Abstract 3455: Prevalence of monoclonal gammopathy of undetermined significance (MGUS) in a Western Nigerian population
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Date
2024-03-15
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Volume 84, Issue 6_Supplement POSTER PRESENTATIONS - PROFFERED ABSTRACTS
Abstract
Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant
condition characterized by plasma cell production of monoclonal (M) protein and is a
requisite precursor to multiple myeloma (MM). African American (AA) individuals have a
two-fold higher incidence of MGUS and MM compared to White individuals. However,
data are limited on individuals from Africa, especially using sensitive MGUS detection
methods. We examined the prevalence of MGUS in a sample of the general population
in Nigeria. Individuals aged 40 and over (n=343) were recruited through health
promotion events in Ado-Odo Ota Local Government Area of Ogun State, Nigeria, and
provided informed consent, a blood sample, and a short questionnaire. Serum was
screened at Mayo Clinic for heavy chain (HC)-MGUS using the matrix-assisted laser
desorption/ionization-time of flight (Mass-Fix) assay, which has high sensitivity for
detection of M-proteins; serum free light chains (FLC) were also measured. FLC was
abnormal if the kappa (>0.26 mg/dL) or lambda (>0.33 mg/dL) light chain (LC) was
elevated and FLC ratio (kappa/lambda) was outside the reference range (0.26-3.10).
LC-MGUS was defined as an abnormal FLC in the absence of a HC. Age- and sex
adjusted prevalence rates were directly standardized to 2010 United States (US)
population for comparison to published studies. Logistic regression was used to
examine the association of age, sex, and BMI with HC-MGUS. The mean age of
participants was 55 years (SD=10.9), and 74.6% were female. Of these, 216 (63%) had
both parents from the Yoruba tribe, 89 (26%) from the Igbo tribe and 38 (11%) from
other tribes. Overall, 33 participants (9.6%) had HC-MGUS, with 8 (2.3%) having an M
protein above 0.2 g/dL; 6 (1.7%) had LC-MGUS. HC-MGUS was predominantly IgG
isotype (48.5%), followed by IgA (27.3%), biclonal (15.2%) and IgM (9.0%). Prevalence
of HC-MGUS was 8.3% for ages 40-49, 7.7% ages 50-69 and 22% ages 70 and above.
Standardized to the US population, age and sex adjusted MGUS prevalence ages 50
and older was 17.3% (95% CI: 9.8%-24.9%) and HC-MGUS was 14.7% (95% CI: 7.7%
21.8%), similar to previously published rates of HC-MGUS using Mass-Fix screening of
AA individuals (16.5%, 95% CI: 12.2%-20.8%) (PMID: 35316833). In models that
included age, sex and BMI, older age was positively associated with HC-MGUS
(OR=3.1, 95% CI: 1.1-8.7 for ages 70+ compared to <50), while female sex (OR=0.53,
95% CI: 0.24-1.2) and overweight/obesity (OR=0.34, 95% CI: 0.16-0.75 for BMI > 25 vs.
<25) were inversely associated with HC-MGUS. We observed similar prevalence of HC
MGUS at ages 50 and above among Western Nigerian and AA populations when
screened using mass-spectrometry. Older age was positively associated with HC
MGUS while overweight and obesity were inversely associated. Studies of MGUS in
indigenous African populations may provide insight to unique cancer risk factors
compared to other populations.