed ART for the management of HIV. Recent evidence suggests that widely prescribed anti-HIV medications, Tenofovir, Emtricitabine, Raltegravir, and Dolutegravir, have been proven to result in reduced in vivo SARS-CoV-2 proliferation [36–39]. It has been further found that, among COVID-19 infected PLWHA, those who took Tenofovir disoproxil fumarate therapy had better clinical outcomes compared to other ARTs [13, 40]. Another possible explanation for this outcome could be that most studies were performed in high-income countries where the majority of PLWHA were more likely to have well-controlled HIV on ART (Table 1). Outcomes in low-income areas having a high burden of HIV might be a little more complex. Another concern is that the patients undergoing ART might be more likely to experience treatment interruptions due to restrictions on non-emergency medical appointments related to physical distancing requirements. It is estimated that approximately 19% of PLWHA were unable to receive ART refills due to the pandemic [41]. Also, many HIV/AIDS prevention and control centers have been converted to COVID-19 centers and refused PLWHA of their ART [41, 42]. Effective action should be taken to help these patients receive their basic ART on time.

Correlation between comorbidities and COVID-19 has recently been in focus. It is reported that approximately two-thirds of COVID-19 co-infected PLWHA had multimorbid complications [43]. In our review, meta-analyses showed that PLWHA who had comorbidities such as- chronic kidney disease, diabetes mellitus, hypertension and chronic cardiac disease, were not associated with a higher risk of contracting COVID-19 compared to non-PLWHA. These results, however, differ from some published studies which showed comorbidities correlated to a higher incidence of COVID-19 in the general population [26, 44]. In fact, the issue of whether comorbidities should be considered the driver of poor outcomes from COVID-19 has been a controversial and much-disputed subject [16, 45], as evidence from most studies was of a single-arm design, not matched, and had a small sample size. The included population for analysis in our study was also not matched, so we might underestimate the magnitude of the effect. Interestingly, our analysis indicated a strong correlation between COVID-19 mortality and comorbidities of chronic kidney disease, diabetes mellitus, and hypertension and chronic cardiac disease in PLWHA (Fig. 6).

These findings contribute to our understanding of the prevalence and mortality rate of COVID-19 in PLWHA. Also, this study has been conducted to confirm that a few comorbidities might drive poor outcomes among COVID-19 co-infected PLWHA. However, this study’s strength is subject to the following disadvantages that possibly limit its external validation: (1) the overall risk of bias assessment for the cohort studies and case series was moderate; however, both types of studies were evaluated to have a high-risk bias in the duration of follow-up, which might likely result in decreased death reporting [46]; (2) most of the included studies used an unmatched population design in assessing the role of comorbidities in contracting COVID-19 between PLWHA and non-PLWHA; the magnitude of the effect might be an underestimate since the sample size of PLWHA in studies was originally small; and (3) few of the included studies were performed in low-income but high-HIV burden areas (e.g., Sub-Saharan Africa). PLWHA living in these areas appeared to have poor HIV management [47]. Since our study included patients from high-income areas with better HIV management, the overall prevalence and mortality for the general population might be underestimated. Careful interpretation of results is, therefore, necessary.

Given the rapid spread of the virus and an exponential increase in cases, a strategy of mass quarantine has been implemented globally. Despite these measures to aid healthcare, a resultant disturbing impact on mental health could arise among PLWHA [48]. It has been evidenced that psycho-social depression could have a negative impact on health and behavior, and is associated with poor health outcomes [49, 50]. None of the included studies investigated mental well-being. Additional research is required to probe psycho-social effects due to COVID-19 among PLWHA.

Limitations

Our analysis faced the following limitations: (1) due to a lack of standardized reporting in included studies, our review was unable to investigate the roles of CD4 count, HIV viral load as well as ART in COVID-19 infection and prognosis; and (2) insufficient data reported in studies led to an inability to gain an insight regarding the incidence of ICU admissions, the need for the use of mechanical ventilation, and the assessing of socio-demographic disparities in COVID-19 co-infection in PLWHA.

Conclusions

Our study gained some insights into the prevalence and mortality of COVID-19 in PLWHA. We also found that comorbidities such as chronic kidney disease, diabetes mellitus, and hypertension and chronic cardiac disease, are responsible for poor outcomes in COVID-19 co-infected PLWHA. Further studies need to be carried out to validate the relationship between COVID-19 outcomes and HIV viral load, CD4 count, ART in diverse settings.

Supplementary Information

Below is the link to the electronic supplementary material.