Skip to main content
. 2024 Oct 10;73(40):896–902. doi: 10.15585/mmwr.mm7340a2

TABLE 2. Odds ratios of mpox associated with reported intimate and nonintimate close contact with a person with mpox — 12 jurisdictions, United States,* August 2022–July 2023.

Characteristic Unadjusted OR (95% CI)
n = 207 p-value Adjusted OR (95% CI)
n = 159 p-value
Age, yrs
1.1 (1.0–1.1)
0.033
1.1 (1.0–1.2)
0.157
Race and ethnicity §
White, non-Hispanic
Ref

Ref

Black or African American, non-Hispanic
1.7 (0.7–3.8)
0.210
0.7 (0.1–3.5)
0.640
Hispanic or Latino
2.4 (1.0–5.4)
0.043
3.4 (0.7–16.5)
0.135
Other, non-Hispanic
1.1 (0.3–3.3)
0.904
0.2 (0–1.6)
0.123
Gender identity
Male
Ref



Transgender female
2.6 (0.3–22.0)
0.375


Transgender male




Another gender identity
0.3 (0.1–1.4)
0.114


No. of sexual partners
0.8 (0.7–1.0)
0.014
0.9 (0.6–1.3)
0.507
HIV status and PrEP/ARV use**
HIV negative, not on PrEP
Ref

Ref

HIV negative, on PrEP
0.2 (0.1–0.6)
0.004
0.3 (0.1–2.2)
0.247
HIV positive, not on ARV
1.0 (0.1–11.2)
0.968
0.3 (0–19.0)
0.586
HIV positive, on ARV but nonadherent
0.7 (0.2–2.6)
0.588
0.4 (0–4.5)
0.469
HIV positive, on ARV and adherent
0.5 (0.2–1.7)
0.279
1.0 (0.1–8.3)
0.985
Immunocompromising condition or medication ††
1.8 (0.5–6.6)
0.393


STI history §§
1.9 (0.9–4.0)
0.105


Mpox vaccination status ¶¶
Not vaccinated
Ref

Ref

Partially vaccinated
0.1 (0–0.2)
<0.001
0 (0–0.1)
<0.001
Fully vaccinated
0.1 (0–0.3)
<0.001
0.1 (0–0.4)
0.005
Intimate contact
Condomless receptive anal sex
3.2 (1.4–7.3)
0.006
5.4 (1.2–24.6)
0.031
Condomless insertive anal sex
2.8 (1.3–6.1)
0.009
1.0 (0.2–5.6)
0.980
Anal sex with a condom
1.6 (0.4–5.8)
0.510
0.5 (0–10.7)
0.661
Received oral sex without a condom
2.7 (1.3–5.4)
0.006
0.8 (0.2–3.4)
0.803
Gave oral sex without a condom
2.0 (1.0–4.1)
0.046
2.6 (0.6–11.2)
0.215
Gave or received oral sex with a condom
0.5 (0.2–1.6)
0.277
0.3 (0–3.7)
0.376
Close contact at a mass gathering where persons were partially undressed and touching
0.3 (0.1–0.7)
0.008
0.3 (0.1–1.3)
0.113
Nonintimate contact
Provided in-home care
0.9 (0.3–3.2)
0.926
4.3 (0.2–79.9)
0.329
Shared food, utensils, or dishes
0.9 (0.4–2.0)
0.851
1.3 (0.3–5.5)
0.682
Shared towels, bedding, or clothing
2.3 (1.1–5.0)
0.034
1.7 (0.4–6.9)
0.480
Shared drug equipment 0.4 (0.2–1.2) 0.108 0.1 (0–1.1) 0.058

Abbreviations: ARV = antiretroviral; OR = odds ratio; PrEP = preexposure prophylaxis; Ref = referent group; STI = sexually transmitted infection.

* Case- and control patients were recruited from the following 12 U.S. jurisdictions: California (excluding Los Angeles County), Colorado, Connecticut, Georgia, District of Columbia, Los Angeles County, Maryland, Minnesota, New York (excluding New York City), New York City, Oregon, and Tennessee.

P-value calculated using logistic regression with a random intercept for jurisdiction.

§ Participants reporting Hispanic ethnicity were categorized as Hispanic or Latino and might be of any race. The Other race category includes Asian, Native Hawaiian or other Pacific Islander, and American Indian or Alaska Native persons.

Participants were asked to report the number of sexual partners they had had during the 3 weeks before completing the survey.

** HIV PrEP use was defined as use at time of survey and was calculated among persons who did not report living with HIV. HIV ARV use was defined as use at time of survey and was calculated among persons who reported living with HIV; nonadherence was defined as missing ≥2 doses during the previous 30 days.

†† Immunocompromising conditions were based on self-report and defined as having a medical condition that weakens the immune response, not including HIV, or taking a medicine that weakens the immune response.

§§ Participants were asked to report STI diagnoses during the 3 weeks before completing the survey.

¶¶ Participants were categorized as not vaccinated if no reported doses were received on or before the index date. Participants were categorized as partially vaccinated if they received 1 dose ≥14 days before the index date and fully vaccinated if they received 2 doses ≥24 days apart (to allow for a 4-day window), with the second dose received ≥14 days before the index date. Participants who received their first vaccine dose ≤13 days before their index date were excluded.