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. 2020 May 22;10:8494. doi: 10.1038/s41598-020-65395-1

Relationship between headaches and tinnitus in a Swedish study

Alessandra Lugo 1,#, Niklas K Edvall 2,#, Andra Lazar 3, Golbarg Mehraei 4, Jose-Antonio Lopez-Escamez 5,6, Jan Bulla 7,8, Inger Uhlen 3, Barbara Canlon 2, Silvano Gallus 1, Christopher R Cederroth 2,
PMCID: PMC7244494  PMID: 32444677

Abstract

The heterogeneity of tinnitus is likely accounting for the lack of effective treatment approaches. Headaches have been related to tinnitus, yet little is known on how headaches impact tinnitus. We use cross-sectional data from the Swedish Tinnitus Outreach Project to i) evaluate the association between headaches and tinnitus (n = 1,984 cases and 1,661 controls) and ii) investigate the phenotypic characteristics of tinnitus subjects with tinnitus (n = 660) or without (n = 1,879) headaches. In a multivariable logistic regression model, headache was significantly associated with any tinnitus (odds ratio, OR = 2.61) and more so with tinnitus as a big problem (as measured by the tinnitus functional index, TFI ≥ 48; OR = 5.63) or severe tinnitus (using the tinnitus handicap inventory, THI ≥ 58; OR = 4.99). When focusing on subjects with tinnitus, the prevalence of headaches was 26% and reached 40% in subjects with severe tinnitus. A large number of socioeconomic, phenotypic and psychological characteristics differed between headache and non-headache subjects with any tinnitus. With increasing tinnitus severity, fewer differences were found, the major ones being vertigo, neck pain and other pain syndromes, as well as stress and anxiety. Our study suggests that headaches could contribute to tinnitus distress and potentially its severity.

Subject terms: Headache, Risk factors, Auditory system

Introduction

Subjective tinnitus is the perception of sounds in absence of external stimuli. Its prevalence ranges from 5–43%, and for about one in ten with tinnitus, the impact is such that individuals seek medical help1. This so-called clinically significant tinnitus is strongly associated with anxiety, depression and stress26. Recent studies revealed an increased risk in suicide attempts in subjects with tinnitus7,8. The combination of these psychological comorbidities with tinnitus has a non-negligible impact on quality of life3. Available treatments are of limited efficacy911, subsequently leading to substantial healthcare costs12. It is now agreed that the heterogeneity of tinnitus could be grounds to treatment failures13, which has led to research programs aimed at identifying means of classifying tinnitus subtypes14. For instance, hyperacusis15 and temporomandibular complaints16,17 have been proposed as potential criteria for subtyping tinnitus.

Headaches have also been recently suggested as an important co-factor for tinnitus subtyping18, but there is limited knowledge on how headaches impact tinnitus. Similar to tinnitus, headaches are very heterogeneous. Migraine is a common primary headache disorder that can be experienced with or without aura, which are defined by episodes of transient focal neurological symptoms. The neural mechanisms of migraine have been reviewed elsewhere19. Recent studies reveal a high prevalence of headache (26–56%) in children, adolescents and patients with tinnitus18,20,21. Indeed, cross-sectional studies show that headache is associated with tinnitus22,23, and this association is greater in presence of migraine headache with aura24. As headache are very prevalent in the population, the co-occurrence of tinnitus and headache or migraine could be coincidental. However, two longitudinal studies show that a history of migraine is a risk factor for the development of tinnitus25,26.

The pathophysiology of tinnitus is thought to derive from a failure to adapt to missing sensory information27. Concomitant with hearing loss, the brain attempts to compensate for the diminished sensory input causing an increased neural activity in the auditory pathway28. Other structures such as the amygdala have been shown to interact with the auditory pathway in tinnitus patients29. Frontostriatal circuits, similar to those involved in chronic pain, have also been evidenced in tinnitus30. Auditory steady-state responses captured using magnetoencephalography reveal that the synchrony between different brain regions, such as the right parietal area and the anterior cingulate cortex correlates strongly with tinnitus intrusiveness31. However, headache and tinnitus also share common mechanisms characterized by changes in oscillatory activity called thalamocortical dysrhythmia3234. Furthermore, alterations in the trigeminal system form a basis for the development of headaches and migraines35,36 as well as for tinnitus16,37.

Using data from the Tinnitus Research Initiative (TRI) database, Langguth et al. evaluated the impact of self-reported headache in tinnitus patients and found that a larger proportion of those with headache complaints were female, with more frequent comorbid vertigo, temporomandibular joint complaints, neck pain and other pain disorders, and depressive symptoms18. Although a number of publications deal with the relationship between tinnitus and headache, only a limited number of these provide a measure of association between headaches and the risk of tinnitus after adjustment for potential confounding factors24,38,39. To our knowledge, none have addressed the risk with severe tinnitus. Here, we investigate this relationship in the Swedish Tinnitus Outreach Projet (STOP), a study designed to investigate the risk factors for tinnitus, and further analyze the phenotypic traits accompanying tinnitus when combined with headaches.

Results

Association study

We subjected STOP participants with (n = 1,984) and without tinnitus (n = 1,661) to the ESIT-SQ in order to evaluate the association between headaches and tinnitus. Within tinnitus cases, 13.3% reported having tinnitus as a big problem according to the TFI cut-off, and 7.9% had severe tinnitus according to the THI cut-off. Subjects with headaches more frequently reported any tinnitus (multivariate OR, 2.61; 95% CI, 2.19–3.12), tinnitus as a big problem (OR, 5.63; 95% CI, 4.10–7.72) and severe tinnitus (OR, 4.99; 95% CI, 3.41–7.32; Table 1). These associations persisted to a similar degree when considering the further adjustment for hearing ability (model 2, Table 1). We also evaluated the association between headache and tinnitus stratifying by sex. The relationship with any tinnitus persisted to the same degree in men (OR, 3.21; 95% CI, 2.22–4.64) and in women (OR, 2.49; 95% CI, 2.03–3.06). The association was greater in men, although not significantly different from women, both for tinnitus as a big problem (men: OR, 7.28; 95% CI, 4.19–12.6 and women: OR, 5.51; 95% CI, 3.69–8.22) and for severe tinnitus (men: OR, 8.14; 95% CI, 4.22–15.7 and women: OR, 4.20; 95% CI, 2.59–6.80). Thus, with increasing severity, the relationship between headache and tinnitus becomes stronger.

Table 1.

Odds ratios (OR) for any tinnitus, tinnitus as a big problem (TFI ≥ 48) and severe tinnitus (THI ≥ 58), and corresponding 95% confidence intervals (CI), according to headache.

No tinnitus Any tinnitus Tinnitus as a big problem (TFI ≥ 48) Severe tinnitus (THI ≥ 58)
N (%) N (%) OR* (95% CI) OR° (95% CI) N (%) OR* (95% CI) OR° (95% CI) N (%) OR* (95% CI) OR° (95% CI)
Both sexes
Total 1661 (100.0) 1984 (100.0) 263 (100.0) 157 (100.0)
Headache
No 1421 (85.6) 1458 (73.5) 1^ 1^ 156 (59.3) 1^ 1^ 94 (59.9) 1^ 1^
Yes 240 (14.4) 526 (26.5) 2.61 (2.19–3.12) 2.19 (1.81–2.64) 107 (40.7) 5.63 (4.10–7.72) 4.29 (2.96–6.22) 63 (40.1) 4.99 (3.41–7.32) 3.80 (2.43–5.94)
Men
Total 563 (100.0) 947 (100.0) 127 (100.0) 71 (100.0)
Headache
No 524 (93.1) 768 (81.1) 1^ 1^ 87 (68.5) 1^ 1^ 46 (64.8) 1^ 1^
Yes 39 (6.9) 179 (18.9) 3.21 (2.22–4.64) 2.64 (1.80–3.87) 40 (31.5) 7.28 (4.19–12.63) 6.09 (3.26–11.35) 25 (35.2) 8.14 (4.22–15.7) 7.47 (3.55–15.7)
Women
Total 1098 (100.0) 1034 (100.0) 135 (100.0) - -— 85 (100.0)
Headache
No 897 (81.7) 689 (66.6) 1^ 1^ 68 (50.4) 1^ 1^ 47 (55.3) 1^ 1^
Yes 201 (18.3) 345 (33.4) 2.49 (2.03–3.06) 2.09 (1.68–2.61) 67 (49.6) 5.51 (3.69–8.22) 4.15 (2.56–6.73) 38 (44.7) 4.20 (2.59–6.80) 2.98 (1.66–5.34)

TFI: Tinnitus Functional Index; THI: Tinnitus Handicap Inventory.

*ORs were estimated using unconditional multiple logistic regression models after adjustment for sex, age, and level of education (model 1). Estimates in bold are statistically significant at 0.05 level.

°ORs were estimated using unconditional multiple logistic regression models after adjustment for sex, age, level of education, and hearing ability (model 2). Estimates in bold are statistically significant at 0.05 level.

^Reference category.

Tinnitus phenotyping study

We next focused on tinnitus subjects only. Among 2,539 subjects with any tinnitus, 26% reported headache. This proportion increased for individuals reporting tinnitus as a big problem (36%), and for those with severe tinnitus (40%). Table 2 describes the sociodemographic characteristics of these three groups. There was a greater proportion of women in the any tinnitus groups with headaches in comparison to those without headaches. This gender bias survived the adjustment for multiple comparisons in the “any tinnitus” group but not in groups with more severe tinnitus. Any tinnitus subjects with headaches significantly differed from those without headaches in age, income, and employment status (p = <0.0001) but not in marital status or education level. In contrast, in the samples with severe tinnitus, no differences were found in all sociodemographic variables after correction for multiple comparisons. We next used a set of questionnaires to assess the global impact of headache on tinnitus-related burden6,40. Subjects with any tinnitus who reported headache were found to have worse scores for all questionnaires (p < 0.0001, Table 3), with the exception of the numerical rating scale for awareness. In subjects with severe tinnitus, the only differences were found in the TFI, stress, anxiety measures, and physical and psychological quality of life (p = 0.039 to 0.025 after correction for multiple comparisons). Thus, headaches contribute to greater psychological burden in tinnitus subjects, regardless of the degree of severity.

Table 2.

Sociodemographic and psychological characteristics for subjects with tinnitus with or without headache.

Any Tinnitus Tinnitus as a big problem Severe tinnitus
Headache (n = 660) No (%) No headache (n = 1879) No (%) Headache (n = 125) No (%) No Headache (n = 218) n (%) Headache (n = 79) No (%) No Headache (n = 119) n (%)
Sex χ²(1) = 94.59, p < 0.0001 (<0.0001) χ²(1) = 23.31, p < 0.0001 (p = 0.0003) χ²(1) = 6.09, p = 0.014 (0.082)
Male 225 (34.1) 1054 (56.1) 43 (34.4) 134 (61.5) 31 (39.2) 68 (57.1)
Female 435 (65.9) 825 (43.9) 82 (65.6) 84 (38.5) 48 (60.8) 51 (42.9)
Age Group χ²(7) = 38.47, p < 0.0001 (<0.0001) χ²(7) = 5.81, p = 0.5619 (0.5619) χ²(7) = 2.84, p = 0.899 (0.899)
<24 19 (2.9) 40 (2.1) 6 (4.8) 4 (1.8) 4 (5.1) 6 (5.1)
25–34 140 (21.3) 350 (18.7) 19 (15.3) 34 (15.7) 13 (16.7) 28 (23.7)
35–44 168 (25.6) 407 (21.7) 25 (20.2) 42 (19.4) 14 (18) 21 (17.8)
45–54 192 (29.2) 487 (26) 39 (31.5) 62 (28.6) 22 (28.2) 26 (22)
55–64 88 (13.4) 272 (14.5) 20 (16.1) 37 (17.1) 14 (18) 21 (17.8)
65–74 43 (6.5) 268 (14.3) 12 (9.7) 24 (11.1) 9 (11.5) 11 (9.3)
75–84 6 (0.9) 48 (2.6) 2 (1.6) 12 (5.5) 2 (2.6) 4 (3.4)
>85 1 (0.2) 3 (0.2) 1 (0.8) 2 (0.9) 0 (0) 1 (0.9)
Marital Status χ²(4) = 7.84, p = 0.0974 (0.0974) χ²(4) = 4.23, p = 0.3757 (0.45084) χ²(4) = 4.36, p = 0.359 (0.539)
Married 268 (40.6) 830 (44.2) 40 (32) 91 (41.7) 29 (36.7) 43 (36.1)
Living with partner 211 (32) 551 (29.3) 41 (32.8) 68 (31.2) 25 (31.7) 44 (37)
Single 132 (20) 320 (17) 28 (22.4) 41 (18.8) 16 (20.3) 25 (21)
Widow/Widower 5 (0.8) 26 (1.4) 3 (2.4) 3 (1.4) 1 (1.3) 3 (2.5)
Divorced 44 (6.7) 152 (8.1) 13 (10.4) 15 (6.9) 8 (10.1) 4 (3.4)
Gross income χ²(3) = 37.56, p < 0.0001 (<0.0001) χ²(3) = 12.72, p = 0.0053 (0.0159) χ²(3) = 5.08, p = 0.166 (0.332)
0–200 000 SEK 90 (13.6) 215 (11.4) 27 (21.6) 36 (16.5) 17 (21.5) 25 (21)
200 001–450 000 SEK 368 (55.8) 877 (46.7) 72 (57.6) 110 (50.5) 49 (62) 60 (50.4)
450 001 SEK or more 162 (24.6) 706 (37.6) 14 (11.2) 59 (27.1) 7 (8.9) 24 (20.2)
Don’t know/don’t want to disclose 40 (6.1) 81 (4.3) 12 (9.6) 13 (6) 6 (7.6) 10 (8.4)
Education Level χ²(3) = 6.8, p = 0.0785 (0.0942) χ²(3) = 5.1, p = 0.1646 (0.2469) χ²(3) = 8, p = 0.046 (0.138)
Middle School 20 (3) 48 (2.6) 8 (6.4) 13 (6) 8 (10.1) 5 (4.2)
High School 138 (20.9) 397 (21.1) 34 (27.2) 70 (32.1) 23 (29.1) 37 (31.1)
University 424 (64.2) 1273 (67.8) 57 (45.6) 109 (50) 32 (40.5) 65 (54.6)
Other 78 (11.8) 161 (8.6) 26 (20.8) 26 (11.9) 16 (20.3) 12 (10.1)
Employment χ²(10) = 75.25, p < 0.0001 (<0.0001) χ²(8) = 19.2, p = 0.0138 (0.0276) χ²(7) = 4.54, p = 0.716 (0.86)
Don’t know 2 (0.3) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0)
Employed 430 (65.2) 1140 (60.7) 59 (47.2) 111 (50.9) 39 (49.4) 59 (49.6)
Unemployed 14 (2.1) 17 (0.9) 7 (5.6) 2 (0.9) 4 (5.1) 2 (1.7)
Running my own business/Working as a partner in a company 67 (10.2) 249 (13.3) 8 (6.4) 30 (13.8) 4 (5.1) 14 (11.8)
Retired 44 (6.7) 286 (15.2) 15 (12) 37 (17) 11 (13.9) 14 (11.8)
Sick leave (for more than two month) or disability pension due to illness or disability 47 (7.1) 49 (2.6) 18 (14.4) 23 (10.6) 12 (15.2) 16 (13.5)
Parental leave (since two months or longer) 13 (2) 27 (1.4) 3 (2.4) 3 (1.4) 1 (1.3) 2 (1.7)
Student 28 (4.2) 79 (4.2) 10 (8) 10 (4.6) 7 (8.9) 10 (8.4)
Sabbatical 3 (0.5) 2 (0.1) 1 (0.8) 0 (0) 0 (0) 0 (0)
Housewife/-Husband 0 (0) 1 (0.1) 0 (0) 0 (0) 0 (0) 0 (0)
Other 12 (1.8) 29 (1.5) 4 (3.2) 2 (0.9) 1 (1.3) 2 (1.7)

Income refers to yearly income in SEK. Pairwise comparisons using Pearson’s Chi-square test are reported. Percentages (%) displayed refer to column percentages. P values adjusted for multiple comparisons are shown between parenthesis. Estimates in bold are statistically significant at 0.05 level.

Table 3.

Questionnaire scores from subjects with tinnitus with or without headache.

Any Tinnitus Tinnitus as a big problem Severe tinnitus
Headache (n = 660) mean (SD) No headache (n = 1879) mean (SD) Headache (n = 125) mean (SD) No headache (n = 218) mean (SD) Headache (n = 79) mean (SD) No headache (n = 119) mean (SD)
NRS Lo 44 (25.5) 39.5 (25.3) 72.4 (19.3) 70.6 (19.1) 76.1 (18.4) 72.8 (20.0)
3.89, p = 0.0001 (0.0001, −0.10) 0.87, p = 0.3829 (0.4248, −0.06) 1.08, p = 0.2816 (0.352, −0.09)
NRS Aw 35.3 (32.3) 32.9 (31.1) 73.5 (27.5) 74 (24.6) 76.1 (25.5) 75 (25.4)
1.87, p = 0.0612 (0.0612, −0.05) 0.36, p = 0.722 (0.722, −0.02) 1.08, p = 0.2816 (0.352, −0.03)
NRS An 23.3 (27.4) 19 (24.8) 62.4 (28.0) 58.9 (26.2) 68.7 (27.2) 64.4 (26.9)
4.6, p < 0.0001 (<0.0001, −0.12) 1.26, p = 0.2059 (0.2574, −0.08) 1.29, p = 0.1978 (0.2697, −0.11)
THI 26.6 (22.9) 19.9 (19.2) 62.4 (19.0) 57.4 (18.3) 75.3 (11.4) 72 (12)
7.09, p < 0.0001 (<0.0001, −0.19) 2.3, p = 0.0212 (0.0353, −0.15) 2.15, p = 0.0319 (0.0684, −0.18)
TFI 26.6 (23.2) 20.2 (19.8) 65.8 (12.4) 62.1 (11.9) 69.6 (14.2) 64.4 (16.2)
6.07, p < 0.0001 (<0.0001, -0.16) 2.91, p = 0.0036 (0.0068, -0.18) 2.48, p = 0.0131 (0.0393, -0.21)
PSQ 0.4 (0.2) 0.3 (0.2) 0.5 (0.2) 0.5 (0.2) 0.6 (0.2) 0.5 (0.2)
13.08, p < 0.0001 (<0.0001, −0.34) 4.54, p < 0.0001 (0.0003, −0.29) 2.94, p = 0.0033 (0.0248, −0.25)
HADS_A 7.8 (4.4) 5.5 (3.9) 10.6 (4.4) 8.7 (4.5) 11.8 (4.2) 10.1 (4.5)
11.59, p < 0.0001 (<0.0001, −0.3) 3.58, p = 0.0003 (0.0011, −0.23) 2.58, p = 0.01 (0.0393, −0.22)
HADS_D 4.7 (3.7) 3.3 (3.2) 7.6 (3.9) 6.4 (3.9) 8.3 (4.0) 7.5 (4.1)
9.15, p < 0.0001 (<0.0001, −0.24) 2.99, p = 0.0028 (0.006, −0.19) 1.66, p = 0.0962 (0.1566, −0.14)
FTQ 5.1 (2.9) 4.6 (2.6) 8.1 (3.2) 8.3 (2.9) 9 (3.0) 9.6 (2.7)
3.85, p = 0.0001 (0.0001, −0.1) −0.85, p = 0.3965 (0.4248, 0.05) −1.63, p = 0.1033 (0.1566, 0.14)
TCS 14.9 (11.5) 11.7 (9.8) 28.1 (11.0) 26.9 (9.4) 31.4 (9.6) 30.4 (8.7)
6.02, p < 0.0001 (<0.0001, −0.16) 1.53, p = 0.1259 (0.1717, −0.1) 0.93, p = 0.3542 (0.4087, −0.08)
HQ 20.2 (9.3) 15.5 (8.9) 26.3 (7.7) 23.3 (8.8) 27.3 (8.0) 25.5 (8.8)
11, p < 0.0001 (<0.0001, −0.29) 3.14, p = 0.0017 (0.0043, −0.2) 1.62, p = 0.1044 (0.1566, −0.14)
QoL Phy 14.4 (2.9) 16.1 (2.5) 12 (2.7) 13.7 (2.7) 11.6 (2.8) 13 (2.7)
13.63, p < 0.0001 (<0.0001, 0.36) 5.29, p < 0.0001 (0.0003, 0.34) 3.14, p = 0.0017 (0.0248, 0.26)
QoL Psy 13.9 (2.9) 15.2 (2.5) 11.8 (2.9) 13 (2.8) 11.1 (2.8) 12.3 (2.8)
10.32, p < 0.0001 (<0.0001, 0.27) 3.55, p = 0.0004 (0.0012, 0.23) 2.49, p = 0.0129 (0.0393, 0.21)
QoL Social 13.6 (3.2) 14.4 (3) 12.2 (3.6) 13.2 (3.3) 12.3 (3.2) 12.7 (3.6)
5.26, p < 0.0001 (<0.0001, 0.14) 2.25, p = 0.0248 (0.0372, 0.14) −0.58, p = 0.5591 (0.599, 0.05)
QoL Env 15.5 (2.4) 16.5 (2.1) 13.9 (2.4) 15 (2.6) 13.9 (2.5) 14.7 (2.7)
9.81, p < 0.0001 (<0.0001, 0.25) 3.99, p < 0.0001 (0.0003, 0.26) −2.25, p = 0.0245 (0.0613, 0.19)

Values are mean (± SD). Pairwise comparisons using Wilcoxon’s tests are reported below the compared values. P values adjusted for multiple comparisons are shown between parenthesis together with Cliff’s δ (noted †). Abbreviations: Numerical Ratings Score (NRS), Tinnitus loudness (Lo), Awareness (Aw), Annoyance (An), Tinnitus Handicap Inventory (THI), Tinnitus Functional Index (TFI), Fear of Tinnitus Questionnaire (FTQ), Tinnitus Catastrophising Scale (TCS), Hyperacusis Questionnaire (HQ), Perceived Stress Questionnaire (PSQ), Hospital Anxiety Depression Scales for Anxiety (HADS A) and depression (HADS D), Quality of Life (QoL) subscales from the World Health Organization: Physical (Phy), Psychological

(Psych), Social (Soc), and Environmental (Env). Estimates in bold are statistically significant at 0.05 level.

When evaluating the tinnitus phenotypic characteristics for the group with any tinnitus, differences were observed in onset-related events (p = 0.006), with subjects more frequently reporting stress as the cause of their tinnitus (Table 4). Such effects were not seen in subjects with tinnitus as a big problem or severe tinnitus. Differences were also found in tinnitus loudness variation from day to day and sound of tinnitus (p = 0.001 to 0.003). Pulsatility was also different between headache and non-headache subjects with “any tinnitus” (p < 0.0001), although this could be due to a larger proportion in the headache group not being able to define it as pulsatile or not. Sounds also had a greater impact on subjects with any tinnitus and headaches, with greater worsening when exposed to loud noise, greater intolerance to sounds, and sounds causing pain and discomfort (p = 0.002 to <0.0001, Tables 4 and 5). The impact of stress, bad night sleep and naps also differed between any tinnitus subjects with or without headaches. A greater proportion of somatosensory impact such as tinnitus being affected by head movement and touch, self-reporting of temporomandibular complaints, vertigo and dizziness, neck pain and other pain syndromes was also found in any tinnitus subjects with headache (p < 0.0001). More subjects with headaches reported a diagnosed disease and were under psychiatric treatment (p < 0.0001), and a greater occurrence of tinnitus in the family was also reported in the headache group (p = 0.03). The proportion of subjects with self-reported hearing problems, hearing aids, and the location of tinnitus (laterality), did not differ between the headache and non-headache groups suggesting a minimal contribution of hearing loss into migraine in tinnitus subjects. Interestingly, in the severe tinnitus group, only vertigo/dizziness, neck pain and other pain syndromes remained different between the headache and non-headache groups (p = 0.014 to 0.002, Table 5).

Table 4.

Phenotypic characteristics for subjects with tinnitus with or without headache.

Any Tinnitus Tinnitus as a big problem Severe tinnitus
Headache (n = 660) No (%) No Headache (n = 1879) No (%) Headache (n = 125) No (%) No Headache (n = 218) No (%) Headache (n = 79) No (%) No Headache (n = 119) No (%)
Tinnitus onset χ²(5) = 5.02, p = 0.414 (0.497) χ²(5) = 1.31, p = 0.934 (0.946) χ²(5) = 3.91, p = 0.562 (0.919)
Don’t know 71 (10.8) 161 (8.6) 3 (2.4) 5 (2.3) 2 (2.5) 2 (1.7)
0 to 6 months 13 (2.0) 39 (2.1) 5 (4.0) 8 (3.7) 4 (5.1) 5 (4.2)
6 months to 3 years 105 (15.9) 265 (14.1) 17 (13.6) 37 (17.0) 14 (17.7) 24 (20.2)
3 to 10 years 183 (27.7) 546 (29.1) 32 (25.6) 61 (28.0) 21 (26.6) 31 (26.1)
10 to 20 years 180 (27.3) 559 (29.8) 39 (31.2) 64 (29.4) 18 (22.8) 38 (31.9)
More than 20 years 108 (16.4) 309 (16.4) 29 (23.2) 43 (19.7) 20 (25.3) 19 (16.0)
Onset-related events χ²(6) = 19.68, p = 0.003 (0.006) χ²(6) = 8.52, p = 0.203 (0.405) χ²(6) = 2.26, p = 0.894 (0.919)
Loud blast of sound 224 (33.9) 759 (40.4) 35 (28) 71 (32.6) 23 (29.1) 33 (27.7)
Stress 117 (17.7) 244 (13) 21 (16.8) 35 (16.1) 12 (15.2) 23 (19.3)
Change in hearing 41 (6.2) 93 (5.0) 16 (12.8) 19 (8.7) 10 (12.7) 10 (8.4)
Head trauma 6 (0.9) 15 (0.8) 0 (0.0) 2 (0.9) 0 (0.0) 1 (0.8)
Whiplash 10 (1.5) 11 (0.6) 4 (3.2) 1 (0.5) 1 (1.3) 1 (0.8)
Other 90 (13.6) 261 (13.9) 20 (16) 46 (21.1) 17 (21.5) 24 (20.2)
Don’t know 172 (26.1) 496 (26.4) 29 (23.2) 44 (20.2) 16 (20.3) 27 (22.7)
Tinnitus occurrence χ²(1) = 3.15, p = 0.076 (0.104) χ²(1) = 4.98, p = 0.026 (0.086) χ²(1) = 0.01, p = 0.913 (0.919)
Occasionally (now and then) 308 (46.7) 802 (42.7) 17 (13.6) 14 (6.4) 5 (6.3) 8 (6.7)
Always (all the time) 352 (53.3) 1077 (57.3) 108 (86.4) 204 (93.6) 74 (93.7) 111 (93.3)
Time of the day of tinnitus emergence χ²(6) = 13.8, p = 0.032 (0.05) χ²(6) = 4.71, p = 0.581 (0.758) χ²(6) = 3.05, p = 0.802 (0.919)
Don’t know 350 (53) 1012 (53.9) 51 (40.8) 85 (39) 28 (35.4) 35 (29.4)
When awakening 34 (5.2) 123 (6.6) 14 (11.2) 31 (14.2) 13 (16.5) 22 (18.5)
In the morning 12 (1.8) 35 (1.9) 6 (4.8) 5 (2.3) 3 (3.8) 4 (3.4)
Around noon 37 (5.6) 125 (6.7) 12 (9.6) 24 (11.0) 9 (11.4) 16 (13.5)
In the afternoon 31 (4.7) 93 (5.0) 7 (5.6) 19 (8.7) 6 (7.6) 16 (13.5)
In the evening 71 (10.8) 238 (12.7) 21 (16.8) 38 (17.4) 15 (19.0) 17 (14.3)
Before sleeping 125 (18.9) 253 (13.5) 14 (11.2) 16 (7.3) 5 (6.3) 9 (7.6)
Perceiving the onset of tinnitus χ²(2) = 6.12, p = 0.047 (0.067) χ²(2) = 0.59, p = 0.744 (0.88) χ²(2) = 0.23, p = 0.891 (0.919)
Don’t know 164 (24.9) 494 (26.3) 14 (11.2) 22 (10.1) 6 (7.6) 7 (5.9)
Gradual 313 (47.4) 790 (42.0) 55 (44.0) 89 (40.8) 29 (36.7) 45 (37.8)
Abrupt 183 (27.7) 595 (31.7) 56 (44.8) 107 (49.1) 44 (55.7) 67 (56.3)
Pulsatility χ²(3) = 22.44, p < 0.0001 (0.0001) χ²(3) = 12.08, p = 0.007 (0.03) χ²(3) = 5.21, p = 0.157 (0.485)
Don’t know 77 (11.7) 138 (7.3) 20 (16.0) 22 (10.1) 5 (6.3) 14 (11.8)
Yes, with heart beat 56 (8.5) 124 (6.6) 19 (15.2) 17 (7.8) 14 (17.7) 10 (8.4)
Yes, different from heart beat 35 (5.3) 62 (3.3) 15 (12.0) 16 (7.3) 10 (12.7) 13 (10.9)
No 492 (74.6) 1555 (82.8) 71 (56.8) 163 (74.8) 50 (63.3) 82 (68.9)
Location of tinnitus χ²(6) = 13.58, p = 0.035 (0.052) χ²(6) = 4.84, p = 0.565 (0.758) χ²(6) = 4.97, p = 0.548 (0.919)
Right ear 50 (7.6) 147 (7.8) 10 (8.0) 22 (10.1) 6 (7.6) 11 (9.2)
Left ear 45 (6.8) 179 (9.5) 14 (11.2) 15 (6.9) 13 (16.5) 10 (8.4)
Both ears, worse in right 141 (21.4) 305 (16.2) 24 (19.2) 35 (16.1) 13 (16.5) 24 (20.2)
Both ears, worse in left 110 (16.7) 316 (16.8) 21 (16.8) 49 (22.5) 15 (19) 27 (22.7)
Both ears equally 197 (29.9) 622 (33.1) 32 (25.6) 51 (23.4) 15 (19) 20 (16.8)
Inside the head 108 (16.4) 289 (15.4) 19 (15.2) 40 (18.4) 12 (15.2) 23 (19.3)
Elsewhere 9 (1.4) 21 (1.1) 5 (4.0) 6 (2.8) 5 (6.3) 4 (3.4)
Sound of tinnitus χ²(9) = 27.04, p = 0.001 (0.003) χ²(7) = 22.48, p = 0.002 (0.013) χ²(7) = 14.21, p = 0.048 (0.204)
Tone 123 (18.9) 414 (22.2) 13 (10.7) 21 (9.7) 10 (13) 12 (10.3)
Noise 65 (10.0) 217 (11.6) 9 (7.4) 26 (12.0) 7 (9.1) 9 (7.7)
Crickets 18 (2.8) 71 (3.8) 2 (1.6) 7 (3.2) 2 (2.6) 5 (4.3)
Heartbeat 5 (0.8) 6 (0.3) 1 (0.8) 1 (0.5) 2 (2.6) 0 (0.0)
Beeping 67 (10.3) 233 (12.5) 6 (4.9) 34 (15.7) 4 (5.2) 17 (14.5)
Morse Code 0 (0.0) 4 (0.2) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
An alarm 9 (1.4) 11 (0.6) 4 (3.3) 2 (0.9) 3 (3.9) 2 (1.7)
Other 11 (1.7) 62 (3.3) 1 (0.8) 13 (6) 1 (1.3) 11 (9.4)
Don’t know 1 (0.2) 1 (0.1) 0 (0) 0 (0.0) 0 (0.0) 0 (0.0)
Complex 352 (54.1) 848 (45.4) 86 (70.5) 112 (51.9) 48 (62.3) 61 (52.1)
Tinnitus loudness variation from day to day χ²(5) = 23.14, p = 0 (0.001) χ²(5) = 3.53, p = 0.62 (0.775) χ²(5) = 4.41, p = 0.493 (0.919)
Don’t know 36 (5.5) 127 (6.8) 4 (3.2) 6 (2.8) 1 (1.3) 2 (1.7)
Never 38 (5.8) 154 (8.2) 10 (8.0) 18 (8.3) 6 (7.6) 6 (5.0)
Seldom 79 (12.0) 301 (16.0) 19 (15.2) 35 (16.1) 11 (13.9) 14 (11.8)
Sometimes 241 (36.5) 710 (37.8) 45 (36.0) 94 (43.1) 27 (34.2) 54 (45.4)
Often 186 (28.2) 397 (21.1) 30 (24.0) 47 (21.6) 19 (24.1) 30 (25.2)
Always 80 (12.1) 190 (10.1) 17 (13.6) 18 (8.3) 15 (19) 13 (10.9)
Pitch of tinnitus χ²(4) = 0.12, p = 0.998 (0.998) χ²(4) = 1.74, p = 0.783 (0.88) χ²(4) = 2.55, p = 0.636 (0.919)
Don’t know 27 (4.1) 72 (3.8) 4 (3.2) 5 (2.3) 2 (2.5) 3 (2.5)
Very high frequency 157 (23.8) 450 (24.0) 39 (31.2) 64 (29.4) 30 (38.0) 38 (31.9)
High frequency 293 (44.4) 838 (44.6) 54 (43.2) 101 (46.3) 30 (38.0) 47 (39.5)
Medium frequency 128 (19.4) 366 (19.5) 24 (19.2) 36 (16.5) 14 (17.7) 20 (16.8)
Low frequency 55 (8.3) 153 (8.1) 4 (3.2) 12 (5.5) 3 (3.8) 11 (9.2)
Reduction of tinnitus by music or environmental sounds χ²(2) = 0.48, p = 0.787 (0.827) χ²(2) = 2.02, p = 0.364 (0.682) χ²(2) = 6.16, p = 0.046 (0.204)
Don’t know 171 (25.9) 470 (25.0) 23 (18.4) 29 (13.3) 15 (19) 10 (8.4)
Yes 367 (55.6) 1074 (57.2) 68 (54.4) 133 (61.0) 45 (57.0) 67 (56.3)
No 122 (18.5) 335 (17.8) 34 (27.2) 56 (25.7) 19 (24.1) 42 (35.3)
Worsening of tinnitus by loud noise χ²(2) = 14.57, p = 0.001 (0.002) χ²(2) = 1.36, p = 0.506 (0.758) χ²(2) = 0.7, p = 0.703 (0.919)
Don’t know 181 (27.4) 525 (27.9) 30 (24.0) 47 (21.6) 21 (26.6) 27 (22.7)
Yes 357 (54.1) 881 (46.9) 77 (61.6) 129 (59.2) 47 (59.5) 71 (59.7)
No 122 (18.5) 473 (25.2) 18 (14.4) 42 (19.3) 11 (13.9) 21 (17.7)
Tinnitus affected by head movement or touch χ²(2) = 38.19, p < 0.0001 (0.0001) χ²(2) = 6.91, p = 0.032 (0.095) χ²(2) = 0.8, p = 0.67 (0.919)
Don’t know 157 (23.8) 361 (19.2) 15 (12.0) 35 (16.1) 8 (10.1) 12 (10.1)
Yes 210 (31.8) 426 (22.7) 61 (48.8) 75 (34.4) 42 (53.2) 56 (47.1)
No 293 (44.4) 1092 (58.1) 49 (39.2) 108 (49.5) 29 (36.7) 51 (42.9)
Tinnitus affected by nap χ²(3) = 9.61, p = 0.022 (0.037) χ²(3) = 1.99, p = 0.574 (0.758) χ²(3) = 0.5, p = 0.919 (0.919)
Don’t know 373 (56.5) 1068 (56.8) 43 (34.4) 88 (40.4) 25 (31.7) 42 (35.3)
It mainly worsens my tinnitus 15 (2.3) 38 (2.0) 7 (5.6) 16 (7.3) 8 (10.1) 12 (10.1)
It mainly reduces my tinnitus 199 (30.2) 633 (33.7) 62 (49.6) 93 (42.7) 39 (49.4) 53 (44.5)
It has no effect 73 (11.1) 140 (7.5) 13 (10.4) 21 (9.6) 7 (8.9) 12 (10.1)
Tinnitus affected by bad nights sleep χ²(5) = 51.73, p < 0.0001 (0.0001) χ²(5) = 7.62, p = 0.179 (0.383) χ²(5) = 6.29, p = 0.279 (0.76)
Don’t know 257 (38.9) 704 (37.5) 25 (20) 42 (19.3) 14 (17.7) 15 (12.6)
Never 53 (8) 315 (16.8) 6 (4.8) 24 (11.0) 3 (3.8) 10 (8.4)
Seldom 43 (6.5) 154 (8.2) 9 (7.2) 20 (9.2) 6 (7.6) 12 (10.1)
Sometimes 145 (22) 419 (22.3) 28 (22.4) 58 (26.6) 14 (17.7) 33 (27.7)
Often 122 (18.5) 221 (11.8) 39 (31.2) 54 (24.8) 27 (34.2) 33 (27.7)
Always 40 (6.1) 66 (3.5) 18 (14.4) 20 (9.2) 15 (19) 16 (13.5)
Tinnitus affected by stress χ²(3) = 69.4, p < 0.0001 (0.0001) χ²(2) = 7.5, p = 0.024 (0.086) χ²(2) = 1.43, p = 0.491 (0.919)
Don’t know 211 (32) 677 (36) 23 (18.4) 50 (22.9) 12 (15.2) 20 (16.8)
Yes, it worsens my tinnitus 369 (55.9) 738 (39.3) 90 (72) 127 (58.3) 62 (78.5) 86 (72.3)
Yes, it reduces my tinnitus 79 (12) 460 (24.5) 12 (9.6) 41 (18.8) 5 (6.3) 13 (10.9)
No, it has no effect 1 (0.2) 4 (0.2) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Tinnitus affected by medication χ²(2) = 0.95, p = 0.623 (0.692) χ²(2) = 0.11, p = 0.946 (0.946) χ²(2) = 0.32, p = 0.854 (0.919)
Don’t know 482 (73) 1380 (73.4) 83 (66.4) 141 (64.7) 46 (58.2) 74 (62.2)
Yes 20 (3.0) 44 (2.3) 9 (7.2) 16 (7.3) 9 (11.4) 12 (10.1)
No 158 (23.9) 455 (24.2) 33 (26.4) 61 (28.0) 24 (30.4) 33 (27.7)
Contacted a clinician due to tinnitus χ²(2) = 1.14, p = 0.566 (0.653) χ²(2) = 1.88, p = 0.391 (0.69) χ²(2) = 0.18, p = 0.916 (0.919)
No 415 (62.9) 1209 (64.3) 32 (25.6) 43 (19.7) 11 (13.9) 17 (14.3)
Yes, because of curiosity 32 (4.9) 102 (5.4) 3 (2.4) 8 (3.7) 2 (2.5) 2 (1.7)
Yes, because I sought for help 213 (32.3) 568 (30.2) 90 (72.0) 167 (76.6) 66 (83.5) 100 (84.0)
Number of tinnitus treatments χ²(3) = 3.18, p = 0.365 (0.456) χ²(3) = 0.83, p = 0.842 (0.902) χ²(3) = 2.29, p = 0.514 (0.919)
None 563 (85.3) 1651 (87.9) 80 (64) 134 (61.5) 42 (53.2) 61 (51.3)
1 41 (6.2) 96 (5.1) 17 (13.6) 30 (13.8) 14 (17.7) 17 (14.3)
2–4 42 (6.4) 94 (5.0) 19 (15.2) 32 (14.7) 16 (20.3) 22 (18.5)
5 or more 14 (2.1) 38 (2.0) 9 (7.2) 22 (10.1) 7 (8.9) 19 (16)
Tinnitus occurence in family χ²(1) = 5.64, p = 0.018 (0.031) χ²(1) = 0.52, p = 0.471 (0.744) χ²(1) = 0.05, p = 0.832 (0.919)
No 518 (78.5) 1553 (82.7) 89 (71.2) 163 (74.8) 56 (70.9) 86 (72.3)
Yes 142 (21.5) 326 (17.4) 36 (28.8) 55 (25.2) 23 (29.1) 33 (27.7)

Pairwise comparisons using Pearson’s Chi-square test are reported. Percentages (%) displayed refer to column percentages. P values adjusted for multiple comparisons are shown between parenthesis. Estimates in bold are statistically significant at 0.05 level.

Table 5.

Comorbidities in subjects with tinnitus with or without headache.

Any Tinnitus Tinnitus as a big problem Severe tinnitus
Headache (n = 660) No (%) No Headache (n = 1879) No (%) Headache (n = 125) No (%) No Headache (n = 218) No (%) Headache (n = 79) No (%) No Headache (n = 119) No (%)
Hearing problem χ²(2) = 2.86, p = 0.24 (0.313) χ²(2) = 1.57, p = 0.456 (0.744) χ²(2) = 0.36, p = 0.836 (0.919)
Don’t know 121 (18.3) 304 (16.2) 14 (11.2) 27 (12.4) 6 (7.6) 12 (10.1)
Yes 309 (46.8) 946 (50.4) 81 (64.8) 151 (69.3) 50 (63.3) 73 (61.3)
No 230 (34.9) 629 (33.5) 30 (24) 40 (18.4) 23 (29.1) 34 (28.6)
Hearing aids χ²(3)=1.01, p = 0.799 (0.827) χ²(3)=1.04, p = 0.792 (0.88) χ²(3)=1.2, p = 0.754 (0.919)
Yes, on both ears 43 (6.5) 115 (6.1) 22 (17.6) 43 (19.7) 12 (15.2) 22 (18.5)
Yes, on the right ear 4 (0.6) 19 (1.0) 4 (3.2) 6 (2.8) 3 (3.8) 4 (3.4)
Yes, on the left ear 8 (1.2) 23 (1.2) 5 (4.0) 5 (2.3) 4 (5.1) 3 (2.5)
No 605 (91.7) 1722 (91.6) 94 (75.2) 164 (75.2) 60 (76.0) 90 (75.6)
Problems tolerating sounds χ²(4) = 70.08, p < 0.0001 (0.0001) χ²(4) = 9.81, p = 0.044 (0.119) χ²(3) = 5.15, p = 0.162 (0.485)
Never 11 (1.7) 95 (5.1) 0 (0.0) 1 (0.5) 0 (0.0) 0 (0.0)
Rarely 61 (9.2) 347 (18.5) 4 (3.2) 16 (7.3) 2 (2.5) 9 (7.6)
Sometimes 248 (37.6) 742 (39.5) 24 (19.2) 66 (30.3) 14 (17.7) 31 (26.1)
Usually 207 (31.4) 469 (25) 49 (39.2) 73 (33.5) 28 (35.4) 39 (32.8)
Always 133 (20.2) 226 (12) 48 (38.4) 62 (28.4) 35 (44.3) 40 (33.6)
Sounds cause pain or physical discomfort χ²(2) = 51.96, p < 0.0001 (0.0001) χ²(2) = 6, p = 0.05 (0.124) χ²(2) = 0.69, p = 0.71 (0.919)
Don’t know 39 (5.9) 115 (6.1) 7 (5.6) 16 (7.3) 3 (3.8) 7 (5.9)
Yes 427 (64.7) 919 (48.9) 98 (78.4) 144 (66.1) 62 (78.5) 88 (74)
No 194 (29.4) 845 (45) 20 (16) 58 (26.6) 14 (17.7) 24 (20.2)
Temporomandibular problems χ²(2) = 168.49, p < 0.0001 (0.0001) χ²(2) = 15.98, p = 0 (0.002) χ²(2) = 9.15, p = 0.01 (0.077)
Don’t know 37 (5.6) 64 (3.4) 11 (8.8) 17 (7.8) 6 (7.6) 7 (5.9)
Yes 231 (35) 245 (13) 50 (40) 45 (20.6) 36 (45.6) 31 (26.1)
No 392 (59.4) 1570 (83.6) 64 (51.2) 156 (71.6) 37 (46.8) 81 (68.1)
Vertigo/dizziness χ²(2) = 177.98, p < 0.0001 (0.0001) χ²(2) = 38.25, p < 0.0001 (0.0005) χ²(2) = 24.39, p < 0.0001 (0.002)
Don’t know 33 (5.0) 64 (3.4) 6 (4.8) 9 (4.1) 1 (1.3) 4 (3.4)
Yes 278 (42.1) 324 (17.2) 67 (53.6) 47 (21.6) 40 (50.6) 21 (17.7)
No 349 (52.9) 1491 (79.4) 52 (41.6) 162 (74.3) 38 (48.1) 94 (79.0)
Neck pain χ²(2) = 339.35, p < 0.0001 (0.0001) χ²(2) = 36.22, p < 0.0001 (0.0005) χ²(2) = 13.17, p = 0.001 (0.014)
Don’t know 14 (2.1) 26 (1.4) 3 (2.4) 6 (2.8) 1 (1.3) 1 (0.8)
Yes 397 (60.2) 410 (21.8) 83 (66.4) 72 (33.0) 51 (64.6) 46 (38.7)
No 249 (37.7) 1443 (76.8) 39 (31.2) 140 (64.2) 27 (34.2) 72 (60.5)
Other pain syndromes χ²(2) = 145.17, p < 0.0001 (0.0001) χ²(2) = 33.37, p < 0.0001 (0.0005) χ²(2) = 17.49, p = 0 (0.003)
Don’t know 24 (3.6) 18 (1.0) 4 (3.2) 2 (0.9) 3 (3.8) 3 (2.5)
Yes 256 (38.8) 341 (18.2) 71 (56.8) 60 (27.5) 43 (54.4) 31 (26.1)
No 380 (57.6) 1520 (80.9) 50 (40) 156 (71.6) 33 (41.8) 85 (71.4)
Under psychatric treatment χ²(2) = 34.43, p < 0.0001 (0.0001) χ²(2) = 5.81, p = 0.055 (0.127) χ²(1) = 3.94, p = 0.047 (0.204)
Don’t know 7 (1.1) 9 (0.5) 0 (0.0) 1 (0.5) 0 (0.0) 0 (0.0)
Yes 89 (13.5) 122 (6.5) 28 (22.4) 28 (12.8) 21 (26.6) 18 (15.1)
No 564 (85.5) 1748 (93) 97 (77.6) 189 (86.7) 58 (73.4) 101 (84.9)
Diagnosed disease χ²(1) = 21.32, p < 0.0001 (0.0001) χ²(1) = 8.01, p = 0.005 (0.023) χ²(1) = 2.15, p = 0.143 (0.485)
Yes 265 (40.2) 570 (30.3) 60 (48) 71 (32.6) 34 (43) 39 (32.8)
No 395 (59.9) 1309 (69.7) 65 (52) 147 (67.4) 45 (57) 80 (67.2)

Pairwise comparisons using Pearson’s Chi-square test are reported. Percentages (%) displayed refer to column percentages. P values adjusted for multiple comparisons are shown between parenthesis. Estimates in bold are statistically significant at 0.05 level.

Discussion

Our study shows a strong relationship between headache and tinnitus with increasing severity. The relationship we found for any tinnitus [OR = 2.19 (95% CI: 1.81–2.64)] is within the range of what has been reported for migraine in another cross-sectional study [multivariable-adjusted OR = 1.77 (1.36–2.30), n = 5729]24. The present work goes beyond this analysis by showing the increasing relationship between headache and tinnitus severity reaching an OR of 5.63 (4.10–7.72) in the group with tinnitus as a big problem, suggesting either that headaches contribute to the distress caused by tinnitus, or that tinnitus distress contribute to headaches – a directionality that remains to be investigated.

Our study goes in line with findings from Langguth et al.18 as we replicate a number of points: vertigo/dizziness, neck pain and other pain syndromes constitute a dominant part of the symptomatology of subjects experiencing headaches, when having tinnitus as a big problem, or in severe tinnitus. A significant number of individuals with vertigo and migraine headache with tinnitus may fulfil diagnostic criteria for migraine41 or vestibular migraine42 and the association between tinnitus and migraine deserves further studies. Our study however included in a large part subjects from the population, rather than patients recruited in a clinical context, as those from the Tinnitus Research Initiative. As a consequence, a greater number of variables were found to differ between tinnitus subjects with or without headaches as we included a larger sample of the population. The any tinnitus group indeed includes subjects experiencing tinnitus occasionally (47%) and permanently (53%), where differences in income and employment could be found, in perception, psychological features (stress, anxiety and depression), fear of tinnitus, hyperacusis and quality of life. These aspects could not all be captured in the study by Langguth and colleagues (2017) most likely due to the fact that as severity increases, fewer differences are seen between the headache and non-headache tinnitus groups. Here, the prevalence of headache in tinnitus subjects started at 26% for the any tinnitus group, up to 40% in the severe tinnitus group as defined by the THI scale. These findings are consistent with the notion that headache, and particularly migraine, could be a facilitator to the development of severe tinnitus, as suggested with the greater risk in developing clinically significant tinnitus with migraines [adjusted Hazard Ratio: 3.30 (2.17–5.00)]26 when compared to self-reported tinnitus of unknown severity [adjusted Recurrence Ratio: 1.28 (1.06, 1.56)]43.

In spite of the sample differences between STOP and the TRI database, the proportion of clinically significant tinnitus subjects with headache is higher in STOP (40%) than in the TRI (27%). Indeed, the county of Stockholm states in their regional guidelines a severe score based on the THI warrants a referral to specialist care44, which hence allows to infer that the severe tinnitus group presented here would be equivalent to clinically significant tinnitus. Differences between the two datasets could be either be regional or due to the fact that a broader range of troublesome tinnitus is included in the TRI. Unlike the Lannguth et al. study (2017), we were not able to perform the analysis according to the laterality of the headache, nor according to subtypes of headache (e.g. migraine, tension-type headache, cluster headache). There, painful sensations upon loud sound exposure were more frequent with bilateral headache, whereas cluster headache was the one most impacting on tinnitus distress. However, common to all types of headaches was the influence on comorbid vertigo, temporomandibular joint (TMJ) complaints, neck pain, and pain in general18, which are also observed in our study.

The frequent co-occurrence of pain symptoms in clinically significant tinnitus with comorbid TMJ complaints16,17 or headache18, is consistent with the hypothesis that tinnitus shares similar neurocircuitry to chronic pain, whereby frontostriatal gating would be affected30. Tinnitus could also emerge as a consequence of vestibular migraine, frequently observed in patients with episodic vertigo45,46. Additional mechanisms may occur such as an increased excitability of the trigeminal system47, also leading to TMJ and neck pain16. An increased occurrence of tinnitus in the family is observed with co-morbid headache, although this increase was not as large as what was found for TMJ complaints17. Recent evidence in twins and adoptees point towards a significant genetic contribution to tinnitus48,49. It is thus possible that the heritability of tinnitus shares common genetic mechanisms with that of pain and migraine. Indeed, genetics of migraine indicate a predisposition towards generalized neuronal excitability due to the inability to regulate glutamate availability19, as it has been recently suggested in a mouse model of tinnitus50. Recently, a genome-wide association studies (GWAS) of 375,000 individuals (including 59,674 cases) identified 38 susceptibility loci for migraine51. However, such large-scale studies in tinnitus are lacking and would be valuable to estimate the overlap between migraine and tinnitus52,53. However, while large biobanks with information on tinnitus do exist, the depth of the phenotyping is often limited which is why large biobanking efforts in ENT clinics have been encouraged54,55.

The phenotypic study on tinnitus-only subjects suggests a sex-bias, whereby the proportion of women with tinnitus increases from 44% to 66% in presence of headaches, as reported by Langguth et al. (2017). Similar sex-bias in women was also recently described in tinnitus with co-morbid TMJ complaints16,17. However, when non-tinnitus controls are included, the sex bias vanishes with instead a trend towards stronger relationship between tinnitus and headache in men, which emphasizes the need to include non-tinnitus controls to infer on sexual dimorphisms. The greater relationship in men did not significantly differ from that of women possibly due to the low sample size of the severe tinnitus groups, which warrants investigation in larger studies. Reasons for the increased proportion of women with tinnitus when reporting headache could also be due to the fact that migraine and TMJ disorders are more frequent in women (3:1 female to male ratio in migraine; and 2:1 in TMJ disorders)56,57. Headaches are indeed among the leading causes of years lived with disability in Scandinavian women58. It is interesting to note though that greater stress due to tinnitus has been reported in women6,59 and that a greater association of tinnitus with suicide attempts was found in women but not in men7, underlying that the greater psychological impact of tinnitus in women should not be disregarded. Our work encourages the need of including sex as a biological variable (SABV) in future tinnitus studies.

There are a number of limitations to our study, which include self-reported tinnitus and headaches. Both of them are complex and heterogeneous conditions that pre-empt clinical examination. Indeed, our study incorporates participants that may not be representative of the clinical setting. Self-reports may yield different prevalence estimates than diagnostic codes from medical records, the latter representing more a severe form of tinnitus for which medical care is sought. Reliance on self-report introduces the possibility of recall bias, that would be otherwise minimized when involving a physician. However, as regional guidelines recommend a referral to specialty care when a severe THI score is reached44, one could – at least in part – infer on the phenotypic characteristics that would be expected in the clinic. Secondly, while STOP participants were recruited from LifeGene, which is representative of the general population, it is unclear whether our findings can be generalized to that of the general population. Not all LifeGene participants with tinnitus joined STOP, and as a consequence, a recruitment bias may have occurred e.g. towards more participants seeking treatment options. Thirdly, as headaches and tinnitus were assessed at one single point in time, it is not possible to understand the direction of the observed relationship.

Overall, our study confirms that tinnitus with co-morbid headaches is accompanied with vertigo, neck and other pain syndromes. The association between headache and tinnitus increases as tinnitus becomes more severe. Thus, an interprofessional approach to care would be warranted in these cases. Future longitudinal studies investigating the conjunct impact of headache with TMJ disorders may offer additional insights into their additive or synergistic contribution to tinnitus.

Materials and Methods

Sample

Participants were invited to join the Swedish Tinnitus Outreach Project via social media channels and through partnerships with local cohorts, including LifeGene60. All participants above 18 years of age were eligible. Voluntary registration was done on a website from STOP (https://stop.ki.se). After providing informed consent for having their data stored in a database and analyzed, participants were invited to fill an online questionnaire, which was answered between November 2015 and January 2018. The first part of this study was performed on a subset of individuals with or without tinnitus who responded to the European School for Interdisciplinary Tinnitus Research – Screening Questionnaire (ESIT-SQ) to investigate the association between headaches and tinnitus. The second part of this study focused only on tinnitus subjects with or without headaches in order to investigate their phenotypic traits. We followed the STROBE guidelines and the checklist is available in the online materials. All subjects gave written informed consent in accordance with the Declaration of Helsinki. The project has been approved by the Regional Ethics Review Board in Stockholm (2015/2129-31/1).

Association study

The ESIT-SQ was designed to be comprehensive with a specific attention to risk factors that could be answered by people with or without tinnitus61. Here the tinnitus question A17 was: “Tinnitus refers to the perception of noise in your head or ears (such as ringing or buzzing) in the absence of any corresponding source of sound external to your head. Over the past year, have you had tinnitus in your head or in one or both ears that lasts for more than five minutes at a time?” with answer options being: “do not know”, “no never”, “no, not in the past year”, “yes, some of the time”, “yes a lot of time”, “yes most of the time”. Those answering “don’t know” or “no, not in the past year” were excluded from the analysis. Question A15 stated “Do you suffer from any of the following pain syndromes?” of which Headache was one of the options. For the present analysis, we thus included 1984 tinnitus cases and 1661 subjects without tinnitus from the STOP project.

Tinnitus phenotyping study

The online survey consisted of a combination of standardized questionnaires translated in Swedish40. Participants were asked the question: “Do you have tinnitus?” with possible answers being: “do not know”, “no”, “yes, occasionally (now and then)”, “yes, always (all the time)”. All of those answering “yes, occasionally” or “yes, always” were considered in this analysis and represent the “any tinnitus” group. The Tinnitus Sample Case History Questionnaire (TSCHQ) measures phenotypic characteristics that may be associated with tinnitus62, and question #30 “Do you suffer from headache?” was adapted in Swedish leading to an intra-class coherent coefficient of 0.77 (good) in a test-retest40. The Tinnitus Handicap Inventory (THI)63, the Tinnitus Functional Index (TFI)64, the Fear of Tinnitus Questionnaire (FTQ)65, the Tinnitus Catastrophizing Scale (TCS)65, the Hyperacusis Questionnaire (HQ)66, the Perceived Stress Questionnaire (PSQ)67, the Hospital Anxiety Depression Scales for Anxiety (HADS A) and depression (HADS D)68, and the World Health Organization’s Quality of Life (WHOQoL)-BREF69 were used. Adaptation of these questionnaires to Swedish and their validity has been reported elsewehere40. Numerical Rating Scales (NRS) for Loudness, Awareness, and Annoyance were obtained via the TSCHQ (questions 12, 16, and 17). Severe tinnitus was operationally defined in two ways. The first used a revised grading system of the original eight-factor 25 item of the TFI70 where a TFI cut-off score ≥ 48 denotes a big problem. The second used a THI cut-off score ≥ 58, since this boundary is used as a criterion for referral to specialty care in the Stockholm County44, here referred to as severe tinnitus according to the terminology used in the THI. Importantly, these two groups both contain the most severe tinnitus cases according to two commonly used clinical tools. Overlap between the groups is expected. We present both groups to maximize comparability with other studies and minimize selection bias that could be introduced from choosing one tool for evaluation. For the present analysis we included 1,879 subjects with tinnitus without headache and 660 subjects with tinnitus with headache.

Statistical analysis

The statistical approach used in the tinnitus phenotyping study has been described elsewhere17. Briefly, phenotypic characteristics such as tinnitus loudness, pitch, onset, whether tinnitus is pulsating or not, what the tinnitus sounds like, and onset-related events were obtained from the TSCHQ. Additional sociodemographic data (i.e. marital status, income, employment status, and education level) were obtained using questions from Svensson et al.71. All statistical analyses were performed in JMP 13 (SAS Institute Inc.) and R (R Core Team, 2019). For nominal variables, Pearson’s Chi-squared test was used. Homoscedasticity between groups was tested for using the Brown-Forsythe test and showed significant differences between subgroups for multiple variables. Multiple questionnaire total scores also deviated from a normal distribution. The non-parametric Wilcoxon’s test and Cliffs delta (δ) for effect size, using the ‘effsize’ package in R, were used for all comparisons to provide easy comparability between different groups for the reader. In order to investigate the potential impact of multiple comparisons on the discovery rates of our tests, we also report p-values adjusted by the method of Benjamini and Hochberg. The adjustments were computed for each set of p-values resulting from multiple tests carried out.

For the association study, we estimated the odds ratios (ORs) and corresponding 95% confidence intervals (CIs) for tinnitus using unconditional multiple logistic regression models after adjustment for sex, age, educational level (model 1) and also self-reported hearing ability (ESIT-SQ question A13) (model 2). Logistic regressions were performed in SAS 9.4 (SAS Institute, Cary, North Carolina).

Supplementary information

Acknowledgements

We gratefully acknowledge the support and generosity of Nancy Pedersen, head of LifeGene. This study was funded by the GENDER-NET Co-Plus Fund (GNP-182, to CRC, SG, JALE and JB). In addition, CRC has received research funding from Decibel Therapeutics, Inc., Svenska Läkaresällskapet (SLS-779681), Tysta Skolan, Hörselforskningsfonden (#503), the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 72204655. BC has received funding from the Swedish Medical Research Council K2014-99×-22478-01-3, Karolinska Institutet and Tysta Skolan. SG is an Honorary Associate Professor at the University of Nottingham, School of Medicine. Open access funding provided by Karolinska Institute.

Author contributions

C.R.C., S.G. and B.C. designed the study. N.K.E. collected, extracted, and processed the STOP data. N.K.E. and A.Lu. analyzed the data and prepared all tables. A.La., G.M., J.A.L.E., J.B. and I.U. helped to develop the scientific arguments and contributed to data interpretation. All authors played a role in writing the manuscript and approved the final version.

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

Competing interests

G.M. is an employee of Decibel Therapeutics. All other authors declare no competing interests.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

These authors contributed equally: Alessandra Lugo and Niklas K. Edvall.

Supplementary information

is available for this paper at 10.1038/s41598-020-65395-1.

References

  • 1.McCormack A, Edmondson-Jones M, Somerset S, Hall D. A systematic review of the reporting of tinnitus prevalence and severity. Hearing Res. 2016;337:70–79. doi: 10.1016/j.heares.2016.05.009. [DOI] [PubMed] [Google Scholar]
  • 2.Dobie RA. Depression and tinnitus. Otolaryngologic Clin. North. Am. 2003;36:383–388. doi: 10.1016/S0030-6665(02)00168-8. [DOI] [PubMed] [Google Scholar]
  • 3.Bartels H, Middel BL, van der Laan BF, Staal MJ, Albers FW. The additive effect of co-occurring anxiety and depression on health status, quality of life and coping strategies in help-seeking tinnitus sufferers. Ear hearing. 2008;29:947–956. doi: 10.1097/AUD.0b013e3181888f83. [DOI] [PubMed] [Google Scholar]
  • 4.Kehrle HM, Sampaio AL, Granjeiro RC, de Oliveira TS, Oliveira CA. Tinnitus Annoyance in Normal-Hearing Individuals: Correlation With Depression and Anxiety. The. Ann. otology, rhinology, laryngology. 2016;125:185–194. doi: 10.1177/0003489415606445. [DOI] [PubMed] [Google Scholar]
  • 5.Hebert S, Canlon B, Hasson D. Emotional exhaustion as a predictor of tinnitus. Psychotherapy Psychosom. 2012;81:324–326. doi: 10.1159/000335043. [DOI] [PubMed] [Google Scholar]
  • 6.Schlee, W. et al. Visualization of Global Disease Burden for the Optimization of Patient Management and Treatment. Front Med (Lausanne) 4:86, 10.3389/fmed.2017.00086 (2017). [DOI] [PMC free article] [PubMed]
  • 7.Lugo, A. et al. Sex-specific influences of tinnitus on suicide attempt. JAMA Otolaryngol Head Neck Surg.145(7), 685–687, 10.1001/jamaoto.2019.0566 (2019). [DOI] [PMC free article] [PubMed]
  • 8.Seo JH, Kang JM, Hwang SH, Han KD, Joo YH. Relationship between tinnitus and suicidal behaviour in Korean men and women: a cross-sectional study. Clin. Otolaryngol. 2016;41:222–227. doi: 10.1111/coa.12500. [DOI] [PubMed] [Google Scholar]
  • 9.Cederroth CR, Canlon B, Langguth B. Hearing loss and tinnitus–are funders and industry listening? Nat. Biotechnol. 2013;31:972–974. doi: 10.1038/nbt.2736. [DOI] [PubMed] [Google Scholar]
  • 10.Cederroth, C. R., Dyhrfjeld-Johnsen, J. & Langguth, B. An update: emerging drugs for tinnitus. Expert Opin Emerg Drugs, 1–10, 10.1080/14728214.2018.1555240 (2018). [DOI] [PubMed]
  • 11.Langguth B, Elgoyhen AB, Cederroth CR. Therapeutic Approaches to the Treatment of Tinnitus. Annu. Rev. Pharmacol. Toxicol. 2019;59:291–313. doi: 10.1146/annurev-pharmtox-010818-021556. [DOI] [PubMed] [Google Scholar]
  • 12.Stockdale D, et al. An economic evaluation of the healthcare cost of tinnitus management in the UK. BMC health Serv. Res. 2017;17:577. doi: 10.1186/s12913-017-2527-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Cederroth CR, et al. Editorial: Towards an Understanding of Tinnitus Heterogeneity. Front. Aging Neurosci. 2019;11:53. doi: 10.3389/fnagi.2019.00053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Schlee W, et al. Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective. Front. Aging Neurosci. 2017;9:447. doi: 10.3389/fnagi.2017.00447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Schecklmann M, Landgrebe M, Langguth B, Group TRIDS. Phenotypic characteristics of hyperacusis in tinnitus. PLoS One. 2014;9:e86944. doi: 10.1371/journal.pone.0086944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Vielsmeier V, et al. Temporomandibular joint disorder complaints in tinnitus: further hints for a putative tinnitus subtype. Plos One. 2012;7:e38887. doi: 10.1371/journal.pone.0038887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Edvall NK, et al. Impact of Temporomandibular Joint Complaints on Tinnitus-Related Distress. Front. Neurosci. 2019;13:879. doi: 10.3389/fnins.2019.00879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Langguth B, Hund V, Landgrebe M, Schecklmann M. Tinnitus Patients with Comorbid Headaches: The Influence of Headache Type and Laterality on Tinnitus Characteristics. Front. Neurol. 2017;8:440. doi: 10.3389/fneur.2017.00440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Burstein R, Noseda R, Borsook D. Migraine: multiple processes, complex pathophysiology. J. neuroscience: Off. J. Soc. Neurosci. 2015;35:6619–6629. doi: 10.1523/JNEUROSCI.0373-15.2015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Brunnberg E, Linden-Bostrom M, Berglund M. Tinnitus and hearing loss in 15-16-year-old students: mental health symptoms, substance use, and exposure in school. Int. J. audiology. 2008;47:688–694. doi: 10.1080/14992020802233915. [DOI] [PubMed] [Google Scholar]
  • 21.Kim YH, et al. Tinnitus in children: association with stress and trait anxiety. Laryngoscope. 2012;122:2279–2284. doi: 10.1002/lary.23482. [DOI] [PubMed] [Google Scholar]
  • 22.Jaramillo CA, et al. A cohort study examining headaches among veterans of Iraq and Afghanistan wars: Associations with traumatic brain injury, PTSD, and depression. Headache. 2016;56:528–539. doi: 10.1111/head.12726. [DOI] [PubMed] [Google Scholar]
  • 23.Pezzoli M, et al. Tinnitus and its relationship with muscle tenderness in patients with headache and facial pain. J. laryngology otology. 2015;129:638–643. doi: 10.1017/S0022215115001425. [DOI] [PubMed] [Google Scholar]
  • 24.Guichard E, Montagni I, Tzourio C, Kurth T. Association Between Headaches and Tinnitus in Young Adults: Cross-Sectional Study. Headache. 2016;56:987–994. doi: 10.1111/head.12845. [DOI] [PubMed] [Google Scholar]
  • 25.Sindhusake D, et al. Risk factors for tinnitus in a population of older adults: the blue mountains hearing study. Ear hearing. 2003;24:501–507. doi: 10.1097/01.AUD.0000100204.08771.3D. [DOI] [PubMed] [Google Scholar]
  • 26.Hwang JH, Tsai SJ, Liu TC, Chen YC, Lai JT. Association of Tinnitus and Other Cochlear Disorders With a History of Migraines. JAMA Otolaryngol. Head. Neck Surg. 2018;144:712–717. doi: 10.1001/jamaoto.2018.0939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Shore SE, Roberts LE, Langguth B. Maladaptive plasticity in tinnitus–triggers, mechanisms and treatment. Nat. reviews. Neurol. 2016;12:150–160. doi: 10.1038/nrneurol.2016.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Auerbach BD, Rodrigues PV, Salvi RJ. Central gain control in tinnitus and hyperacusis. Front. Neurol. 2014;5:206. doi: 10.3389/fneur.2014.00206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Rauschecker JP, Leaver AM, Muhlau M. Tuning out the noise: limbic-auditory interactions in tinnitus. Neuron. 2010;66:819–826. doi: 10.1016/j.neuron.2010.04.032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Rauschecker JP, May ES, Maudoux A, Ploner M. Frontostriatal Gating of Tinnitus and Chronic Pain. Trends Cognit. Sci. 2015;19:567–578. doi: 10.1016/j.tics.2015.08.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Schlee W, Weisz N, Bertrand O, Hartmann T, Elbert T. Using auditory steady state responses to outline the functional connectivity in the tinnitus brain. Plos One. 2008;3:e3720. doi: 10.1371/journal.pone.0003720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.De Ridder D, Vanneste S, Langguth B, Llinas R. Thalamocortical Dysrhythmia: A Theoretical Update in Tinnitus. Front. Neurol. 2015;6:124. doi: 10.3389/fneur.2015.00124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.de Tommaso M, et al. Altered processing of sensory stimuli in patients with migraine. Nature reviews. Neurology. 2014;10:144–155. doi: 10.1038/nrneurol.2014.14. [DOI] [PubMed] [Google Scholar]
  • 34.Vanneste S, Song JJ, De Ridder D. Thalamocortical dysrhythmia detected by machine learning. Nat. Commun. 2018;9:1103. doi: 10.1038/s41467-018-02820-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Akerman S, Romero-Reyes M. Insights into the pharmacological targeting of the trigeminocervical complex in the context of treatments of migraine. Expert. Rev. Neurother. 2013;13:1041–1059. doi: 10.1586/14737175.2013.827472. [DOI] [PubMed] [Google Scholar]
  • 36.May A. Diagnosis and clinical features of trigemino-autonomic headaches. Headache. 2013;53:1470–1478. doi: 10.1111/head.12213. [DOI] [PubMed] [Google Scholar]
  • 37.Haider HF, et al. Pathophysiology, Diagnosis and Treatment of Somatosensory Tinnitus: A Scoping Review. Front. Neurosci. 2017;11:207. doi: 10.3389/fnins.2017.00207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Kim, S. Y., Jeon, Y. J., Lee, J.-Y. & Kim, Y. H. In The Laryngoscope Vol. 127 2113–2119 (Wiley-Blackwell, 2017). [DOI] [PubMed]
  • 39.Swan, A. A. et al. In Hearing research Vol. 349 04-dic (2017).
  • 40.Müller K, et al. Validation of Online Versions of Tinnitus Questionnaires Translated into Swedish. Front. Aging Neurosci. 2016;8:272. doi: 10.3389/fnagi.2016.00272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.IHS. Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition. Cephalalgia: an international journal of headache38, 1–211, 10.1177/0333102417738202 (2018). [DOI] [PubMed]
  • 42.Lempert T, et al. Vestibular migraine: diagnostic criteria. J. Vestib. Res. 2012;22:167–172. doi: 10.3233/VES-2012-0453. [DOI] [PubMed] [Google Scholar]
  • 43.Sindhusake D, et al. Prevalence and characteristics of tinnitus in older adults: the Blue Mountains Hearing Study. Int. J. audiology. 2003;42:289–294. doi: 10.3109/14992020309078348. [DOI] [PubMed] [Google Scholar]
  • 44.Idrizbegovic, E., Kjerulf, E. & Team for Diagnostics Hearing Habilitation Children and Youth and Hearing Rehabilitation for Adults. Tinnitus Care Program [Tinnitus Vårdprogram] (ed. Karolinska Sjukhuset) (Stockholm, 2011).
  • 45.Lopez-Escamez JA, et al. Accompanying Symptoms Overlap during Attacks in Meniere’s Disease and Vestibular Migraine. Front. Neurol. 2014;5:265. doi: 10.3389/fneur.2014.00265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Eggers SD, Neff BA, Shepard NT, Staab JP. Comorbidities in vestibular migraine. J. Vestib. Res. 2014;24:387–395. doi: 10.3233/VES-140525. [DOI] [PubMed] [Google Scholar]
  • 47.Langguth B, et al. Tinnitus and Headache. BioMed. Res. Int. 2015;2015:797416. doi: 10.1155/2015/797416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Maas IL, et al. Genetic susceptibility to bilateral tinnitus in a Swedish twin cohort. Genet. medicine: Off. J. Am. Coll. Med. Genet. 2017;19:1007–1012. doi: 10.1038/gim.2017.4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Cederroth, C. R. et al. Association of Genetic vs Environmental Factors in Swedish Adoptees With Clinically Significant Tinnitus. JAMA Otolaryngol Head Neck Surg, 10.1001/jamaoto.2018.3852 (2019). [DOI] [PMC free article] [PubMed]
  • 50.Yu, H. et al. GLAST Deficiency in Mice Exacerbates Gap Detection Deficits in a Model of Salicylate-Induced Tinnitus. Frontiers inBehavioral Neuroscience10, 10.3389/fnbeh.2016.00158 (2016). [DOI] [PMC free article] [PubMed]
  • 51.Gormley P, et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 2016;48:856–866. doi: 10.1038/ng.3598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Vona B, Nanda I, Shehata-Dieler W, Haaf T. Genetics of Tinnitus: Still in its Infancy. Front. Neurosci. 2017;11:236. doi: 10.3389/fnins.2017.00236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Lopez-Escamez, J. A. et al. Genetics of tinnitus: an emerging area for molecular diagnosis and drug development. Frontiers in Neuroscience10, 10.3389/fnins.2016.00377 (2016). [DOI] [PMC free article] [PubMed]
  • 54.Cederroth CR, Kähler A, Sullivan PF, Lopez-Escamez JA. Genetics of tinnitus: time to biobank phantom sounds. Front. Genet. 2017;8:110. doi: 10.3389/fgene.2017.00110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Szczepek AJ, et al. Recommendations on Collecting and Storing Samples for Genetic Studies in Hearing and Tinnitus Research. Ear hearing. 2019;40:219–226. doi: 10.1097/AUD.0000000000000614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Bueno CH, Pereira DD, Pattussi MP, Grossi PK, Grossi ML. Gender differences in temporomandibular disorders in adult populational studies: A systematic review and meta-analysis. J. Oral. Rehabil. 2018;45:720–729. doi: 10.1111/joor.12661. [DOI] [PubMed] [Google Scholar]
  • 57.Leonardi M, Steiner TJ, Scher AT, Lipton RB. The global burden of migraine: measuring disability in headache disorders with WHO’s Classification of Functioning. Disability Health . J. Headache Pain. 2005;6:429–440. doi: 10.1007/s10194-005-0252-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58. Nordic Burden of Disease, C. Life expectancy and disease burden in the Nordic countries: results from the Global Burden of Diseases, Injuries, and Risk Factors Study 2017. Lancet Public Health4, e658-e669, 10.1016/S2468-2667(19)30224-5 (2019). [DOI] [PMC free article] [PubMed]
  • 59.Seydel C, Haupt H, Olze H, Szczepek AJ, Mazurek B. Gender and chronic tinnitus: differences in tinnitus-related distress depend on age and duration of tinnitus. Ear hearing. 2013;34:661–672. doi: 10.1097/AUD.0b013e31828149f2. [DOI] [PubMed] [Google Scholar]
  • 60.Almqvist C, et al. LifeGene–a large prospective population-based study of global relevance. Eur. J. Epidemiol. 2011;26:67–77. doi: 10.1007/s10654-010-9521-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Genitsaridi E, et al. Standardised profiling for tinnitus research: The European School for Interdisciplinary Tinnitus Research Screening Questionnaire (ESIT-SQ) Hearing Res. 2019 doi: 10.1016/j.heares.2019.02.017. [DOI] [PubMed] [Google Scholar]
  • 62.Landgrebe M, et al. The Tinnitus Research Initiative (TRI) database: a new approach for delineation of tinnitus subtypes and generation of predictors for treatment outcome. BMC Med. Inform. Decis. Mak. 2010;10:42. doi: 10.1186/1472-6947-10-42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Newman CW, Jacobson GP, Spitzer JB. Development of the Tinnitus Handicap Inventory. Arch. Otolaryngol. Head. Neck Surg. 1996;122:143–148. doi: 10.1001/archotol.1996.01890140029007. [DOI] [PubMed] [Google Scholar]
  • 64.Meikle MB, et al. The tinnitus functional index: development of a new clinical measure for chronic, intrusive tinnitus. Ear hearing. 2012;33:153–176. doi: 10.1097/AUD.0b013e31822f67c0. [DOI] [PubMed] [Google Scholar]
  • 65.Cima RF, Crombez G, Vlaeyen JW. Catastrophizing and fear of tinnitus predict quality of life in patients with chronic tinnitus. Ear hearing. 2011;32:634–641. doi: 10.1097/AUD.0b013e31821106dd. [DOI] [PubMed] [Google Scholar]
  • 66.Khalfa, S. et al. Psychometric normalization of a hyperacusis questionnaire. ORL; journal for oto-rhino-laryngology and its related specialties64, 436-442, doi:67570 (2002). [DOI] [PubMed]
  • 67.Levenstein S, et al. Development of the Perceived Stress Questionnaire: a new tool for psychosomatic research. J. Psychosom. Res. 1993;37:19–32. doi: 10.1016/0022-3999(93)90120-5. [DOI] [PubMed] [Google Scholar]
  • 68.Andersson G, Kaldo-Sandstrom V, Strom L, Stromgren T. Internet administration of the Hospital Anxiety and Depression Scale in a sample of tinnitus patients. J. Psychosom. Res. 2003;55:259–262. doi: 10.1016/S0022-3999(02)00575-5. [DOI] [PubMed] [Google Scholar]
  • 69.The WHOQOL Group. Development of the World Health Organization WHOQOL-BREF quality of life assessment.. Psychological medicine28, 551-558 (1998). [DOI] [PubMed]
  • 70.Fackrell K, Hall DA, Barry JG, Hoare DJ. Performance of the Tinnitus Functional Index as a diagnostic instrument in a UK clinical population. Hearing Res. 2017 doi: 10.1016/j.heares.2017.10.016. [DOI] [PubMed] [Google Scholar]
  • 71.Svensson AC, et al. Cohort profile: The Stockholm Public Health Cohort. Int. J. Epidemiol. 2013;42:1263–1272. doi: 10.1093/ije/dys126. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.


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