Literature DB >> 25436894

Comparison of self-reported alcohol consumption to phosphatidylethanol measurement among HIV-infected patients initiating antiretroviral treatment in southwestern Uganda.

Francis Bajunirwe1, Jessica E Haberer2, Yap Boum3, Peter Hunt4, Rain Mocello4, Jeffrey N Martin5, David R Bangsberg2, Judith A Hahn5.   

Abstract

BACKGROUND: Alcohol consumption among HIV-infected patients may accelerate HIV disease progression or reduce antiretroviral therapy adherence. Self-reported alcohol use is frequently under-reported due to social desirability and recall bias. The aim of this study was to compare self-reported alcohol consumption to phosphatidylethanol (PEth), a biomarker of alcohol consumption, and to estimate the correlation between multiple measures of self-reported alcohol consumption with PEth.
METHODS: The Uganda AIDS Rural Treatment Outcomes (UARTO) cohort is located in southwestern Uganda and follows patients on ART to measure treatment outcomes. Patients complete standardized questionnaires quarterly including questions on demographics, health status and alcohol consumption. Baseline dried blood spots (DBS) were collected and retrieved to measure PEth.
RESULTS: One hundred fifty samples were tested, and 56 (37.3%) were PEth positive (≥8 ng/mL). Of those, 51.7% did not report alcohol use in the past month. Men were more likely to under-report compared to women, OR 2.9, 95% CI = 1.26, 6.65) and those in the higher economic asset categories were less likely to under-report compared to those in the lowest category (OR = 0.41 95% CI: 0.17, 0.94). Among self-reported drinkers (n = 31), PEth was highly correlated with the total number of drinking days in the last 30 (Spearman R = 0.73, p<0.001).
CONCLUSIONS: Approximately half of HIV infected patients initiating ART and consuming alcohol under-report their use of alcohol. Given the high prevalence, clinicians should assess all patients for alcohol use with more attention to males and those in lower economic asset categories who deny alcohol use. Among those reporting current drinking, self-reported drinking days is a useful quantitative measure.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25436894      PMCID: PMC4249861          DOI: 10.1371/journal.pone.0113152

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Uganda faces a dual burden of HIV and unhealthy alcohol use. The country is ranked among the top per capita consumers of alcohol in the world [1] and also has a high prevalence of HIV of 7.3% among the adults [2]. This dual burden of heavy alcohol use and HIV may present challenges because alcohol use among HIV patients has been associated with increased progression of HIV disease [3], potentially due to the effect of alcohol on the immune system [4]. Alcohol is known to interact with certain antiretroviral treatments hence reducing treatment efficacy [5], and alcohol consumption is associated with poor adherence to antiretroviral medication [6]–[8] and with excess mortality [9]–[11]. Effective treatments in the form of behavioral or pharmacological therapy [12] exist to reduce the negative effects of alcohol among those with alcohol use disorders; while screening and brief interventions may reduce alcohol consumption among problem drinkers who are not alcohol dependent [13]. To identify patients who consume alcohol, counselors and clinicians often rely on self-reported measures of alcohol consumption which may be biased toward under-report by social desirability to report what the counselor or clinician wants to hear, or out of fear of being denied ART [14] or simply recall bias. The frequency of under-reporting has been explored in very few studies, however in a nested case control from our cohort, the frequency of self-reported prior 3-month alcohol use increased from 20% to 41% when alcohol biomarker and breathalyzer testing was included as part of the study protocol and discussed during the informed consent process [15]. There are also challenges in quantifying alcohol consumption in resource limited settings such as Uganda, where drinks are often served in non-standard containers such as gourds or consumed communally. In order to accurately measure alcohol consumption, biomarkers of alcohol such as phosphatidylethanol (PEth), a phospholipid which is formed by the action of a phospholipase enzyme only in the presence of alcohol, may be useful. PEth has been tested in Uganda and shown to be highly sensitive (88%) and specific (89%) for any alcohol consumption in the prior 21 days [16]. Thus this biomarker provides a tool to estimate under report. The aim of this study was to determine the frequency of alcohol under-reporting among patients receiving HIV treatment, the characteristics of the patients who underreport, and examine the correlation of quantitative PEth results with various self-reported measures of alcohol consumption in rural Uganda.

Methods

Setting and study procedures

Participants in this study were part of the Uganda AIDS Rural Treatment Outcomes (UARTO) cohort study located in Mbarara, which is in southwestern Uganda. The UARTO cohort began in July 2005 and recruited treatment-naïve patients initiating ART at Mbarara Hospital's HIV clinic. A study representative approached individuals collecting new antiretroviral prescriptions from the pharmacy, and determined their eligibility and interest in participation. Those who were at least 18 years of age and lived within 50 kilometers of the clinic were eligible for the study. The cohort is fully recruited now but follow-up is still ongoing.

Ethics statement

All study procedures were approved by the Institutional review Boards of the Mbarara University of Science and Technology, Partners HealthCare, the University of California, San Francisco, and the Uganda National Council of Science and Technology. All participants enrolled in the study provided written informed consent. As part of the consent process, participants agreed to have their blood samples stored, and were told that the blood may be tested to see if they had consumed alcohol. Upon recruitment, UARTO participants underwent a baseline interview and phlebotomy. Participants completed standardized interviewer-administered surveys detailing demographics, household socioeconomic profile, alcohol use, mental and physical health status and depression scores among other variables, as well as CD4 cell count and HIV RNA quantification, on a quarterly basis.

Measurement of alcohol consumption

We asked study participants when they last consumed alcohol, and how many days in the prior 30 they consumed alcohol. We additionally asked the typical number of drinks consumed per drinking day for those drinking alcohol in forms other than gourds or non-standard drink containers. The number of drinks per day was used to calculate the total number of drinks in the last 30 days. We asked the total amount of money (in Ugandan shillings) that the participants spent on their own alcohol in the prior 30 days. Lastly, we asked the number of days the participants drank until they reached the following stages of intoxication (in descending order of severity): drinking until feeling stuporous or becoming unconscious; drinking until it was difficult to speak or see clearly or walk; drinking until it was difficult to think clearly; and drinking until feeling uninhibited or a false sense of confidence. We added the number of days the participants reported these to create a variable representing the number of days of drinking until intoxication.

Covariates

Depression was assessed using the 15-items of the Hopkins Symptoms checklist depression scale (HSCL) that screen for depression [17]. The tool has been used widely in the region and has been found to have high validity and reliability [18]. We used a cut-off of average value of greater than or equal to 1.75 to indicate a positive screen for clinical depression. Literacy levels were assessed using simple reading cards in the local language and English. Socio-economic status was assessed using education, electricity in the home, asset category and land ownership. Economic asset categories to indicate household wealth were constructed using Principal components analysis [19]. Low represents the bottom two quintiles and the rest were classified in a single category representing medium to high assets.

Dried blood spot collection and phosphatidylethanol testing

Phospatidylethanol (PEth) is a metabolite of alcohol and is a highly sensitive and specific biomarker for alcohol consumption and has been shown to have the highest sensitivity for detecting alcohol intake over the last 21 days compared to the other biomarkers such as carbohydrate deficient transferin (CDT), mean corpuscular volume (MCV) and gamma-glutamyl transferase [20]. In a previous study of persons with HIV attending the Mbarara Hospital HIV Clinic different from those enrolled in the current study, we found that PEth was 88% sensitive and 89% specific for any alcohol consumption in the prior 21 days. [16] In that study any alcohol consumption was defined as either detectable alcohol use on any daily breathalyzer test conducted at home or a pre-arranged drinking establishment, or any and alcohol use self-reported on a daily survey. In addition, the study found that PEth was highly correlated with several quantitative measures of alcohol consumption, such as number of days drinking (Spearman r = 0.74); others have shown similar results in HIV uninfected populations. [21], [22] We collected dried blood spots (DBS) at all study visits beginning July 2011, and retrieved those for the baseline visits for the first 150 patients in August 2013, therefore samples were stored for a maximum of two years. PEth testing was conducted at the United States Drug Testing Laboratory, Des Plaines, IL, using a previously published method. [23] PEth was detected in standard dried blood spot punches (3.1 mm) using an Agilent 6460 liquid chromatography-tandem mass spectrometry (LC-MS/MS) system following extraction into methanol. The most prevalent PEth isomer, palmitoyl (PEth 16∶0)/oleoyl (PEth 18∶1), was detected. Positive tests were confirmed with a repeat test, and the average of the two results was used. The limit of detection was 2 ng/mL, the limit of quantitation was 8 ng/mL, and the assay was linear up to 800 ng/mL.

Statistical analysis

We calculated the proportions for categorical variables and means or medians for continuous variables. We determined the sensitivity of self-reported alcohol use compared to PEth. Participants were considered to have under-reported alcohol consumption if they tested positive for PEth (≥8 ng/mL, the current limit of quantification) but report no alcohol consumption in the last 30 days. We use logistic regression to determine the factors associated with under-reporting. We conducted 3 sets of logistic regression in which the outcome variable was a PEth positive result. These regressions were conducted (1) among all participants, (2) among those who reported prior 30 day drinking and/or those who were PEth positive, collectively called drinkers, and (3), among those who reported no drinking in the prior 30 days. We used the Wilcoxon rank sum test (Mann-Whitney) to compare the median PEth values of those who did to those who did not report any 30 day drinking, overall and by sex, among those who tested positive for PEth. Lastly, we calculated Spearman's rank correlations between the quantitative PEth values and several self-reported measures of alcohol consumption among those who reported any 30 day drinking.

Results

Baseline characteristics

Of the 150 participants, 65% were female, 43% were aged 31 to 45 years and 53% were of Protestant religion (Table 1). Almost one quarter (23%) of the respondents could not read a sentence and 26% screened positive for depression.
Table 1

Baseline characteristics (n = 150).

CharacteristicN (%)
Gender
Male52 (34.6)
Female98 (65.4)
Age
18–3063 (42.0)
31–4565 (43.3)
Over 4522 (14.7)
Religion
Protestant79 (52.7)
Catholic45 (30.0)
Moslem17 (11.3)
Pentecostal9 (6.0)
Education
None28 (18.6)
Primary78 (52.0)
Secondary and above44 (29.3)
Own land
No63 (42.0)
Yes87 (58.0)
Literacy
Cannot read at all34 (23.3)
Able to read parts of a sentence26 (17.8)
Able to read whole sentence86 (58.9)
Electricity in the home
Yes38 (25.4)
No112 (74.6)
Economic asset category*
Low43 (28.7)
Medium to High107 (71.3)
Screened positive for depression (Hopkins Symptoms Checklist)
No111 (74.0)
Yes39 (26.0)
Health status (missing = 7)
No serious illness134 (93.7)
Serious illness9 (6.3)
Self reported alcohol consumption in past 30 days
None119 (79.3)
Some31 (20.7)
PEth
Negative94 (62.7)
Positive (≥8 ng/ml)56 (37.3)

*Low = bottom 2 quintiles.

*Low = bottom 2 quintiles.

Alcohol consumption

Overall, 21% reported consuming alcohol in the past 30 days, but 37% tested positive for PEth. Of those reporting no alcohol consumption in the prior 30 days, 25% were positive for PEth (Table 2). Thirty-one patients reported use of alcohol and of these, 4 or 13% of them tested negative for PEth. Among the 60 drinkers (by self-report and/or PEth results), 31 reported having consumed alcohol, giving self-report a sensitivity of 48.2% (95% CI 34.7, 62%). The sensitivity by sex was 48.4% (95% CI 30.2, 66.9) for the men and 48% (95% CI 27.8, 68.7) for the women and the two were not statistically different from each other (Fisher's exact 2-sided p-value = 1.0).
Table 2

Sensitivity for self reported alcohol use, overall and by sex.

PEth results
Self report alcohol use, prior 30 daysPositiveNegativeTotal
Overall, n = 150
Yes 27 (48.2)4 (4.4) 31
No 29 (51.8)90 (95.6) 119
Total 56 94 150
Among women, n = 98
Yes 12 (48.0)4 (5.5) 16
No 13 (52.0)69 (94.5) 82
Total 25 73 98
Among men, n = 52
Yes 15 (48.3)0 (0.0) 15
No 16 (51.7)21 (100) 37
Total 31 21 52

PEth levels by self report

Among those testing PEth positive, the median PEth value was higher among those reporting alcohol use (median = 477) compared to those who did not report any use of alcohol (median = 135.5) in the prior 30 days (Wilcoxon rank sum test p = 0.02, Table 3). The difference in the medians was statistically significant among the men (p = 0.01) but not the women (p = 0.14).
Table 3

PEth results among those with PEth>8 ng/mL, by self-reported alcohol consumption and by sex.

Self report alcohol use, prior 30 daysMedian PEth ng/mL (25th, 75th percentile)Wilcoxon rank sum test (Self report yes vs no)
Overall
Yes, n = 27477.0 (51.8, 850)
No, n = 29135.5 (31.5, 322) z = −2.43, p = 0.02
Total, n = 56 191.3 (47.4, 683)
Among women
Yes, n = 12111.2 (34.5, 608.8)
No, n = 1331.5 (15.9, 116.0) z = −1.46, p = 0.14
Total, n = 25 51.8 (19.2, 432.5)
Among men
Yes, n = 15733.5 (338.5, 1228)
No, n = 16191.3 (132.5, 360.3) z = −2.53, p = 0.01
Total, n = 31 351.5 (136.0, 850.0)

Predictors of under-reporting

Age, level of education, health status and history of depression were not associated with alcohol under-reporting in any of the bivariate logistic regression analyses (Table 4). In the entire sample, the odds of under reporting are almost three fold among men compared to women (OR = 2.93, 95%CI 1.26, 6.65), and even higher when the analysis was restricted to those not reporting any drinking (OR = 4.04, 95% CI 1.67, 9.74). The odds of under-report were 60% lower in the high/medium asset category compared to the low one (OR = 0.41, 95% CI 0.17, 0.94). Among drinkers, there was no significant association between gender and under-report (OR = 1.33 and 95% CI 0.48, 3.62). The odds of under-reporting were lower among those with partial literacy compared to no ability to read a sentence in the entire sample (OR = 0.17 and 95% CI 0.03, 0.87) and among those not reporting drinking (OR = 0.17 and 95% CI 0.03, 0.89).
Table 4

Bivariate logistic regression to determine the predictors of under-reporting alcohol use.

CharacteristicUnder-report* in the entire sample (29 of 150) OR(95% CI)Under-report* among drinkers (Self-reported and/or PEth positive) (29 of 60) OR(95% CI)Under-report* among those not reporting drinking (29 of 119) OR (95% CI)
Gender
Female1.001.001.00
Male 2.93 (1.26, 6.65) 1.33 (0.48, 3.62) 4.04 (1.67, 9.74)
Age
18–301.001.001.00
31–451.12 (0.43, 2.64)0.94 (0.31, 2.85)1.11 (0.44, 2.84)
Over 451.74 (0.56, 5.55)2.36 (0.48, 11.72)1.64 (0.51, 5.31)
Education
None1.001.001.00
Primary school0.42 (0.16,1.14)0.45 (0.12, 1.68)0.41 (0.15, 1.16)
Secondary and above0.39 (0.13, 1.23)0.38 (0.09, 1.67)0.40 (0.12, 1.31)
Literacy
Cannot read a sentence1.001.001.00
Read parts of a sentence 0.17 (0.03, 0.87) 0.18 (0.03, 1.19) 0.17 (0.03, 0.89)
Read a whole sentence0.41 (0.16, 1.01)0.42 (0.13, 1.43)0.40 (0.15, 1.04)
Own land
No1.001.001.00
Yes0.62 (0.27, 1.38)0.67 (0.24, 1.86)0.59 (0.255, 1.38)
Electricity in the home
No1.001.001.00
Yes1.26 (0.46, 2.82)1.09 (0.35, 3.44)1.18 (0.45, 3.03)
Economic asset category
Low1.001.001.00
Medium to High 0.41 (0.17, 0.94) 0.58 (0.21, 1.67) 0.35 (0.14, 0.85)
Screened positive for depression (Hopkins Symptoms Checklist)
No1.001.001.00
Yes0.88(0.34, 2.27)0.91 (0.28, 2.95)0.88 (0.33, 2.31)
Health status (serious illness)
None1.001.001.00
Present1.13 (0.22, 5.76)1.78 (0.15, 20.86)0.97 (0.18, 5.12)
*Under-report defined as PEth+ but no self-reported drinking in the prior 30 days

Quantitative results

The median values for PEth and for self-reported measures of alcohol consumption among those reporting any alcohol consumption are reported in Table 5, along with the Spearman correlations between self-reported alcohol consumption and PEth. PEth was significantly correlated with the total number of days of drinking in the past 30 days (Spearman correlation  = 0.73, p<0.01), the total number of drinks in the past 30 days (Spearman correlation  = 0.72, p<0.01), and the amount of money spent on alcohol (Spearman correlation  = 0.43, p = 0.02).
Table 5

Measures of alcohol consumption and correlations with PEth, among those reporting any alcohol consumption, prior 30 days (n = 31).

Measure of alcohol consumptionMedian (25th, 75th percentile)Spearman correlation with PEth valuep value
PEth (ng/mL)405.5 (37.1, 796.5)
Number of days drinking3.0 (2.0, 8.0)0.73<0.01
Typical number of drinks per drinking day* 3.5 (2.5, 7.0)0.350.09
Total number of drinks (# days drinking x # drinks per drinking day)* 10.5 (6, 40)0.72<0.01
Total amount of money spent on alcohol (USD)4.0 (1.2, 10)0.430.02
Number of days drinking until uninhibited or more intoxicated0 (0,0)0.240.19

*n = 24 due to missing values for those drinking from shared or non-standard vessels.

*n = 24 due to missing values for those drinking from shared or non-standard vessels.

Discussion

Our study used a sensitive and specific alcohol biomarker to demonstrate that a high proportion of clients initiating ART at an HIV clinic at a large urban center in Uganda under-report their alcohol consumption. At the time of study recruitment, HIV clinic patients received counseling for at least 2 weekly sessions before initiation of therapy; this counseling included instructions to avoid alcohol consumption while on treatment. It is therefore not surprising that a significant proportion of patients under-reported their alcohol consumption. This is likely because of social desirability bias. Other authors have noted this concern. [14], [24] Our findings are consistent with our previous study in which we used %carbohydrate specific transferrin (%CDT), a biomarker for heavy alcohol use to examine under-reporting. [25] In that study, we found that 7% of those denying alcohol use were %CDT positive, a percent lower than found here but likely due to the low sensitivity of %CDT. [26] This study adds to the literature by using PEth, a more sensitive marker, demonstrating that 25% of those denying recent use were PEth positive and slightly over 50% of those who were PEth positive denied recent use. Gender and economic asset index were significant predictors of under-reporting alcohol use overall and among those not reporting alcohol use. To the best of our knowledge, no other studies have demonstrated this before. Among drinkers, men were no more likely than women to under report. The high prevalence of alcohol use warrants screening for all patients, however the results suggest that men and particularly those with fewer assets may need more scrutiny for possible under-reporting if they deny any alcohol use. These patients may need reassurance that disclosure of alcohol use will in no way jeopardize their chances of initiating ART. Currently, clinics in Uganda do not have any strategies in place to reduce under-reporting. No other characteristic was associated with under-reporting alcohol use. Our data also show a strong correlation between PEth and self-report measures of alcohol consumption among those who did report any alcohol consumption. The number of days of drinking in the past 30 days showed the strongest correlation (Spearman = 0.73) with the quantitative PEth result. This suggests that among those reporting any recent alcohol consumption, reporting of the frequency of consuming alcohol is highly valid, and also suggests that PEth may be a useful quantitative measure when self-report is unavailable or difficult to obtain. It is also notable that even among self-reported drinkers, the level of alcohol consumption was fairly low, with a median of 3 drinking days in the prior month. This is consistent with our previous findings of a large number of drinkers reporting reducing their alcohol consumption at the time of ART initiation in a previous wave of this same cohort [27]. Our data shows low correlation between number of days drinking until intoxicated and typical number of drinks per day with PEth probably because of under-report. However, the low correlation does not necessarily mean these measures are less useful. PEth was detectable though results were significantly lower among those not reporting any alcohol consumption. This may imply that under-reporters may be lighter drinkers than those reporting drinking. In an analysis stratified by gender, the difference remained statistically significant among men but not the women. This may imply that women drinkers have similar levels of alcohol consumption whether they under-report or correctly report their alcohol consumption. However, this may be because of the small sample size. Also, because the women's PEth values are lower overall, even among those reporting alcohol use, their data represents the end of the scale where the difference is small. Regardless, the level of PEth was high among all those with detectable PEth, with a median of 191 ng/ml, which is well above the recent cutoff of 80 ng/ml which indicated drinking> = 4 drinks daily in a recent study among a group of patients with liver disease [28]. Our study has some weaknesses. PEth may not be completely sensitive and specific, therefore we may have under or over-estimated under-report. Secondly, there were some who reported drinking but were PEth negative, although these were very few. Our self-report measure spans 30 days while the biomarker spans 21 days; hence self-report may have reflected alcohol use beyond the window detectable by PEth. Also, it is still unclear whether PEth when assessed using LC/MS/MS is measuring any alcohol use or heavy alcohol use. [29] We took a conservative approach and used positive PEth results to suggest any alcohol use; however, it is possible that some PEth negatives may have consumed alcohol although moderately. This is supported by a recent study where participants with a negative PEth and reporting alcohol use were mainly light drinkers. [28] Our study also warrants the necessity for clinicians to screen HIV infected patients initiating ART for alcohol use, especially in countries such as Uganda where alcohol consumption is high among drinkers. The high cost and limited availability of biomarkers restricts their use to research and limits their application in clinical settings. In conclusion, our study has shown that many of HIV infected patients receiving ART under-report their alcohol consumption. Clinicians should screen the men more for possible under-reporting of alcohol consumption. Interventions depend on the reporting of alcohol use, therefore future research should develop ways to increase self-report.
  25 in total

1.  PHosphatidylethanol (PEth) concentrations in blood are correlated to reported alcohol intake in alcohol-dependent patients.

Authors:  Steina Aradottir; Gulber Asanovska; Stefan Gjerss; Per Hansson; Christer Alling
Journal:  Alcohol Alcohol       Date:  2006-04-19       Impact factor: 2.826

2.  A temporal and dose-response association between alcohol consumption and medication adherence among veterans in care.

Authors:  R Scott Braithwaite; Kathleen A McGinnis; Joseph Conigliaro; Stephen A Maisto; Stephen Crystal; Nancy Day; Robert L Cook; Adam Gordon; Michael W Bridges; Jason F S Seiler; Amy C Justice
Journal:  Alcohol Clin Exp Res       Date:  2005-07       Impact factor: 3.455

3.  Constructing socio-economic status indices: how to use principal components analysis.

Authors:  Seema Vyas; Lilani Kumaranayake
Journal:  Health Policy Plan       Date:  2006-10-09       Impact factor: 3.344

4.  Mortality among participants in the Multicenter AIDS Cohort Study and the Women's Interagency HIV Study.

Authors:  Nancy A Hessol; Ann Kalinowski; Lorie Benning; Joanne Mullen; Mary Young; Frank Palella; Kathryn Anastos; Roger Detels; Mardge H Cohen
Journal:  Clin Infect Dis       Date:  2006-12-12       Impact factor: 9.079

5.  Validation of blood phosphatidylethanol as an alcohol consumption biomarker in patients with chronic liver disease.

Authors:  Scott H Stewart; David G Koch; Ira R Willner; Raymond F Anton; Adrian Reuben
Journal:  Alcohol Clin Exp Res       Date:  2014-05-21       Impact factor: 3.455

6.  Phosphatidylethanol as a sensitive and specific biomarker: comparison with gamma-glutamyl transpeptidase, mean corpuscular volume and carbohydrate-deficient transferrin.

Authors:  Susanne Hartmann; Steina Aradottir; Marc Graf; Gerhard Wiesbeck; Otto Lesch; Katrin Ramskogler; Manfred Wolfersdorf; Christer Alling; Friedrich Martin Wurst
Journal:  Addict Biol       Date:  2007-03       Impact factor: 4.280

7.  Combined pharmacotherapies and behavioral interventions for alcohol dependence: the COMBINE study: a randomized controlled trial.

Authors:  Raymond F Anton; Stephanie S O'Malley; Domenic A Ciraulo; Ron A Cisler; David Couper; Dennis M Donovan; David R Gastfriend; James D Hosking; Bankole A Johnson; Joseph S LoCastro; Richard Longabaugh; Barbara J Mason; Margaret E Mattson; William R Miller; Helen M Pettinati; Carrie L Randall; Robert Swift; Roger D Weiss; Lauren D Williams; Allen Zweben
Journal:  JAMA       Date:  2006-05-03       Impact factor: 56.272

Review 8.  Biochemical markers of alcoholism.

Authors:  Minna L Hannuksela; Marja K Liisanantti; Antti E T Nissinen; Markku J Savolainen
Journal:  Clin Chem Lab Med       Date:  2007       Impact factor: 3.694

9.  Alcohol consumption and antiretroviral adherence among HIV-infected persons with alcohol problems.

Authors:  Jeffrey H Samet; Nicholas J Horton; Seville Meli; Kenneth A Freedberg; Anita Palepu
Journal:  Alcohol Clin Exp Res       Date:  2004-04       Impact factor: 3.455

10.  Alcohol consumption and HIV disease progression.

Authors:  Jeffrey H Samet; Debbie M Cheng; Howard Libman; David P Nunes; Julie K Alperen; Richard Saitz
Journal:  J Acquir Immune Defic Syndr       Date:  2007-10-01       Impact factor: 3.731

View more
  52 in total

1.  Phosphatidylethanol in Comparison to Self-Reported Alcohol Consumption Among HIV-Infected Women in a Randomized Controlled Trial of Naltrexone for Reducing Hazardous Drinking.

Authors:  Yan Wang; Xinguang Chen; Judith A Hahn; Babette Brumback; Zhi Zhou; Maria J Miguez; Robert L Cook
Journal:  Alcohol Clin Exp Res       Date:  2017-12-05       Impact factor: 3.455

2.  Alcohol use and relationship quality among South African couples.

Authors:  Sarah E Woolf-King; Amy A Conroy; Katherine Fritz; Mallory O Johnson; Victoria Hosegood; Heidi van Rooyen; Lynae Darbes; Nuala McGrath
Journal:  Subst Use Misuse       Date:  2018-11-08       Impact factor: 2.164

3.  Concordance of Self- and Partner-Reported Alcohol Consumption Among Couples Experiencing Intimate Partner Violence in Zambia.

Authors:  Jeremy C Kane; Sarah M Murray; Michael J Vinikoor; M Claire Greene; Shoshanna L Fine; Ravi Paul; Laura K Murray
Journal:  Alcohol Clin Exp Res       Date:  2019-10-20       Impact factor: 3.455

4.  Alcohol Use and HIV Disease Progression in an Antiretroviral Naive Cohort.

Authors:  Judith A Hahn; Debbie M Cheng; Nneka I Emenyonu; Christine Lloyd-Travaglini; Robin Fatch; Starley B Shade; Christine Ngabirano; Julian Adong; Kendall Bryant; Winnie R Muyindike; Jeffrey H Samet
Journal:  J Acquir Immune Defic Syndr       Date:  2018-04-15       Impact factor: 3.731

5.  Declining and rebounding unhealthy alcohol consumption during the first year of HIV care in rural Uganda, using phosphatidylethanol to augment self-report.

Authors:  Judith A Hahn; Nneka I Emenyonu; Robin Fatch; Winnie R Muyindike; Allen Kekiibina; Adam W Carrico; Sarah Woolf-King; Stephen Shiboski
Journal:  Addiction       Date:  2015-11-05       Impact factor: 6.526

6.  The Association Between Changes in Alcohol Use and Changes in Antiretroviral Therapy Adherence and Viral Suppression Among Women Living with HIV.

Authors:  Nikita Barai; Anne Monroe; Catherine Lesko; Bryan Lau; Heidi Hutton; Cui Yang; Anika Alvanzo; Mary Elizabeth McCaul; Geetanjali Chander
Journal:  AIDS Behav       Date:  2017-07

Review 7.  Alcohol Use and Human Immunodeficiency Virus (HIV) Infection: Current Knowledge, Implications, and Future Directions.

Authors:  Emily C Williams; Judith A Hahn; Richard Saitz; Kendall Bryant; Marlene C Lira; Jeffrey H Samet
Journal:  Alcohol Clin Exp Res       Date:  2016-09-22       Impact factor: 3.455

8.  Alcohol Use and Food Insecurity Among People Living with HIV in Mbarara, Uganda and St. Petersburg, Russia.

Authors:  Gregory J Patts; Debbie M Cheng; Nneka Emenyonu; Carly Bridden; Natalia Gnatienko; Christine A Lloyd-Travaglini; Christine Ngabirano; Tatiana Yaroslavtseva; Winnie R Muyindike; Sheri D Weiser; Evgeny M Krupitsky; Judith A Hahn; Jeffrey H Samet
Journal:  AIDS Behav       Date:  2017-03

9.  Alcohol Interactive Toxicity Beliefs and ART Non-adherence Among HIV-Infected Current Drinkers in Mbarara, Uganda.

Authors:  Robin Fatch; Nneka I Emenyonu; Winnie Muyindike; Allen Kekibiina; Sarah Woolf-King; Judith A Hahn
Journal:  AIDS Behav       Date:  2017-07

10.  Natural language processing and machine learning to identify alcohol misuse from the electronic health record in trauma patients: development and internal validation.

Authors:  Majid Afshar; Andrew Phillips; Niranjan Karnik; Jeanne Mueller; Daniel To; Richard Gonzalez; Ron Price; Richard Cooper; Cara Joyce; Dmitriy Dligach
Journal:  J Am Med Inform Assoc       Date:  2019-03-01       Impact factor: 4.497

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.