Maria Gabriella Donà

Dr. Maria Gabriella Donà

STI/HIV Unit, San Gallicano Dermatological Institute, IRCCS, Rome, Rome, Lazio, Italy
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2021 in The Lancet HIV
Verified
Journal Article
Open access
FWFeixue Wei
Feixue Wei
MGMichael M Gaisa
Michael M Gaisa
GDGypsyamber D'SOuza
Gypsyamber D'SOuza
NXNingshao Xia
Ningshao Xia
AGAnna R Giuliano
Anna R Giuliano
GCGary M Clifford
Gary M Clifford
Robust age-specific estimates of anal human papillomavirus (HPV) and high-grade squamous intraepithelial lesions (HSIL) in men can inform anal cancer prevention efforts. We aimed to evaluate the age-specific prevalence of anal HPV, HSIL, and their combination, in men, stratified by HIV status and sexuality. We did a systematic review for studies on anal HPV infection in men and a pooled analysis of individual-level data from eligible studies across four groups: HIV-positive men who have sex with men (MSM), HIV-negative MSM, HIV-positive men who have sex with women (MSW), and HIV-negative MSW. Studies were required to inform on type-specific HPV infection (at least HPV16), detected by use of a PCR-based test from anal swabs, HIV status, sexuality (MSM, including those who have sex with men only or also with women, or MSW), and age. Authors of eligible studies with a sample size of 200 participants or more were invited to share deidentified individual-level data on the above four variables. Authors of studies including 40 or more HIV-positive MSW or 40 or more men from Africa (irrespective of HIV status and sexuality) were also invited to share these data. Pooled estimates of anal high-risk HPV (HR-HPV, including HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and 68), and HSIL or worse (HSIL+), were compared by use of adjusted prevalence ratios (aPRs) from generalised linear models. The systematic review identified 93 eligible studies, of which 64 contributed data on 29 900 men to the pooled analysis. Among HIV-negative MSW anal HPV16 prevalence was 1·8% (91 of 5190) and HR-HPV prevalence was 6·9% (345 of 5003); among HIV-positive MSW the prevalences were 8·7% (59 of 682) and 26·9% (179 of 666); among HIV-negative MSM they were 13·7% (1455 of 10 617) and 41·2% (3798 of 9215), and among HIV-positive MSM 28·5% (3819 of 13 411) and 74·3% (8765 of 11 803). In HIV-positive MSM, HPV16 prevalence was 5·6% (two of 36) among those age 15-18 years and 28·8% (141 of 490) among those age 23-24 years (ptrend=0·0091); prevalence was 31·7% (1057 of 3337) among those age 25-34 years and 22·8% (451 of 1979) among those age 55 and older (ptrend<0·0001). HPV16 prevalence in HIV-negative MSM was 6·7% (15 of 223) among those age 15-18 and 13·9% (166 of 1192) among those age 23-24 years (ptrend=0·0076); the prevalence plateaued thereafter (ptrend=0·72). Similar age-specific patterns were observed for HR-HPV. No significant differences for HPV16 or HR-HPV were found by age for either HIV-positive or HIV-negative MSW. HSIL+ detection ranged from 7·5% (12 of 160) to 54·5% (61 of 112) in HIV-positive MSM; after adjustment for heterogeneity, HIV was a significant predictor of HSIL+ (aPR 1·54, 95% CI 1·36-1·73), HPV16-positive HSIL+ (1·66, 1·36-2·03), and HSIL+ in HPV16-positive MSM (1·19, 1·04-1·37). Among HPV16-positive MSM, HSIL+ prevalence increased with age. High anal HPV prevalence among young HIV-positive and HIV-negative MSM highlights the benefits of gender-neutral HPV vaccination before sexual activity over catch-up vaccination. HIV-positive MSM are a priority for anal cancer screening research and initiatives targeting HPV16-positive HSIL+. International Agency for Research on Cancer.

1 May 2014 in Oral Oncology
Verified
Journal Article
Closed access
CNCecilia Nordfors
Cecilia Nordfors
AVAndrea Vlastos
Andrea Vlastos
Juan DuJuan Du
Juan Du
AÄAndreas Ährlund-Richter
Andreas Ährlund-Richter
NTNikolaos Tertipis
Nikolaos Tertipis
Tina DalianisTina Dalianis
Tina Dalianis

1 June 2012 in Journal of Clinical Virology
Verified
Journal Article
Closed access
Maria Gabriella DonàMaria Gabriella Donà
Maria Gabriella Donà
GPGuido Palamara
Guido Palamara
ACAldo Di Carlo
Aldo Di Carlo
Alessandra LatiniAlessandra Latini
Alessandra Latini
AVAmina Vocaturo
Amina Vocaturo
Massimo GiulianiMassimo Giuliani
Massimo Giuliani

23 July 2022 in Clinical Infectious Diseases
Verified
Journal Article
Closed access
PDF file
FWFeixue Wei
Feixue Wei
MGMarc T Goodman
Marc T Goodman
NXNingshao Xia
Ningshao Xia
JZJun Zhang
Jun Zhang
AGAnna R Giuliano
Anna R Giuliano
GCGary M Clifford
Gary M Clifford
Background: Understanding the natural history of anal high-risk human papillomavirus (hrHPV) infection is key for designing anal cancer prevention programs but has not been systematically characterized. Methods: We reanalyzed data from 34 studies including 16 164 individuals in 6 risk groups defined by human immunodeficiency virus (HIV) status, sex, and male sexuality: men who have sex with men (MSM) and people with HIV (MSMWH), HIV-negative MSM, women with HIV (WWH), HIV-negative women, men who have sex with women (MSW) with HIV (MSWWH), and HIV-negative MSW. We used Markov models to estimate incidence and clearance of 13 hrHPV types and their determinants. Results: Human papillomavirus (HPV) 16 had the highest incidence-clearance ratio of the hrHPV types. MSMWH had the highest hrHPV incidence (eg, 15.5% newly HPV-16 infected within 2 years), followed by HIV-negative MSM (7.5%), WWH (6.6%), HIV-negative women (2.9%), MSWWH (1.7%), and HIV-negative MSW (0.7%). Determinants of HPV-16 incidence included HIV status and number of sexual partners for MSM, women, and MSW, and anal sex behavior for MSM only. HPV-16 clearance was lower for people with HIV (PWH) and lower for prevalent than incident infection. Among MSM, increasing age was associated with lower clearance of prevalent, but not incident, HPV-16 infection. Conclusions: This robust and unifying analysis of anal hrHPV natural history is essential to designing and predicting the impact of HPV vaccination and HPV-based screening programs on anal cancer prevention, particularly in MSM and PWH. Importantly, it demonstrates the higher carcinogenic potential of longstanding anal prevalent hrHPV infection than more recent incident infection.


27 July 2020 in Sexually Transmitted Infections
Verified
Journal Article
Open access
PDF file
Alessandra LatiniAlessandra Latini
Alessandra Latini
FMFrancesca Magri
Francesca Magri
Maria Gabriella DonàMaria Gabriella Donà
Maria Gabriella Donà
MGMassimo Giuliani
Massimo Giuliani
ACAntonio Cristaudo
Antonio Cristaudo
MZMauro Zaccarelli
Mauro Zaccarelli