Hirsutism is excess terminal hair in a male pattern affecting 5 - 10% of women aged from 18 to 45 years (
7). Although this is generally associated with hyperandrogenemia, one-half of women with mild symptoms have normal androgen levels. While the most common cause is PCOS, many medications can also cause hirsutism. In patients whose hirsutism is not related to medication use, evaluation is focused on testing for endocrinopathies and neoplasms, such as PCOS, adrenal hyperplasia, thyroid dysfunction, Cushing syndrome, and androgen-secreting tumors (
8).
Hirsutism is often classified in terms of the distribution and degree of hair growth. We used the Ferriman-Gallwey scale, which is the most widely recognized scoring method that evaluates hair growth in nine androgen-dependent body areas (upper lip, chin, chest, upper and lower back, upper and lower abdomen, thighs, and upper arms). Although it is fairly user-friendly, this scale is limited by its subjective nature and its failure to take into consideration all androgenic areas (e.g., sideburns and buttocks), focal hirsutism, ongoing use of cosmetic measures, and above all, the effect on the patients’ quality of life. To obviate these shortcomings, some experts recommend the term “patient-important hirsutism” to indicate symptoms significant enough to cause distress, irrespective of the severity of clinical findings. We found few similar studies regarding quality of life in Asian women with variable results. The mean age (37.10 ± 9.02 years) in our study was higher compared to a study by Baig et al. (
9) in 200 women with hirsutism (26.12 ± 5.83 years) and Kiran et al. (
10) in 100 women with hirsutism (24.41 years). The proportion of unmarried women in our study was larger than both of the studies, including Baig et al. (51.5%) and Kiran et al. (65%) (
9,
10).
Hirsutism is cosmetically disconcerting and is frequently associated with embarrassment, depression, anxiety, and social withdrawal. Moreover, it may be a cutaneous clue to underlying diseases like metabolic syndrome and PCOS. It has been linked with decreased quality of life as an outcome, including (but not limited to) undermined perception of the feminine identity, by self as well as society (
11). In our study, all of the 40 patients had mild hirsutism i.e., F-G score >8 but <15. However, Kiran et al. and Hodeeb et al. (
10,
12) reported mild hirsutism at 21% and 29%, respectively. The definitions of F-G grading used were different in both of these studies. Thirty percent of our subjects had PCOS, which was higher than in Kiran et al.’s study (23%), whereas lower than in Sharma et al.’s study (
8) (38%), which was a study of clinico-investigative profiles of 50 patients with hirsutism. These differences in the severity of hirsutism can be attributed to regional variations among Indian women, as most of the previous studies have been from Northern and Southern India, while ours was set in Western India.
The mean DLQI of our study was 5.55 ± 1.501, which was less than mean scores of the study by Kiran et al., Baig et al., and Loo and Lanigan (
9,
10,
13), where it was 6.67 ± 4.57, 17.9 ± 5.71, and 12.8 ± 8.5, respectively. Thus, the effect of quality of life on our study participants was small (52%) to moderate (45%), which probably might be due to the lower F-G scores.
We found an insignificant weak positive correlation between F-G score and DLQI, indicating that hirsutism itself had a negative impact on the quality of life irrespective of severity. On the other hand, this lack of correlation between DLQI and F-G scores may be attributed to the fact that all our patients had mild hirsutism with a narrow interval between minimum and maximum F-G scores. Baig et al. (
9) also found that DLQI scores were very close in moderate and severe groups through different criteria used for grading. These results suggest that hirsutism is emotionally disturbing regardless of the degree, and effect on the quality of life is almost equivalent in women with moderate and severe hirsutism. Most of our subjects perceived hirsutism as an impediment to multiple routine activities related to occupation, leisure, and personal relationships. There was no significant correlation between DLQI and variables like age, marital status, occupation, and presence of PCOS, which might be due to small sample size in our study.
Some interesting findings in our study were that F-G score decreased with increasing age, which may be due to the waning hormonal effects. On the other hand, DLQI increased (indicating poorer quality of life), which is contrary to the belief that younger subjects are more cosmetically conscious. We also found higher F-G scores and DLQI in unmarried subjects, which might be due to effect of negative body image as well as social stigma. We observed lower F-G scores and DLQI in housewives compared to working women, but marital status could be a confounding factor here. According to the Rotterdam criteria, PCOS is a constellation of two out of three symptoms and signs, chiefly clinical and/or biochemical signs of androgen excess, oligo/anovulation, and radiological evidence of PCOS (12 or more antral follicles per ovary and/or ovarian volume greater than 10 mL). In our study, PCOS did not influence DLQI, which could be the limitation of a small sample size. Similarly, in the study by Kiran et al. (
10), the quality of life was not affected by marital status, religious background, education, and socio-economic status. However, they observed that quality of life of hirsute women with PCOS was poorer when compared to those without this endocrine disorder.
Previous studies have demonstrated a discordance between perception of hirsutism between patients and clinicians, with patients considering their hirsutism as more severe than clinicians. Since it is likely that self-ratings may be more consistently associated with poor quality of life than clinician ratings, it has been recommended that treatment goals take into account patient distress and subjective perceptions of unwanted hair growth (
14).
The strength and novelty of our study was the attempt to analyze the contribution of a host of subject-related (age, occupation, and marital status) and disease-related (severity) factors on the effect of hirsutism on the quality of life. A thorough search through published English literature did not yield any similar studies from our part of India. However, it was limited by a small sample size. Hence, we can conclude that hirsutism had a small to moderate effect on the quality of life of our study subjects, affecting both young and old, married and unmarried, working women and housewives equally and independent of severity. The domain of “symptoms and feelings” of our subjects was affected the most. Therefore, compassionate counseling deserves to be an integral part of a holistic management strategy for all women with hirsutism. Moreover, these women should be treated with courtesy and civility during professional and social interactions. Most importantly, it would be useful to conduct multi-centric studies from various parts of the world to gain deeper insight into the impact of hirsutism (addressing both patient and health care provider perspectives) on multiple ethnic and cultural groups residing in diverse regions.